Search research articles
Contact Us
Filters
Showing results (111-120 of 333) with videos related to
Page
of 34
Sort By:
Developmental Medicine and Child Neurology
|
April 19, 2018
Preliteracy impairments in children with neurofibromatosis type 1
Shelley S Arnold, Jonathan M Payne, Jennifer Lorenzo, et al.
Journal of the International Neuropsychological Society : JINS
|
November 16, 2020
Profiling the Word Reading Abilities of School-Age Children with Neurofibromatosis Type 1
Shelley S Arnold, Jonathan M Payne, Genevieve McArthur, et al.
Neuromuscular Disorders : NMD
|
January 24, 2006
Autosomal dominant nemaline myopathy with intranuclear rods due to mutation of the skeletal muscle ACTA1 gene: clinical and pathological variability within a kindred
David O Hutchinson, Amanda Charlton, Nigel G Laing, et al.
Neuromuscular Disorders : NMD
|
April 7, 2009
Cap disease due to mutation of the beta-tropomyosin gene (TPM2)
Nigel F Clarke, Ana Domazetovska, Leigh Waddell, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
February 15, 2007
T2 hyperintensities in children with neurofibromatosis type 1 and their relationship to cognitive functioning
Shelley L Hyman, Deepak S Gill, Edwin Arthur Shores, et al.
Biochimica Et Biophysica Acta
|
January 24, 2016
How does α-actinin-3 deficiency alter muscle function? Mechanistic insights into ACTN3, the 'gene for speed'
Fiona X Z Lee, Peter J Houweling, Kathryn N North, et al.
Nature Genetics
|
April 7, 1999
A common nonsense mutation results in alpha-actinin-3 deficiency in the general population
K N North, N Yang, D Wattanasirichaigoon, et al.
Journal of Neuropathology and Experimental Neurology
|
April 27, 2010
In vitro analysis of rod composition and actin dynamics in inherited myopathies
Aurélie Vandebrouck, Ana Domazetovska, Nancy Mokbel, et al.
Traffic (Copenhagen, Denmark)
|
August 16, 2011
Ferlins: regulators of vesicle fusion for auditory neurotransmission, receptor trafficking and membrane repair
Angela Lek, Frances J Evesson, R Bryan Sutton, et al.
Muscle & Nerve
|
July 15, 2011
Using complementary DNA from MyoD-transduced fibroblasts to sequence large muscle genes
Leigh B Waddell, Nicole Monnier, Sandra T Cooper, et al.
Page
of 34
Search research articles
Search
Showing results (111-120 of 333) with videos related to
Sort By:
Page
of 34
Developmental Medicine and Child Neurology
|
April 19, 2018
Preliteracy impairments in children with neurofibromatosis type 1
Shelley S Arnold, Jonathan M Payne, Jennifer Lorenzo, et al.
Journal of the International Neuropsychological Society : JINS
|
November 16, 2020
Profiling the Word Reading Abilities of School-Age Children with Neurofibromatosis Type 1
Shelley S Arnold, Jonathan M Payne, Genevieve McArthur, et al.
Neuromuscular Disorders : NMD
|
January 24, 2006
Autosomal dominant nemaline myopathy with intranuclear rods due to mutation of the skeletal muscle ACTA1 gene: clinical and pathological variability within a kindred
David O Hutchinson, Amanda Charlton, Nigel G Laing, et al.
Neuromuscular Disorders : NMD
|
April 7, 2009
Cap disease due to mutation of the beta-tropomyosin gene (TPM2)
Nigel F Clarke, Ana Domazetovska, Leigh Waddell, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
February 15, 2007
T2 hyperintensities in children with neurofibromatosis type 1 and their relationship to cognitive functioning
Shelley L Hyman, Deepak S Gill, Edwin Arthur Shores, et al.
Biochimica Et Biophysica Acta
|
January 24, 2016
How does α-actinin-3 deficiency alter muscle function? Mechanistic insights into ACTN3, the 'gene for speed'
Fiona X Z Lee, Peter J Houweling, Kathryn N North, et al.
Nature Genetics
|
April 7, 1999
A common nonsense mutation results in alpha-actinin-3 deficiency in the general population
K N North, N Yang, D Wattanasirichaigoon, et al.
Journal of Neuropathology and Experimental Neurology
|
April 27, 2010
In vitro analysis of rod composition and actin dynamics in inherited myopathies
Aurélie Vandebrouck, Ana Domazetovska, Nancy Mokbel, et al.
Traffic (Copenhagen, Denmark)
|
August 16, 2011
Ferlins: regulators of vesicle fusion for auditory neurotransmission, receptor trafficking and membrane repair
Angela Lek, Frances J Evesson, R Bryan Sutton, et al.
Muscle & Nerve
|
July 15, 2011
Using complementary DNA from MyoD-transduced fibroblasts to sequence large muscle genes
Leigh B Waddell, Nicole Monnier, Sandra T Cooper, et al.
Page
of 34