Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Anne Rutkowski

Showing results (11-20 of 27) with videos related to

Pageof 3
Sort By:
Archives of Pathology & Laboratory Medicine|July 2, 2015
Common Data Elements for Muscle Biopsy ReportingJahannaz Dastgir, Anne Rutkowski, Rachel Alvarez, et al.
BMC Pediatrics|February 8, 2020
Hypoglycemia in patients with congenital muscle diseaseLeslie H Hayes, Pomi Yun, Payam Mohassel, et al.
Pediatric Neurology|February 11, 2014
Congenital muscular dystrophy with dropped head linked to the LMNA gene in a Brazilian cohortLívia M A Pasqualin, Umbertina C Reed, Thais V M M Costa, et al.
Neuromuscular Disorders : NMD|July 18, 2012
Report on the Myomatrix Conference April 22-24, 2012, University of Nevada, Reno, Nevada, USAAnne Rutkowski, Carsten Bönnemann, Susan Brown, et al.
Neuromuscular Disorders : NMD|March 4, 2014
Diagnostic approach to the congenital muscular dystrophiesCarsten G Bönnemann, Ching H Wang, Susana Quijano-Roy, et al.
Journal of Neuromuscular Diseases|May 28, 2017
Improving Reproducibility of Phenotypic Assessments in the DyW Mouse Model of Laminin-α2 Related Congenital Muscular DystrophyRaffaella Willmann, Heather Gordish-Dressman, Sarina Meinen, et al.
Archives of Physical Medicine and Rehabilitation|May 28, 2014
English cross-cultural translation and validation of the neuromuscular score: a system for motor function classification in patients with neuromuscular diseasesCarole Vuillerot, Katherine G Meilleur, Minal Jain, et al.
Pediatric Pulmonology|January 14, 2017
Comparison of sitting and supine forced vital capacity in collagen VI-related dystrophy and laminin α2-related dystrophyKatherine G Meilleur, Melody M Linton, Joseph Fontana, et al.
Neurology|April 1, 2015
Evidence-based guideline summary: evaluation, diagnosis, and management of congenital muscular dystrophy: Report of the Guideline Development Subcommittee of the American Academy of Neurology and the Practice Issues Review Panel of the American Association of Neuromuscular & Electrodiagnostic MedicinePeter B Kang, Leslie Morrison, Susan T Iannaccone, et al.
Muscle & Nerve|February 23, 2017
Electrical impedance myography in individuals with collagen 6 and laminin α-2 congenital muscular dystrophy: a cross-sectional and 2-year analysisCarmel Nichols, Minal S Jain, Katherine G Meilleur, et al.
Pageof 3

Showing results (11-20 of 27) with videos related to

Sort By:
Pageof 3
Archives of Pathology & Laboratory Medicine|July 2, 2015
Common Data Elements for Muscle Biopsy ReportingJahannaz Dastgir, Anne Rutkowski, Rachel Alvarez, et al.
BMC Pediatrics|February 8, 2020
Hypoglycemia in patients with congenital muscle diseaseLeslie H Hayes, Pomi Yun, Payam Mohassel, et al.
Pediatric Neurology|February 11, 2014
Congenital muscular dystrophy with dropped head linked to the LMNA gene in a Brazilian cohortLívia M A Pasqualin, Umbertina C Reed, Thais V M M Costa, et al.
Neuromuscular Disorders : NMD|July 18, 2012
Report on the Myomatrix Conference April 22-24, 2012, University of Nevada, Reno, Nevada, USAAnne Rutkowski, Carsten Bönnemann, Susan Brown, et al.
Neuromuscular Disorders : NMD|March 4, 2014
Diagnostic approach to the congenital muscular dystrophiesCarsten G Bönnemann, Ching H Wang, Susana Quijano-Roy, et al.
Journal of Neuromuscular Diseases|May 28, 2017
Improving Reproducibility of Phenotypic Assessments in the DyW Mouse Model of Laminin-α2 Related Congenital Muscular DystrophyRaffaella Willmann, Heather Gordish-Dressman, Sarina Meinen, et al.
Archives of Physical Medicine and Rehabilitation|May 28, 2014
English cross-cultural translation and validation of the neuromuscular score: a system for motor function classification in patients with neuromuscular diseasesCarole Vuillerot, Katherine G Meilleur, Minal Jain, et al.
Pediatric Pulmonology|January 14, 2017
Comparison of sitting and supine forced vital capacity in collagen VI-related dystrophy and laminin α2-related dystrophyKatherine G Meilleur, Melody M Linton, Joseph Fontana, et al.
Neurology|April 1, 2015
Evidence-based guideline summary: evaluation, diagnosis, and management of congenital muscular dystrophy: Report of the Guideline Development Subcommittee of the American Academy of Neurology and the Practice Issues Review Panel of the American Association of Neuromuscular & Electrodiagnostic MedicinePeter B Kang, Leslie Morrison, Susan T Iannaccone, et al.
Muscle & Nerve|February 23, 2017
Electrical impedance myography in individuals with collagen 6 and laminin α-2 congenital muscular dystrophy: a cross-sectional and 2-year analysisCarmel Nichols, Minal S Jain, Katherine G Meilleur, et al.
Pageof 3