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Teresinha Evangelista

Assistance Publique - Hôpitaux de Paris

France

Research Interests

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Professors in France

Articles (23)

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2026

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2024

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2024

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2022

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2021

Collaborators (13)

Anna Kostera-Pruszczyk

Head of Department/Prof

Medical University of Warsaw

POLAND

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Ana Rosa Soares

Universidade de Lisboa Instituto de Medicina Molecular João Lobo Antunes

PORTUGAL

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DOURAIED BEN SALEM

Professor

Centre Hospitalier Universitaire de Nantes

FRANCE

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Jonathan Baets

University of Antwerp

BELGIUM

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Patrick Chinnery

Professor of Neurology

Newcastle University

UNITED KINGDOM

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Mallory Freeberg

Human Genomics Team lead

European Bioinformatics Institute

UNITED KINGDOM

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Janet R. Vos

Radboud University Medical Center

NETHERLANDS

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roberta battini

University of Pisa

ITALY

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Marina Grandis

Docenti di ruolo di IIa fascia

University of Genoa

ITALY

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Edoardo Malfatti

Full Professor

FRANCE

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Davide Gabellini

Group Leader

Vita-Salute San Raffaele University

ITALY

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Hani Kushlaf

Associate Professor of Neurology & Pathology

University of Cincinnati

UNITED STATES

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Michael Way

Professor of Virology

Imperial College London

UNITED KINGDOM

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Teresinha Evangelista

Research Interests

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Articles (23)

The actomyosin cortex controls t-tubule remodeling in skeletal muscle

A toolkit for new facioscapulohumeral muscular dystrophy trial sites

Respiratory insufficiency and sleep impairment in facioscapulohumeral muscular dystrophy

Muscle Biopsy Findings in Valosin-Containing Protein Multisystem Proteinopathy.

Describing phenotypes in FSHD: an update of the comprehensive clinical evaluation form

Awareness of bone strength in patients with neuromuscular disorders

Genomic reanalysis of a pan-European rare-disease resource yields new diagnoses

A novel XPNPEP3 gene variant manifesting as rhabdomyolysis and exercise intolerance

Glycogenosis type XI, a rare association between muscle and skin manifestations - the contribution of proteomics for the understanding of the underlying myopathology

Lysosomal damage is a therapeutic target in Duchenne Muscular Dystrophy

Publisher Correction: Genomic reanalysis of a pan-European rare-disease resource yields new diagnoses.

Transition from childhood to adulthood in neuromuscular disorders: results from the ERN EURO-NMD survey

Chronic pain as a presenting feature of dysferlinopathy

Co-occurrence of myositis and neuropathy after anti-CD30 therapy in a late-adolescent Hodgkin lymphoma patient

Generation and characterization of three human induced pluripotent stem cell lines from patients with glycogen storage disease type II

High prevalence of facioscapulohumeral muscular dystrophy (FSHD) and inflammatory myopathies association: Is there an interplay?

MYH7 -related myopathies: Clinical, myopathological and genotypic spectrum in a multicentre French cohort

SMCHD1 genetic variants in type 2 facioscapulohumeral dystrophy and challenges in predicting pathogenicity and disease penetrance

The most bothersome symptoms in neuromuscular diseases: the ERN EURO NMD Survey

Dysregulation of muscle cholesterol transport in amyotrophic lateral sclerosis.

Rapidly progressive myopathy: unveiling light chain amyloidosis as an initial manifestation of multiple myeloma: a case report and literature review

Comprehensive morphometric assessment of deltoid muscle development in children: A cross-sectional study

Survey on patients’ organisations’ knowledge and position paper on screening for inherited neuromuscular diseases in Europe

Collaborators (13)

Anna Kostera-Pruszczyk

Ana Rosa Soares

DOURAIED BEN SALEM

Jonathan Baets

Patrick Chinnery

Mallory Freeberg

Janet R. Vos

roberta battini

Marina Grandis

Edoardo Malfatti

Davide Gabellini

Hani Kushlaf

Michael Way

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