المؤلفون: Alisa Mo, Afshin Saffari, Melanie Kellner, Marion Döbler‐Neumann, Catherine Jordan, Siddharth Srivastava, Bo Zhang, Mustafa Sahin, John K. Fink, Linsley Smith, Jennifer E. Posey, Katharine E. Alter, Camilo Toro, Craig Blackstone, Ariane G. Soldatos, Michelle Christie, Rebecca Schüle, Darius Ebrahimi‐Fakhari

المصدر: Movement disorders 37(12), 2440-2446 (2022). doi:10.1002/mds.29225
Mov Disord

مصطلحات موضوعية: Adult, cerebral palsy, Spastin, Adolescent, Spastic Paraplegia, Hereditary, childhood-onset movement disorders, Article, diagnosis [Spastic Paraplegia, Hereditary], Young Adult, Cross-Sectional Studies, Phenotype, Neurology, Muscle Spasticity, Child, Preschool, genetics [Spastic Paraplegia, Hereditary], Mutation, Humans, genetics [Spastin], SPAST, Neurology (clinical), ddc:610, hereditary spastic paraplegia, Child, neurogenetics

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fb27dd83920485e0a4b88794a230e52cTest
https://pub.dzne.de/record/165247Test

المؤلفون: Boston Children's Hospital - Children's Rare Disease Cohorts Initiative

المساهمون: Darius Ebrahimi-Fakhari, Principal Investigator

المصدر: Investigating the Genetic Basis of Hereditary Spastic Paraplegia

الوصول الحر: https://clinicaltrials.gov/ct2/show/NCT05354622Test

المؤلفون: CureAP4 Foundation

المساهمون: Darius Ebrahimi-Fakhari, Director, Movement Disorders Program

المصدر: Registry and Natural History Study for Early Onset Hereditary Spastic Paraplegia (HSP)

الوصول الحر: https://clinicaltrials.gov/ct2/show/NCT04712812Test