Nigel Clarke - JoVE Visualize

Search research articles

ABOUT JoVE

Overview Leadership Blog JoVE Help Center

AUTHORS

Publishing Process Editorial Board Scope & Policies Peer Review FAQ Submit

LIBRARIANS

Testimonials Subscriptions Access Resources Library Advisory Board FAQ

RESEARCH

JoVE Journal Methods Collections JoVE Encyclopedia of Experiments Archive

EDUCATION

JoVE Core JoVE Business JoVE Science Education JoVE Lab Manual Faculty Resource Center Faculty Site

Terms & Conditions of Use

Policies

Search research articles

ABOUT JoVE

Overview Leadership Blog JoVE Help Center

AUTHORS

Publishing Process Editorial Board Scope & Policies Peer Review FAQ Submit

LIBRARIANS

Testimonials Subscriptions Access Resources Library Advisory Board FAQ

RESEARCH

JoVE Journal Methods Collections JoVE Encyclopedia of Experiments Archive

EDUCATION

JoVE Core JoVE Business JoVE Science Education JoVE Lab Manual Faculty Resource Center Faculty Site

Terms & Conditions of Use

Policies

Filters

Nigel Clarke

Showing results (71-80 of 76) with videos related to

Pageof 8

Sort By:

You have reached the last page of results.This site can display upto 76 results.

European Journal of Medical Genetics|January 14, 2009

POMT2 intragenic deletions and splicing abnormalities causing congenital muscular dystrophy with mental retardationAkiko Yanagisawa, Céline Bouchet, Susana Quijano-Roy, et al.

Neuromuscular Disorders : NMD|January 25, 2014

Approach to the diagnosis of congenital myopathiesKathryn N North, Ching H Wang, Nigel Clarke, et al.

Plos One|March 5, 2015

Temporal relationship between vitamin D status and parathyroid hormone in the United StatesMartin H Kroll, Caixia Bi, Carl C Garber, et al.

Neurology|January 1, 2016

Mutations in HSPB8 causing a new phenotype of distal myopathy and motor neuropathyRoula Ghaoui, Johanna Palmio, Janice Brewer, et al.

Journal of Child Neurology|March 21, 2012

Consensus statement on standard of care for congenital myopathiesChing H Wang, James J Dowling, Kathryn North, et al.

Clinical Chemistry|January 1, 2016

Recommendations for the Generation, Quantification, Storage, and Handling of Peptides Used for Mass Spectrometry-Based AssaysAndrew N Hoofnagle, Jeffrey R Whiteaker, Steven A Carr, et al.

Pageof 8

Search research articles

Showing results (71-80 of 76) with videos related to

Sort By:

Pageof 8

You have reached the last page of results.This site can display upto 76 results.

European Journal of Medical Genetics|January 14, 2009

POMT2 intragenic deletions and splicing abnormalities causing congenital muscular dystrophy with mental retardationAkiko Yanagisawa, Céline Bouchet, Susana Quijano-Roy, et al.

Neuromuscular Disorders : NMD|January 25, 2014

Approach to the diagnosis of congenital myopathiesKathryn N North, Ching H Wang, Nigel Clarke, et al.

Plos One|March 5, 2015

Temporal relationship between vitamin D status and parathyroid hormone in the United StatesMartin H Kroll, Caixia Bi, Carl C Garber, et al.

Neurology|January 1, 2016

Mutations in HSPB8 causing a new phenotype of distal myopathy and motor neuropathyRoula Ghaoui, Johanna Palmio, Janice Brewer, et al.

Journal of Child Neurology|March 21, 2012

Consensus statement on standard of care for congenital myopathiesChing H Wang, James J Dowling, Kathryn North, et al.

Clinical Chemistry|January 1, 2016

Recommendations for the Generation, Quantification, Storage, and Handling of Peptides Used for Mass Spectrometry-Based AssaysAndrew N Hoofnagle, Jeffrey R Whiteaker, Steven A Carr, et al.

Pageof 8