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62 results on '"Hardwick DF"'

52. Hyperprolinemia type II.

Author

Applegarth DA, Ingram P, Hingston J, and Hardwick DF

Subjects
Alanine Transaminase blood, Alkaline Phosphatase blood, Amino Acids blood, Asparagine urine, Aspartate Aminotransferases blood, Blood Protein Electrophoresis, Body Height, Body Weight, Borohydrides, Child, Child, Preschool, Chromatography, Ion Exchange, Chromatography, Paper, Creatinine metabolism, Electroencephalography, Female, Glutamine urine, Humans, Immunoglobulin A analysis, Immunoglobulin G analysis, L-Lactate Dehydrogenase blood, Male, Spectrophotometry, Spectrophotometry, Ultraviolet, Amino Acid Metabolism, Inborn Errors blood, Proline metabolism
Published
1974
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53. Congenital osteopetrosis: an unusual cause of hydrocephalus.

Author

Baird PA, Robinson GC, Hardwick DF, and Sovereign AE

Subjects
Alkaline Phosphatase blood, Calcium blood, Humans, Hydrocephalus diagnostic imaging, Infant, Infant, Newborn, Male, Osteopetrosis diagnostic imaging, Osteopetrosis pathology, Phosphorus blood, Radiography, Hydrocephalus etiology, Osteopetrosis complications, Osteopetrosis congenital
Published
1968

54. Liver glycogen phosphorylase deficiency.

Author

Drummond GI, Hardwick DF, and Israels S

Subjects
Blood Glucose analysis, Carbohydrate Metabolism, Inborn Errors diagnosis, Female, Glucagon analysis, Hepatomegaly etiology, Histocytochemistry, Humans, Hypoglycemia etiology, Infant, Leukocytes enzymology, Liver pathology, Carbohydrate Metabolism, Inborn Errors enzymology, Glucosyltransferases analysis, Liver enzymology, Liver Glycogen metabolism
Published
1970

55. Pathogenesis of methionine-induced toxicity.

Author

Hardwick DF, Applegarth DA, Cockcroft DM, Ross PM, and Cder RJ

Subjects
Amino Acids blood, Animals, Fatty Liver chemically induced, Female, Guinea Pigs, Hypoglycemia chemically induced, Hypothermia mortality, Kidney metabolism, Liver drug effects, Liver Glycogen metabolism, Male, Methionine metabolism, Nucleosides metabolism, Rats, Spasm mortality, Stereoisomerism, Adenosine Triphosphate metabolism, Liver metabolism, Methionine toxicity
Published
1970
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57. Cerebro-hepato-renal syndrome of Zellweger.

Author

Jan JE, Hardwick DF, Lowry RB, and McCormick AQ

Subjects
Chondrodysplasia Punctata complications, Eye Abnormalities, Facial Expression, Female, Hematopoiesis, Humans, Infant, Newborn, Iron metabolism, Kidney Diseases, Cystic complications, Liver Diseases complications, Metabolism, Inborn Errors complications, Pregnancy, Abnormalities, Multiple complications, Central Nervous System Diseases complications, Muscular Diseases complications
Published
1970
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58. Cystathioninuria in two healthy siblings.

Author

Perry TL, Hardwick DF, Hansen S, Love DL, and Israels S

Subjects
Amino Acid Metabolism, Inborn Errors drug therapy, Amino Acids blood, Amino Acids cerebrospinal fluid, Child, Child, Preschool, Female, Humans, Male, Methionine, Pyridoxine therapeutic use, Amino Acid Metabolism, Inborn Errors genetics, Amino Acids urine
Published
1968
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59. Hyperprolinaemia in two successive generations of a North American Indian family.

Author

Perry TL, Hardwick DF, Lowry RB, and Hansen S

Subjects
Adult, Amino Acid Metabolism, Inborn Errors complications, British Columbia, Child, Child, Preschool, Female, Humans, Infant, Intellectual Disability complications, Male, Middle Aged, Pedigree, Proline blood, Proline cerebrospinal fluid, Wilms Tumor complications, Amino Acid Metabolism, Inborn Errors genetics, Indians, North American, Proline metabolism
Published
1968
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60. Thalassemic hydrops fetalis in two Chinese-Canadian families.

Author

Gray GR, Towell ME, Wright VJ, and Hardwick DF

Subjects
Acid-Base Equilibrium, Asian People, Canada, Carbon Dioxide blood, China, Electrophoresis, Starch Gel, Erythrocytes enzymology, Female, Glucosephosphate Dehydrogenase Deficiency, Hemoglobinometry, Humans, Inclusion Bodies, Infant, Newborn, Osmotic Fragility, Oxygen blood, Pregnancy, Thalassemia congenital, Edema congenital, Fetal Diseases genetics, Infant, Newborn, Diseases genetics, Thalassemia genetics
Abstract

Two unrelated Chinese-Canadian families with recurrent hydrops fetalis are described. The investigation, acid-base and blood gas studies, and clinical course of one hydropic fetus with large amounts of hemoglobin Bart's who survived for three hours are described. Data for the parents of both families, consistent with the alphathalassemia carrier state, are presented.

Published
1972

61. Methionine induction of experimental tyrosinaemia.

Author

Perry TL, Hardwick DF, Hansen S, Pohlmann L, and Warrington PD

Subjects
Amino Acids blood, Animals, Chromosome Aberrations, Chromosome Disorders, Guinea Pigs, Pancreas pathology, Tyrosine metabolism, Tyrosine urine, Amino Acid Metabolism, Inborn Errors chemically induced, Methionine metabolism, Tyrosine blood
Published
1967
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