L. G. Goldfarb - Concepedia

Author

L. G. Goldfarb

National Institute of Neurological Disorders and Stroke

Also Known As

L G Goldfarb, L Goldfarb, L. G. Goldfarb, L. Goldfarb, L.G. Goldfarb, LevG Goldfarb, LevG. Goldfarb

Publications

1.6K

Citations

H-Index

Concepts

All Affiliations

National Institute of Neurological Disorders and Stroke National Institutes of Health Tel Aviv University

About

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

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	9	9	511
2	Public Health	2	2	193
3	Molecular Biology	2	2	83
4	Molecular Genetics	2	2	193
5	Social Sciences	1	1	14

L. G. Goldfarb

Publications

904

Citations

H-Index

Page 1

	Year	Citations
Iatrogenic Creutzfeldt‐Jakob disease Paul A. Brown, Larisa Červen̆áková, L. G. Goldfarb, Neurology	1994	149
Creutzfeldt-Jacob disease associated with the PRNP codon 200LYS mutation: An analysis of 45 families L. G. Goldfarb, Paul Brown, E. Mitrov�, European Journal of Epidemiology Creutzfeldt-jacob DiseaseMendelian DisorderCreutzfeldt-jakob DiseaseGenetic DisorderMedicine	1991	128
Clinical heterogeneity and unusual presentations of Creutzfeldt-Jakob disease in Jewish patients with the PRNP codon 200 mutation. Joab Chapman, Paul Brown, L. G. Goldfarb, Journal of Neurology Neurosurgery & Psychiatry Creutzfeldt-jakob DiseaseNeurological DisorderGeneticsGenetic EpidemiologyPathology	1993	76
Clinical and molecular genetic study of a large German kindred with Gerstmann‐Straussler‐Scheinker syndrome Paul Brown, L. G. Goldfarb, W. Ted Brown, Neurology	1991	74
Clinical and genetic studies of fatal familial insomnia Anthony T. Reder, A. S. Mednick, Paul Brown, Neurology Fatal Familial InsomniaSleep DisordersGeneticsGenetic EpidemiologyNeurochemical Biomarkers	1995	71
A new (two‐repeat) octapeptide coding insert mutation in Creutzfeldt‐Jakob disease L. G. Goldfarb, Paul Brown, B W Little, Neurology	1993	70
Familial Creutzfeldt-Jakob disease with a five-repeat octapeptide insert mutation Elizabeth J. Cochran, David A. Bennett, Larisa Červen̆áková, Neurology	1996	69
The phenotypic expression of different mutations in transmissible familial Creutzfeldt-Jakob disease Paul Brown, L. G. Goldfarb, Clarence J. Gibbs, European Journal of Epidemiology Mendelian DisorderPhenotypic ExpressionCreutzfeldt-jakob DiseaseGenetic DisorderGenetics	1991	65
Fatal insomnia in a case of familial Creutzfeldt-Jakob disease with the codon 200 <sup>Lys</sup> mutation Joab Chapman, A Arlazoroff, L. G. Goldfarb, Neurology Creutzfeldt-jakob DiseaseGeneticsGenetic EpidemiologyPathologyFatal Insomnia	1996	61
Atypical Creutzfeldt‐Jakob disease in an American family with an insert mutation in the PRNP amyloid precursor gene P. Brown, L. G. Goldfarb, W. Richard McCombie, Neurology Creutzfeldt-jakob DiseaseGeneticsGenetic EpidemiologyPathologyNeurochemical Biomarkers	1992	59

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