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

262 related items for PubMed ID: 22587661

  • 1.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 2.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

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

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

  • 5. Non-insulinoma persistent hyperinsulinaemic hypoglycaemia caused by an activating glucokinase mutation: hypoglycaemia unawareness and attacks.
    Christesen HB, Brusgaard K, Beck Nielsen H, Brock Jacobsen B.
    Clin Endocrinol (Oxf); 2008 May; 68(5):747-55. PubMed ID: 18208578
    [Abstract] [Full Text] [Related]

  • 6.
    ; . PubMed ID:
    [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. Insulinoma presenting as postprandial hypoglycaemia.
    Madathil A, Weaver J.
    BMJ Case Rep; 2011 Aug 24; 2011():. PubMed ID: 22678942
    [Abstract] [Full Text] [Related]

  • 11. Seizures and epilepsy in hypoglycaemia caused by inborn errors of metabolism.
    Gataullina S, Delonlay P, Lemaire E, Boddaert N, Bulteau C, Soufflet C, Laín GA, Nabbout R, Chiron C, Dulac O.
    Dev Med Child Neurol; 2015 Feb 24; 57(2):194-9. PubMed ID: 25145506
    [Abstract] [Full Text] [Related]

  • 12. Lack of genotype-phenotype correlations and outcome in MCAD deficiency diagnosed by newborn screening in New York State.
    Arnold GL, Saavedra-Matiz CA, Galvin-Parton PA, Erbe R, Devincentis E, Kronn D, Mofidi S, Wasserstein M, Pellegrino JE, Levy PA, Adams DJ, Nichols M, Caggana M.
    Mol Genet Metab; 2010 Mar 24; 99(3):263-8. PubMed ID: 20036593
    [Abstract] [Full Text] [Related]

  • 13.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 14.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 15. [Inborn errors of metabolism in adult neurology].
    Sedel F.
    Rev Neurol (Paris); 2013 Feb 24; 169 Suppl 1():S63-9. PubMed ID: 23452774
    [Abstract] [Full Text] [Related]

  • 16. Inborn defects of fatty acid oxidation: a preventable cause of SIDS.
    Keppen LD, Randall B.
    S D J Med; 1999 Jun 24; 52(6):187-8; disscussion 188-9. PubMed ID: 10388343
    [Abstract] [Full Text] [Related]

  • 17. Milder childhood form of very long-chain acyl-CoA dehydrogenase deficiency in a 6-year-old Japanese boy.
    Doi T, Abo W, Tateno M, Hayashi K, Hori T, Nakada T, Fukao T, Takahashi Y, Terada N.
    Eur J Pediatr; 2000 Dec 24; 159(12):908-11. PubMed ID: 11131350
    [Abstract] [Full Text] [Related]

  • 18.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 19. Severe hypoglycaemia in isolated 3-methylcrotonyl-CoA carboxylase deficiency; a rare, severe clinical presentation.
    Oude Luttikhuis HG, Touati G, Rabier D, Williams M, Jakobs C, Saudubray JM.
    J Inherit Metab Dis; 2005 Dec 24; 28(6):1136-8. PubMed ID: 16435207
    [Abstract] [Full Text] [Related]

  • 20.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 14.