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Proceedings of the National Academy of Sciences of the United States of America
|
October 28, 1998
Phenotype-genotype studies in kuru: implications for new variant Creutzfeldt-Jakob disease
L Cervenáková, L G Goldfarb, R Garruto, et al.
Annales Francaises D'Anesthesie Et De Reanimation
|
January 1, 1989
[Incidence of headache after continuous spinal anesthesia: a prospective study]
E T Ang, D Kry, S Khon, et al.
Archives of Disease in Childhood
|
May 25, 2004
Lower respiratory tract illness and RSV prophylaxis in very premature infants
T Lacaze-Masmonteil, P Truffert, D Pinquier, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
October 1, 1993
Clinical heterogeneity and unusual presentations of Creutzfeldt-Jakob disease in Jewish patients with the PRNP codon 200 mutation
J Chapman, P Brown, L G Goldfarb, et al.
Neurology
|
August 23, 2000
Inherited prion encephalopathy associated with the novel PRNP H187R mutation: a clinical study
C M Bütefisch, P Gambetti, L Cervenakova, et al.
Genomics
|
February 1, 1991
Support of linkage of Gerstmann-Sträussler-Scheinker syndrome to the prion protein gene on chromosome 20p12-pter
M C Speer, D Goldgaber, L G Goldfarb, et al.
The American Journal of Tropical Medicine and Hygiene
|
March 1, 1980
An epidemiological model of Crimean hemorrhagic fever
L G Goldfarb, M P Chumakov, A A Myskin, et al.
Occupational and Environmental Medicine
|
January 12, 2023
Development of a job-exposure matrix (JEM) for exposure to smoke particle mass among firefighters of the Fire Department of the City of New York (FDNY)
David G Goldfarb, David J Prezant, Rachel Zeig-Owens, et al.
Acta Neuropathologica
|
March 11, 2005
The enlarging spectrum of desminopathies: new morphological findings, eastward geographic spread, novel exon 3 desmin mutation
Alexandra Vrabie, Lev G Goldfarb, Alexey Shatunov, et al.
Bratislavske Lekarske Listy
|
January 7, 2005
A case of Rett syndrome from Ukraine--clinical diagnosis confirmed by mutation analysis of the MECP2 gene
V Bzduch, D Zahorakova, E Grechanina, et al.
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Showing results (91-100 of 244) with videos related to
Sort By:
Page
of 25
Proceedings of the National Academy of Sciences of the United States of America
|
October 28, 1998
Phenotype-genotype studies in kuru: implications for new variant Creutzfeldt-Jakob disease
L Cervenáková, L G Goldfarb, R Garruto, et al.
Annales Francaises D'Anesthesie Et De Reanimation
|
January 1, 1989
[Incidence of headache after continuous spinal anesthesia: a prospective study]
E T Ang, D Kry, S Khon, et al.
Archives of Disease in Childhood
|
May 25, 2004
Lower respiratory tract illness and RSV prophylaxis in very premature infants
T Lacaze-Masmonteil, P Truffert, D Pinquier, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
October 1, 1993
Clinical heterogeneity and unusual presentations of Creutzfeldt-Jakob disease in Jewish patients with the PRNP codon 200 mutation
J Chapman, P Brown, L G Goldfarb, et al.
Neurology
|
August 23, 2000
Inherited prion encephalopathy associated with the novel PRNP H187R mutation: a clinical study
C M Bütefisch, P Gambetti, L Cervenakova, et al.
Genomics
|
February 1, 1991
Support of linkage of Gerstmann-Sträussler-Scheinker syndrome to the prion protein gene on chromosome 20p12-pter
M C Speer, D Goldgaber, L G Goldfarb, et al.
The American Journal of Tropical Medicine and Hygiene
|
March 1, 1980
An epidemiological model of Crimean hemorrhagic fever
L G Goldfarb, M P Chumakov, A A Myskin, et al.
Occupational and Environmental Medicine
|
January 12, 2023
Development of a job-exposure matrix (JEM) for exposure to smoke particle mass among firefighters of the Fire Department of the City of New York (FDNY)
David G Goldfarb, David J Prezant, Rachel Zeig-Owens, et al.
Acta Neuropathologica
|
March 11, 2005
The enlarging spectrum of desminopathies: new morphological findings, eastward geographic spread, novel exon 3 desmin mutation
Alexandra Vrabie, Lev G Goldfarb, Alexey Shatunov, et al.
Bratislavske Lekarske Listy
|
January 7, 2005
A case of Rett syndrome from Ukraine--clinical diagnosis confirmed by mutation analysis of the MECP2 gene
V Bzduch, D Zahorakova, E Grechanina, et al.
Page
of 25