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Maria Teresa Sanz Martinez

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Institutions of which they are part

Predoctoral researcher
Translational Immunology
Vall Hebron Institut de Recerca
Doctor
Immunology
Cross-departmental services

Maria Teresa Sanz Martinez

Institutions of which they are part

Predoctoral researcher
Translational Immunology
Vall Hebron Institut de Recerca
Doctor
Immunology
Cross-departmental services

.

.

Projects

Evaluación objetiva de la afectación gastrointestinal en pacientes esclerodermia y síntomas de reflujo gastroesofágico refractario a inhibidores de la bomba de protones.

IP: Luis Gerardo Alcala Gonzalez
Collaborators: Carmen Pilar Simeón i Aznar, Alfredo Guillen Del Castillo, Jorge Serra Pueyo, Evaluación objetiva de la afectación gastrointestinal en pacientes esclerodermia y síntomas de reflujo gastroesofágico refractar, Laura Viñas Gimenez, Claudia Barber Caselles, Maria Teresa Sanz Martinez
Funding agency: Instituto de Salud Carlos III
Funding: 105000
Reference: PI25/00647
Duration: 01/01/2026 - 31/12/2028

Determinació de nous anticossos en síndrome de Sjögren.

IP: Jaume Mestre Torres
Collaborators: Roser Solans Laque, Laura Viñas Gimenez, Maria Teresa Sanz Martinez
Funding agency: Instituto de Salud Carlos III
Funding: 43625
Reference: PI24/01620
Duration: 01/01/2025 - 31/12/2027

CARACTERIZACIÓNDE LA FARMACOCINÈTICA DE RITUXIMAB EN PACIENTS AMB MALALTIES RENALS AMB AFECTACIÓ GLOMERULAR

IP: Maria Larrosa Garcia
Collaborators: Mónica Martínez Gallo, J. Bruno Montoro Ronsano, Maria Queralt Gorgas Torner, Irene Agraz Pamplona, Carla Alonso Martinez, Maria Teresa Sanz Martinez, Sonia García García
Funding agency: Societat Catalana de Farmàcia Clínica
Funding: 12000
Reference: SCFC/JOAQUIM.BONAL/2022/LARROSA
Duration: 01/09/2022 - 30/08/2024

Related news

A Vall d’Hebron team demonstrates, for the first time, the potential of optical genome mapping to detect genetic alterations associated with this rare disease that are not identified using conventional methods.

The study describes the first documented case worldwide of hereditary angioedema transmission through assisted reproduction.

The paper describes the case of a patient in whom, years after a bone marrow transplant, two immune cell lines corrected the original genetic defect.

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