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

R Matalon

Showing results (91-100 of 185) with videos related to

Pageof 19
Sort By:
The Journal of Biological Chemistry|September 3, 1998
A novel mutation in the switch 3 region of Gsalpha in a patient with Albright hereditary osteodystrophy impairs GDP binding and receptor activationD R Warner, G Weng, S Yu, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|March 4, 2000
Novel splice site mutation of aspartoacylase gene in a Turkish patient with Canavan diseaseP L Rady, J M Penzien, T Vargas, et al.
Archives of Pathology & Laboratory Medicine|September 1, 1983
Hunter' syndrome. Ultrastructural features in young childrenJ V Murphy, A E Hodach, E F Gilbert, et al.
The Journal of Infectious Diseases|December 1, 1971
The use of gentamicin in peritoneal dialysis. I. Pharmacologic resultsT Smithivas, P J Hyams, R Matalon, et al.
Journal of Investigative Medicine High Impact Case Reports|February 8, 2023
Creatine Transporter Deficiency Presenting as Failure to Thrive: A Case Report of a Novel <i>SLC6A8</i> Variant Causing a Treatable but Likely Underdiagnosed Genetic DisorderChristina G Tise, Melinda J Palma, Kristina P Cusmano-Ozog, et al.
American Journal of Diseases of Children (1960)|November 1, 1993
The North American Collaborative Study of Maternal Phenylketonuria. Status report 1993R Koch, H L Levy, R Matalon, et al.
Annals of Internal Medicine|April 1, 1974
Glomerular sclerosis in adults with nephrotic syndromeR Matalon, L Katz, G Gallo, et al.
Journal of Inherited Metabolic Disease|September 16, 2003
Danger of high-protein dietary supplements to persons with hyperphenylalaninaemiaR Koch, K D Moseley, R Moats, et al.
The Journal of Pediatrics|January 1, 1993
Prospective management of a child with neonatal citrullinemiaA R Melnyk, R Matalon, B W Henry, et al.
The Journal of Biological Chemistry|August 24, 1999
MCD encodes peroxisomal and cytoplasmic forms of malonyl-CoA decarboxylase and is mutated in malonyl-CoA decarboxylase deficiencyK A Sacksteder, J C Morrell, R J Wanders, et al.
Pageof 19

Showing results (91-100 of 185) with videos related to

Sort By:
Pageof 19
The Journal of Biological Chemistry|September 3, 1998
A novel mutation in the switch 3 region of Gsalpha in a patient with Albright hereditary osteodystrophy impairs GDP binding and receptor activationD R Warner, G Weng, S Yu, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|March 4, 2000
Novel splice site mutation of aspartoacylase gene in a Turkish patient with Canavan diseaseP L Rady, J M Penzien, T Vargas, et al.
Archives of Pathology & Laboratory Medicine|September 1, 1983
Hunter' syndrome. Ultrastructural features in young childrenJ V Murphy, A E Hodach, E F Gilbert, et al.
The Journal of Infectious Diseases|December 1, 1971
The use of gentamicin in peritoneal dialysis. I. Pharmacologic resultsT Smithivas, P J Hyams, R Matalon, et al.
Journal of Investigative Medicine High Impact Case Reports|February 8, 2023
Creatine Transporter Deficiency Presenting as Failure to Thrive: A Case Report of a Novel <i>SLC6A8</i> Variant Causing a Treatable but Likely Underdiagnosed Genetic DisorderChristina G Tise, Melinda J Palma, Kristina P Cusmano-Ozog, et al.
American Journal of Diseases of Children (1960)|November 1, 1993
The North American Collaborative Study of Maternal Phenylketonuria. Status report 1993R Koch, H L Levy, R Matalon, et al.
Annals of Internal Medicine|April 1, 1974
Glomerular sclerosis in adults with nephrotic syndromeR Matalon, L Katz, G Gallo, et al.
Journal of Inherited Metabolic Disease|September 16, 2003
Danger of high-protein dietary supplements to persons with hyperphenylalaninaemiaR Koch, K D Moseley, R Moats, et al.
The Journal of Pediatrics|January 1, 1993
Prospective management of a child with neonatal citrullinemiaA R Melnyk, R Matalon, B W Henry, et al.
The Journal of Biological Chemistry|August 24, 1999
MCD encodes peroxisomal and cytoplasmic forms of malonyl-CoA decarboxylase and is mutated in malonyl-CoA decarboxylase deficiencyK A Sacksteder, J C Morrell, R J Wanders, et al.
Pageof 19