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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

214 related articles for article (PubMed ID: 6264784)

  • 1. Niemann-Pick disease type B: prenatal diagnosis and enzymatic and chemical studies on fetal brain and liver.
    Wenger DA; Kudoh T; Sattler M; Palmieri M; Yudkoff M
    Am J Hum Genet; 1981 May; 33(3):337-44. PubMed ID: 6264784
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Clinical and biochemical diagnostics of Niemann-Pick disease.
    Maciejko D; Tylki-Szymańska A
    Klin Padiatr; 1986; 198(2):103-6. PubMed ID: 3009958
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Niemann-Pick disease, Type C: evidence for the deficiency of an activating factor stimulating sphingomyelin and glucocerebroside degradation.
    Christomanou H
    Hoppe Seylers Z Physiol Chem; 1980 Oct; 361(10):1489-502. PubMed ID: 6256275
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A profound deficiency of (CH3-14C)choline sphingomyelin-cleaving enzyme in Niemann-Pick disease type B.
    Orii T; Nakamura F; Kudoh T; Tsuchihashi K; Nakao T
    Tohoku J Exp Med; 1975 Oct; 117(2):193-5. PubMed ID: 174246
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. Chronic Niemann-Pick disease with sphingomyelinase deficiency in two brothers with mental retardation.
    Sogawa H; Horino K; Nakamura F; Kudoh T; Oyanagi K; Yamanouchi T; Minami R; Nakao T; Watanabe A; Matsuura Y
    Eur J Pediatr; 1978 Jul; 128(4):235-40. PubMed ID: 208852
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Activators for sphingohydrolases and the nature of the sphingomyelinase deficiency in Niemann-Pick disease types A, B and C (author's transl)].
    Baraton G; Revol A
    Clin Chim Acta; 1977 May; 76(3):339-43. PubMed ID: 192496
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. Niemann-Pick disease: prenatal diagnoses and studies of sphingomyelinase activities.
    Wenger DA; Wharton C; Sattler M; Clark C
    Am J Med Genet; 1978; 2(4):345-56. PubMed ID: 233699
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Niemann-Pick disease revealed late by miliary tuberculosis: diagnosis by leukocyte determination of sphingomyelinase deficiency].
    Kofman J; Chevalier JP; Brun J
    Nouv Presse Med; 1978 Dec; 7(45):4147. PubMed ID: 218165
    [No Abstract]   [Full Text] [Related]  

  • 11. 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]  

  • 12. Sphingomyelinase isozymes of human tissues: a phpothesis on enzymatic differentiation of the neuropathic and non-neuropathic forms of Niemann-Pick disease.
    Yamaguchi S; Suzuki K
    Biochem Biophys Res Commun; 1977 Aug; 77(3):999-1003. PubMed ID: 197954
    [No Abstract]   [Full Text] [Related]  

  • 13. [Niemann-Pick disease type C (subacute neurovisceral lipidosis). Problems of altered sphingomyelinase activity in the brain (author's transl)].
    Harzer K; Peiffer J
    Arch Psychiatr Nervenkr (1970); 1981; 230(1):71-9. PubMed ID: 6266371
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Subcellular localization of acid sphingomyelinase and lipid in Niemann-Pick mice.
    Sakiyama T; Akashi K; Akatsuka A; Owada M; Miyawaki S; Kitagawa T
    J Inherit Metab Dis; 1987; 10(3):301-4. PubMed ID: 2828764
    [No Abstract]   [Full Text] [Related]  

  • 15. Enzymatic hydrolysis of sphingomyelin liposomes by normal tissues and tissues from patients with Niemann-Pick disease.
    Poulos A; Shankaran P; Jones CS; Callahan JW
    Biochim Biophys Acta; 1983 May; 751(3):428-31. PubMed ID: 6303435
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Chemical and biochemical studies in fetuses affected with Nieman-Pick disease type A.
    Schoenfeld A; Ovadia J; Neri A; Abramovici A; Klibanski C
    Prenat Diagn; 1982 Jul; 2(3):177-83. PubMed ID: 6292890
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Importance of fluorescent lipid substrates for the study of hereditary lysosomal lipidoses. Application to the diagnosis of Niemann-Pick disease].
    Douste-Blazy L; Levade T; Salvayre R; Gatt S
    Bull Acad Natl Med; 1988 Jun; 172(6):807-13. PubMed ID: 2847857
    [No Abstract]   [Full Text] [Related]  

  • 18. 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]  

  • 19. Specific enzymatic diagnosis and ultrastructural analysis of peripheral leukocytes in infantile form of Niemann-Pick sphingomyelinosis.
    László A; Klujber L; Streitmann K; Barb E
    Acta Paediatr Hung; 1990; 30(1):99-105. PubMed ID: 2156543
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 11.