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Year
2014
Referencia
Transpl Infect Dis. 2014 Aug;16(4):642-7. doi: 10.1111/tid.12246. Epub 2014 Jul 2.
Tipus publicació
Review in international publication
DOI
http://dx.doi.org/10.1111/tid.12246
Revista
Transplant Infectious Disease
Títol Complet
Extensive emphysematous pyelonephritis in a renal allograft: case report and review of literature.
Codi
55498
PMID
https://pubmed.ncbi.nlm.nih.gov/24984587
Nom Autors
Agreda Castaneda, F; Gasanz Serrano, C; Iztueta Saavedra, I; Lorente, D; Morote Robles, J; Servian Vives, P; Trilla Herrera, E et al.
DOI número
10.1111/tid.12246
Year
2014
Referencia
Arch Esp Urol. 2014 Jun;67(5):442-51.
Tipus publicació
Letter or abstract
DOI
http://dx.doi.org/
Revista
Archivos españoles de urología
Títol Complet
[Optimization of follow up in prostate cancer active surveillance].
Codi
55497
PMID
https://pubmed.ncbi.nlm.nih.gov/24914843
Nom Autors
Celma Domenech, Ana; Morote Robles, Juan; Planas Morin, Jacques et al.
Year
2014
Referencia
Rheumatol Int. 2014 Oct;34(10):1419-25. doi: 10.1007/s00296-014-2977-3. Epub 2014 Mar 11.
Tipus publicació
Paper in international publication
DOI
http://dx.doi.org/10.1007/s00296-014-2977-3
Revista
RHEUMATOLOGY INTERNATIONAL
Títol Complet
Bone mass behavior after 1 year of different treatment strategies in prostate cancer patients subjected to androgen deprivation therapy.
Codi
55496
PMID
https://pubmed.ncbi.nlm.nih.gov/24615021
Nom Autors
Carles Galceran, J; Celma Domenech, A; Lorente Garcia, D; Morote Robles, J; Placer Santos, J; Planas Morin, J; Regis, L; Salvador Lacambra, C; Trilla Herrera, E et al.
DOI número
10.1007/s00296-014-2977-3
Year
2014
Referencia
Eur Urol. 2014 Oct;66(4):655-63. doi: 10.1016/j.eururo.2014.05.037. Epub 2014 Jun 18.
Tipus publicació
Clinical Trials
DOI
http://dx.doi.org/10.1016/j.eururo.2014.05.037
Revista
EUROPEAN UROLOGY
Títol Complet
Degarelix as an intermittent androgen deprivation therapy for one or more treatment cycles in patients with prostate cancer.
Codi
55495
PMID
https://pubmed.ncbi.nlm.nih.gov/24954791
Nom Autors
Albers, Peter; Boccon-Gibod, Laurent; de la Rosette, Jean; Malmberg, Anders; Montorsi, Francesco; Morote, Juan; Neijber, Anders; van Poppel, Hendrik; Villers, Arnauld et al.
DOI número
10.1016/j.eururo.2014.05.037
Year
2014
Referencia
Actas Urol Esp. 2014 Dec;38(10):685-93. doi: 10.1016/j.acuro.2014.05.003. Epub 2014 Jun 14.
Tipus publicació
Paper in national publication
DOI
http://dx.doi.org/10.1016/j.acuro.2014.05.003
Revista
Actas Urologicas Espanolas
Títol Complet
Bone health in patients with prostate cancer.
Codi
55494
PMID
https://pubmed.ncbi.nlm.nih.gov/24934457
Nom Autors
Alcaraz, A; Carballido, J; Cozar, J M; Gomez-Veiga, F J; Minana, B; Morote, J; Rodriguez-Antolin, A; Solsona, E et al.
DOI número
10.1016/j.acuro.2014.05.003
Year
2014
Referencia
Actas Urol Esp. 2014 Sep;38(7):419-20. doi: 10.1016/j.acuro.2014.02.016. Epub 2014 May 25.
