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1.
Compound heterozygosity for an expanded (GAA) and a (GAAGGA) repeat at FXN locus: from a diagnostic pitfall to potential clues to the pathogenesis of Friedreich ataxia.
Neurogenetics;
21(4): 279-287, 2020 10.
Artículo
en Inglés
| MEDLINE | ID: mdl-32638185
2.
Neurological Erdheim-Chester Disease Manifesting with Subacute or Progressive Cerebellar Ataxia: Novel Case Series and Review of the Literature.
Brain Sci;
13(1)2022 Dec 22.
Artículo
en Inglés
| MEDLINE | ID: mdl-36672008
3.
High Prevalence and Gender-Related Differences of Gastrointestinal Manifestations in a Cohort of DM1 Patients: A Perspective, Cross-Sectional Study.
Front Neurol;
11: 394, 2020.
Artículo
en Inglés
| MEDLINE | ID: mdl-32595582
4.
Response to "Autosomal recessive axonal neuropathy caused by HINT1 mutation: New association of a psychiatric disorder to the neurological phenotype".
Neuromuscul Disord;
30(3): 265-266, 2020 03.
Artículo
en Inglés
| MEDLINE | ID: mdl-32171572
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