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Found 25 studies with search of: | "leukoencephalopathy with vanishing white matter" OR "Hereditary Central Nervous System Demyelinating Diseases" |
Rank | Status | Study | ||||
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1 | Active, not recruiting |
Study of Pulmonary Complications in Pediatric Patients With Storage Disorders Undergoing Allogeneic Hematopoietic Stem Cell Transplantation
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2 | Recruiting |
Oral Glyceryl Triacetate (GTA) in Newborns With Canavan
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3 | Completed |
Stem Cell Transplant for Inborn Errors of Metabolism
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4 | Active, not recruiting |
GTA-Glyceryltriacetate for Canavan Disease
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5 | Enrolling by invitation |
Compassionate Use of Metazym in Patients With Late Infantile Metachromatic Leukodystrophy
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6 | Completed |
Phase III Randomized, Double-Blind, Placebo-Controlled Study of Dehydroepiandrosterone Replacement for Primary Adrenal Insufficiency
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7 | Recruiting |
Study of Glyceryl Trierucate and Glyceryl Trioleate (Lorenzo's Oil) Therapy in Male Children With Adrenoleukodystrophy
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8 | Completed |
Survey in Patients With Chronic Adrenal Insufficiency in Germany
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9 | Completed |
Study of Oral Cholic Acid in Patients With Inborn Errors of Bile Acid Synthesis
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10 | Recruiting |
The Natural History of Metachromatic Leukodystrophy
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11 | Recruiting |
Adrenal Function After Living Kidney Donation
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12 | Completed |
Long-Term Metazym Treatment of Patients With Late Infantile Metachromatic Leukodystrophy (MLD)
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13 | Not yet recruiting |
Study of Bile Acids in Patients With Peroxisomal Disorders
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14 | Recruiting |
Clinical Study and Gene Mutation Analysis of Adrenoleukodystrophy in Taiwanese Children
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15 | Recruiting |
HSCT for High Risk Inherited Inborn Errors
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16 | Suspended |
Lithium and Acetate for Canavan Disease
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17 | Completed |
Randomized Study of Beta Interferon and Thalidomide in Patients With Adrenoleukodystrophy
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18 | Completed |
Diagnostic and Screening Study of Genetic Disorders
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19 | Completed |
Metazym for the Treatment of Patients With Late Infantile Metachromatic Leukodystrophy (MLD)
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20 | Recruiting |
Hematopoietic Stem Cell Transplantation (HCT) for Inborn Errors of Metabolism
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