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.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

91 related items for PubMed ID: 2986935

  • 1. [Pseudohypertriglyceridemia in glycerokinase deficiency].
    Wirth A, Heuck CC, Bieger W, Schlierf G.
    Dtsch Med Wochenschr; 1985 May 24; 110(21):843-7. PubMed ID: 2986935
    [Abstract] [Full Text] [Related]

  • 2. [Pseudohypertriglyceridemia due to hyperglycerolemia caused by glycerol kinase deficiency].
    Chanu B, Bakir R, Goussault Y, Neel D, Turpin E, Dreux C, Rouffy J.
    Nouv Presse Med; 1982 Apr 24; 11(19):1498-9. PubMed ID: 6281724
    [No Abstract] [Full Text] [Related]

  • 3.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 4.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 5.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 6. [Glycerol kinase deficiency].
    Matsumoto T, Niikawa N.
    Tanpakushitsu Kakusan Koso; 1988 Apr 24; 33(5):678-81. PubMed ID: 2855951
    [No Abstract] [Full Text] [Related]

  • 7.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 8.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 9.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 10. Complex glycerol kinase deficiency: molecular-genetic, cytogenetic, and clinical studies of five Japanese patients.
    Matsumoto T, Kondoh T, Yoshimoto M, Fujieda K, Matsuura N, Matsuda I, Miike T, Yano K, Okuno A, Aoki Y.
    Am J Med Genet; 1988 Nov 24; 31(3):603-16. PubMed ID: 2852474
    [Abstract] [Full Text] [Related]

  • 11. Two cases of isolated glycerol kinase deficiency with heterogeneous neurological symptoms.
    Illsinger S, Marquardt I, Lücke T, Hellerud C, Korenke C, Das AM.
    Dev Med Child Neurol; 2007 May 24; 49(5):396-7. PubMed ID: 17489818
    [No Abstract] [Full Text] [Related]

  • 12. [Pseudohypertriglyceridemia due to hyperglycerolaemia].
    Raynaud E, Perez-Martin A, Lalande O, Solere M.
    Ann Biol Clin (Paris); 2000 May 24; 58(5):607-9. PubMed ID: 11022104
    [No Abstract] [Full Text] [Related]

  • 13. Human glycerol kinase deficiency: an inborn error of compartmental metabolism.
    McCabe ER.
    Biochem Med; 1983 Oct 24; 30(2):215-30. PubMed ID: 6316939
    [Abstract] [Full Text] [Related]

  • 14. Novel mutation (Gly280Ala) in the ATP-binding domain of glycerol kinase causes severe hyperglycerolemia.
    Wibmer T, Otto J, Parhofer KG, Otto C.
    Exp Clin Endocrinol Diabetes; 2005 Jul 24; 113(7):396-403. PubMed ID: 16025401
    [Abstract] [Full Text] [Related]

  • 15. Pseudo-hypertriglyceridaemia: a measurement artefact due to glycerol kinase deficiency.
    Walmsley TA, Potter HC, George PM, Florkowski CM.
    Postgrad Med J; 2008 Oct 24; 84(996):552-4. PubMed ID: 19017842
    [Abstract] [Full Text] [Related]

  • 16. Fine mapping of glycerol kinase deficiency and congenital adrenal hypoplasia within Xp21 on the short arm of the human X chromosome.
    Davies KE, Patterson MN, Kenwrick SJ, Bell MV, Sloan HR, Westman JA, Elsas LJ, Mahan J.
    Am J Med Genet; 1988 Mar 24; 29(3):557-64. PubMed ID: 2837087
    [Abstract] [Full Text] [Related]

  • 17. Deficiency of glycerol kinase (EC 2.7.1.30).
    Eriksson A, Lindstedt S, Ransnäs L, von Wendt L.
    Clin Chem; 1983 Apr 24; 29(4):718-22. PubMed ID: 6299616
    [Abstract] [Full Text] [Related]

  • 18. [Case of adrenal insufficiency, nonspecific myopathy, psychomotor retardation and glyceroluria--glycerol kinase deficiency?].
    Yoshimoto M, Takayanagi T, Nagayoshi T, Baba T, Tsuji Y.
    No To Hattatsu; 1984 Jul 24; 16(4):328-9. PubMed ID: 6091705
    [No Abstract] [Full Text] [Related]

  • 19. Pseudo-pseudohypertriglyceridemia: a case of increased free glycerol without evidence for glycerol kinase deficiency.
    Nauck M, Winkler K, Siekmeier R, Marangos N, Richter B, März W, Wieland H.
    Clin Chem; 1995 Apr 24; 41(4):619-20. PubMed ID: 7720256
    [Abstract] [Full Text] [Related]

  • 20. Aland Island eye disease (Forsius-Eriksson ocular albinism) and an Xp21 deletion in a patient with Duchenne muscular dystrophy, glycerol kinase deficiency, and congenital adrenal hypoplasia.
    Pillers DA, Weleber RG, Powell BR, Hanna CE, Magenis RE, Buist NR.
    Am J Med Genet; 1990 May 24; 36(1):23-8. PubMed ID: 2159212
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 5.