Skip to main content

Pediatric Neurology

The Pediatric Neurology Research group is mainly involved in the study of genetic diseases of the developing nervous system. The main emphasis is on paroxysmal neurological disorders and neuromuscular disorders. A common theme across the different projects, besides the identification of the molecular basis of several of these rare disorders, is the investigation of molecules involved in their pathophysiological mechanisms and the effective translation of these findings into the fields of molecular diagnosis, genetic counselling and newly developed gene or drug therapies.

Team

Mireia del Toro Riera

Mireia del Toro Riera

Pediatric Neurology
Read more
Ana Felipe Rucián

Ana Felipe Rucián

Predoctoral researcher
Pediatric Neurology
Read more
Leal Roca, Nuria

Leal Roca, Nuria

Research technician
Pediatric Neurology
Read more
Lungo Peccorini, Ana Gabriela

Lungo Peccorini, Ana Gabriela

Research technician
Pediatric Neurology
Read more
María Delgado Muñoz

María Delgado Muñoz

Read more
Rebecca Herzog

Rebecca Herzog

Research technician
Pediatric Neurology
Read more
Mireia del Toro Riera

Mireia del Toro Riera

Pediatric Neurology
Read more
Ana Felipe Rucián

Ana Felipe Rucián

Predoctoral researcher
Pediatric Neurology
Read more
Leal Roca, Nuria

Leal Roca, Nuria

Research technician
Pediatric Neurology
Read more
Lungo Peccorini, Ana Gabriela

Lungo Peccorini, Ana Gabriela

Research technician
Pediatric Neurology
Read more
María Delgado Muñoz

María Delgado Muñoz

Read more
Rebecca Herzog

Rebecca Herzog

Research technician
Pediatric Neurology
Read more

Research lines

Pediatric neurogenetics

Neurogenetics of paroxysmal neurological disorders (neuronal channelopathies)

Genetic and epigenetic basis of neural tube defects and Chiari type I malformation 

Clinical researchers have collected samples from more than 2000 patients with paroxysmal neurological disorders (migraine, epilepsy, paroxysmal movement disorders and episodic ataxias) and over 300 patients with Chiari I malformation. Current strategies include whole-genome linkage analysis, exome sequencing, customized array re-sequencing, SNP-based genetic association studies and expression analysis in fetal tissues. The goals in this area are:


- to identify novel genetic variants responsible for these diseases

- to establish a correlation between the genetic variants and the clinical forms of the disease

- to perform functional studies of the mutant proteins

- to design an animal model of cortical spreading depression, with emphasis in epigenetic modification of susceptibility genes.


IP: Alfons Macaya Ruíz

Pediatric Neuromuscular Disorders

1. DUCHENNE MUSCULAR DYSTROPHY (DMD)

THERAPEUTIC POTENTIAL OF ESTROGENS IN DMD, EFFECTS AND MECHANISMS OF ACTION ON SATELLITE CELLS AND MACROPHAGES

We have found that estradiol has beneficial effects on myogenesis and inflammation. We aim to characterize the estradiol effects on satellite cells and their interaction with macrophages and the ability of estrogens to increase the efficiency of cell therapy based on satellite cell transplant to restore the expression of dystrophin in the dystrophic muscle in vivo.


IN VITRO TESTING OF GENE THERAPIES TO REPAIR DYSTROPHIN IN HUMAN MYOBLASTS AND DEVELOPMENT OF NANIOPARTICLES FOR MUSCLE DELIVERY

Compounds with readthrough activity are currently used for DMD patients with nonsense mutations with highly variable results. We are testing the efficacy of several drugs with read-through action (PTC124, RTC14, RTC13, Geneticin) to restore protein levels in myoblasts and differentiated myotubes obtained from DMD patients carrying nonsense mutations with variable codon composition and different location.

We are testing the possibility to use modified nanopaticles for muscle delivery of specific drugs.


2. USE OF NEW TECHNOLOGIES FOR DIAGNOSTIC OPTIMISATION IN INHERITED MYOPATHIES

We used exome capture and massive sequencing technologies for the diagnosis of patients with neuromuscular disorders, to deliver a proof-of-concept of the superior diagnostic accuracy, speed and costeffectiveness of these novel technologies over current approaches.

IP: Francina Munell Casadesus

Projects

Predictores de eficacia clínica, genética y radiológica en niños y adolescentes con distonía tratados mediante estimulación cerebral profunda

IP: Belen Perez Dueñas
Collaborators: Anna Marcé Grau, Manel Alberich Jordà, Ana Laura Cazurro Gutierrez, Lucy Dougherty de Miguel
Funding agency: Instituto de Salud Carlos III
Funding: 140000
Reference: PI24/01083
Duration: 01/01/2025 - 31/12/2027

HUB D'INNOVACIÓ PEDIÀTRICA - I4KIDS

IP: Ramon Martí Seves
Collaborators: Alfons Macaya Ruíz, Lucas Moreno Martín-Retortillo
Funding agency: Agència Gestió Ajuts Universitaris i de Recerca
Funding: 0.01
Reference: 2022 XARDI 00006
Duration: 01/01/2023 - 31/12/2025

Neurologia infantil

IP: Alfons Macaya Ruíz
Collaborators: Laia Ventura i Expósito, Belen Perez Dueñas, Laura Costa Comellas, Neurologia infantil, Francina Munell Casadesus, Anna Marcé Grau, Miquel Raspall Chaure, Mireia del Toro Riera, Julia Sala Coromina, Ana Felipe Rucián, Ana Laura Cazurro Gutierrez, David Gómez Andrés, Amaia Lasa Aranzasti, Lucy Dougherty de Miguel
Funding agency: Agència Gestió Ajuts Universitaris i de Recerca
Funding: 0.01
Reference: 2021 SGR 01171
Duration: 01/01/2022 - 30/06/2025

Distrofia muscular congénita tipo 1A: inhibición de la fibrosis y corrección mediante edición génica

IP: Jordi Barquinero Mañez
Collaborators: Laura Costa Comellas, Francina Munell Casadesus, David Gómez Andrés, Rocío Piñera Moreno, Maria Pallares Masmitja
Funding agency: Instituto de Salud Carlos III
Funding: 117370
Reference: PI22/01027
Duration: 01/01/2023 - 31/12/2025

Publications

Developmental outcome of electroencephalographic findings in SYNGAP1 encephalopathy.

