المؤلفون: Imis Dogan, Chantal Depondt, Manuel Dafotakis, Sandra Benaich, Ralf-Dieter Hilgers, Paola Giunti, Dagmar Timmann, Perrine Charles, Jörg B. Schulz, Lorenzo Nanetti, Katrin Bürk, Claire Didszun, Claire Ewenczyk, Ummehan Ermis, Marta Panzeri, Myriam Rai, Ludger Schöls, Michael H Parkinson, Wolfgang Nachbauer, Massimo Pandolfo, Kathrin Reetz, Caterina Mariotti, Ilaria Giordano, Claudia Stendel, Sylvia Boesch, Marie-Lorraine Monin, Thomas Klockgether, Ivan Karin, Kathrin Fedosov, Javier Arpa, Andreas Eigentler, Irene Sanz-Gallego, Mary G. Sweeney, Christiane Neuhofer, Anna Castaldo, Jennifer Müller vom Hagen, Francisco Javier Rodriguez de Rivera, Julia Wolf, Thomas Klopstock, Alexandra Durr

المصدر: The lancet / Neurology 15(13), 1346-1354 (2016). doi:10.1016/S1474-4422(16)30287-3
The lancet / Neurology Neurology 15(13), 1346-1354 (2016). doi:10.1016/S1474-4422(16)30287-3

مصطلحات موضوعية: 0301 basic medicine, Gerontology, Adult, Male, Pediatrics, medicine.medical_specialty, Ataxia, physiopathology [Friedreich Ataxia], Severity of Illness Index, Cohort Studies, 03 medical and health sciences, 0302 clinical medicine, Severity of illness, Activities of Daily Living, diagnosis [Friedreich Ataxia], Outcome Assessment, Health Care, Clinical endpoint, Medicine, Humans, ddc:610, Registries, Age of Onset, business.industry, Middle Aged, medicine.disease, Prognosis, genetics [Friedreich Ataxia], Clinical trial, Europe, 030104 developmental biology, Friedreich Ataxia, Cohort, Spinocerebellar ataxia, Disease Progression, Female, Neurology (clinical), medicine.symptom, Age of onset, business, 030217 neurology & neurosurgery, Cohort study

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2815590671fafeddeba2f5c49a05e8ea

المؤلفون: Daniel Rabier, Fanny Mochel, Sandra Benaich, Alexandra Durr

المصدر: Archives of neurology. 68(2)

مصطلحات موضوعية: Adult, Male, Heterozygote, Genotype, Nerve Tissue Proteins, Disease, Biology, Severity of Illness Index, Arts and Humanities (miscellaneous), Huntington's disease, Valine, Leucine, Predictive Value of Tests, medicine, Huntingtin Protein, Humans, Isoleucine, Aged, chemistry.chemical_classification, Nuclear Proteins, Middle Aged, medicine.disease, Amino acid, Early Diagnosis, Huntington Disease, chemistry, Biochemistry, Linear Models, Female, Neurology (clinical), Trinucleotide repeat expansion, Trinucleotide Repeat Expansion, Amino Acids, Branched-Chain, Biomarkers

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7f3c9ba43d24a952560c7fea4d948870
https://pubmed.ncbi.nlm.nih.gov/21320997