Tipus publicació
Editorial in national publication
DOI
http://dx.doi.org/10.1016/j.acuro.2014.02.016
Revista
Actas Urologicas Espanolas
Títol Complet
Non-metastatic castration-resistant prostate cancer (CPRCM0), an old scenario with renewed clinical interest.
Codi
55493
PMID
https://pubmed.ncbi.nlm.nih.gov/24866537
Nom Autors
Carles, J; Maldonado, X; Morote, J; Planas, J et al.
DOI número
10.1016/j.acuro.2014.02.016
Year
2014
Referencia
Urology. 2014 Jun;83(6):1217-22. doi: 10.1016/j.urology.2014.02.001. Epub 2014 Apr 6.
Tipus publicació
Review in international publication
DOI
http://dx.doi.org/10.1016/j.urology.2014.02.001
Revista
UROLOGY
Títol Complet
Maximal testosterone suppression in prostate cancer--free vs total testosterone.
Codi
55492
PMID
https://pubmed.ncbi.nlm.nih.gov/24713136
Nom Autors
Andriole, Gerald L; Crawford, E David; Eisenberger, Mario A; Klotz, Laurence; Lange, Paul H; Matsumoto, Alvin M; Morote, Juan; Perachino, Massimo; Reis, Leonardo O; Rove, Kyle O et al.
DOI número
10.1016/j.urology.2014.02.001
Year
2014
Referencia
Med Clin (Barc). 2014 Dec 23;143(12):e23. doi: 10.1016/j.medcli.2014.05.016. Epub 2014 Jul 9.
Tipus publicació
Paper in national publication
DOI
http://dx.doi.org/10.1016/j.medcli.2014.05.016
Revista
MEDICINA CLINICA
Títol Complet
[Imperfect osteogenesis].
Codi
55491
PMID
https://pubmed.ncbi.nlm.nih.gov/25015250
Nom Autors
Cueto Gonzalez, Ana Maria; de Pablo Marquez, Bernat; May Llanes, Maria Elena; Yela Verdu, Christian et al.
DOI número
10.1016/j.medcli.2014.05.016
Year
2014
Referencia
Cytogenet Genome Res. 2014;144(4):290-3. doi: 10.1159/000375184. Epub 2015 Feb 14.
Tipus publicació
Paper in international publication
DOI
http://dx.doi.org/10.1159/000375184
Revista
CYTOGENETIC AND GENOME RESEARCH
Títol Complet
Intrachromosomal 3p insertion as a cause of reciprocal pure interstitial deletion and duplication in two siblings: further delineation of the emerging proximal 3p deletion syndrome.
Codi
55490
PMID
https://pubmed.ncbi.nlm.nih.gov/25720458
Nom Autors
Castells, Neus; Cueto, Ana; Del Campo, Miguel; Fernandez, Asuncion; Hernando, Cristina; Lloveras, Elisabet; Plaja, Alberto; Vendrell, Teresa; Villa, Olaya et al.
DOI número
10.1159/000375184
Year
2014
Referencia
Med Care. 2014 Nov;52(11):975-81. doi: 10.1097/MLR.0000000000000233.
Tipus publicació
Paper in international publication
DOI
http://dx.doi.org/10.1097/MLR.0000000000000233
Revista
MEDICAL CARE
Títol Complet
Nurses' shift length and overtime working in 12 European countries: the association with perceived quality of care and patient safety.
Codi
55489
PMID
https://pubmed.ncbi.nlm.nih.gov/25226543
Nom Autors
Aiken, Linda; Aiken, Linda H; Alenius, Lisa Smeds; Ball, Jane; Ball, Jane; Blumel, Miriam; Bruyneel, Luk; Brzostek, Tomasz; Brzyski, Piotr; Busse, Reinhard et al.
DOI número
10.1097/MLR.0000000000000233
Year
2014
Referencia
Lancet. 2014 May 24;383(9931):1824-30. doi: 10.1016/S0140-6736(13)62631-8. Epub 2014 Feb 26.
Tipus publicació
Paper in international publication
DOI
http://dx.doi.org/10.1016/S0140-6736(13)62631-8
Revista
LANCET
Títol Complet
Nurse staffing and education and hospital mortality in nine European countries: a retrospective observational study.
