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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 activation
D 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 disease
P L Rady, J M Penzien, T Vargas, et al.
Archives of Pathology & Laboratory Medicine
|
September 1, 1983
Hunter' syndrome. Ultrastructural features in young children
J 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 results
T 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 Disorder
Christina 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 1993
R Koch, H L Levy, R Matalon, et al.
Annals of Internal Medicine
|
April 1, 1974
Glomerular sclerosis in adults with nephrotic syndrome
R Matalon, L Katz, G Gallo, et al.
Journal of Inherited Metabolic Disease
|
September 16, 2003
Danger of high-protein dietary supplements to persons with hyperphenylalaninaemia
R Koch, K D Moseley, R Moats, et al.
The Journal of Pediatrics
|
January 1, 1993
Prospective management of a child with neonatal citrullinemia
A 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 deficiency
K A Sacksteder, J C Morrell, R J Wanders, et al.
Page
of 19
Search research articles
Search
Showing results (91-100 of 185) with videos related to
Sort By:
Page
of 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 activation
D 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 disease
P L Rady, J M Penzien, T Vargas, et al.
Archives of Pathology & Laboratory Medicine
|
September 1, 1983
Hunter' syndrome. Ultrastructural features in young children
J 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 results
T 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 Disorder
Christina 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 1993
R Koch, H L Levy, R Matalon, et al.
Annals of Internal Medicine
|
April 1, 1974
Glomerular sclerosis in adults with nephrotic syndrome
R Matalon, L Katz, G Gallo, et al.
Journal of Inherited Metabolic Disease
|
September 16, 2003
Danger of high-protein dietary supplements to persons with hyperphenylalaninaemia
R Koch, K D Moseley, R Moats, et al.
The Journal of Pediatrics
|
January 1, 1993
Prospective management of a child with neonatal citrullinemia
A 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 deficiency
K A Sacksteder, J C Morrell, R J Wanders, et al.
Page
of 19