Elisa De La Cruz

6PUBLICATIONS
33CO-AUTHORS
Neurology and neuromuscular diseasesImmunogenetics (incl. genetic immunology)Cancer diagnosisDevelopmental genetics (incl. sex determination)Cardiovascular medicine and haematology not elsewhere classified
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Publications (6)

|Feb 26, 2025
Comparative Performances of 4 Serum NfL Assays, pTau181, and GFAP in Patients With Amyotrophic Lateral Sclerosis.

Etienne Mondesert, Constance Delaby, Elisa De La Cruz

|Oct 24, 2024
MYH7-related myopathies: clinical, myopathological and genotypic spectrum in a multicentre French cohort.

Marie Bahout, Gianmarco Severa, Emna Kamoun

|Jul 02, 2024
Author Correction: The SOD1-mediated ALS phenotype shows a decoupling between age of symptom onset and disease duration.

Sarah Opie-Martin, Alfredo Iacoangeli, Simon D Topp

|Jun 26, 2024
Most SOD1 mutations are pathogenic, and their identification can lead to early access to treatment.

Elisa De La Cruz, Florence Esselin, Anne Polge

|Nov 13, 2022
The SOD1-mediated ALS phenotype shows a decoupling between age of symptom onset and disease duration.

Sarah Opie-Martin, Alfredo Iacoangeli, Simon D Topp

|Dec 17, 2020
A rare cause of midbrain haemorrhage.

Kristin S Lange, Guillaume Taieb, Pierre Lepretre

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Frequent Collaborators

2 joint publications

Nicola Ticozzi

2 joint publications

Garth A Nicholson

2 joint publications

Lyndal Henden

2 joint publications

Alfredo Iacoangeli