المؤلفون: Esmaeilzadeh, Niloofar, aref, parissa, Ashrafi, Mahmoud Reza, Ardakani, Hossein Shojaaldini, Seraj, Bahman

المصدر: Iranian Journal of Child Neurology; Vol. 16 No. 1 (2022): winter; 135-142 ; 2008-0700 ; 1735-4668

مصطلحات موضوعية: Hereditary sensory and autonomic neuropathy, Oral ulcer, Self-mutilation

وصف الملف: application/pdf

العلاقة: https://journals.sbmu.ac.ir/ijcn/article/view/32016/28114Test; https://journals.sbmu.ac.ir/ijcn/article/view/32016Test

الإتاحة: https://doi.org/10.22037/ijcn.v15i4.32016Test
https://journals.sbmu.ac.ir/ijcn/article/view/32016Test

المصدر: Natural History of Familial Dysautonomia

الوصول الحر: https://clinicaltrials.gov/ct2/show/NCT03920774Test

المساهمون: Florian Eichler, Assistant Professor of Neurology

المصدر: Garofalo K, Penno A, Schmt BP, Lee HJ, Frosch MP, von Eckardste A, Brown RH, Hornemann T, Ehler FS. Oral L-sere supplementatn reduces productn of neurotox deoxysphgols me and humans wh heredary sensory autonom neuropathy type 1. J Cl vest. 2011 Dec;121(12):4735-45. do 10.1172/JC7549.
A Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Efficacy of L-Serine in Subjects With Hereditary Sensory Neuropathy Type 1

الوصول الحر: https://clinicaltrials.gov/ct2/show/NCT01733407Test

المؤلفون: National Ataxia Foundation, International WAGR Syndrome Association, 4p- Support Group, ML4 Foundation, Cornelia de Lange Syndrome Foundation, Stickler Involved People, Kawasaki Disease Foundation, Klippel-Feil Syndrome Alliance, Klippel-Feil Syndrome Freedom, Hyperacusis Research Limited, Hypersomnia Foundation, Kabuki Syndrome Network, Kleine-Levin Syndrome Foundation, Leiomyosarcoma Direct Research Foundation, Marinesco-Sjogren Syndrome Support Group - NORD, Mucolipidosis Type IV (ML4) Foundation, People with Narcolepsy 4 People with Narcolepsy (PWN4PWN), Soft Bones Incorporated, American Multiple Endocrine Neoplasia Support, Atypical Hemolytic Uremic Syndrome Foundation, All Things Kabuki, Wiedemann-Steiner Syndrome Foundation, Breast Implant Victim Advocates, PROS Foundation, American Behcet's Disease Association, Alstrom United Kingdom, Athymia, Curing Retinal Blindness Foundation, HSAN1E Society, 1p36 Deletion Support and Awareness, The Alagille Syndrome Alliance, Autoinflammatory Alliance, Beyond Batten Disease Foundation, Bohring-Opitz Syndrome Foundation, INC, Cockayne Syndrome Network (Share and Care), CRMO Foundation, Cure VCP Disease,INC, FOD Support, Cystinosis Research Foundation, Global DARE Foundation, Hypnic Jerk-Sleep Myoclonus Support Group, Jansen's Foundation, KCNMA1 Channelopathy International Advocacy Foundation, Kawasaki Disease Foundation Australia, Life with LEMS Foundation, Lowe Syndrome Association, The Malan Syndrome Foundation, Maple Syrup Urine Disease Family Support Group, International Association for Muscle Glycogen Storage Disease (IamGSD), Myhre Syndrome Foundation, DNM1 Families, Nicolaides Baraitser Syndrome (NCBRS) Worldwide Foundation, The PBCers Organization, Pitt Hopkins Research Foundation, Recurrent Meningitis Association, Recurrent Respiratory Papillomatosis Foundation, Remember the Girls, Smith-Kingsmore Syndrome Foundation, SPG Research Foundation, Team Telomere, Transient Global Amnesia Project, The Charlotte & Gwenyth Gray Foundation, The Cute Syndrome Foundation, The Maddi Foundation, White Sutton Syndrome Foundation, Zmynd11 Gene Disorder, Cauda Equina Foundation, Inc, Tango2 Research Foundation, Noah's Hope - Hope4Bridget Foundation, Project Sebastian, SMC1A Epilepsy Foundation, International Foundation for Gastrointestinal Disorders, Endosalpingiosis Foundation, Inc, International Sacral Agenesis/Caudal Regression Association (ISACRA), Scheuermann's Disease Fund, Batten Disease Support and Research Association, Kennedy's Disease Association, Cure Mito Foundation, Warburg Micro Research Foundation, Cure Mucolipidosis, Riaan Research Initiative, CureARS A NJ Nonprofit Corporation, CACNA1H Alliance, IMBS Alliance, SHINE-Syndrome Foundaion, Non- Ketotic Hyperglycinemia (NKH) Crusaders, Hypertrophic Olivary Degeneration Association (HODA), National Organization for Disorders of the Corpus Callosum (NODCC), Team4Travis, Taylor's Tale Foundation, Lambert Eaton (LEMS) Family Association, BARE Inc, STAG1 Gene Foundation, Coffin Lowry Syndrome Foundation, BLFS Incorporate, Aniridia North America, Cure Blau Syndrome Foundation, ARG1D Foundation, CURE HSPB8 Myopathy, International Society of Mannosidosis and Related Disorders, TBX4Life, Cure DHDDS, MANDKind Foundation, Krishnan Family Foundation, SPATA Foundation

المصدر: Coordination of Rare Diseases at Sanford

الوصول الحر: https://clinicaltrials.gov/ct2/show/NCT01793168Test

Other URLs: http://www.sanfordresearch.org/SpecialPrograms/cordsTest/
https://cordsconnect.sanfordresearch.org/BayaPES/sf/screeningForm?id=SFSFLTest#
https://cordsconnect.sanfordresearch.org/BayaPES/pp/participantLoginTest#