Genotype-phenotype correlation in Tunisian patients with Amyotrophic Lateral Sclerosis-Reference-Cited by-同舟云学术

Genotype-phenotype correlation in Tunisian patients with Amyotrophic Lateral Sclerosis

Published:2022-12 Issue: Volume:120 Page:27-33
ISSN:0197-4580
Container-title:Neurobiology of Aging
language:en
Short-container-title:Neurobiology of Aging

Author:

Kacem Imen,Sghaier Ikram^ORCID,Peverelli Silvia,Souissi Emira,Ticozzi Nicola^ORCID,Gharbi Alya^ORCID,Ratti Antonia,Berrechid Amina Gargouri^ORCID,Silani Vincenzo,Gouider Riadh

Funder

Ministero della Salute

Publisher

Elsevier BV

Subject

Geriatrics and Gerontology,Developmental Biology,Neurology (clinical),Aging,General Neuroscience

Reference39 articles.

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4. Hereditary motor system diseases (chronic juvenile amyotrophic lateral sclerosis). Conditions combining a bilateral pyramidal syndrome with limb and bulbar amyotrophy;Ben Hamida;Brain J. Neurol.,1990

5. El Escorial revisited: revised criteria for the diagnosis of amyotrophic lateral sclerosis;Brooks;Amyotroph. Lateral Scler. Mot. Neuron Disord. Off. Publ. World Fed. Neurol. Res. Group Mot. Neuron Dis.,2000

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