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Annals of Neurology
|
January 23, 1999
Effects of PMP22 duplication and deletions on the axonal cytoskeleton
Z Sahenk, L Chen, J R Mendell
Human Mutation
|
March 1, 2000
Novel compound heterozygous laminina2-chain gene (LAMA2) mutations in congenital muscular dystrophy. Mutations in brief no. 159. Online
J T Mendell, S G Panicker, C Y Tsao, et al.
Brain Research
|
February 26, 1990
Immunocytochemical evidence for the retrograde transport of intraaxonal cathepsin D: possible relevance to the dying-back process
Z Sahenk, J N Whitaker, J R Mendell
Journal of Child Neurology
|
July 17, 2001
High mitochondrial DNA T8993G mutation (<90%) without typical features of Leigh's and NARP syndromes
C Y Tsao, J R Mendell, D Bartholomew
Neuroscience Letters
|
January 15, 2008
Casein kinase 1 alpha associates with the tau-bearing lesions of inclusion body myositis
Theresa J Kannanayakal, Jerry R Mendell, Jeff Kuret
Journal of Neurophysiology
|
February 1, 1995
Properties of regenerated primary afferents and their functional connections
H R Koerber, K Mirnics, L M Mendell
Journal of Clinical Neuromuscular Disease
|
December 17, 2008
Fatal group a streptococcal necrotizing myopathy
Yelena Lindenbaum, N Stanley Nahman, Jerry R Mendell
Journal of Clinical Pharmacology
|
June 11, 2010
Effects of food on the pharmacokinetics of edoxaban, an oral direct factor Xa inhibitor, in healthy volunteers
Jeanne Mendell, Masaya Tachibana, Minggao Shi, et al.
Journal of Exposure Science & Environmental Epidemiology
|
April 21, 2026
The impact of portable air cleaners on indoor particulate matter concentrations and perceptions of indoor air quality: a randomized crossover trial in three multifamily buildings
Alexander Y Mendell, Seungjae Lee, Jeffrey A Siegel
American Journal of Medical Genetics
|
October 21, 1998
Identification of a missense mutation in a Friedreich's ataxia patient: implications for diagnosis and carrier studies
C Bartolo, J R Mendell, T W Prior
Page
of 89
Search research articles
Search
Showing results (131-140 of 889) with videos related to
Sort By:
Page
of 89
Annals of Neurology
|
January 23, 1999
Effects of PMP22 duplication and deletions on the axonal cytoskeleton
Z Sahenk, L Chen, J R Mendell
Human Mutation
|
March 1, 2000
Novel compound heterozygous laminina2-chain gene (LAMA2) mutations in congenital muscular dystrophy. Mutations in brief no. 159. Online
J T Mendell, S G Panicker, C Y Tsao, et al.
Brain Research
|
February 26, 1990
Immunocytochemical evidence for the retrograde transport of intraaxonal cathepsin D: possible relevance to the dying-back process
Z Sahenk, J N Whitaker, J R Mendell
Journal of Child Neurology
|
July 17, 2001
High mitochondrial DNA T8993G mutation (<90%) without typical features of Leigh's and NARP syndromes
C Y Tsao, J R Mendell, D Bartholomew
Neuroscience Letters
|
January 15, 2008
Casein kinase 1 alpha associates with the tau-bearing lesions of inclusion body myositis
Theresa J Kannanayakal, Jerry R Mendell, Jeff Kuret
Journal of Neurophysiology
|
February 1, 1995
Properties of regenerated primary afferents and their functional connections
H R Koerber, K Mirnics, L M Mendell
Journal of Clinical Neuromuscular Disease
|
December 17, 2008
Fatal group a streptococcal necrotizing myopathy
Yelena Lindenbaum, N Stanley Nahman, Jerry R Mendell
Journal of Clinical Pharmacology
|
June 11, 2010
Effects of food on the pharmacokinetics of edoxaban, an oral direct factor Xa inhibitor, in healthy volunteers
Jeanne Mendell, Masaya Tachibana, Minggao Shi, et al.
Journal of Exposure Science & Environmental Epidemiology
|
April 21, 2026
The impact of portable air cleaners on indoor particulate matter concentrations and perceptions of indoor air quality: a randomized crossover trial in three multifamily buildings
Alexander Y Mendell, Seungjae Lee, Jeffrey A Siegel
American Journal of Medical Genetics
|
October 21, 1998
Identification of a missense mutation in a Friedreich's ataxia patient: implications for diagnosis and carrier studies
C Bartolo, J R Mendell, T W Prior
Page
of 89