Search research articles
Contact Us
Filters
Showing results (101-110 of 175) with videos related to
Page
of 18
Sort By:
Annals of the New York Academy of Sciences
|
January 1, 1985
Biotin deficiency complicating parenteral alimentation: diagnosis, metabolic repercussions, and treatment
D M Mock, D L Baswell, H Baker, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1989
3-Ketothiolase deficiency: heterogeneity in a defect of mitochondrial acetoacetyl-CoA thiolase biosynthesis in fibroblasts from four patients
H Nagasawa, S Yamaguchi, T Orii, et al.
European Journal of Pediatrics
|
September 1, 1984
A child with acute pancreatitis and recurrent hypoglycemia due to 3-hydroxy-3-methylglutaryl-CoA lyase deficiency
W G Wilson, M B Cass, O Søvik, et al.
Biophysical Journal
|
May 12, 2009
Nature of the individual Ca binding sites in Ca-regenerated bacteriorhodopsin
Y N Zhang, L L Sweetman, E S Awad, et al.
American Journal of Medical Genetics
|
April 1, 1990
Pyridoxine-unresponsive homocystinuria with an unusual clinical course
F B Cochran, L Sweetman, K Schmidt, et al.
The New England Journal of Medicine
|
April 2, 1981
Biotin deficiency: an unusual complication of parenteral alimentation
D M Mock, A A deLorimer, W M Liebman, et al.
The Journal of Pediatrics
|
May 1, 1985
Biotin deficiency complicating parenteral alimentation: diagnosis, metabolic repercussions, and treatment
D M Mock, D L Baswell, H Baker, et al.
Pediatric Research
|
August 1, 1979
Abnormal pyruvate and alpha-ketoglutarate dehydrogenase complexes in a patient with lactic acidemia
Y Kuroda, J J Kline, L Sweetman, et al.
The Journal of Pediatrics
|
June 1, 1980
Glutaric aciduria Type II
L Sweetman, W L Nyhan, D A Tauner, et al.
Monographs in Human Genetics
|
January 1, 1978
The diagnosis and management of propionic acidemia
C de Cespedes, A R Loria, Y Estrada, et al.
Page
of 18
Search research articles
Search
Showing results (101-110 of 175) with videos related to
Sort By:
Page
of 18
Annals of the New York Academy of Sciences
|
January 1, 1985
Biotin deficiency complicating parenteral alimentation: diagnosis, metabolic repercussions, and treatment
D M Mock, D L Baswell, H Baker, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1989
3-Ketothiolase deficiency: heterogeneity in a defect of mitochondrial acetoacetyl-CoA thiolase biosynthesis in fibroblasts from four patients
H Nagasawa, S Yamaguchi, T Orii, et al.
European Journal of Pediatrics
|
September 1, 1984
A child with acute pancreatitis and recurrent hypoglycemia due to 3-hydroxy-3-methylglutaryl-CoA lyase deficiency
W G Wilson, M B Cass, O Søvik, et al.
Biophysical Journal
|
May 12, 2009
Nature of the individual Ca binding sites in Ca-regenerated bacteriorhodopsin
Y N Zhang, L L Sweetman, E S Awad, et al.
American Journal of Medical Genetics
|
April 1, 1990
Pyridoxine-unresponsive homocystinuria with an unusual clinical course
F B Cochran, L Sweetman, K Schmidt, et al.
The New England Journal of Medicine
|
April 2, 1981
Biotin deficiency: an unusual complication of parenteral alimentation
D M Mock, A A deLorimer, W M Liebman, et al.
The Journal of Pediatrics
|
May 1, 1985
Biotin deficiency complicating parenteral alimentation: diagnosis, metabolic repercussions, and treatment
D M Mock, D L Baswell, H Baker, et al.
Pediatric Research
|
August 1, 1979
Abnormal pyruvate and alpha-ketoglutarate dehydrogenase complexes in a patient with lactic acidemia
Y Kuroda, J J Kline, L Sweetman, et al.
The Journal of Pediatrics
|
June 1, 1980
Glutaric aciduria Type II
L Sweetman, W L Nyhan, D A Tauner, et al.
Monographs in Human Genetics
|
January 1, 1978
The diagnosis and management of propionic acidemia
C de Cespedes, A R Loria, Y Estrada, et al.
Page
of 18