- ICH GCP
- US Clinical Trials Registry
- Researchers
- Canada
- Chondrodysplasia Punctata, Rhizomelic
Medical specialists from Canada tagged as investigators in clinical trials studying Chondrodysplasia Punctata, Rhizomelic
Total 1 results
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Nancy E Braverman, MD, MSSeen in:
- Quebec, Montreal, Frederique Arnaud
- Quebec, Montreal, Research Institute of the McGill University Health Center
Trials:- NCT01668186 (Principal Investigator)
- NCT06190626 (Principal Investigator)
Conditions:- Peroxisome Biogenesis Disorder;
- Zellweger Spectrum Disorder;
- RCDP - Rhizomelic Chondrodysplasia Punctata;
- D-Bifunctional Protein Deficiency;
- Alpha-Methylacyl-CoA Racemase Deficiency;
- Peroxisomal Acyl-CoA Oxidase Deficiency;
- Peroxisomal Acyl-CoA Oxidase 2 Deficiency;
- ATP Binding Cassette Subfamily D Member 3 Gene Mutation;
- ACBD5 (AcylCoA Binding Domain 5) Deficiency;
- Adult Refsum Disease;
- Sterol Carrier Protein 2 Deficiency
Clinical Trials on Chondrodysplasia Punctata, Rhizomelic
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Nemours Children's ClinicRhizoKids InternationalRecruitingRCDP - Rhizomelic Chondrodysplasia Punctata | RCDP1 | RCDP2 | RCDP3 | RCDP4 | RCDP5United States
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MED-LIFE DISCOVERIES LPUnknown
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MED-LIFE DISCOVERIES LPBioPharma Services, IncRecruitingRhizomelic Chondrodysplasia PunctataCanada
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McGill University Health Centre/Research Institute...RecruitingPeroxisome Biogenesis Disorder | Zellweger Spectrum Disorder | RCDP - Rhizomelic Chondrodysplasia Punctata | D-Bifunctional Protein Deficiency | Alpha-Methylacyl-CoA Racemase Deficiency | Peroxisomal Acyl-CoA Oxidase Deficiency | Peroxisomal Acyl-CoA Oxidase 2 Deficiency | ATP Binding Cassette Subfamily... and other conditionsCanada
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ProgenaBiomeRecruitingPsoriasis | Psoriasis Vulgaris | Psoriasis of Scalp | Psoriatic Plaque | Psoriasis Universalis | Psoriasis Face | Psoriasis Nail | Psoriasis Diffusa | Psoriasis Punctata | Psoriasis Palmaris | Psoriasis Circinata | Psoriasis Annularis | Psoriasis Genital | Psoriasis GeographicaUnited States
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Foundation Fighting BlindnessRecruitingRetinitis Pigmentosa | Choroideremia | Usher Syndrome | Batten Disease | Leber Congenital Amaurosis | Goldmann-Favre Syndrome | Kearns-Sayre Syndrome | Retinal Disease | Bardet-Biedl Syndrome | Stargardt Disease | Cone Dystrophy | Retinoschisis | Achromatopsia | Gyrate Atrophy | Eye Diseases Hereditary | Bassen-Kornzweig... and other conditionsUnited States
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Sanford HealthNational Ataxia Foundation; Beyond Batten Disease Foundation; Pitt Hopkins Research... and other collaboratorsRecruitingMitochondrial Diseases | Retinitis Pigmentosa | Myasthenia Gravis | Eosinophilic Gastroenteritis | Multiple System Atrophy | Leiomyosarcoma | Leukodystrophy | Anal Fistula | Spinocerebellar Ataxia Type 3 | Friedreich Ataxia | Kennedy Disease | Lyme Disease | Hemophagocytic Lymphohistiocytosis | Spinocerebellar Ataxia... and other conditionsUnited States, Australia