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G Goldfarb

Showing results (151-160 of 244) with videos related to

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Annals of the American Thoracic Society|March 24, 2023
Association of Lung Function Decline with All-Cause and Cancer-Cause Mortality after World Trade Center Dust ExposureDavid G Goldfarb, Charles B Hall, Jaeun Choi, et al.
Muscle & Nerve|November 25, 2010
Nemaline myopathy type 6: clinical and myopathological featuresMontse Olivé, Lev G Goldfarb, Hee-Suk Lee, et al.
European Journal of Immunogenetics : Official Journal of the British Society for Histocompatibility and Immunogenetics|June 9, 2004
Evaluating association and transmission of eight inflammatory genes with Viliuisk encephalomyelitis susceptibilityT K Oleksyk, L G Goldfarb, T Sivtseva, et al.
Clinical Genetics|July 25, 2000
Sporadic cardiac and skeletal myopathy caused by a de novo desmin mutationK Y Park, M C Dalakas, C Semino-Mora, et al.
Neurology|April 1, 1998
Creutzfeldt-Jakob disease in a husband and wifeP Brown, L Cervenáková, L McShane, et al.
Anesthesiology|February 26, 2005
Screening of the entire ryanodine receptor type 1 coding region for sequence variants associated with malignant hyperthermia susceptibility in the north american populationNyamkhishig Sambuughin, Heather Holley, Sheila Muldoon, et al.
European Neurology|October 12, 2012
Clinical and myopathological characteristics of desminopathy caused by a mutation in desmin tail domainPaul Maddison, Maxwell S Damian, Caroline Sewry, et al.
Neuromuscular Disorders : NMD|May 13, 2009
Severe infantile-onset cardiomyopathy associated with a homozygous deletion in desminGerard Piñol-Ripoll, Alexey Shatunov, Ana Cabello, et al.
Annals of Neurology|March 1, 1992
Creutzfeldt-Jakob disease cosegregates with the codon 178Asn PRNP mutation in families of European originL G Goldfarb, P Brown, M Haltia, et al.
BMC Neurology|March 22, 2013
Exome sequencing identifies titin mutations causing hereditary myopathy with early respiratory failure (HMERF) in families of diverse ethnic originsCamilo Toro, Montse Olivé, Marinos C Dalakas, et al.
Pageof 25

Showing results (151-160 of 244) with videos related to

Sort By:
Pageof 25
Annals of the American Thoracic Society|March 24, 2023
Association of Lung Function Decline with All-Cause and Cancer-Cause Mortality after World Trade Center Dust ExposureDavid G Goldfarb, Charles B Hall, Jaeun Choi, et al.
Muscle & Nerve|November 25, 2010
Nemaline myopathy type 6: clinical and myopathological featuresMontse Olivé, Lev G Goldfarb, Hee-Suk Lee, et al.
European Journal of Immunogenetics : Official Journal of the British Society for Histocompatibility and Immunogenetics|June 9, 2004
Evaluating association and transmission of eight inflammatory genes with Viliuisk encephalomyelitis susceptibilityT K Oleksyk, L G Goldfarb, T Sivtseva, et al.
Clinical Genetics|July 25, 2000
Sporadic cardiac and skeletal myopathy caused by a de novo desmin mutationK Y Park, M C Dalakas, C Semino-Mora, et al.
Neurology|April 1, 1998
Creutzfeldt-Jakob disease in a husband and wifeP Brown, L Cervenáková, L McShane, et al.
Anesthesiology|February 26, 2005
Screening of the entire ryanodine receptor type 1 coding region for sequence variants associated with malignant hyperthermia susceptibility in the north american populationNyamkhishig Sambuughin, Heather Holley, Sheila Muldoon, et al.
European Neurology|October 12, 2012
Clinical and myopathological characteristics of desminopathy caused by a mutation in desmin tail domainPaul Maddison, Maxwell S Damian, Caroline Sewry, et al.
Neuromuscular Disorders : NMD|May 13, 2009
Severe infantile-onset cardiomyopathy associated with a homozygous deletion in desminGerard Piñol-Ripoll, Alexey Shatunov, Ana Cabello, et al.
Annals of Neurology|March 1, 1992
Creutzfeldt-Jakob disease cosegregates with the codon 178Asn PRNP mutation in families of European originL G Goldfarb, P Brown, M Haltia, et al.
BMC Neurology|March 22, 2013
Exome sequencing identifies titin mutations causing hereditary myopathy with early respiratory failure (HMERF) in families of diverse ethnic originsCamilo Toro, Montse Olivé, Marinos C Dalakas, et al.
Pageof 25