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Journal Abstract Search
153 related items for PubMed ID: 4110774
21. Inborn errors of metabolism in neurology (Wilson's disease, Refsum's disease and lipidoses). Cumings JN. Proc R Soc Med; 1971 Mar; 64(3):313-22. PubMed ID: 4101505 [No Abstract] [Full Text] [Related]
22. [Metachromatic leucodystrophy or sulfatidosis in children]. Marchal C, Vidailhet M, Vidailhet C, Humbel R, Grignon G, Floquet J. Arch Fr Pediatr; 1970 Nov; 27(9):996. PubMed ID: 5510699 [No Abstract] [Full Text] [Related]
23. Simple biochemical methods for the study of lipidoses and aminoacidopathies. Adriaenssens K, Karcher D. Riv Patol Nerv Ment; 1970 Oct; 91(5):274-6. PubMed ID: 5525772 [No Abstract] [Full Text] [Related]
24. Genetics and the sphingolipidoses. Brady RO. Med Clin North Am; 1969 Jul; 53(4):827-38. PubMed ID: 4892639 [No Abstract] [Full Text] [Related]
25. [Recent biochemical research on some types of cerebral lipid thesaurismosis]. Ionăşescu V. Stud Cercet Neurol; 1966 Oct; 11(5):431-42. PubMed ID: 4166985 [No Abstract] [Full Text] [Related]
26. The sphingolipidoses. Brady RO. N Engl J Med; 1966 Aug 11; 275(6):312-8. PubMed ID: 5940695 [No Abstract] [Full Text] [Related]
27. [Recent findings in lipidoses]. Yokoi S. Shinkei Kenkyu No Shimpo; 1968 Aug 11; 12(1):159-76. PubMed ID: 4972824 [No Abstract] [Full Text] [Related]
28. Inherited neuropathies related to disorders of lipid metabolism. Thomas PK. Adv Neurol; 1988 Aug 11; 48():133-44. PubMed ID: 2446477 [No Abstract] [Full Text] [Related]
29. [Genetic, biochemical and morphopathological bases for the current classification of neurolipidoses]. Predescu V, Alexianu M, Milea S, Christodorescu D. Rev Med Interna Neurol Psihiatr Neurochir Dermatovenerol Neurol Psihiatr Neurochir; 1977 Aug 11; 22(1):1-14. PubMed ID: 406655 [No Abstract] [Full Text] [Related]
32. [Histocytochemistry of the demyelinating disease, leukodystrophy]. Yokoi S. No To Shinkei; 1968 Oct 11; 20(10):986-90. PubMed ID: 4180410 [No Abstract] [Full Text] [Related]
35. Fatty acid composition of cholesterol esters in brains of patients with Schilder's disease, G M1 -gangliosidosis and Tay-Sachs disease, and its possible relationship to the -position fatty acids of lecithin. Eto Y, Suzuki K. J Neurochem; 1971 Jun 11; 18(6):1007-16. PubMed ID: 5567894 [No Abstract] [Full Text] [Related]
36. Studies on neuronal lipid dystrophies. Seitelberger F, Sluga E, Bernhelmer H. Pathol Eur; 1968 Jun 11; 3(2):230-47. PubMed ID: 5688460 [No Abstract] [Full Text] [Related]
38. [A case of neurovisceral gangliosidosis]. Hooghwinkel GJ, Bots GT. Ned Tijdschr Geneeskd; 1968 Oct 26; 112(43):1952-8. PubMed ID: 5687137 [No Abstract] [Full Text] [Related]
39. Study of hereditary metabolic diseases using in vitro techniques. Hsia DY. Metabolism; 1970 Apr 26; 19(4):309-39. PubMed ID: 4190983 [No Abstract] [Full Text] [Related]
40. A case of GM2-gangliosidosis with total hexosaminidase deficiency. Suzuki Y, Jacob JC, Suzuki K, Suzuki K. Neurology; 1970 Apr 26; 20(4):388. PubMed ID: 5535009 [No Abstract] [Full Text] [Related] Page: [Previous] [Next] [New Search]