Inborn Errors of Metabolism in Man, Issue 9Oded Sperling, André De Vries, J. E. Seegmiller S. Karger, 1978 - Metabolism, Inborn errors of |
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Page 56
... protein metabolism ; pp . 299-387 ( Academic Press , New York 1970 ) . 8 Nyhan , W.I. and Childs , B ... protein synthesis in humans . II . Measurement of the metabolic pool and the rate of protein synthesis . J. Biol . Chem . 201 : 457 ...
... protein metabolism ; pp . 299-387 ( Academic Press , New York 1970 ) . 8 Nyhan , W.I. and Childs , B ... protein synthesis in humans . II . Measurement of the metabolic pool and the rate of protein synthesis . J. Biol . Chem . 201 : 457 ...
Page 81
... PROTEIN . G / KG / DAY R. B. 1.0 0.5 H BIOTIN , Mg./DAY- 10 0.15 5 0.15 5 Mg . 100 KETONURIA 4+ 4+ 4 + 0 4 + 0 4+ 4+ 4+ -8 90 -62 -5.5 -5.5 -5 -7 -8.5 -52 80 % 70 -32-7 32 BRONCHITIS TONSILLITIS MILD ACIDOSIS BRIGHTER AND PIGMENTED HAIR ...
... PROTEIN . G / KG / DAY R. B. 1.0 0.5 H BIOTIN , Mg./DAY- 10 0.15 5 0.15 5 Mg . 100 KETONURIA 4+ 4+ 4 + 0 4 + 0 4+ 4+ 4+ -8 90 -62 -5.5 -5.5 -5 -7 -8.5 -52 80 % 70 -32-7 32 BRONCHITIS TONSILLITIS MILD ACIDOSIS BRIGHTER AND PIGMENTED HAIR ...
Page 82
... protein / kg / day was initiated . After a few months on this diet , the girl showed alternating pigmented and unpigmented bands in the hair , the flag sign of protein malnutrition . She was hypotonic and the skin was doughy , although ...
... protein / kg / day was initiated . After a few months on this diet , the girl showed alternating pigmented and unpigmented bands in the hair , the flag sign of protein malnutrition . She was hypotonic and the skin was doughy , although ...
Contents
Structural Mutation of Aldolase B | 2 |
Prenatal Diagnosis of Fucosidosis | 7 |
Erythrocyte Glutathione | 16 |
Copyright | |
26 other sections not shown
Common terms and phrases
abnormal Acta aldolase amino acid amniotic fluid assay B12 deficient Basel biochemical Biol biopsy blood brain cell cultures cell lines cholate choline Clin clinical concentration contamination cystathionine cystine defect dehydrogenase demonstrated diabetes diet dietary disorders elevated enzymatic enzyme enzyme activity errors of metabolism erythrocytes excretion fetal fibroblasts FIGLU Gaucher's disease Genet glucocerebrosidase glucocerebrosidase activity glucose glutamate glutathione glycine Glycogen GSD-I heterozygotes hexosaminidase homocystinuria human inactivation inborn errors increased Karger lactate leukocyte HAA leukocytes levels lipid liver lysosomal Medical membrane methionine method mg/dl molecular Monogr muscle Mutant Cell mycoplasma newborn NIG therapy nonketotic hyperglycinemia normal patients Pediat phenylalanine phenylketonuria phosphatase plasma population pregnancies prenatal diagnosis protein pyruvate range renal Repository retardation samples Sandhoff disease screening serum Storage disease studies substrate syndrome Table Tay-Sachs disease tissue treatment Tween Type tyrosine urinary urine vitamin