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Journal Abstract Search

99 related items for PubMed ID: 1941377

  • 21. A Japanese case of congenital hyperinsulinism with hyperammonemia due to a mutation in glutamate dehydrogenase (GLUD1) gene.
    Yasuda K, Koda N, Kadowaki H, Ogawa Y, Kimura S, Kadowaki T, Akanuma Y.
    Intern Med; 2001 Jan; 40(1):32-7. PubMed ID: 11201367
    [Abstract] [Full Text] [Related]

  • 22. Surgical treatment of organic hyperinsulinism in infancy. Surgical procedure in the absence of a demonstrable insulinoma and a peroperative diagnosis of nesidioblastosis.
    Goudswaard WB, Zwierstra RP, Houthoff HJ, Rouwé C, Kootstra G.
    Z Kinderchir; 1984 Apr; 39(2):91-5. PubMed ID: 6328789
    [Abstract] [Full Text] [Related]

  • 23. [Familial hyperinsulinism].
    Lásztity N, Balogh L.
    Orv Hetil; 1995 Jul 23; 136(30):1611-3. PubMed ID: 7637980
    [Abstract] [Full Text] [Related]

  • 24. [Preoperative localization in organic hyperinsulinism--useful or superfluous].
    Böttger T, Weber W, Beyer J, Junginger T.
    Langenbecks Arch Chir Suppl II Verh Dtsch Ges Chir; 1990 Jul 23; ():1003-6. PubMed ID: 1983474
    [Abstract] [Full Text] [Related]

  • 25. The laparoscopic approach toward hyperinsulinism in children.
    Bax KN, van der Zee DC.
    Semin Pediatr Surg; 2007 Nov 23; 16(4):245-51. PubMed ID: 17933666
    [Abstract] [Full Text] [Related]

  • 26. Familial hyperinsulinism presenting in adults.
    Burman WJ, McDermott MT, Bornemann M.
    Arch Intern Med; 1992 Oct 23; 152(10):2125-7. PubMed ID: 1358043
    [Abstract] [Full Text] [Related]

  • 27. Congenital hyperinsulinism: pancreatic [18F]fluoro-L-dihydroxyphenylalanine (DOPA) positron emission tomography and immunohistochemistry study of DOPA decarboxylase and insulin secretion.
    de Lonlay P, Simon-Carre A, Ribeiro MJ, Boddaert N, Giurgea I, Laborde K, Bellanné-Chantelot C, Verkarre V, Polak M, Rahier J, Syrota A, Seidenwurm D, Nihoul-Fékété C, Robert JJ, Brunelle F, Jaubert F.
    J Clin Endocrinol Metab; 2006 Mar 23; 91(3):933-40. PubMed ID: 16403819
    [Abstract] [Full Text] [Related]

  • 28. Role of initial near total (95%) pancreatectomy in persistent neonatal hyperinsulinism (PNH).
    Haddad MJ, Mathew PM.
    Eur J Pediatr Surg; 1996 Apr 23; 6(2):82-5. PubMed ID: 8740129
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  • 30. Recombinant mapping of the familial hyperinsulinism gene to an 0.8 cM region on chromosome 11p15.1 and demonstration of a founder effect in Ashkenazi Jews.
    Glaser B, Chiu KC, Liu L, Anker R, Nestorowicz A, Cox NJ, Landau H, Kaiser N, Thornton PS, Stanley CA.
    Hum Mol Genet; 1995 May 23; 4(5):879-86. PubMed ID: 7633448
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  • 33. The surgical approach to hyperinsulinism and hypoglycemia in children.
    Kamiński W, Cedro A, Pronicka E, Gruszczyńska B, Husein N, Kaliciński P, Kamiński A, Prokurat A.
    Mater Med Pol; 1990 May 23; 22(2):97-100. PubMed ID: 2102986
    [Abstract] [Full Text] [Related]

  • 34. Pancreatic exocrine and endocrine function after pancreatectomy for persistent hyperinsulinaemic hypoglycaemia of infancy.
    Cade A, Walters M, Puntis JW, Arthur RJ, Stringer MD.
    Arch Dis Child; 1998 Nov 23; 79(5):435-9. PubMed ID: 10193259
    [Abstract] [Full Text] [Related]

  • 35. Preoperative evaluation of infants with focal or diffuse congenital hyperinsulinism by intravenous acute insulin response tests and selective pancreatic arterial calcium stimulation.
    Stanley CA, Thornton PS, Ganguly A, MacMullen C, Underwood P, Bhatia P, Steinkrauss L, Wanner L, Kaye R, Ruchelli E, Suchi M, Adzick NS.
    J Clin Endocrinol Metab; 2004 Jan 23; 89(1):288-96. PubMed ID: 14715863
    [Abstract] [Full Text] [Related]

  • 36. Inheritance of Indian childhood cirrhosis.
    Agarwal SS, Lahori UC, Mehta SK, Smith DG, Bajpai PC.
    Hum Hered; 1979 Jan 23; 29(2):82-9. PubMed ID: 437795
    [Abstract] [Full Text] [Related]

  • 37. Hyperinsulinism and hyperammonemia in infants with regulatory mutations of the glutamate dehydrogenase gene.
    Stanley CA, Lieu YK, Hsu BY, Burlina AB, Greenberg CR, Hopwood NJ, Perlman K, Rich BH, Zammarchi E, Poncz M.
    N Engl J Med; 1998 May 07; 338(19):1352-7. PubMed ID: 9571255
    [Abstract] [Full Text] [Related]

  • 38. Evidence for autosomal recessive inheritance of infantile dilated cardiomyopathy: studies from the Eastern Province of Saudi Arabia.
    Seliem MA, Mansara KB, Palileo M, Ye X, Zhang Z, Benson DW.
    Pediatr Res; 2000 Dec 07; 48(6):770-5. PubMed ID: 11102545
    [Abstract] [Full Text] [Related]

  • 39. The genetics of neonatal hyperinsulinism.
    Fournet JC, Junien C.
    Horm Res; 2003 Dec 07; 59 Suppl 1():30-4. PubMed ID: 12566718
    [Abstract] [Full Text] [Related]

  • 40. An autosomal dominant form of familial persistent hyperinsulinemic hypoglycemia of infancy, not linked to the sulfonylurea receptor locus.
    Kukuvitis A, Deal C, Arbour L, Polychronakos C.
    J Clin Endocrinol Metab; 1997 Apr 07; 82(4):1192-4. PubMed ID: 9100595
    [Abstract] [Full Text] [Related]

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