James V. Leonard - Concepedia

Author

James V. Leonard

University College London

Also Known As

, J Leonard, J V LEONARD, J V Leonard, J. LEONARD, J. Leonard, J. V. LEONARD, J. V. Leonard, J.V Leonard, J.V. Leonard

1.2K

Publications

11.5K

Citations

H-Index

167

Concepts

All Affiliations

University College London Great Ormond Street Hospital Institute of Child Health National Hospital for Neurology and Neurosurgery The Royal Free Hospital

About

James V. Leonard is an author at University College London specializing in medicine, pathology, and metabolism.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	42	74	5.7K
2	Health Sciences	12	12	604
3	Arts	1	1	12
4	Education	1	1	12
5	Engineering	1	1	21

James V. Leonard

118

Publications

8.2K

Citations

H-Index

Page 1

	Year	Citations
A Lethal Defect of Mitochondrial and Peroxisomal Fission Hans R. Waterham, Janet Koster, Carlo W.T. van Roermund, New England Journal of Medicine MitophagyGeneticsMolecular BiologyOxidative StressMitochondrial Biogenesis	2007	739
Glycogen storage disease type I: diagnosis, management, clinical course and outcome. Results of the European Study on Glycogen Storage Disease Type I (ESGSD I) Jan Peter Rake, Gepke Visser, Philippe Labrune, European Journal of Pediatrics Clinical CourseInherited Metabolic DiseaseDiabetesEuropean StudyMedicine	2002	320
Glycogen storage disease type I: diagnosis, management, clinical course and outcome. Results of the European study on glycogen storage disease type I (ESGSD I) Jan Peter Rake, Gepke Visser, Philippe Labrune, European Journal of Pediatrics Clinical CourseInherited Metabolic DiseaseDiabetesEuropean StudyMedicine	2002	294
Natural History, Outcome, and Treatment Efficacy in Children and Adults with Glutaryl-CoA Dehydrogenase Deficiency Stefan Kölker, Sven F. Garbade, Cheryl R. Greenberg, Pediatric Research NutritionMetabolic DisorderPediatric HematologyTreatment EfficacyHematology	2006	266
Neutropenia, neutrophil dysfunction, and inflammatory bowel disease in glycogen storage disease type Ib: Results of the European Study on Glycogen Storage Disease Type I Gepke Visser, J. P. Rake, John Fernandes, The Journal of Pediatrics GastroenterologyPathologyClinical GastroenterologyNeutrophil DysfunctionUlcerative Colitis	2000	253
Impaired endothelial function occurs in the systemic arteries of children with homozygous homocystinuria but not in their heterozygous parents David S. Celermajer, Keld E. Sørensen, Michael Ryalls, Journal of the American College of Cardiology Homozygous HomocystinuriaVascular DiseasePhysiologyEndothelial DysfunctionPediatrics	1993	252
Guidelines for management of glycogen storage disease type I—European study on glycogen storage disease type I (ESGSD I) Jan Peter Rake, Gepke Visser, Philippe Labrune, European Journal of Pediatrics Global HealthInherited Metabolic DiseaseClinical EpidemiologyPublic HealthMedicine	2002	196
The mutation spectrum of the facilitative glucose transporter gene SLC2A2 (GLUT2) in patients with Fanconi-Bickel syndrome René Santer, Sebastian Groth, Martina Kinner, Human Genetics Mendelian DisorderGenetic DisorderGeneticsInherited Metabolic DiseaseDiabetes	2001	170
Guideline for the diagnosis and management of glutaryl‐CoA dehydrogenase deficiency (glutaric aciduria type I) S. Kölker, E. Christensen, James V. Leonard, Journal of Inherited Metabolic Disease	2007	145
A Missense Mutation of Cytochrome Oxidase Subunit II Causes Defective Assembly and Myopathy Shamima Rahman, Jan‐Willem Taanman, Jonathan M. Cooper, The American Journal of Human Genetics Mendelian DisorderMitochondrial FunctionGenetic DisorderGeneticsMissense Mutation	1999	139

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