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Showing results (261-270 of 333) with videos related to

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JAMA Psychiatry|October 21, 2016
Disease Burden and Symptom Structure of Autism in Neurofibromatosis Type 1: A Study of the International NF1-ASD Consortium Team (INFACT)Stephanie M Morris, Maria T Acosta, Shruti Garg, et al.
Neuromuscular Disorders : NMD|November 8, 2008
Muscular dystrophy associated with alpha-dystroglycan deficiency in Sphynx and Devon Rex catsPaul T Martin, G Diane Shelton, Peter J Dickinson, et al.
The Medical Journal of Australia|November 3, 2017
The kids are OK: it is discrimination not same-sex parents that harms childrenKen W Knight, Sarah Em Stephenson, Sue West, et al.
Stem Cell Research|February 15, 2025
Generation of an iPSC line (with isogenic control) from the PBMCs of a COL6A1 (c.1056 + 2T > A) Bethlem myopathy patientVanessa G Crossman, Chrystal F Tiong, Chantal A Coles, et al.
Child Neuropsychology : a Journal on Normal and Abnormal Development in Childhood and Adolescence|September 30, 2021
The mediating role of ADHD symptoms between executive function and social skills in children with neurofibromatosis type 1Kristina M Haebich, Duy P Dao, Natalie A Pride, et al.
Human Molecular Genetics|May 4, 2011
Deficiency of α-actinin-3 is associated with increased susceptibility to contraction-induced damage and skeletal muscle remodelingJane T Seto, Monkol Lek, Kate G R Quinlan, et al.
Neurology|February 26, 2003
Clinical course correlates poorly with muscle pathology in nemaline myopathyM M Ryan, B Ilkovski, C D Strickland, et al.
Annals of Neurology|February 27, 2008
Mutations in TPM3 are a common cause of congenital fiber type disproportionNigel F Clarke, Hanna Kolski, Danielle E Dye, et al.
Human Molecular Genetics|January 8, 2008
An Actn3 knockout mouse provides mechanistic insights into the association between alpha-actinin-3 deficiency and human athletic performanceDaniel G MacArthur, Jane T Seto, Stephen Chan, et al.
European Journal of Human Genetics : EJHG|January 28, 2016
Prominent scapulae mimicking an inherited myopathy expands the phenotype of CHD7-related diseaseGina L O'Grady, Alan Ma, Deborah Sival, et al.
Pageof 34

Showing results (261-270 of 333) with videos related to

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Pageof 34
JAMA Psychiatry|October 21, 2016
Disease Burden and Symptom Structure of Autism in Neurofibromatosis Type 1: A Study of the International NF1-ASD Consortium Team (INFACT)Stephanie M Morris, Maria T Acosta, Shruti Garg, et al.
Neuromuscular Disorders : NMD|November 8, 2008
Muscular dystrophy associated with alpha-dystroglycan deficiency in Sphynx and Devon Rex catsPaul T Martin, G Diane Shelton, Peter J Dickinson, et al.
The Medical Journal of Australia|November 3, 2017
The kids are OK: it is discrimination not same-sex parents that harms childrenKen W Knight, Sarah Em Stephenson, Sue West, et al.
Stem Cell Research|February 15, 2025
Generation of an iPSC line (with isogenic control) from the PBMCs of a COL6A1 (c.1056 + 2T > A) Bethlem myopathy patientVanessa G Crossman, Chrystal F Tiong, Chantal A Coles, et al.
Child Neuropsychology : a Journal on Normal and Abnormal Development in Childhood and Adolescence|September 30, 2021
The mediating role of ADHD symptoms between executive function and social skills in children with neurofibromatosis type 1Kristina M Haebich, Duy P Dao, Natalie A Pride, et al.
Human Molecular Genetics|May 4, 2011
Deficiency of α-actinin-3 is associated with increased susceptibility to contraction-induced damage and skeletal muscle remodelingJane T Seto, Monkol Lek, Kate G R Quinlan, et al.
Neurology|February 26, 2003
Clinical course correlates poorly with muscle pathology in nemaline myopathyM M Ryan, B Ilkovski, C D Strickland, et al.
Annals of Neurology|February 27, 2008
Mutations in TPM3 are a common cause of congenital fiber type disproportionNigel F Clarke, Hanna Kolski, Danielle E Dye, et al.
Human Molecular Genetics|January 8, 2008
An Actn3 knockout mouse provides mechanistic insights into the association between alpha-actinin-3 deficiency and human athletic performanceDaniel G MacArthur, Jane T Seto, Stephen Chan, et al.
European Journal of Human Genetics : EJHG|January 28, 2016
Prominent scapulae mimicking an inherited myopathy expands the phenotype of CHD7-related diseaseGina L O'Grady, Alan Ma, Deborah Sival, et al.
Pageof 34