PMID: 38505260
Journal: Frontiers in Cell and Developmental Biology
Year: 2024
Reference: Front Cell Dev Biol. 2024 Mar 5;12:1321282. doi: 10.3389/fcell.2024.1321282. eCollection 2024.
Impact factor:
Publication type: Paper in international publication
Authors: Alonso, Xenia; Alonso-Colmenero, Itziar; Bayes, Alex; Camacho, Ana; Camino Leon, Rafael; Campistol Plana, Jaume; Cazorla, Maria Rosario; Cueto-Gonzalez, Anna Ma; Del Castillo-Berges, Diego; Fernandez-Jaen, Alberto et al.
DOI: 10.3389/fcell.2024.1321282

Biallelic PI4KA Mutations Disrupt B-Cell Metabolism and Cause B-Cell Lymphopenia and Hypogammaglobulinemia.

PMID: 39312004
Journal: JOURNAL OF CLINICAL IMMUNOLOGY
Year: 2024
Reference: J Clin Immunol. 2024 Sep 23;45(1):15. doi: 10.1007/s10875-024-01793-8.
Impact factor:
Publication type: Paper in international publication
Authors: Adam, Margaret P; Adams, David; Amel, Hassan; Baple, Emma L; Barberis, Matteo; Barredo, Estibaliz; Bhatia, Sanil; Biondi, Andrea; Borkhardt, Arndt; Brusco, Alfredo et al.
DOI: 10.1007/s10875-024-01793-8

Influence of initial clinical suspicion on the diagnostic yield of laboratory enzymatic testing in lysosomal storage disorders. Experience from a multispecialty hospital.

PMID: 36265282
Journal: BLOOD CELLS MOLECULES AND DISEASES
Year: 2023
Reference: Blood Cells Mol Dis. 2023 Jan;98:102704. doi: 10.1016/j.bcmd.2022.102704. Epub 2022 Oct 5.
Impact factor:
Publication type: Paper in international publication
Authors: Agraz-Pamplona, Irene; Arranz-Amo, Jose Antonio; Barquin-Del-Pino, Raquel; Camprodon-Gomez, Maria; Carnicer-Caceres, Clara; Castillo-Ribelles, Laura; Del-Toro-Riera, Mireia; Felipe-Rucian, Ana; Garcia-Serra, Anna; Hernandez-Vara, Jorge et al.
DOI: 10.1016/j.bcmd.2022.102704

Expanding allelic and phenotypic spectrum of ZC4H2-related disorder: A novel hypomorphic variant and high prevalence of tethered cord.

PMID: 36250278
Journal: CLINICAL GENETICS
Year: 2023
Reference: Clin Genet. 2023 Feb;103(2):167-178. doi: 10.1111/cge.14248. Epub 2022 Oct 31.
Impact factor:
Publication type: Paper in international publication
Authors: Balak, Chris; Casadesus, Francina Munell; Choi, Tae-Ik; Cueto-Gonzalez, Anna Maria; Kim, Cheol-Hee; Kim, Oc-Hee; Koeberl, Dwight; Narayanan, Vinodh; Ramsey, Keri; Riley, Kacie et al.
DOI: 10.1111/cge.14248

De novo KCNA6 variants with attenuated KV 1.6 channel deactivation in patients with epilepsy.

PMID: 36318112
Journal: EPILEPSIA
Year: 2023
Reference: Epilepsia. 2023 Feb;64(2):443-455. doi: 10.1111/epi.17455. Epub 2022 Dec 5.
Impact factor:
Publication type: Paper in international publication
Authors: Accogli, Andrea; Alesandrini, Marie; Au, P Y Billie; Blevins, Amy; Cogne, Benjamin; Efthymiou, Stephanie; Fortuna, Sara; Galassi-Deforie, Valentina; Hanna, Michael G; Houlden, Henry et al.
DOI: 10.1111/epi.17455

Early recognition of SGCE-myoclonus-dystonia in children.

PMID: 35723607
Journal: DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY
Year: 2023
Reference: Dev Med Child Neurol. 2023 Feb;65(2):207-214. doi: 10.1111/dmcn.15298. Epub 2022 Jun 20.
Impact factor:
Publication type: Paper in international publication
Authors: Alvarez, Ramiro; Carvalho, Joao; Cazurro-Gutierrez, Ana; Correa-Vela, Marta; Ferrero-Turrion, Julia; Gonzalez, Victoria; Macaya-Ruiz, Alfons; Marce-Grau, Anna; Moreno, Antonio; Perez-Duenas, Belen et al.
DOI: 10.1111/dmcn.15298

Real-World Evidence Study on the Long-Term Safety of Everolimus in Patients With Tuberous Sclerosis Complex: Final Analysis Results.

PMID: 35462939
Journal: Frontiers in Pharmacology
Year: 2022
Reference: Front Pharmacol. 2022 Apr 8;13:802334. doi: 10.3389/fphar.2022.802334. eCollection 2022.
Impact factor:
Publication type: Paper in international publication
Authors: Feucht, Martha; Hahn, Andreas; Hirschberg, Yulia; Kingswood, John Chris; Maamari, Ricardo; Macaya, Alfons; Ridolfi, Antonia; Ruiz-Falco Rojas, Maria Luz; Wilken, Bernd et al.
DOI: 10.3389/fphar.2022.802334

Acetazolamide Improves Episodic Ataxia in a Patient with Non-Verbal Autism and Paroxysmal Dyskinesia Due To PRRT2 Biallelic Variants.

PMID: 36247910
Journal: Movement Disorders Clinical Practice
Year: 2022
Reference: Mov Disord Clin Pract. 2022 Aug 22;9(7):979-982. doi: 10.1002/mdc3.13528. eCollection 2022 Oct.
Impact factor:
Publication type: Letter or abstract
Authors: Macaya, Alfons; Martorell, Loreto; Ortigoza-Escobar, Juan Dario; Perez-Duenas, Belen et al.
DOI: 10.1002/mdc3.13528

Neurological Short-Term Outcomes of a Cohort of Children Born to Zika Virus-Infected Mothers in Barcelona.

