Page 1 of Clinical Trials for "Hereditary Central Nervous System Demyelinating Diseases", 37 Total Matches
- 1RecruitingLast Updated: February 21, 2012Condition(s): Leukodystrophy, Metachromatic; Hereditary Central Nervous System Demyelinating Diseases; Brain Diseases, Metabolic, Inborn; Sphingolipidoses; Lysosomal Storage Diseases, Nervous System
- 2RecruitingLast Updated: February 6, 2012Condition(s): Lysosomal Storage Diseases; Krabbe Disease
- 3Active, not recruitingLast Updated: June 23, 2005Condition(s): I Cell Disease; Fucosidosis; Globoid Cell Leukodystrophy; Adrenoleukodystrophy; Mannosidosis; Niemann-Pick Disease; Pulmonary Complications; Mucopolysaccharidosis I; Mucopolysaccharidosis VI; Metachromatic Leukodystrophy; Gaucher's Disease; Wolman Disease
- 4RecruitingLast Updated: June 20, 2011Condition(s): Canavan Disease
- 5CompletedLast Updated: June 14, 2011Condition(s): Adrenoleukodystrophy; Metachromatic Leukodystrophy; Globoid Cell Leukodystrophy; Gaucher's Disease; Fucosidosis; Wolman Disease; Niemann-Pick Disease; Batten Disease; GM1 Gangliosidosis; Tay Sachs Disease; Sandhoff Disease
- 6Active, not recruitingLast Updated: March 29, 2012Condition(s): Pelizaeus-Merzbacher Disease
- 7WithdrawnLast Updated: October 6, 2010Condition(s): Leukodystrophy, Globoid Cell
- 8Active, not recruitingLast Updated: August 11, 2006Condition(s): Infantile Canavan Disease; Deficiency Disease, Aspartoacylase
- 9TerminatedLast Updated: March 16, 2012Condition(s): Late Infantile Metachromatic Leukodystrophy
- 10RecruitingLast Updated: June 15, 2009Condition(s): Adrenoleukodystrophy
- 11CompletedLast Updated: September 21, 2011Condition(s): Infantile Refsum's Disease; Zellweger Syndrome; Adrenoleukodystrophy; Peroxisomal Disorders; Cholestasis
- 12RecruitingLast Updated: November 21, 2011Condition(s): Late Infantile Metachromatic Leukodystrophy
- 13Active, not recruitingLast Updated: April 3, 2012Condition(s): Leukodystrophy, Metachromatic
- 14RecruitingLast Updated: January 6, 2011Condition(s): Metachromatic Leukodystrophy
- 15Active, not recruitingLast Updated: July 8, 2011Condition(s): Pelizaeus-Merzbacher Disease; PMD
- 16CompletedLast Updated: December 3, 2008Condition(s): Late Infantile Metachromatic Leukodystrophy
- 17RecruitingLast Updated: April 4, 2012Condition(s): Mucopolysaccharidosis; Hurler Syndrome; Hunter Syndrome; Maroteaux-Lamy Syndrome; Sly Syndrome; Alpha Mannosidosis; Fucosidosis; Aspartylglucosaminuria; Adrenoleukodystrophy (ALD); Globoid Cell Leukodystrophy (GLD); Krabbe Disease; Metachromatic Leukodystrophy (MLD); Sphingolipidoses; Peroxisomal Disorders
- 18Not yet recruitingLast Updated: June 23, 2005Condition(s): Infantile Refsum's Disease; Zellweger Syndrome; Bifunctional Enzyme Deficiency; Adrenoleukodystrophy
- 19RecruitingLast Updated: February 6, 2009Condition(s): Adrenoleukodystrophy
- 20RecruitingLast Updated: April 17, 2012Condition(s): Hematological Malignancies; Certain Lysosomal Storage and Peroxisomal Enzyme Deficiency Disorders; Hurler Syndrome (MPS I); Krabbe Disease (Globoid Leukodystrophy); X-linked Adrenoleukodystrophy; Primary Immunodeficiency Diseases; Bone Marrow Failure; Beta-thalassemia
Clinical Trials content is provided directly by the U.S. National Institutes of Health via ClinicalTrials.gov and is not reviewed separately by ClinicalTrialsFeeds.org. Every page of specific clinical trials information contains a unique identifier which can be used to find further details directly from the National Institutes of Health.
The URL of this page is: http://clinicaltrialsfeeds.org/clinical-trials/results/?cond=%22Hereditary+Central+Nervous+System+Demyelinating+Diseases%22