Codi
55488
PMID
https://pubmed.ncbi.nlm.nih.gov/24581683
Nom Autors
Aiken, Linda; Aiken, Linda H; Ball, Jane; Blumel, Miriam; Bruyneel, Luk; Bruyneel, Luk; Brzostek, Tomasz; Brzyski, Piotr; Busse, Reinhard; Busse, Reinhard et al.
DOI número
10.1016/S0140-6736(13)62631-8
Year
2014
Referencia
J Neuropathol Exp Neurol. 2014 Jun;73(6):559-67. doi: 10.1097/NEN.0000000000000078.
Tipus publicació
Paper in international publication
DOI
http://dx.doi.org/10.1097/NEN.0000000000000078
Revista
JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY
Títol Complet
Abnormalities in early markers of muscle involvement support a delay in myogenesis in spinal muscular atrophy.
Codi
55487
PMID
https://pubmed.ncbi.nlm.nih.gov/24806300
Nom Autors
Alias, Laura; Bernal, Sara; Martinez-Hernandez, Rebeca; Tizzano, Eduardo F et al.
DOI número
10.1097/NEN.0000000000000078
Year
2014
Referencia
Amyotroph Lateral Scler Frontotemporal Degener. 2014 Dec;15(7-8):563-8. doi: 10.3109/21678421.2014.929148. Epub 2014 Jul 7.
Tipus publicació
Paper in international publication
DOI
http://dx.doi.org/10.3109/21678421.2014.929148
Revista
Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration
Títol Complet
Analysis of the C9orf72 gene in spinal muscular atrophy patients.
Codi
55486
PMID
https://pubmed.ncbi.nlm.nih.gov/24998634
Nom Autors
Alias, Laura; Baiget, Montserrat; Barcelo, Maria J; Bernal, Sara; Martinez, Elisabeth; Martinez-Hernandez, Rebeca; Tizzano, Eduardo F et al.
DOI número
10.3109/21678421.2014.929148
Year
2014
Referencia
Hum Mol Genet. 2014 Jun 1;23(11):2888-900. doi: 10.1093/hmg/ddu002. Epub 2014 Jan 8.
Tipus publicació
Paper in international publication
DOI
http://dx.doi.org/10.1093/hmg/ddu002
Revista
HUMAN MOLECULAR GENETICS
Títol Complet
Loss-of-function HDAC8 mutations cause a phenotypic spectrum of Cornelia de Lange syndrome-like features, ocular hypertelorism, large fontanelle and X-linked inheritance.
Codi
55485
PMID
https://pubmed.ncbi.nlm.nih.gov/24403048
Nom Autors
Amor, David J; Ansari, Morad; Atwal, Paldeep S; Bahlo, Melanie; Bando, Masashige; Bowman, Christine M; Bradley, Jacquelyn J; Braunholz, Diana; Brunner, Han G; Christianson, David W et al.
DOI número
10.1093/hmg/ddu002
Year
2014
Referencia
Hum Mutat. 2014 Dec;35(12):1436-41. doi: 10.1002/humu.22689.
Tipus publicació
Paper in international publication
DOI
http://dx.doi.org/10.1002/humu.22689
Revista
HUMAN MUTATION
Títol Complet
A new overgrowth syndrome is due to mutations in RNF125.
Codi
55484
PMID
https://pubmed.ncbi.nlm.nih.gov/25196541
Nom Autors
Acosta, Angelina; Alija Merillas, M Jesus; Alonso, Almudena; Antolin, Eugenia; Aragon Fernandez, Carmen; Arberas, Claudia; Arcas, Javier; Arias, Pedro; Armengod, Carmen Gonzalez; Armenta, Daniel et al.
DOI número
10.1002/humu.22689
Year
2014
Referencia
Rev Esp Cardiol (Engl Ed). 2014 Oct;67(10):861-3. doi: 10.1016/j.rec.2014.06.003. Epub 2014 Sep 8.
