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G Lennox

Showing results (111-120 of 121) with videos related to

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Journal of Intellectual Disability Research : JIDR|January 17, 2017
Intellectual disability and patient activation after release from prison: a prospective cohort studyJ T Young, C Cumming, K van Dooren, et al.
Brain : a Journal of Neurology|June 1, 1993
The mitochondrial DNA transfer RNA(Lys)A-->G(8344) mutation and the syndrome of myoclonic epilepsy with ragged red fibres (MERRF). Relationship of clinical phenotype to proportion of mutant mitochondrial DNAS R Hammans, M G Sweeney, M Brockington, et al.
Transactions - American Society for Artificial Internal Organs|January 1, 1983
Reducing patient morbidity from high-efficiency hemodialysis: a double-blind crossover trialA G Shimizu, D W Taylor, D L Sackett, et al.
Nature|July 20, 1989
Ubiquitin and dementiaR J Mayer, M Landon, F J Doherty, et al.
Pharmacotherapy|February 25, 1999
Lack of a pharmacokinetic interaction at steady state between ropinirole and L-dopa in patients with Parkinson's diseaseA C Taylor, A Beerahee, D R Citerone, et al.
F1000Research|February 25, 2014
Identification and molecular characterization of a novel Chlamydomonas reinhardtii mutant defective in chlorophyll biosynthesisPhillip B Grovenstein, Darryel A Wilson, Cameron G Lennox, et al.
BMJ Open|December 7, 2019
Cohort profile: the Australian Longitudinal Study of Adults with Autism (ALSAA)Samuel Arnold, Kitty-Rose Foley, Ye In Jane Hwang, et al.
American Journal of Human Genetics|April 16, 1998
ATM mutations and phenotypes in ataxia-telangiectasia families in the British Isles: expression of mutant ATM and the risk of leukemia, lymphoma, and breast cancerT Stankovic, A M Kidd, A Sutcliffe, et al.
Archives of Neurology|May 21, 2003
Expanding the phenotypic spectrum of the CACNA1A gene T666M mutation: a description of 5 families with familial hemiplegic migraineE E Kors, J Haan, N J Giffin, et al.
Brain : a Journal of Neurology|February 9, 2002
Two large British kindreds with familial Parkinson's disease: a clinico-pathological and genetic studyD J Nicholl, J R Vaughan, N L Khan, et al.
Pageof 13

Showing results (111-120 of 121) with videos related to

Sort By:
Pageof 13
Journal of Intellectual Disability Research : JIDR|January 17, 2017
Intellectual disability and patient activation after release from prison: a prospective cohort studyJ T Young, C Cumming, K van Dooren, et al.
Brain : a Journal of Neurology|June 1, 1993
The mitochondrial DNA transfer RNA(Lys)A-->G(8344) mutation and the syndrome of myoclonic epilepsy with ragged red fibres (MERRF). Relationship of clinical phenotype to proportion of mutant mitochondrial DNAS R Hammans, M G Sweeney, M Brockington, et al.
Transactions - American Society for Artificial Internal Organs|January 1, 1983
Reducing patient morbidity from high-efficiency hemodialysis: a double-blind crossover trialA G Shimizu, D W Taylor, D L Sackett, et al.
Nature|July 20, 1989
Ubiquitin and dementiaR J Mayer, M Landon, F J Doherty, et al.
Pharmacotherapy|February 25, 1999
Lack of a pharmacokinetic interaction at steady state between ropinirole and L-dopa in patients with Parkinson's diseaseA C Taylor, A Beerahee, D R Citerone, et al.
F1000Research|February 25, 2014
Identification and molecular characterization of a novel Chlamydomonas reinhardtii mutant defective in chlorophyll biosynthesisPhillip B Grovenstein, Darryel A Wilson, Cameron G Lennox, et al.
BMJ Open|December 7, 2019
Cohort profile: the Australian Longitudinal Study of Adults with Autism (ALSAA)Samuel Arnold, Kitty-Rose Foley, Ye In Jane Hwang, et al.
American Journal of Human Genetics|April 16, 1998
ATM mutations and phenotypes in ataxia-telangiectasia families in the British Isles: expression of mutant ATM and the risk of leukemia, lymphoma, and breast cancerT Stankovic, A M Kidd, A Sutcliffe, et al.
Archives of Neurology|May 21, 2003
Expanding the phenotypic spectrum of the CACNA1A gene T666M mutation: a description of 5 families with familial hemiplegic migraineE E Kors, J Haan, N J Giffin, et al.
Brain : a Journal of Neurology|February 9, 2002
Two large British kindreds with familial Parkinson's disease: a clinico-pathological and genetic studyD J Nicholl, J R Vaughan, N L Khan, et al.
Pageof 13