These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
134 related articles for article (PubMed ID: 6295665)
21. A practical chromogenic procedure for the detection of homozygotes and heterozygous carriers of Niemann-Pick disease. Gal AE; Brady RO; Hibbert SR; Pentchev PG N Engl J Med; 1975 Sep; 293(13):632-6. PubMed ID: 239343 [TBL] [Abstract][Full Text] [Related]
22. Deficiency of phospholipase C acting on phosphatidylglycerol in Niemann-Pick disease. Huterer S; Wherrett JR; Poulos A; Callahan JW Neurology; 1983 Jan; 33(1):67-73. PubMed ID: 6681561 [TBL] [Abstract][Full Text] [Related]
23. [Adult Niemann-Pick disease: a 26 years follow-up. Report of a case with isolated visceral involvement, excess of tissue sphingomyelin, and deficient sphingomyelinase activity (author's transl)]. Brière J; Calman F; Lageron A; Hinglais N; Emerit J; Bernard J Nouv Rev Fr Hematol Blood Cells; 1976; 16(2):185-202. PubMed ID: 184433 [TBL] [Abstract][Full Text] [Related]
24. Sphingomyelinase activity levels in human peripheral blood leukocytes, using [3H]sphingomyelin as substrate: study of heterozygotes and homozygotes for Niemann-Pick disease variants. Zitman D; Chazan S; Klibansky C Clin Chim Acta; 1978 May; 86(1):37-43. PubMed ID: 26487 [TBL] [Abstract][Full Text] [Related]
25. Diagnosis of Niemann-Pick disease using a simple and sensitive fluorimetric assay of sphingomyelinase activity. Besley GT Clin Chim Acta; 1978 Dec; 90(3):269-78. PubMed ID: 31994 [TBL] [Abstract][Full Text] [Related]
26. A family with visceral course of Niemann-Pick disease, macular halo syndrome and low sphingomyelin degradation rate. Sperl W; Bart G; Vanier MT; Christomanou H; Baldissera I; Steichen-Gersdorf E; Paschke E J Inherit Metab Dis; 1994; 17(1):93-103. PubMed ID: 8051942 [TBL] [Abstract][Full Text] [Related]
27. Uptake and metabolism of radioactively labeled sphingomyelin in cultured skin fibroblasts from controls and patients with Niemann-Pick disease and other lysosomal storage diseases. Kudoh T; Velkoff MA; Wenger DA Biochim Biophys Acta; 1983 Nov; 754(1):82-92. PubMed ID: 6626569 [TBL] [Abstract][Full Text] [Related]
28. Synthesis of pyrenesulfonylamido-sphingomyelin and its use as substrate for determining sphingomyelinase activity and diagnosing Niemann-Pick disease. Klar R; Levade T; Gatt S Clin Chim Acta; 1988 Sep; 176(3):259-67. PubMed ID: 2846208 [TBL] [Abstract][Full Text] [Related]
29. Sphingomyelinase activities of various human tissues in control subjects and in Niemann-Pick disease - development and evaluation of a microprocedure. Vanier MT; Revol A; Fichet M Clin Chim Acta; 1980 Oct; 106(3):257-67. PubMed ID: 6251986 [TBL] [Abstract][Full Text] [Related]
30. Studies on pyrophosphate diesterase activity in cultured human fibroblasts: a deficiency in Niemann-Pick disease. Besley GT; Moss SE Clin Chim Acta; 1981 Nov; 117(1):75-84. PubMed ID: 6277531 [TBL] [Abstract][Full Text] [Related]
31. A new variant of sphingomyelinase deficiency (Niemann-Pick): visceromegaly, minimal neurological lesions and low in vivo degradation rate of sphingomyelin. Elleder M; Nevoral J; Spicáková V; Hyniová H; Kraus J; Krásný J; Vanier MT J Inherit Metab Dis; 1986; 9(4):357-66. PubMed ID: 3104673 [TBL] [Abstract][Full Text] [Related]
32. Studies on sphingomyelinase and beta-glucosidase activities in Niemann-Pick disease variants. Phosphodiesterase activities measured with natural and artificial substrates. Besley GT; Moss SE Biochim Biophys Acta; 1983 Jun; 752(1):54-64. PubMed ID: 6303436 [TBL] [Abstract][Full Text] [Related]
33. Gelastic cataplexy in Niemann-Pick disease group C and related variants without generalized sphingomyelinase deficiency. Philippart M; Engel J; Zimmerman EG Ann Neurol; 1983 Oct; 14(4):492-3. PubMed ID: 6314876 [No Abstract] [Full Text] [Related]
34. Fibroblast phosphodiesterase deficiency in Niemann-Pick disease. Fensom AH; Benson PF; Babarik AW; Grant AR; Jacobs L Biochem Biophys Res Commun; 1977 Feb; 74(3):877-83. PubMed ID: 191016 [No Abstract] [Full Text] [Related]
35. Chemical and biochemical studies in human fetuses affected with Niemann-Pick disease type A. Klibansky C; Chazan S; Schoenfeld A; Abramovici A Clin Chim Acta; 1979 Feb; 91(3):243-50. PubMed ID: 761400 [TBL] [Abstract][Full Text] [Related]
36. Immunological studies on lysosomal sphingomyelinase: identification of a 28 000-Da component deficient in urine from patients with Niemann-Pick disease types A and B. Schram AW; Dreissen M; Bastiaannet J; Donker-Koopman WE; Brouwer-Kelder EM; Weitz G; Barranger JA; Sandhoff K; Tager JM Biosci Rep; 1984 Dec; 4(12):1051-7. PubMed ID: 6099155 [TBL] [Abstract][Full Text] [Related]
37. Lack of acid sphingomyelinase in the mitochondria-lysosome fraction of brain from Niemann-Pick mice. Tsuda M; Owada M; Kitagawa T; Miyawaki S J Inherit Metab Dis; 1985; 8(3):147-8. PubMed ID: 3027450 [No Abstract] [Full Text] [Related]
38. An animal model of human acid sphingomyelinase deficiency (Niemann-Pick disease) and the study of its enzyme replacement (the Japan Society of Human Genetics award lecture). Kitagawa T Jinrui Idengaku Zasshi; 1987 Jun; 32(2):55-69. PubMed ID: 2830422 [No Abstract] [Full Text] [Related]
39. Sphingomyelinase and nonspecific phosphodiesterase activities in Epstein-Barr virus-transformed lymphoid cell lines from Niemann-Pick disease A, B and C. Levade T; Salvayre R; Lenoir G; Douste-Blazy L Biochim Biophys Acta; 1984 Apr; 793(2):321-4. PubMed ID: 6324871 [TBL] [Abstract][Full Text] [Related]
40. Studies on the activation of sphingomyelinase activity in Niemann-Pick type A, B, and C fibroblasts: enzymological differentiation of types A and B. Poulos A; Ranieri E; Shankaran P; Callahan JW Pediatr Res; 1984 Nov; 18(11):1088-93. PubMed ID: 6096798 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]