PMID: 36291474
Journal: Children-Basel
Year: 2022
Reference: Children (Basel). 2022 Oct 9;9(10). pii: children9101537. doi: 10.3390/children9101537.
Impact factor:
Publication type: Paper in international publication
Authors: Espiau, Maria; Felipe-Rucian, Ana; Frick, Marie Antoinette; Giaquinto, Carlo; Pieras, Maria; Rodo, Carlota; Romani, Natalia; Silgado, Aroa; Soler-Palacin, Pere; Soriano-Arandes, Antoni et al.
DOI: 10.3390/children9101537

Novel Splicing Mutation in MTM1 Leading to Two Abnormal Transcripts Causes Severe Myotubular Myopathy.

PMID: 36142184
Journal: INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES
Year: 2022
Reference: Int J Mol Sci. 2022 Sep 7;23(18). pii: ijms231810274. doi: 10.3390/ijms231810274.
Impact factor:
Publication type: Letter or abstract
Authors: Bertini, Enrico; Bosco, Luca; Costa Comellas, Laura; D'Amico, Adele; Fattori, Fabiana; Leone, Daniela; Mercuri, Eugenio; Monforte, Mauro; Pane, Marika et al.
DOI: 10.3390/ijms231810274

Correction: Solving unsolved rare neurological diseases-a Solve-RD viewpoint.

PMID: 34429526
Journal: EUROPEAN JOURNAL OF HUMAN GENETICS
Year: 2021
Reference: Eur J Hum Genet. 2021 Sep;29(9):1462-1465. doi: 10.1038/s41431-021-00935-5.
Impact factor:
Publication type: Letter or abstract
Authors: 't Hoen, Peter A C; Alexander, Elizabeth; Allamand, Valerie; Aretz, Stefan; Atalaia, Antonio; Baets, Jonathan; Balicza, Peter; Balicza, Peter; Banfi, Sandro; Banka, Siddharth et al.
DOI: 10.1038/s41431-021-00935-5

Author Correction: The utility of Next Generation Sequencing for molecular diagnostics in Rett syndrome.

PMID: 34493777
Journal: Scientific Reports
Year: 2021
Reference: Sci Rep. 2021 Sep 7;11(1):18146. doi: 10.1038/s41598-021-97262-y.
Impact factor:
Publication type: Letter or abstract
Authors: Aguirre, Francisco Javier; Aleu, Montserrat; Alonso, Xenia; Alsius, Merce; Antinolo, Guillermo; Antonio, Victoria San; Aquino, Lourdes; Arellano, Carmen; Armstrong, Judith; Arriola, Gema et al.
DOI: 10.1038/s41598-021-97262-y

Solving unsolved rare neurological diseases-a Solve-RD viewpoint.

PMID: 33972714
Journal: EUROPEAN JOURNAL OF HUMAN GENETICS
Year: 2021
Reference: Eur J Hum Genet. 2021 Sep;29(9):1332-1336. doi: 10.1038/s41431-021-00901-1. Epub 2021 May 10.
Impact factor:
Publication type: Letter whit IF
Authors: 't Hoen, Peter A C; Alexander, Elizabeth; Allamand, Valerie; Aretz, Stefan; Atalaia, Antonio; Baets, Jonathan; Balicza, Peter; Balicza, Peter; Banfi, Sandro; Banka, Siddharth et al.
DOI: 10.1038/s41431-021-00901-1

Solve-RD: systematic pan-European data sharing and collaborative analysis to solve rare diseases.

PMID: 34075208
Journal: EUROPEAN JOURNAL OF HUMAN GENETICS
Year: 2021
Reference: Eur J Hum Genet. 2021 Sep;29(9):1325-1331. doi: 10.1038/s41431-021-00859-0. Epub 2021 Jun 1.
Impact factor:
Publication type: Letter whit IF
Authors: 't Hoen, Peter A C; Alexander, Elizabeth; Allamand, Valerie; Aretz, Stefan; Atalaia, Antonio; Baets, Jonathan; Balicza, Peter; Banfi, Sandro; Banka, Siddharth; Beeson, David et al.
DOI: 10.1038/s41431-021-00859-0

The European Reference Network for Rare Neurological Diseases.

PMID: 33519696
Journal: Frontiers in Neurology
Year: 2020
Reference: Front Neurol. 2021 Jan 14;11:616569. doi: 10.3389/fneur.2020.616569. eCollection 2020.
Impact factor:
Publication type: Review in international publication
Authors: Bachoud-Levi, Anne-Catherine; Baumer, Tobias; Bertini, Enrico; Brunelle, Alicia; Buizer, Annemieke I; Federico, Antonio; Gasser, Thomas; Graessner, Holm; Groeschel, Samuel; Hermanns, Sanja et al.
DOI: 10.3389/fneur.2020.616569

[50 years of the Neonatal Screening Program in Catalonia.]

PMID: 33323926
Journal: Revista Espanola de Salud Publica
Year: 2020
Reference: Rev Esp Salud Publica. 2020 Dec 16;94.
Impact factor:
Publication type: Paper in national publication
Authors: Argudo Ramirez, Ana; Armelles Sebastia, Merce; Arranz Amo, Jose Antonio; Artuch Iriberri, Rafael; Asensio de la Cruz, Oscar; Asso Ministral, Laia; Badenas Orquin, Celia; Beneitez Pastor, David; Blanco Alvarez, Adoracion; Cabezas Pena, Carmen et al.
DOI:

Tic disorders and premonitory urges: validation of the Spanish-language version of the Premonitory Urge for Tics Scale in children and adolescents.

PMID: 33317967
Journal: NEUROLOGIA
Year: 2020
Reference: Neurologia (Engl Ed). 2020 Dec 11:S0213-4853(20)30427-8. doi: 10.1016/j.nrl.2020.09.006.
Impact factor:
Publication type: Paper in national publication
Authors: Cordovilla, C; Correa-Vela, M; Forcadell, E; Garcia-Delgar, B; Ibanez, L; Lazaro, L; Madruga-Garrido, M; Mir, P; Morer, A; Nicolau, R et al.
DOI: 10.1016/j.nrl.2020.09.006

Clinical disease progression and biomarkers in Niemann-Pick disease type C: a prospective cohort study.

PMID: 33228797
Journal: Orphanet Journal of Rare Diseases
Year: 2020
Reference: Orphanet J Rare Dis. 2020 Nov 23;15(1):328. doi: 10.1186/s13023-020-01616-0.
Impact factor:
Publication type: Paper in international publication
Authors: Bembi, Bruno; Day, Simon; Del Toro, Mireia; Deodato, Federica; Gautschi, Matthias; Gronborg, Sabine; Grunewald, Stephanie; Guldberg, Christina; Heron, Benedicte; Hudgens, Stacie et al.
DOI: 10.1186/s13023-020-01616-0

Migraine polygenic risk score associates with efficacy of migraine-specific drugs.

