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G N Donnell

Showing results (61-70 of 73) with videos related to

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Radiology|July 11, 1992
Galactosemia: evaluation with MR imagingM D Nelson, J A Wolff, C A Cross, et al.
Pediatric Research|February 1, 1989
Galactose metabolism in human ovarian tissueY K Xu, W G Ng, F R Kaufman, et al.
American Journal of Ophthalmology|November 1, 1972
Galactokinase-deficiency cataracts in identical twinsA E Oberman, W A Wilson, S D Frasier, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|August 31, 1995
HPLC analysis of uridine diphosphate sugars: decreased concentrations of uridine diphosphate galactose in erythrocytes and cultured skin fibroblasts from classical galactosemia patientsY K Xu, F R Kaufman, G N Donnell, et al.
Journal of Inherited Metabolic Disease|January 1, 1983
Neonatal pyruvate carboxylase deficiency with renal tubular acidosis and cystinuriaJ Oizumi, K N Shaw, T A Giudici, et al.
Birth Defects Original Article Series|January 1, 1975
A syndrome of systemic hyalinosis, short-limb dwarfism and possible thymic dysplasiaO S Alfi, E T Heuser, B H Landing, et al.
Clinical Genetics|June 1, 1984
Partial ornithine transcarbamylase deficiency associated with recurrent hyperammonemia, lethargy and depressed sensoriumJ Oizumi, W G Ng, R Koch, et al.
Biochemical Medicine and Metabolic Biology|June 1, 1986
Methylmalonic and propionic acidemias: lipid profiles of normal and affected human skin fibroblasts incubated with [1-14C]propionateT A Giudici, R G Chen, J Oizumi, et al.
Cytogenetics and Cell Genetics|January 1, 1984
Congenital lactic acidosis associated with pyruvate carboxylase deficiency. Repository identification No. GM6056J Oizumi, G N Donnell, W G Ng, et al.
Acta Endocrinologica|February 1, 1989
Gonadal function and ovarian galactose metabolism in classic galactosemiaF R Kaufman, Y K Xu, W G Ng, et al.
Pageof 8

Showing results (61-70 of 73) with videos related to

Sort By:
Pageof 8
Radiology|July 11, 1992
Galactosemia: evaluation with MR imagingM D Nelson, J A Wolff, C A Cross, et al.
Pediatric Research|February 1, 1989
Galactose metabolism in human ovarian tissueY K Xu, W G Ng, F R Kaufman, et al.
American Journal of Ophthalmology|November 1, 1972
Galactokinase-deficiency cataracts in identical twinsA E Oberman, W A Wilson, S D Frasier, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|August 31, 1995
HPLC analysis of uridine diphosphate sugars: decreased concentrations of uridine diphosphate galactose in erythrocytes and cultured skin fibroblasts from classical galactosemia patientsY K Xu, F R Kaufman, G N Donnell, et al.
Journal of Inherited Metabolic Disease|January 1, 1983
Neonatal pyruvate carboxylase deficiency with renal tubular acidosis and cystinuriaJ Oizumi, K N Shaw, T A Giudici, et al.
Birth Defects Original Article Series|January 1, 1975
A syndrome of systemic hyalinosis, short-limb dwarfism and possible thymic dysplasiaO S Alfi, E T Heuser, B H Landing, et al.
Clinical Genetics|June 1, 1984
Partial ornithine transcarbamylase deficiency associated with recurrent hyperammonemia, lethargy and depressed sensoriumJ Oizumi, W G Ng, R Koch, et al.
Biochemical Medicine and Metabolic Biology|June 1, 1986
Methylmalonic and propionic acidemias: lipid profiles of normal and affected human skin fibroblasts incubated with [1-14C]propionateT A Giudici, R G Chen, J Oizumi, et al.
Cytogenetics and Cell Genetics|January 1, 1984
Congenital lactic acidosis associated with pyruvate carboxylase deficiency. Repository identification No. GM6056J Oizumi, G N Donnell, W G Ng, et al.
Acta Endocrinologica|February 1, 1989
Gonadal function and ovarian galactose metabolism in classic galactosemiaF R Kaufman, Y K Xu, W G Ng, et al.
Pageof 8