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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
Genetics of Charcot Marie Tooth (CMT) - Modifiers of CMT1A, New Causes of CMT2Charcot-Marie-Tooth disease, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, central nervous system malformation, hereditary disease, hereditary motor and sensory neuropathy, inherited neurodegenerative disorder, nervous system disorder, neurodegenerative disease, neuromuscular disease, peripheral nervous system disorder, polyneuropathyRecruitingNot stated2025-10-07NCT01193088

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22 results · Page 1 of 1

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Research sitesCityCountryLinked trials
C. Besta Neurological InstituteMilanItaly1
Cedars-Sinai Medical CenterLos AngelesUnited States392
Children's Hospital of PhiladelphiaPhiladelphiaUnited States434
Children's Hospital of WestmeadSydneyAustralia1
Connecticut Children's Medical CenterHartfordUnited States106
Dubowitz Neuromuscular CentreLondonUnited Kingdom1
Harvard/Massachusetts General HospitalBostonUnited States2
Houston Methodist HospitalHoustonUnited States260
Johns Hopkins UniversityBaltimoreUnited States60
National Hospital of Neurology and NeurosurgeryLondonUnited Kingdom2
Seattle Children's HospitalSeattleUnited States281
St. Jude Children's Research HospitalMemphisUnited States194
Stanford UniversityPalo AltoUnited States161
The Hospital For Sick ChildrenTorontoCanada94
University Of Colorado HospitalAuroraUnited States106
University of IowaIowa CityUnited States284
University of MiamiMiamiUnited States327
University of MichiganAnn ArborUnited States538
University of MinnesotaMaple GroveUnited States1
University of North CarolinaChapel HillUnited States101
University of PennsylvaniaPhiladelphiaUnited States507
University of RochesterRochesterUnited States360