Tipus publicació
Letter or abstract
DOI
http://dx.doi.org/10.1016/j.rec.2014.06.003
Revista
REVISTA ESPANOLA DE CARDIOLOGIA
Títol Complet
Nonsyndromic familial aortic disease: an underdiagnosed entity.
Codi
55483
PMID
https://pubmed.ncbi.nlm.nih.gov/25200617
Nom Autors
Borregan, Mar; del Campo, Miguel; Evangelista, Artur; Gutierrez, Laura; Teixido-Tura, Gisela; Valenzuela, Irene et al.
DOI número
10.1016/j.rec.2014.06.003
Year
2014
Referencia
Pediatr Nephrol. 2014 Feb;29(2):223-34. doi: 10.1007/s00467-013-2657-7. Epub 2013 Oct 27.
Tipus publicació
Paper in international publication
DOI
http://dx.doi.org/10.1007/s00467-013-2657-7
Revista
PEDIATRIC NEPHROLOGY
Títol Complet
Cost-effective PKHD1 genetic testing for autosomal recessive polycystic kidney disease.
Codi
55482
PMID
https://pubmed.ncbi.nlm.nih.gov/24162162
Nom Autors
Ars, Elisabet; Ballarin, Jose; Camacho, Juan Antonio; Ejarque, Laia; Krall, Paola; Mendizabal, Santiago; Oliver, Artur; Pineda, Cristina; Ruiz, Patricia; Torra, Roser et al.
DOI número
10.1007/s00467-013-2657-7
Year
2014
Referencia
J Clin Immunol. 2014 Jul;34(5):521-3. doi: 10.1007/s10875-014-0042-3. Epub 2014 Apr 24.
Tipus publicació
Paper in international publication
DOI
http://dx.doi.org/10.1007/s10875-014-0042-3
Revista
JOURNAL OF CLINICAL IMMUNOLOGY
Títol Complet
A novel splice site mutation in the SERPING1 gene leads to haploinsufficiency by complete degradation of the mutant allele mRNA in a case of familial hereditary angioedema.
Codi
55481
PMID
https://pubmed.ncbi.nlm.nih.gov/24760113
Nom Autors
Colobran, Roger; Guilarte, Mar; Hernandez-Gonzalez, Manuel; Pujol-Borrell, Ricardo et al.
DOI número
10.1007/s10875-014-0042-3
Year
2014
Referencia
J Immunol. 2014 Oct 15;193(8):3872-9. doi: 10.4049/jimmunol.1400223. Epub 2014 Sep 12.
Tipus publicació
Paper in international publication
DOI
http://dx.doi.org/10.4049/jimmunol.1400223
Revista
JOURNAL OF IMMUNOLOGY
Títol Complet
Autoimmune predisposition in Down syndrome may result from a partial central tolerance failure due to insufficient intrathymic expression of AIRE and peripheral antigens.
Codi
55480
PMID
https://pubmed.ncbi.nlm.nih.gov/25217160
Nom Autors
Armengol, Maria del Pilar; Casteras, Anna; Colobran, Roger; Correa, Paula A; Gimenez-Barcons, Mireia; Marin, Ana; Porta, Eduard; Pujol-Borrell, Ricardo et al.
DOI número
10.4049/jimmunol.1400223
Year
2014
Referencia
Multidiscip Respir Med. 2014 Nov 4;9(1):54. doi: 10.1186/2049-6958-9-54. eCollection 2014.
Tipus publicació
Letter or abstract
DOI
http://dx.doi.org/10.1186/2049-6958-9-54
Revista
Multidisciplinary Respiratory Medicine
Títol Complet
Metabolomic profile of amniotic fluid to evaluate lung maturity: the diaphragmatic hernia lamb model.
Codi
55479
PMID
https://pubmed.ncbi.nlm.nih.gov/25419460
Nom Autors
Andreatta, Erika; Ballico, Maurizio; Calcaterra, Valeria; Federico, Costanzo; Marotta, Mario; Mimmi, Maria Chiara; Nakib, Ghassan; Peiro, Jose Louis; Pelizzo, Gloria; Sampaolesi, Maurilio et al.
DOI número
10.1186/2049-6958-9-54