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 H Walter

Showing results (41-50 of 96) with videos related to

Pageof 10
Sort By:
Journal of the American Podiatric Medical Association|April 1, 1990
Anatomical and histologic investigation of the syndesmotic area in the ankle jointK A Sabacinski, J H Walter, G M Saffo
The Journal of Foot and Ankle Surgery : Official Publication of the American College of Foot and Ankle Surgeons|March 1, 1995
Subcapital talar osteotomy to correct transverse plane structural flatfoot deformitiesJ H Walter, M A Bailey, M R Kressler
Archives of Disease in Childhood. Fetal and Neonatal Edition|May 1, 1995
Absence of acidosis in the initial presentation of propionic acidaemiaJ H Walter, J E Wraith, M A Cleary
The Journal of Foot Surgery|July 1, 1989
Use of the cannulated bone screw in rearfoot surgeryW A Chieppa, K H Sydnor, J H Walter
Journal of Inherited Metabolic Disease|January 1, 1986
3-Hydroxy-3-methylglutaryl-CoA lyase deficiencyJ H Walter, P T Clayton, J V Leonard
Neuroreport|February 24, 2001
Disappearance of beta2-adrenergic receptors on astrocytes in canine distemper encephalitis: possible implications for the pathogenesis of multiple sclerosisJ De Keyser, N Wilczak, J H Walter, et al.
Archives of Disease in Childhood|January 25, 2005
Maternal phenylketonuria: report from the United Kingdom Registry 1978-97P J Lee, D Ridout, J H Walter, et al.
Lancet (London, England)|October 28, 1989
Propionate production in methylmalonic acidemiaJ H Walter, G N Thompson, J V Leonard, et al.
European Journal of Pediatrics|October 1, 1993
Biochemical control, genetic analysis and magnetic resonance imaging in patients with phenylketonuriaJ H Walter, L A Tyfield, J B Holton, et al.
Journal of Inherited Metabolic Disease|January 1, 1994
Immune function in prolidase deficiencyM A Cleary, M Heaney, J M Couriel, et al.
Pageof 10

Showing results (41-50 of 96) with videos related to

Sort By:
Pageof 10
Journal of the American Podiatric Medical Association|April 1, 1990
Anatomical and histologic investigation of the syndesmotic area in the ankle jointK A Sabacinski, J H Walter, G M Saffo
The Journal of Foot and Ankle Surgery : Official Publication of the American College of Foot and Ankle Surgeons|March 1, 1995
Subcapital talar osteotomy to correct transverse plane structural flatfoot deformitiesJ H Walter, M A Bailey, M R Kressler
Archives of Disease in Childhood. Fetal and Neonatal Edition|May 1, 1995
Absence of acidosis in the initial presentation of propionic acidaemiaJ H Walter, J E Wraith, M A Cleary
The Journal of Foot Surgery|July 1, 1989
Use of the cannulated bone screw in rearfoot surgeryW A Chieppa, K H Sydnor, J H Walter
Journal of Inherited Metabolic Disease|January 1, 1986
3-Hydroxy-3-methylglutaryl-CoA lyase deficiencyJ H Walter, P T Clayton, J V Leonard
Neuroreport|February 24, 2001
Disappearance of beta2-adrenergic receptors on astrocytes in canine distemper encephalitis: possible implications for the pathogenesis of multiple sclerosisJ De Keyser, N Wilczak, J H Walter, et al.
Archives of Disease in Childhood|January 25, 2005
Maternal phenylketonuria: report from the United Kingdom Registry 1978-97P J Lee, D Ridout, J H Walter, et al.
Lancet (London, England)|October 28, 1989
Propionate production in methylmalonic acidemiaJ H Walter, G N Thompson, J V Leonard, et al.
European Journal of Pediatrics|October 1, 1993
Biochemical control, genetic analysis and magnetic resonance imaging in patients with phenylketonuriaJ H Walter, L A Tyfield, J B Holton, et al.
Journal of Inherited Metabolic Disease|January 1, 1994
Immune function in prolidase deficiencyM A Cleary, M Heaney, J M Couriel, et al.
Pageof 10