PMID: 31872049
Journal: Neurology-Genetics
Year: 2019
Reference: Neurol Genet. 2019 Oct 24;5(6):e364. doi: 10.1212/NXG.0000000000000364. eCollection 2019 Dec.
Impact factor:
Publication type: Paper in international publication
Authors: Awasthi, Swapnil; Davidsson, Olafur B; Erikstrup, Christian; Esserlind, Ann-Louise; Folkmann Hansen, Thomas; Francke Christensen, Anne; Hjalgrim, Henrik; Ingason, Andres; Kogelman, Lisette J A; Macaya Ruíz, Alfons et al.
DOI: 10.1212/NXG.0000000000000364

Galloping tongue syndrome in a PRRT2 mutation carrier.

PMID: 31872056
Journal: Neurology-Genetics
Year: 2019
Reference: Neurol Genet. 2019 Nov 11;5(6):e377. doi: 10.1212/NXG.0000000000000377. eCollection 2019 Dec.
Impact factor:
Publication type: Paper in international publication
Authors: Macaya, Alfons; Marce-Grau, Anna; Tolosa, Eduard; Valls-Sole, Josep; Vilas, Dolores et al.
DOI: 10.1212/NXG.0000000000000377

Epilepsy with migrating focal seizures: KCNT1 mutation hotspots and phenotype variability.

PMID: 31872048
Journal: Neurology-Genetics
Year: 2019
Reference: Neurol Genet. 2019 Oct 25;5(6):e363. doi: 10.1212/NXG.0000000000000363. eCollection 2019 Dec.
Impact factor:
Publication type: Paper in international publication
Authors: Auvin, Stephane; Bahi-Buisson, Nadia; Barcia, Giulia; Barthez, Marie-Anne; Billette de Villemeur, Thierry; Boddaert, Nathalie; Bonnefont, Jean-Paul; Chemaly, Nicole; Ciorna, Viorica; Doummar, Diane et al.
DOI: 10.1212/NXG.0000000000000363

The TOSCA Registry for Tuberous Sclerosis-Lessons Learnt for Future Registry Development in Rare and Complex Diseases.

PMID: 31798515
Journal: Frontiers in Neurology
Year: 2019
Reference: Front Neurol. 2019 Nov 13;10:1182. doi: 10.3389/fneur.2019.01182. eCollection 2019.
Impact factor:
Publication type: Paper in international publication
Authors: Beaure d'Augeres, Guillaume; Belousova, Elena; Benedik, Mirjana P; Carter, Tom; Cottin, Vincent; Curatolo, Paolo; D'Amato, Lisa; Dahlin, Maria; de Vries, Petrus J; Ferreira, Jose C et al.
DOI: 10.3389/fneur.2019.01182

Machine learning applied to neuroimaging for diagnosis of adult classic Chiari malformation: role of the basion as a key morphometric indicator.

PMID: 29053075
Journal: JOURNAL OF NEUROSURGERY
Year: 2018
Reference: J Neurosurg. 2018 Sep;129(3):779-791. doi: 10.3171/2017.3.JNS162479. Epub 2017 Oct 20.
Impact factor:
Publication type: Paper in international publication
Authors: Espanol, Malena I; Macaya, Alfons; Martin, Bryn A; Moncho, Dulce; Poca, Maria A; Rovira, Alex; Sahuquillo, Juan; Urbizu, Aintzane et al.
DOI: 10.3171/2017.3.JNS162479

Common Variant Burden Contributes to the Familial Aggregation of Migraine in 1,589 Families.

PMID: 29731251
Journal: NEURON
Year: 2018
Reference: Neuron. 2018 May 16;98(4):743-753.e4. doi: 10.1016/j.neuron.2018.04.014. Epub 2018 May 3.
Impact factor:
Publication type: Paper in international publication
Authors: Agee, Michelle; Alipanahi, Babak; Anttila, Verneri; Anttila, Verneri; Artto, Ville; Artto, Ville; Auton, Adam; Belin, Andrea Carmine; Belin, Andrea Carmine; Bell, Robert K et al.
DOI: 10.1016/j.neuron.2018.04.014

Common Variant Burden Contributes to the Familial Aggregation of Migraine in 1,589 Families.

PMID: 30189203
Journal: NEURON
Year: 2018
Reference: Neuron. 2018 Sep 5;99(5):1098. doi: 10.1016/j.neuron.2018.08.029.
Impact factor:
Publication type: Letter or abstract
Authors: Agee, Michelle; Alipanahi, Babak; Anttila, Verneri; Anttila, Verneri; Artto, Ville; Artto, Ville; Auton, Adam; Belin, Andrea Carmine; Belin, Andrea Carmine; Bell, Robert K et al.
DOI: 10.1016/j.neuron.2018.08.029

Analysis of shared heritability in common disorders of the brain.

PMID: 29930110
Journal: SCIENCE
Year: 2018
Reference: Science. 2018 Jun 22;360(6395). pii: 360/6395/eaap8757. doi: 10.1126/science.aap8757.
Impact factor:
Publication type: Paper in international publication
Authors: Adams, Hieab H H; Air, Tracy; Al-Chalabi, Ammar; Alda, Martin; Alegret, Montserrat; Alfredsson, Lars; Amouyel, Philippe; Andlauer, Till F M; Andreassen, Ole A; Anjorin, Adebayo et al.
DOI: 10.1126/science.aap8757

Rufinamide in children and adults in routine clinical practice.

PMID: 26923380
Journal: ACTA NEUROLOGICA SCANDINAVICA
Year: 2017
Reference: Acta Neurol Scand. 2017 Jan;135(1):122-128. doi: 10.1111/ane.12572. Epub 2016 Feb 29.
Impact factor:
Publication type: Paper in international publication
Authors: Becerra, J L; Burcet, J; Cano, A; Falip, M; Fernandez, S; Fossas, P; Jaraba, S; Miravet, E; Miro, J; Molins, A et al.
DOI: 10.1111/ane.12572

Intrathecal cyclodextrin in the treatment of Niemann-Pick disease type C.

