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1. Abnormal Hypermethylation at Imprinting Control Regions in Patients with S-Adenosylhomocysteine Hydrolase (AHCY) Deficiency.

2. Molecular and biochemical investigations of patients with intermediate or severe hyperhomocysteinemia

3. Two patients with hepatic mtDNA depletion syndromes and marked elevations of S-adenosylmethionine and methionine

4. Hypermethioninemias of genetic and non-genetic origin: A review

5. Liver transplantation for treatment of severe S-adenosylhomocysteine hydrolase deficiency

6. Infantile hypermethioninemia and hyperhomocysteinemia due to high methionine intake: a diagnostic trap

7. Progressive cerebral edema associated with high methionine levels and betaine therapy in a patient with cystathionine β-synthase (CBS) deficiency

8. Biochemical Basis for the Dominant Inheritance of Hypermethioninemia Associated with the R264H Mutation of theMAT1A Gene

9. Isolated hypermethioninemia: Measurements of S-adenosylmethionine and choline

10. Neurologically normal development of a patient with severe methionine adenosyltransferase I/III deficiency after continuing dietary methionine restriction

11. Abnormal Hypermethylation at Imprinting Control Regions in Patients with S-Adenosylhomocysteine Hydrolase (AHCY) Deficiency

12. Metabolic profiling of total homocysteine and related compounds in hyperhomocysteinemia: utility and limitations in diagnosing the cause of puzzling thrombophilia in a family

13. Enzymatic activity of methionine adenosyltransferase variants identified in patients with persistent hypermethioninemia

14. S-adenosylhomocysteine hydrolase deficiency: two siblings with fetal hydrops and fatal outcomes

15. A revisit to the natural history of homocystinuria due to cystathionine beta-synthase deficiency

16. S-Adenosylhomocysteine Hydrolase (AHCY) Deficiency: Two Novel Mutations with Lethal Outcome

17. HIES

18. Hereditary Motor and Sensory Neuropathy

19. Hyperostosis Corticalis Deformans Juvenilis

20. Human Transmissible Spongiform Encephalopathies

21. Hereditary Nephritis

22. Hearing Loss, Noise-induced and Acoustic Trauma

23. Hypersensitivity Type I

24. Hypoglycemia, Non-islet Cell

25. Hyper-IgE Recurrent Infection Syndrome

26. Hypermobility Syndrome

27. Hyperostose en Coulée

28. Hyperekplexia, Hereditary

29. Hand-Heart Syndrome

30. Hyperostosis, Infantile Cortical

31. Hyperparathyroidism, Primary

32. Hypothyroidism, Nongoitrous Congenital

33. β-Hexosaminidase α-Subunit Deficiency

34. Hypoxic Ischemia

35. High Blood Triglycerides

36. Hypersensitivity Vasculitis

37. Hyperthyroidism due to Thyroid Autonomy

38. Hyperhomocysteinemia: Genetic Basis and Arterial Thrombosis

39. Hyperthyroidism, Sporadic Non-autoimmune

40. Hereditary Renal Hypouricemia

41. Huntington’s Chorea

42. Hepatitis, Acute

43. Hauptmann-Thannhauser Muscular Dystrophy

44. High Triglycerides

45. Hemophilia B

46. Human RSV

47. Hypotrichosis-Lymphedema-Telangiectasia Syndrome

48. Hypertrophic Pulmonary Osteoarthropathy

49. Hyperostosis Calvaria Interna

50. Hypovitaminosis E

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