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Neuromuscular Disorders : NMD
|
August 30, 2001
Identification and functional characterization of a novel ryanodine receptor mutation causing malignant hyperthermia in North American and South American families
N Sambuughin, T E Nelson, J Jankovic, et al.
Journal of Medical Genetics
|
November 10, 2000
Desmin splice variants causing cardiac and skeletal myopathy
K Y Park, M C Dalakas, H H Goebel, et al.
Neuromuscular Disorders : NMD
|
October 25, 2008
Transcription-terminating mutation in telethonin causing autosomal recessive muscular dystrophy type 2G in a European patient
Montse Olivé, Alexey Shatunov, Laura Gonzalez, et al.
CA: a Cancer Journal for Clinicians
|
March 24, 2022
Cancer risk among World Trade Center rescue and recovery workers: A review
Paolo Boffetta, Charles B Hall, Andrew C Todd, et al.
Annals of Neurology
|
May 1, 1994
Human spongiform encephalopathy: the National Institutes of Health series of 300 cases of experimentally transmitted disease
P Brown, C J Gibbs, P Rodgers-Johnson, et al.
Amyotrophic Lateral Sclerosis : Official Publication of the World Federation of Neurology Research Group on Motor Neuron Diseases
|
May 5, 2009
Mutational analysis of glycyl-tRNA synthetase (GARS) gene in Hirayama disease
Sergiu C Blumen, Vivian E Drory, Menachem Sadeh, et al.
European Journal of Epidemiology
|
September 1, 1991
Creutzfeldt-Jacob disease associated with the PRNP codon 200Lys mutation: an analysis of 45 families
L G Goldfarb, P Brown, E Mitrovà, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
October 24, 1995
Nonsense mutation in the phosphofructokinase muscle subunit gene associated with retention of intron 10 in one of the isolated transcripts in Ashkenazi Jewish patients with Tarui disease
O Vasconcelos, K Sivakumar, M C Dalakas, et al.
The Journal of Infectious Diseases
|
September 1, 1993
Belgrade virus, a cause of hemorrhagic fever with renal syndrome in the Balkans, is closely related to Dobrava virus of field mice
A M Taller, S Y Xiao, M S Godec, et al.
Bone Marrow Transplantation
|
December 5, 2025
Age 60 or older is an independent predictor of outcomes after thiotepa-based autologous transplant in primary CNS lymphoma: a CIBMTR analysis
Neela Easton, David G Goldfarb, Ahmed El-Naas, et al.
Page
of 25
Search research articles
Search
Showing results (141-150 of 244) with videos related to
Sort By:
Page
of 25
Neuromuscular Disorders : NMD
|
August 30, 2001
Identification and functional characterization of a novel ryanodine receptor mutation causing malignant hyperthermia in North American and South American families
N Sambuughin, T E Nelson, J Jankovic, et al.
Journal of Medical Genetics
|
November 10, 2000
Desmin splice variants causing cardiac and skeletal myopathy
K Y Park, M C Dalakas, H H Goebel, et al.
Neuromuscular Disorders : NMD
|
October 25, 2008
Transcription-terminating mutation in telethonin causing autosomal recessive muscular dystrophy type 2G in a European patient
Montse Olivé, Alexey Shatunov, Laura Gonzalez, et al.
CA: a Cancer Journal for Clinicians
|
March 24, 2022
Cancer risk among World Trade Center rescue and recovery workers: A review
Paolo Boffetta, Charles B Hall, Andrew C Todd, et al.
Annals of Neurology
|
May 1, 1994
Human spongiform encephalopathy: the National Institutes of Health series of 300 cases of experimentally transmitted disease
P Brown, C J Gibbs, P Rodgers-Johnson, et al.
Amyotrophic Lateral Sclerosis : Official Publication of the World Federation of Neurology Research Group on Motor Neuron Diseases
|
May 5, 2009
Mutational analysis of glycyl-tRNA synthetase (GARS) gene in Hirayama disease
Sergiu C Blumen, Vivian E Drory, Menachem Sadeh, et al.
European Journal of Epidemiology
|
September 1, 1991
Creutzfeldt-Jacob disease associated with the PRNP codon 200Lys mutation: an analysis of 45 families
L G Goldfarb, P Brown, E Mitrovà, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
October 24, 1995
Nonsense mutation in the phosphofructokinase muscle subunit gene associated with retention of intron 10 in one of the isolated transcripts in Ashkenazi Jewish patients with Tarui disease
O Vasconcelos, K Sivakumar, M C Dalakas, et al.
The Journal of Infectious Diseases
|
September 1, 1993
Belgrade virus, a cause of hemorrhagic fever with renal syndrome in the Balkans, is closely related to Dobrava virus of field mice
A M Taller, S Y Xiao, M S Godec, et al.
Bone Marrow Transplantation
|
December 5, 2025
Age 60 or older is an independent predictor of outcomes after thiotepa-based autologous transplant in primary CNS lymphoma: a CIBMTR analysis
Neela Easton, David G Goldfarb, Ahmed El-Naas, et al.
Page
of 25