PMID: 31156935
Journal: European Journal of Hospital Pharmacy-Science and Practice
Year: 2017
Reference: Eur J Hosp Pharm. 2017 May;24(3):185-188. doi: 10.1136/ejhpharm-2016-001067. Epub 2016 Nov 4.
Impact factor:
Publication type: Paper in international publication
Authors: Cabanas Poy, Maria Josep; Canete Ramirez, Carme; Clemente Bautista, Susana; Del Toro Riera, Mireia; Fernandez Polo, Aurora; Roch Santed, Maria et al.
DOI: 10.1136/ejhpharm-2016-001067

Proxy-reported quality of life in adolescents and adults with dyskinetic cerebral palsy is associated with executive functions and cortical thickness.

PMID: 27766516
Journal: QUALITY OF LIFE RESEARCH
Year: 2017
Reference: Qual Life Res. 2017 May;26(5):1209-1222. doi: 10.1007/s11136-016-1433-0. Epub 2016 Oct 20.
Impact factor:
Publication type: Paper in international publication
Authors: Ballester-Plane, J; Botellero, V L; Delgado, I; Laporta-Hoyos, O; Macaya, A; Melendez-Plumed, M; Narberhaus, A; Poo, P; Pueyo, R; Segarra, D et al.
DOI: 10.1007/s11136-016-1433-0

Intracranial Hypertension in Cystinosis Is a Challenge: Experience in a Children's Hospital.

PMID: 27858370
Journal: JIMD reports
Year: 2017
Reference: JIMD Rep. 2017;35:17-22. doi: 10.1007/8904_2016_18. Epub 2016 Nov 18.
Impact factor:
Publication type: Paper in international publication
Authors: Alarcon, Silvia; Ariceta, Gema; Cano, Paola; Del Toro, Mireia; Lara, Luis Enrique; Madrid, Alvaro; Martin-Begue, Nieves; Wolley-Dod, Charlotte et al.
DOI: 10.1007/8904_2016_18

[Outbreak of acute neurological disease associated to enterovirus in Catalonia: neuropaediatric aspects].

PMID: 27345273
Journal: REVISTA DE NEUROLOGIA
Year: 2016
Reference: Rev Neurol. 2016 Jul 1;63(1):3-4.
Impact factor:
Publication type: Paper in national publication
Authors: Felipe-Rucian, A; Macaya-Ruiz, A et al.
DOI:

Levetiracetam and Valproate Retention Rate in Juvenile Myoclonic Epilepsy.

PMID: 27438183
Journal: CLINICAL NEUROPHARMACOLOGY
Year: 2016
Reference: Clin Neuropharmacol. 2016 Nov/Dec;39(6):299-301.
Impact factor:
Publication type: Paper in international publication
Authors: Gonzalez-Cuevas, Montserrat; Quintana, Manolo; Raspall-Chaure, Miquel; Sala-Padro, Jacint; Salas-Puig, Xavier; Santamarina, Estevo; Sueiras-Gil, Maria; Toledo, Manuel et al.
DOI: 10.1097/WNF.0000000000000177

[Transition process from paediatric to adult care in patients with inborn errors of metabolism. Consensus statement].

PMID: 27816186
Journal: MEDICINA CLINICA
Year: 2016
Reference: Med Clin (Barc). 2016 Dec 2;147(11):506.e1-506.e7. doi: 10.1016/j.medcli.2016.09.018. Epub 2016 Nov 3.
Impact factor:
Publication type: Paper in national publication
Authors: Aldamiz Echevarri Azuara, Luis Jose; Campistol, Jaume; Ceberio-Hualde, Leticia; Couce, M Luz; Del Toro, Mireia; Garcia Morillo, Jose Salvador; Garcia-Silva, Maria Teresa; Gonzalez Gutierrez-Solana, Luis; Grau-Junyent, Josep M; Hermida Ameijeiras, Alvaro et al.
DOI: 10.1016/j.medcli.2016.09.018

Carglumic acid enhances rapid ammonia detoxification in classical organic acidurias with a favourable risk-benefit profile: a retrospective observational study.

PMID: 27030250
Journal: Orphanet Journal of Rare Diseases
Year: 2016
Reference: Orphanet J Rare Dis. 2016 Mar 31;11:32. doi: 10.1186/s13023-016-0406-2.
Impact factor:
Publication type: Clinical guide
Authors: Baruteau, Julien; Cano, Aline; Chakrapani, Anupam; Coker, Mahmut; Couce, Maria L; Del Toro, Mireia; Delgado, Maria Bueno; Donati, Maria Alice; Garcia-Cazorla, Angeles; Gil-Ortega, David et al.
DOI: 10.1186/s13023-016-0406-2

[Concordance between a head circumference growth function and intellectual disability in relation with the cause of microcephaly].

PMID: 25534043
Journal: AN PEDIATR
Year: 2015
Reference: An Pediatr (Barc). 2015 Aug;83(2):109-16. doi: 10.1016/j.anpedi.2014.10.030. Epub 2014 Dec 19.
Impact factor:
Publication type: Paper in national publication
Authors: Coronado, R; Giraldo Arjonilla, J; Macaya Ruiz, A; Roig-Quilis, M et al.
DOI: 10.1016/j.anpedi.2014.10.030

Antenatal corticosteroids and perinatal outcomes in infants born at 23-25 weeks of gestation.

PMID: 25367557
Journal: J MATERN-FETAL NEO M
Year: 2015
Reference: J Matern Fetal Neonatal Med. 2015;28(17):2084-9. doi: 10.3109/14767058.2014.978280. Epub 2014 Nov 25.
Impact factor:
Publication type: Paper in international publication
Authors: Cabero, L; Camba, F; Capote, S; Carreras, E; Cespedes, M C; Felipe, A; Gorraiz, V; Goya, M; Gracia, A; Halachian, C et al.
DOI: 10.3109/14767058.2014.978280

Candidate-gene association study searching for genetic factors involved in migraine chronification.

PMID: 25169732
Journal: CEPHALALGIA
Year: 2015
Reference: Cephalalgia. 2015 May;35(6):500-7. doi: 10.1177/0333102414547141. Epub 2014 Aug 28.
Impact factor:
Publication type: Paper in international publication
Authors: Alvarez-Sabin, J; Anttila, V; Cormand, B; de Vries, B; Fernandez-Cadenas, I; Fernandez-Morales, J; Ferrari, Md; Louter, Ma; Macaya, A; Montaner, J et al.
DOI: 10.1177/0333102414547141

Autoimmune post-herpes simplex encephalitis of adults and teenagers.

