Lev G. Goldfarb - Concepedia

Author

Lev G. Goldfarb

National Institute of Neurological Disorders and Stroke

Also Known As

Dieter O. Fürst, L G Goldfarb, L Goldfarb, L. G Goldfarb, L. G. GOLDFARB, L. G. Goldfarb, L. Goldfarb, L.G. Goldfarb, LEV G. GOLDFARB, LEV GOLDFARB

358

Publications

11.4K

Citations

H-Index

114

Concepts

All Affiliations

National Institute of Neurological Disorders and Stroke National Institutes of Health Bellvitge University Hospital Institut d'Investigació Biomédica de Bellvitge Sorbonne Université

About

Lev G. Goldfarb is an author at National Institute of Neurological Disorders and Stroke specializing in medicine, pathology, and genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	39	68	5.4K
2	Natural Sciences	7	7	400
3	Public Health	7	7	899
4	Health Sciences	3	3	93
5	Engineering	1	1	15

Lev G. Goldfarb

112

Publications

10.3K

Citations

H-Index

Page 1

	Year	Citations
Human spongiform encephalopathy: The national institutes of health series of 300 cases of experimentally transmitted disease Paul S. Brown, Clarence J. Gibbs, Pamela Rodgers‐Johnson, Annals of Neurology	1994	816
Fatal Familial Insomnia and Familial Creutzfeldt-Jakob Disease: Disease Phenotype Determined by a DNA Polymorphism Lev G. Goldfarb, Robert B. Petersen, Massimo Tabaton, Science	1992	716
Glycyl tRNA Synthetase Mutations in Charcot-Marie-Tooth Disease Type 2D and Distal Spinal Muscular Atrophy Type V Anthony Antonellis, Rachel E. Ellsworth, Nyamkhishig Sambuughin, The American Journal of Human Genetics Mendelian DisorderGenetic DisorderGeneticsMolecular BiologyDegenerative Disease	2003	555
Missense mutations in desmin associated with familial cardiac and skeletal myopathy Lev G. Goldfarb, Kyeyoon Park, Larisa Červen̆áková, Nature Genetics Missense MutationsCardiomyopathyMendelian DisorderGenetic DisorderSkeletal Myopathy	1998	503
Apolipoprotein E &isin;4 allele distributions in late-onset Alzheimer's disease and in other amyloid-forming diseases Ann M. Saunders, Allen D. Roses, Jeffery M. Vance, The Lancet Allele DistributionsAlzheimer's DiseaseApolipoprotein EGenetic EpidemiologyDegenerative Pathology	1993	500
Natural History of Fabry Renal Disease Mary H. Branton, Raphael Schiffmann, Sharda G. Sabnis, Medicine	2002	456
Desmin Myopathy, a Skeletal Myopathy with Cardiomyopathy Caused by Mutations in the Desmin Gene Marinos C. Dalakas, Kyeyoon Park, Cristina Semino‐Mora, New England Journal of Medicine	2000	449
Transmissible familial Creutzfeldt-Jakob disease associated with five, seven, and eight extra octapeptide coding repeats in the PRNP gene. Lev G. Goldfarb, Paul Brown, W. Richard McCombie, Proceedings of the National Academy of Sciences Neurodegenerative DiseasesMendelian DisorderCreutzfeldt-jakob DiseaseGenetic DisorderMedicine	1991	329
Distinct muscle imaging patterns in myofibrillar myopathies Dirk Fischer, Rudolf A. Kley, Katharina Strach, Neurology	2008	252
Myotilinopathy: refining the clinical and myopathological phenotype Montse Olivé, Lev G. Goldfarb, Dirk Fischer, Brain	2005	172

Page 1