Cure Research for Niemann-Pick disease

Cure Research discussion for Niemann-Pick disease:

The gene that is altered in the majority of patients with type C (and D) was identified by investigators at NINDS. A second (different) gene that is mutated in a minority of patients with type C Niemann-Pick disease was discovered in 2000. (Source: excerpt from NINDS Niemann-Pick Disease Information Page: NINDS)

Clinical Trials for Niemann-Pick disease

Some of the clinical trials for Niemann-Pick disease include:

• Study of Pulmonary Complications in Pediatric Patients With Storage Disorders Undergoing Allogeneic Hematopoietic Stem Cell Transplantation - This study is no longer recruiting patients (Current: 23 Nov 2006)
• PET Scan of Brain Metabolism in Relation to Age and Disease - This study has been completed (Current: 23 Nov 2006) - 15 O Water
• Saccadic Eye Movements in Patients With Niemann-Pick Type C Disease - This study is no longer recruiting patients (Current: 23 Nov 2006) - OGT918
• Stem Cell Transplant for Inborn Errors of Metabolism - This study is currently recruiting patients (Current: 23 Nov 2006) - Busulfan,Cyclophosphamide,ATG
• Evaluation of Biochemical Markers and Clinical Investigation of Niemann-Pick Disease, Type C - This study is currently recruiting patients (Current: 23 Nov 2006)
• more trials...»

Evidence Based Medicine Research for Niemann-Pick disease

Medical research papers related to Niemann-Pick disease include:

• Niemann-Pick Disease (Diagnosis)
• Niemann-Pick Disease (Follow-up)
• Niemann-Pick Disease (Treatment)
• Niemann-Pick Disease (Overview)
• Niemann-Pick Disease (Follow-up)
• Niemann-Pick Disease (Diagnosis)
• Niemann-Pick Disease (Treatment)
• Niemann-Pick Disease (Overview)
• Niemann-Pick Syndrome
• Beta Hex Deficiency
• Inborn Errors of Metabolism in Infancy and Early Childhood: An Update
• Gastrointestinal History and Examination
• Lysosomal Storage Disease (Overview)
• Generalised Lymphadenopathy
• Splenomegaly (Diagnosis)
• Lipid Storage Disorders (Diagnosis)
• Lymphadenopathy (Diagnosis)
• Lymphadenopathy (Overview)
• Lipid Storage Disorders (Follow-up)
• Lymphadenitis (Follow-up)
• Lymphadenopathy (Treatment)
• Mongolian Spot (Overview)
• Lymphadenopathy (Follow-up)
• Lymphadenitis (Treatment)
• Lymphadenitis (Diagnosis)
• Gaucher Disease (Diagnosis)
• Lipid Storage Disorders (Treatment)
• GM1 Gangliosidosis (Overview)
• Glycogen-Storage Disease Type I (Diagnosis)
• Splenomegaly (Diagnosis)

Click here to find more evidence-based articles on the TRIP Database

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