EURO-NMD REGISTRY HUB. European reference network for neuromuscular disease.

Datos básicos

Código:
EURO-NMD registry
Protocolo:
EURO-NMD registry
EUDRACT:
NCT:
Centro:
HOSPITAL UNIVERSITARI I POLITÈCNIC LA FE
Dotación:
Año de incio:
2024
Año de finalización:
PI BIOMÉDICA

Documentos

  • No hay documentos

Participantes

Grupos

Financiadores - Promotores

EUROPEAN REFERENCE NETWORK FOR RARE NEUROMUSCULAR DISEASES (ERN EURO-NMD)

Resultados del Ensayo Clínico


A description of variant transthyretin amyloidosis (ATTRv) stage 1 patients and asymptomatic carriers in Spain: the EMPATIa study

Davila, Lucia Galan; (...); Tarilonte, Patricia

Article. 10.1186/s13023-024-03304-9. 2024


Advances in the early diagnosis of amyotrophic lateral sclerosis.

Garcia-Casanova, Pilar H, Vazquez-Costa, Juan F

Article. 10.1080/14737175.2025.2471556. 2025


Asymptomatic HyperCKemia in the Pediatric Population A Prospective Study Utilizing Next-Generation Sequencing and Ancillary Tests

Marti, Pilar; (...); Vilchez, Juan Jesus

Article. 10.1212/WNL.0000000000210116. 2025


Clinical features, mutation spectrum and factors related to reaching molecular diagnosis in a cohort of patients with distal myopathies.

Muelas, Nuria; (...); Vilchez, Juan J

Article. 10.1007/s00415-024-12821-3. 2025


Deletion of exons 45 to 55 in the DMD gene: from the therapeutic perspective to the in vitro model

Poyatos-Garcia, Javier; (...); Vilchez, Juan J

Article. 10.1186/s13395-024-00353-3. 2024


Descriptive analysis of the spinal muscular atrophy population treated with Nusinersen included in the CuidAME project

Sotoca Fernandez, J.; (...); Fernandez-Garcia, M.

Meeting Abstract. 10.1016/j.nmd.2024.07.462. 2024

  • Open Access.

Effects of Spinal Cord Stimulation in Patients with Small Fiber and Associated Comorbidities from Neuropathy After Multiple Etiologies

Canos-Verdecho, Angeles; (...); Morales-Suarez-Varela, Maria

Article. 10.3390/jcm14020652. 2025


Hereditary transthyretin amyloidosis caused by the Val142Ile variant in Spain.

de Frutos, Fernando; (...); Gonzalez-Costello, Jose

Article. 10.1016/j.rec.2024.12.012. 2025


Hereditary transthyretin amyloidosis caused by Val142Ile variant in Spain: phenotypic characteristics, geographic distribution and population frequency

Seminario, F. De Frutos; (...); Gonzalez-Costello, J.

Meeting Abstract. 10.1093/eurheartj/ehae666.2073. 2024

  • Open Access.

Impact of SARS-CoV-2 infection and COVID-19 pandemic on the morbidity and mortality of amyotrophic lateral sclerosis patients in Valencia, Spain

Garcia-Casanova, Pilar H.; (...); Vazquez-Costa, Juan F.

Article. 10.1111/ene.16465. 2024

  • Open Access.

Insights into phenotypic variability caused by GARS1 pathogenic variants.

Jiménez-Jiménez J; (...); Sivera R

Article. 10.1111/ene.16416. 2024


ITPR3-associated neuropathy: Report of a further family with adult onset intermediate Charcot-Marie-Tooth disease.

Cabello-Murgui, Javier; (...); Sivera, Rafael

Article. 10.1111/ene.16485. 2024

  • Open Access.

Management of Hereditary Transthyretin Amyloidosis (ATTRv) Patients and Asymptomatic Carriers in Spain: The EMPATIa Study.

Losada Lopez, Ines; (...); Setaro, Francesca

Article. 10.3390/jcm13247587. 2024


Muscle MRI-phenotyping of patients with likely pathogenic anoctamin 5 variants

Poulsen, N.; (...); Vissing, J.

Meeting Abstract. 10.1016/j.nmd.2024.07.187. 2024

  • Open Access.

Outcomes of a Pilot Newborn Screening Program for Spinal Muscular Atrophy in the Valencian Community.

Berzal-Serrano, Alba; (...); Millan, Jose M

Article. 10.3390/ijns11010007. 2025


Safety and efficacy of nipocalimab in adults with generalised myasthenia gravis (Vivacity-MG3): a phase 3, randomised double-blind, placebo-controlled study

Antozzi, Carlo; (...); Sun, Hong

Article. 2025


Short-term and long-term safety profile of Givinostat in Duchenne muscular dystrophy

Vucinic, D.; (...); Muelas, N.

Meeting Abstract. 10.1016/j.nmd.2024.07.289. 2024

  • Open Access.

Spanish Pompe Registry: overview based on the 130 patients included

Marin, R. Martinez; (...); Manera, J. Diaz

Meeting Abstract. 10.1016/j.nmd.2024.07.732. 2024

  • Open Access.

STUB1 Mutations as Possible Genetic Modifiers in Spinocerebellar Ataxia Type 8.

Baviera-Munoz, Raquel; (...); Aller, Elena

Article. 10.1002/mds.29910. 2024


The cross-sectional area of the median nerve: An independent prognostic biomarker in amyotrophic lateral sclerosis

Martinez-Paya, J. J.; (...); Vazquez-Costa, J. F.

Article. 10.1016/j.nrl.2022.01.008. 2024


The cross-sectional area of the median nerve: An independent prognostic biomarker in amyotrophic lateral sclerosis.

Martinez-Paya, J J; (...); Vazquez-Costa, J F

Article. 10.1016/j.nrleng.2024.07.003. 2024


Validation of Neuromyotype: A smart keyboard for the evaluation of spinal muscular atrophy patients

Lizandra Cortes, P.; (...); Vazquez-Costa, J. F.

Article. 10.1016/j.nrl.2022.05.004. 2024


Campos de estudio

Compartir