PMID: 26491084
Journal: NEUROLOGY
Year: 2015
Reference: Neurology. 2015 Nov 17;85(20):1736-43. doi: 10.1212/WNL.0000000000002125. Epub 2015 Oct 21.
Impact factor:
Publication type: Paper in international publication
Authors: Aguilar, Esther; Aguilera-Albesa, Sergio; Armangue, Thais; Arratibel, Izaskun; Bataller, Luis; Bosch, Beatriz; Cantarin-Extremera, Veronica; Casado-Naranjo, Ignacio; Cervera, Carlos; Conde, Carlos Enrique et al.
DOI: 10.1212/WNL.0000000000002125

Urea cycle disorders in Spain: an observational, cross-sectional and multicentric study of 104 cases.

PMID: 25433810
Journal: Orphanet Journal of Rare Diseases
Year: 2014
Reference: Orphanet J Rare Dis. 2014 Nov 30;9:187. doi: 10.1186/s13023-014-0187-4.
Impact factor:
Publication type: Paper in international publication
Authors: Aldamiz-Echevarria, Luis; Balmaseda-Serrano, Elena; Belanger-Quintana, Amaya; Bueno-Delgado, Maria Amor; Castejon-Ponce, Esperanza; Couce, Maria Luz; Dalmau, Jaime; Del Toro-Riera, Mirella; Garcia-Jimenez, Inmaculada; Garcia-Silva, Maria Teresa et al.
DOI: 10.1186/s13023-014-0187-4

TOSCA inverted question mark first international registry to address knowledge gaps in the natural history and management of tuberous sclerosis complex.

PMID: 25424195
Journal: Orphanet Journal of Rare Diseases
Year: 2014
Reference: Orphanet J Rare Dis. 2014 Nov 26;9:182. doi: 10.1186/s13023-014-0182-9.
Impact factor:
Publication type: Paper in international publication
Authors: Belousova, Elena; Benedik, Mirjana; Bruzzi, Paolo; Carter, Tom; Castellana, Ramon; Comis, Silvia; Cottin, Vincent; Crippa, Stefania; Curatolo, Paolo; D Augeres, Guillaume et al.
DOI: 10.1186/s13023-014-0182-9

Clinical and genetic analysis in alternating hemiplegia of childhood: ten new patients from Southern Europe.

PMID: 24996492
Journal: JOURNAL OF THE NEUROLOGICAL SCIENCES
Year: 2014
Reference: J Neurol Sci. 2014 Sep 15;344(1-2):37-42. doi: 10.1016/j.jns.2014.06.014. Epub 2014 Jun 17.
Impact factor:
Publication type: Paper in international publication
Authors: Carreno, Oriel; Cormand, Bru; Macaya, Alfons; Marce-Grau, Anna; Pineda-Marfa, Merce; Pons, Roser; Raspall-Chaure, Miquel; Sintas, Celia; Vila-Pueyo, Marta et al.
DOI: 10.1016/j.jns.2014.06.014

Herpes simplex virus encephalitis is a trigger of brain autoimmunity.

PMID: 24318406
Journal: ANNALS OF NEUROLOGY
Year: 2014
Reference: Ann Neurol. 2014 Feb;75(2):317-23. doi: 10.1002/ana.24083. Epub 2014 Feb 25.
Impact factor:
Publication type: Paper in international publication
Authors: Armangue, Thais; Dalmau, Josep; Glaser, Carol; Hoftberger, Romana; Ke, Michael; Lafuente-Hidalgo, Miguel; Leypoldt, Frank; Macaya, Alfons; Malaga, Ignacio; Marti, Itxaso et al.
DOI: 10.1002/ana.24083

Leigh Syndrome and the Mitochondrial m.13513G>A Mutation: Expanding the Clinical Spectrum.

PMID: 23034978
Journal: JOURNAL OF CHILD NEUROLOGY
Year: 2013
Reference: J Child Neurol. 2013 Nov;28(11):1531-1534. doi: 10.1177/0883073812460580. Epub 2012 Oct 3.
Impact factor:
Publication type: Paper in international publication
Authors: Bornstein, Belen; Del Toro, Mireia; Garcia-Arumi, Elena; Monlleo-Neila, Laura; Munell, Francina; Roig-Quilis, Manuel; Sarrias, Axel et al.
DOI: 10.1177/0883073812460580

Protein expression profiles in patients carrying NFU1 mutations. Contribution to the pathophysiology of the disease.

PMID: 23179554
Journal: JOURNAL OF INHERITED METABOLIC DISEASE
Year: 2013
Reference: J Inherit Metab Dis. 2013 Sep;36(5):841-7. doi: 10.1007/s10545-012-9565-z. Epub 2012 Nov 22.
Impact factor:
Publication type: Paper in international publication
Authors: Arranz, Jose Antonio; Briones, Paz; Bujan, Nuria; Campistol, Jaume; Del Toro, Mireia; Ferrer-Cortes, Xenia; Font, Aida; Garcia-Cazorla, Angels; Matalonga, Leslie; Navarro-Sastre, Aleix et al.
DOI: 10.1007/s10545-012-9565-z

Biallelic SZT2 mutations cause infantile encephalopathy with epilepsy and dysmorphic corpus callosum.

PMID: 23932106
Journal: AMERICAN JOURNAL OF HUMAN GENETICS
Year: 2013
Reference: Am J Hum Genet. 2013 Sep 5;93(3):524-9. doi: 10.1016/j.ajhg.2013.07.005. Epub 2013 Aug 8.
Impact factor:
Publication type: Paper in international publication
Authors: Basel-Vanagaite, Lina; Bode, Harald; Borck, Guntram; Dahary, Dvir; Gothelf, Doron; Haviv, Ami; Hershkovitz, Tova; Heyman, Eli; Hubshman, Monika Weisz; Kakar, Naseebullah et al.
DOI: 10.1016/j.ajhg.2013.07.005

Assessment of interferon-related biomarkers in Aicardi-Goutieres syndrome associated with mutations in TREX1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, and ADAR: a case-control study.

