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Lev G Goldfarb

Showing results (21-30 of 51) with videos related to

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Muscle & Nerve|November 25, 2010
Nemaline myopathy type 6: clinical and myopathological featuresMontse Olivé, Lev G Goldfarb, Hee-Suk Lee, 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.
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.
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.
Journal of Diabetes|December 14, 2011
Genetic variants in potassium channels are associated with type 2 diabetes in a Mongolian populationZagaa Odgerel, Hee S Lee, Narnygerel Erdenebileg, et al.
Human Genetics|July 29, 2003
Allelic variation at alcohol metabolism genes ( ADH1B, ADH1C, ALDH2) and alcohol dependence in an American Indian populationConnie J Mulligan, Robert W Robin, Michael V Osier, et al.
International Journal of Cardiology|August 8, 2006
Restrictive cardiomyopathy with atrioventricular conduction block resulting from a desmin mutationPiotr Pruszczyk, Anna Kostera-Pruszczyk, Alexey Shatunov, et al.
Muscle & Nerve|May 27, 2003
Respiratory insufficiency in desminopathy patients caused by introduction of proline residues in desmin c-terminal alpha-helical segmentAyush Dagvadorj, Bertrand Goudeau, David Hilton-Jones, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|October 13, 2006
Functional analyses of glycyl-tRNA synthetase mutations suggest a key role for tRNA-charging enzymes in peripheral axonsAnthony Antonellis, Shih-Queen Lee-Lin, Amy Wasterlain, et al.
Pageof 6

Showing results (21-30 of 51) with videos related to

Sort By:
Pageof 6
Muscle & Nerve|November 25, 2010
Nemaline myopathy type 6: clinical and myopathological featuresMontse Olivé, Lev G Goldfarb, Hee-Suk Lee, 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.
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.
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.
Journal of Diabetes|December 14, 2011
Genetic variants in potassium channels are associated with type 2 diabetes in a Mongolian populationZagaa Odgerel, Hee S Lee, Narnygerel Erdenebileg, et al.
Human Genetics|July 29, 2003
Allelic variation at alcohol metabolism genes ( ADH1B, ADH1C, ALDH2) and alcohol dependence in an American Indian populationConnie J Mulligan, Robert W Robin, Michael V Osier, et al.
International Journal of Cardiology|August 8, 2006
Restrictive cardiomyopathy with atrioventricular conduction block resulting from a desmin mutationPiotr Pruszczyk, Anna Kostera-Pruszczyk, Alexey Shatunov, et al.
Muscle & Nerve|May 27, 2003
Respiratory insufficiency in desminopathy patients caused by introduction of proline residues in desmin c-terminal alpha-helical segmentAyush Dagvadorj, Bertrand Goudeau, David Hilton-Jones, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|October 13, 2006
Functional analyses of glycyl-tRNA synthetase mutations suggest a key role for tRNA-charging enzymes in peripheral axonsAnthony Antonellis, Shih-Queen Lee-Lin, Amy Wasterlain, et al.
Pageof 6