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

J Philpot

Showing results (41-50 of 48) with videos related to

Pageof 5
Sort By:
You have reached the last page of results.This site can display upto 48 results.
Biochemical Society Transactions|May 1, 1996
The protein defect in congenital muscular dystrophyC A Sewry, I Naom, M D'Alessandro, et al.
The Journal of Pediatrics|March 1, 1983
Progeria: insulin resistance and hyperglycemiaA L Rosenbloom, M S Kappy, F L DeBusk, et al.
ASAIO Journal (American Society for Artificial Internal Organs : 1992)|October 15, 2019
A Protocol that Mandates Postoxygenator and Arterial Blood Gases to Confirm Brain Death on Venoarterial Extracorporeal Membrane OxygenationJoshua F Ihle, Aidan J C Burrell, Steve J Philpot, et al.
Neuropediatrics|June 1, 1995
Minor neurological and perceptuo-motor deficits in children with congenital muscular dystrophy: correlation with brain MRI changesE Mercuri, L Dubowitz, A Berardinelli, et al.
Human Molecular Genetics|September 1, 1994
Localization of merosin-negative congenital muscular dystrophy to chromosome 6q2 by homozygosity mappingD Hillaire, A Leclerc, S Fauré, et al.
Lancet (London, England)|March 2, 1996
Diagnosis of merosin (laminin-2) deficient congenital muscular dystrophy by skin biopsyC A Sewry, J Philpot, L M Sorokin, et al.
Neuromuscular Disorders : NMD|November 2, 1999
Cognitive abilities in children with congenital muscular dystrophy: correlation with brain MRI and merosin statusE Mercuri, J Gruter-Andrew, J Philpot, et al.
Journal of Medical Genetics|February 1, 1997
Refinement of the laminin alpha2 chain locus to human chromosome 6q2 in severe and mild merosin deficient congenital muscular dystrophyI S Naom, M D'Alessandro, H Topaloglu, et al.
Pageof 5

Showing results (41-50 of 48) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 48 results.
Biochemical Society Transactions|May 1, 1996
The protein defect in congenital muscular dystrophyC A Sewry, I Naom, M D'Alessandro, et al.
The Journal of Pediatrics|March 1, 1983
Progeria: insulin resistance and hyperglycemiaA L Rosenbloom, M S Kappy, F L DeBusk, et al.
ASAIO Journal (American Society for Artificial Internal Organs : 1992)|October 15, 2019
A Protocol that Mandates Postoxygenator and Arterial Blood Gases to Confirm Brain Death on Venoarterial Extracorporeal Membrane OxygenationJoshua F Ihle, Aidan J C Burrell, Steve J Philpot, et al.
Neuropediatrics|June 1, 1995
Minor neurological and perceptuo-motor deficits in children with congenital muscular dystrophy: correlation with brain MRI changesE Mercuri, L Dubowitz, A Berardinelli, et al.
Human Molecular Genetics|September 1, 1994
Localization of merosin-negative congenital muscular dystrophy to chromosome 6q2 by homozygosity mappingD Hillaire, A Leclerc, S Fauré, et al.
Lancet (London, England)|March 2, 1996
Diagnosis of merosin (laminin-2) deficient congenital muscular dystrophy by skin biopsyC A Sewry, J Philpot, L M Sorokin, et al.
Neuromuscular Disorders : NMD|November 2, 1999
Cognitive abilities in children with congenital muscular dystrophy: correlation with brain MRI and merosin statusE Mercuri, J Gruter-Andrew, J Philpot, et al.
Journal of Medical Genetics|February 1, 1997
Refinement of the laminin alpha2 chain locus to human chromosome 6q2 in severe and mild merosin deficient congenital muscular dystrophyI S Naom, M D'Alessandro, H Topaloglu, et al.
Pageof 5