PMID: 24183309
Journal: LANCET NEUROLOGY
Year: 2013
Reference: Lancet Neurol. 2013 Dec;12(12):1159-69. doi: 10.1016/S1474-4422(13)70258-8. Epub 2013 Oct 30.
Impact factor:
Publication type: Paper in international publication
Authors: Abdel-Hamid, Mohamed S; Abdel-Salam, Ghada M H; Ackroyd, Sam; Aeby, Alec; Aglan, Mona S; Allcock, Rebecca; Bailey, Kathryn M; Balottin, Umberto; Barnerias, Christine; Bernard, Genevieve et al.
DOI: 10.1016/S1474-4422(13)70258-8

[Reversible encephalopathy caused by valproic acid in an adolescent with idiopathic generalised epilepsy].

PMID: 23172093
Journal: REVISTA DE NEUROLOGIA
Year: 2012
Reference: Rev Neurol. 2012 Dec 1;55(11):663-8.
Impact factor:
Publication type: Paper in national publication
Authors: Lainez, Elena; Macaya-Ruiz, Alfons; Raspall-Chaure, Miquel; Roig-Quilis, Manuel; Salas-Puig, Javier; Toledo, Manuel et al.
DOI: 10.33588/rn.5511.2012374

Efficacy and tolerability of rizatriptan in pediatric migraineurs: results from a randomized, double-blind, placebo-controlled trial using a novel adaptive enrichment design.

PMID: 22711898
Journal: CEPHALALGIA
Year: 2012
Reference: Cephalalgia. 2012 Jul;32(10):750-65. Epub 2012 Jun 18.
Impact factor:
Publication type: Paper in international publication
Authors: Abrahim, Alber; Adler, Lawrence; Agarwal, Sandeep; Aguado, Mario; Almadani, Mahmud; Anand, Ish; Annequin, Daniel; Arthur, Charles Peter; Artigas Pallares, Josep; Assaid, Christopher et al.
DOI: 10.1177/0333102412451358

Prognostic value of X-chromosome inactivation in symptomatic female carriers of dystrophinopathy.

PMID: 23092449
Journal: Orphanet Journal of Rare Diseases
Year: 2012
Reference: Orphanet J Rare Dis. 2012 Oct 23;7:82. doi: 10.1186/1750-1172-7-82.
Impact factor:
Publication type: Paper in international publication
Authors: Baiget, Montserrat; Colomer, Jaume; Diaz-Manera, Jorge; Gallano, Pia; Gallardo, Eduard; Gonzalez-Mera, Laura; Gonzalez-Quereda, Lidia; Hernandez-Lain, Aurelio; Jimenez-Mallebrera, Cecilia; Jou, Cristina et al.
DOI: 10.1186/1750-1172-7-82

Mutations in ADAR1 cause Aicardi-Goutieres syndrome associated with a type I interferon signature.

PMID: 23001123
Journal: NATURE GENETICS
Year: 2012
Reference: Nat Genet. 2012 Sep 23;44(11):1243-8. doi: 10.1038/ng.2414. Epub 2012 Sep 23.
Impact factor:
Publication type: Paper in international publication
Authors: Bacino, Carlos A; Battini, Roberta; Bertini, Enrico; Bhaskar, Sanjeev S; Briggs, Tracy A; Brogan, Paul A; Brueton, Louise A; Carpanelli, Marialuisa; Crow, Yanick J; De Laet, Corinne et al.
DOI: 10.1038/ng.2414

Etanercept-induced myelopathy in a pediatric case of blau syndrome.

PMID: 22937436
Journal: Case Rep Rheumatol
Year: 2011
Reference: Case Rep Rheumatol. 2011;2011:134106. doi: 10.1155/2011/134106. Epub 2012 Jan 15.
Impact factor:
Publication type: Paper in international publication
Authors: Caracseghi, Fabiola; Izquierdo-Blasco, Jaume; Melendo-Perez, Susana; Modesto, Consuelo; Roig-Quilis, Manuel; Sanchez-Montanez, Angel et al.
DOI: 10.1155/2011/134106

Incidence and timing of infusion-related reactions in patients with mucopolysaccharidosis type II (Hunter syndrome) on idursulfase therapy in the real-world setting: a perspective from the Hunter Outcome Survey (HOS).

PMID: 21439875
Journal: MOLECULAR GENETICS AND METABOLISM
Year: 2011
Reference: Mol Genet Metab. 2011 Jun;103(2):113-20. Epub 2011 Mar 4.
Impact factor:
Publication type: Paper in international publication
Authors: Abdul-Rahman, O; Acosta, A; Alcalde, C; Aldamiz, L; Aleck, K; Almassy, Z; Baldellou, A; Baric, I; Barisic, I; Beck, M et al.
DOI: 10.1016/j.ymgme.2011.02.018

Tyrosinemia type 1 in Spain: mutational analysis, treatment and long-term outcome.

PMID: 21752152
Journal: PEDIATRICS INTERNATIONAL
Year: 2011
Reference: Pediatr Int. 2011 Dec;53(6):985-9. doi: 10.1111/j.1442-200X.2011.03427.x.
Impact factor:
Publication type: Paper in international publication
Authors: Aldamiz-Echevarria, Luis; Blasco, J; Bueno, M A; Campos, M Gil; Couce, Maria Luz; Dalmau, Jaime; del Toro, Mireia; Gomez, L; Manzanares, J; Ortega, A Gil et al.
DOI: 10.1111/j.1442-200X.2011.03427.x

Screening for nuclear genetic defects in the ATP synthase-associated genes TMEM70, ATP12 and ATP5E in patients with 3-methylglutaconic aciduria.

PMID: 21815885
Journal: CLINICAL GENETICS
Year: 2011
Reference: Clin Genet. 2011 Sep;80(3):297-300. doi: 10.1111/j.1399-0004.2011.01650.x.
Impact factor:
Publication type: Letter or abstract
Authors: Arranz, J A; Briones, P; Bujan, N; Del Toro, M; Fernandez-Burriel, M; Font, A; Lissens, W; Lopez-Gallardo, E; Montoya, J; Navarro-Sastre, A et al.
DOI: 10.1111/j.1399-0004.2011.01650.x

Home treatment with intravenous enzyme replacement therapy with idursulfase for mucopolysaccharidosis type II - data from the Hunter Outcome Survey.

