44 results on '"Brandt, Ira K."'
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2. Linkage analysis using heterozygote detection in phenylketonuria
3. Unusual association of Saethre-Chotzen syndrome and congenital adrenal hyperplasia
4. Propionicacidemia (Ketotic Hyperglycinemia): Dietary Treatment Resulting in Normal Growth and Development.
5. Nonketotic hyperglycinemia.
6. Linkage analysis using heterozygote detection in phenylketonuria.
7. Unusual association of Saethre-Chotzen syndrome and congenital adrenal hyperplasia.
8. A residential camp for children with phenylketonuria.
9. Clinical Atlas of Human Chromosomes Jean de Grouchy Catherine Turleau
10. Genetic Screening: Programs, Principles, and Research Committee for the Study of Inborn Errors of Metabolism of the National Research Council
11. INTRA-AORTIC TRANSFUSION OF OXYGENATED BLOOD AND ENDOTRACHEAL INSUFFLATION OF OXYGEN IN THE RESUSCITATION OF SEVERELY ANOXIC NEWBORN LAMBS.
12. Infectious and Bleeding Complications in Patients With Glycogenosis lb
13. Hurler Syndrome: a-L-Iduronidase Activity in Leukocytes as a Method for Heterozygote Detection
14. Hurler Syndrome α-L-Iduronidase Activity in Leukocytes as a Method for Heterozygote Detection
15. New Syndrome of Neonatal Hypoglycemia - Association with Visceromegaly, Macroglossia, Microcephaly and Abnormal Umbilicus
16. PSEUDO-HYPOALDOSTERONISM DUE TO SWEAT GLAND DYSFUNCTION
17. An artifact in the gas chromatographic analysis of urinary organic acids from phenylketonuric children: Decarboxylation of phenylpyruvic acid during extraction
18. A NEW VARIANT OF GALACTOSEMIA
19. Letter to the Editor: White Cell Ornithine Transcarbamylase Activity Cannot Detect the Liver Enzyme Deficiency
20. Mevalonate Kinase in Lysates of Cultured Human Fibroblasts and Lymphoblasts: Kinetic Properties, Assay Conditions, Carrier Detection and Measurement of Residual Activity in a Patient with Mevalonic Aciduria
21. Mevalonic Aciduria — An Inborn Error of Cholesterol and Nonsterol Isoprene Biosynthesis
22. Reply to Dr. Pinsky
23. Endogenous glucose production in type I glycogen storage disease
24. Kaufman syndrome (hydrometrocolpos, polydactyly, and congenital heart disease) with pituitary dysplasia, choanal atresia, and vertebral anomalies
25. Morquio's syndrome: Deficiency of a chondroitin sulfate N-acetylhexosamine sulfate sulfatase
26. Type III glycogenosis
27. Amino acids in muscle and kidney of potassium-deficient rats
28. Glycine acyltransferase activity in developing rat liver
29. Incorporation of Labeled Amino Acids into the Protein of Muscle and Liver Mitochondria
30. Hematologic Reactions to Diazoxide
31. Hepatolenticular degeneration: The comparative effectiveness of D-penicillamine, potassium sulfide, and diethyldithiocarbamate as decoppering agents
32. Copper Content of Some Low-Copper Foods
33. Carbohydrate, Electrolyte and Amino Acid Metabolism in the Anoxic Newborn Lamb
34. Hepatolenticular degeneration: Observations on a case treated with d-penicillamine
35. Rat liver glycine acyltransferase: Partial purification and some properties
36. Circulatory Phenomena During Anoxia in the Newborn Lamb
37. The development of the hippuric acid-synthesizing system in the rat
38. Transient hyperphenylalaninemia
39. Microtechniques of Clinical Chemistry for the Routine Laboratory
40. Genes, Enzymes, and Inherited Diseases
41. Genetics Today
42. Physiology of Prematurity
43. Protein and Amino Acid Requirements in Early Life
44. PSEUDOHYPOALDOSTERONISM DUE TO SWEAT GLAND DYSFUNCTION
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