Research Impact

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Research impact score

Publications

0

Total publications

Trial Results

0

Published trial results

Citations

0

Total citations

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Trial Phases

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Trial Status

Recruiting1

Role Distribution

Other Roles1

Activity Timeline

Clinical Trials (1)

NCT01403402Recruiting

Congenital Muscle Disease Study of Patient and Family Reported Medical Information

Alpha-Dystroglycanopathy (Congenital Muscular Dystrophy and Abnormal Glycosylation of Dystroglycan With Severe Epilepsy)Alpha-Dystroglycanopathy (Congenital Muscular Dystrophy With Fatty Liver and Infantile-onset Cataract Caused by TRAPPC11 Mutations)Alpha-Dystroglycanopathy (Congenital Muscular Dystrophy With Hypoglycosylation of Dystroglycan and Epilepsy)+49 more

StudychairStart date: 2009-09-01

Research Network

Collaboration Network

1 collaborators·0 connections

Network Legend

KOL

Current Investigator

CO

High-influence Collaborator

CO

Collaborator

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Research Areas & Affiliations

Therapeutic Areas

Alpha-Dystroglycanopathy (Congenital Muscular Dystrophy and Abnormal Glycosylation of Dystroglycan With Severe Epilepsy)1 Alpha-Dystroglycanopathy (Congenital Muscular Dystrophy With Fatty Liver and Infantile-onset Cataract Caused by TRAPPC11 Mutations)1 Alpha-Dystroglycanopathy (Congenital Muscular Dystrophy With Hypoglycosylation of Dystroglycan)1 Alpha-Dystroglycanopathy (Congenital Muscular Dystrophy With Hypoglycosylation of Dystroglycan and Epilepsy)1 Alpha-Dystroglycanopathy (Dystroglycanopathy, Congenital With or Without Mental Retardation (Formerly MDC1C))1 Alpha-Dystroglycanopathy (Fukuyama CMD)1 Alpha-Dystroglycanopathy (LGMDR09 FKRP Related (Formerly LGMD2I))1 Alpha-Dystroglycanopathy (LGMDR11 POMT1 Related (Formerly LGMD2K))1

Affiliations

CureCMD, CMDIR

Similar Key Opinion Leaders

Discover other key opinion leaders with similar research profiles, therapeutic areas, and collaboration networks.

10 similar investigators found

Céline BONNYAUD, PhD

Laboratoire d'analyse du mouvement, Service d'explorations fonctionnelles, Hôpital Raymond Poincaré, APHP

Shared therapeutic areas:

Muscular Dystrophies, Limb-Girdle

Similarity Score1%

Simon Edvardson

Hadassah Medical Organization

Shared therapeutic areas:

Myasthenic Syndromes, Congenital

Similarity Score1%

William J. Powers, MD

University of North Carolina

Shared therapeutic areas:

Muscular Dystrophies, Limb-Girdle

Similarity Score1%

Sofie T Østergaard, Bsc.

Copenhagen Neuromuscular Center, Department of Neurology, Rigshospitalet, Copenhagen University

Shared therapeutic areas:

Muscular Dystrophies, Limb-Girdle

Similarity Score1%

Jayashri Srinivasan, MD,MCRP,PhD

Lahey Clinic

Shared therapeutic areas:

Myasthenic Syndromes, Congenital

Similarity Score1%

Ricardo Maselli, MD

University of California, Davis

Shared therapeutic areas:

Myasthenic Syndromes, Congenital

Similarity Score1%

Jerry R. Mendell, M.D.

Nationwide Children's Hospital

Shared therapeutic areas:

Muscular Dystrophies, Limb-Girdle

Similarity Score1%

Kjell Arne Arntzen, ph.d

University Hospital of North Norway

Shared therapeutic areas:

Muscular Dystrophies, Limb-Girdle

Similarity Score1%

Cristobal Passalacqua, MD

PTC Therapeutics

Shared therapeutic areas:

Muscular Dystrophies, Limb-Girdle

Similarity Score1%

Samuel POUPLIN

Plateforme Nouvelles Technologies, Hôpital Raymond Poincaré, APHP

Shared therapeutic areas:

Muscular Dystrophies, Limb-Girdle

Similarity Score1%

Publications (0)

No publications found for this investigator.

Clinical Trials (1)

Showing 1 of 1 trials

NCT01403402StudyChair

Congenital Muscle Disease Study of Patient and Family Reported Medical Information

Alpha-Dystroglycanopathy (Congenital Muscular Dystrophy and Abnormal Glycosylation of Dystroglycan With Severe Epilepsy)Alpha-Dystroglycanopathy (Congenital Muscular Dystrophy With Fatty Liver and Infantile-onset Cataract Caused by TRAPPC11 Mutations)Alpha-Dystroglycanopathy (Congenital Muscular Dystrophy With Hypoglycosylation of Dystroglycan and Epilepsy)+49 more

Recruiting

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