PMID: 20638311
Journal: MOLECULAR GENETICS AND METABOLISM
Year: 2010
Reference: Mol Genet Metab. 2010 Oct-Nov;101(2-3):123-9. Epub 2010 Jun 23.
Impact factor:
Publication type: Paper in international publication
Authors: Abdul-Rahman, O; Acosta, A; Alcalde, C; Aldamiz, L; Aleck, K; Almassy, Z; Baldellou, A; Baric, I; Barisic, I; Beck, M et al.
DOI: 10.1016/j.ymgme.2010.06.011

Human SHBG mRNA Translation Is Modulated by Alternative 5'-Non-Coding Exons 1A and 1B.

PMID: 21079794
Journal: PLoS One
Year: 2010
Reference: PLoS One. 2010 Nov 4;5(11):e13844.
Impact factor:
Publication type: Paper in international publication
Authors: ; ; ; ; ; ; et al.
DOI: 10.1371/journal.pone.0013844

Paroxysmal exercise-induced dyskinesia, writer's cramp, migraine with aura and absence epilepsy in twin brothers with a novel SLC2A1 missense mutation.

PMID: 20621801
Journal: JOURNAL OF THE NEUROLOGICAL SCIENCES
Year: 2010
Reference: J Neurol Sci. 2010 Aug 15;295(1-2):110-3. Epub 2010 Jun 8.
Impact factor:
Publication type: Paper in international publication
Authors: Conill, Joan; Cuenca-Leon, Ester; Gratacos, Margarida; Macaya, Alfons; Raspall-Chaure, Miquel; Redecillas, Susana; Roig-Quilis, Manuel; Urbizu, Aintzane et al.
DOI: 10.1016/j.jns.2010.05.017

[Recommendations and management of Type I hereditary or hepatorenal Tyrosinemia.]

PMID: 20813594
Journal: ANALES DE PEDIATRIA
Year: 2010
Reference: An Pediatr (Barc). 2010 Nov;73(5):279.e1-4. Epub 2010 Sep 1.
Impact factor:
Publication type: Paper in national publication
Authors: ; ; ; ; ; ; ; ; ; et al.
DOI: 10.1016/j.anpedi.2010.03.005

Proteomic analysis in cerebrospinal fluid of patients with atypical nonketotic hyperglycinemia and pulmonary hypertension - A pilot study.

PMID: 21136962
Journal: Proteomics Clinical Applications
Year: 2009
Reference: Proteomics Clin Appl. 2009 Dec;3(12):1430-9. doi: 10.1002/prca.200800251. Epub 2009 Oct 7.
Impact factor:
Publication type: Paper in international publication
Authors: Arranz, Jose A; Bech-Serra, Joan J; Canals, Francesc; Colome, Nuria; Del Toro, Mireia; Riudor, Encarnacio; Rodriguez, Carlos E et al.
DOI: 10.1002/prca.200800251

[Intracranial hypertension associated with cerebral venous sinus thrombosis and mastoiditis. Two paediatric case reports]

PMID: 19859877
Journal: REVISTA DE NEUROLOGIA
Year: 2009
Reference: Rev Neurol. 2009 Nov 16-30;49(10):529-32.
Impact factor:
Publication type: Paper in national publication
Authors: Boronat-Guerrero, S; del Toro-Riera, M; Roig-Quilis, M; Vazquez-Mendez, E; Velasco-Puyo, P et al.
DOI:

Mortality and cause of death in mucopolysaccharidosis type II-a historical review based on data from the Hunter Outcome Survey (HOS).

PMID: 19597960
Journal: JOURNAL OF INHERITED METABOLIC DISEASE
Year: 2009
Reference: J Inherit Metab Dis. 2009 Aug;32(4):534-43.
Impact factor:
Publication type: Paper in international publication
Authors: Aldamiz, Luis; Aleck, Kirk; Almassy, Z; Almassy, Zsuzsanna; Baldellou, Antonio; Baric, Ivo; Barisic, Ingeborg; Beck, M; Beck, Michael; Bodamer, Olaf et al.
DOI: 10.1007/s10545-009-1119-7

Long-term efficacy and tolerability of 4-monthly versus yearly botulinum toxin type A treatment for lower-limb spasticity in children with cerebral palsy.

PMID: 19563586
Journal: DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY
Year: 2009
Reference: Dev Med Child Neurol. 2009 Jun;51(6):436-45.
Impact factor:
Publication type: Paper in international publication
Authors: Bares, Martin; Benetin, J; Bonikowski, M; Cardo, E; Fontan, D; Jasinski, M; Jozwiak, M; Kanovsky, P; Kanovsky, Petr; Kraus, J et al.
DOI: 10.1111/j.1469-8749.2008.03264.x

Estrogen receptor beta displays cell cycle-dependent expression and regulates the G1 phase through a non-genomic mechanism in prostate carcinoma cells.

PMID: 18607069
Journal: CELLULAR ONCOLOGY
Year: 2008
Reference: Cell Oncol. 2008;30(4):349-65.
Impact factor:
Publication type: Paper in international publication
Authors: Barbosa-Desongles, Anna; Barquinero, Jordi; Bellmunt, Joaquim; de Torres, Ines; Hurtado, Antoni; Lopez-Aviles, Sandra; Morote, Joan; Munell, Francina; Petriz, Jordi; Pinos, Tomas et al.
DOI:

Thesis

Diagnòstic dels trastorns genètics de la substància blanca cerebral i identificació de noves malalties mitjançant tècniques de sequ?enciació massiva

PhD student: Agusti Rodriguez Palmero Seuma
Director/s: Alfons Macaya Ruíz, Aurora Pujol Onofre
University: Universitat Autònoma de Barcelona
Year: 2022

Seqüenciació exòmica en l'estudi molecular de les encefalopaties epilèptiques d'inici precoç

PhD student: Anna Marcé Grau
Director/s: Alfons Macaya Ruíz
University: Universidad Autònoma de Barcelona
Year: 2018

Factors influencing psychiatric outcome in children with neurological conditions: focus on acquired brain injury epilepsy

PhD student: María Teresa Lax Pericall
Director/s:
University: Universidad Autònoma de Barcelona
Year: 2016

Blog

News

The ClinPrior algorithm achieved a positive diagnosis rate of 70% in two minority diseases of neurodegenerative origin, which represents double the number of cases that are diagnosed with current tools.

Over the course of two days, experts presented the latest advances in vectors, different gene modification techniques and their transfer to clinical practice.

El 20% dels pacients en els quals s’havia trobat alguna predisposició genètica van ser diagnosticats amb algun tipus de tumor i van poder iniciar el tractament de manera precoç.