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Journal Abstract Search

221 related items for PubMed ID: 23585210

  • 1. Recurrent infantile hypoglycemia due to combined fructose-1,6-diphosphatase deficiency and growth hormone deficiency.
    Takagi D, Ben-Ari J, Nemet D, Zeharia A, Eliakim A.
    J Pediatr Endocrinol Metab; 2013; 26(7-8):761-3. PubMed ID: 23585210
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  • 2. Fructose-1,6-diphosphatase deficiency: a rare cause of prolonged prothrombin time.
    Nitzan O, Saliba WR, Goldstein LH, Elias MS.
    Ann Hematol; 2004 May; 83(5):302-3. PubMed ID: 15064857
    [Abstract] [Full Text] [Related]

  • 3. [Recurrent acidosis with hypoglycemia in an infant: fructose-1,6-diphosphatase deficiency].
    Fischer PJ, Hecker W.
    Klin Padiatr; 1990 May; 202(2):73-5. PubMed ID: 2325353
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  • 4. Hepatic fructose-1,6-diphosphatase deficiency. A cause of lactic acidosis and hypoglycemia in infancy.
    Pagliara AS, Karl IE, Keating JP, Brown BI, Kipnis DM.
    J Clin Invest; 1972 Aug; 51(8):2115-23. PubMed ID: 4341015
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  • 5. [Hypoglycemia and hyperlactacidemia in relation with a new case of fructose-1,6-diphosphatase deficiency. Determination of enzymatic activity in leukocytes].
    Rayet I, Teyssier G, Berlioux F, Maire I, Freycon MT.
    Pediatrie; 1986 Aug; 41(1):49-55. PubMed ID: 3014428
    [Abstract] [Full Text] [Related]

  • 6. Fructose-1,6-diphosphatase deficiency in Israel.
    Moses SW, Bashan N, Flasterstein BF, Rachmel A, Gutman A.
    Isr J Med Sci; 1991 Jan; 27(1):1-4. PubMed ID: 1995492
    [Abstract] [Full Text] [Related]

  • 7. Fructose-1,6-bisphosphatase deficiency as a cause of recurrent hypoglycemia and metabolic acidosis: Clinical and molecular findings in Malaysian patients.
    Moey LH, Abdul Azize NA, Yakob Y, Leong HY, Keng WT, Chen BC, Ngu LH.
    Pediatr Neonatol; 2018 Aug; 59(4):397-403. PubMed ID: 29203193
    [Abstract] [Full Text] [Related]

  • 8. Gluconeogenesis defect presenting with resistant hyperglycemia and acidosis mimicking diabetic ketoacidosis.
    Paksu MŞ, Kalkan G, Asilioglu N, Paksu S, Dinler G.
    Pediatr Emerg Care; 2011 Dec; 27(12):1180-1. PubMed ID: 22158280
    [Abstract] [Full Text] [Related]

  • 9. [Neonatal lactic acidosis and hypoglycemia due to a congenital hepatic fructose-1,6-diphosphatase deficiency].
    Retbi JM, Gabilan JC, Marsac C.
    Arch Fr Pediatr; 1975 Apr; 32(4):367-80. PubMed ID: 169761
    [Abstract] [Full Text] [Related]

  • 10. Recurrent hypoglycemia due to growth hormone deficiency in an infant with Turner syndrome.
    Bonfig W, Salem NJ, Heiliger K, Hempel M, Lederer G, Bornkamm M, Wieland K, Lohse P, Burdach S, Oexle K.
    J Pediatr Endocrinol Metab; 2012 Apr; 25(9-10):991-5. PubMed ID: 23426831
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  • 16. [Characteristics of a case of hepatic fructose-1,6-diphosphatase deficiency].
    Largillière C, Amédée-Manesme O, Marsac C, Reguet C, Lefebvre R, Farriaux JP.
    Arch Fr Pediatr; 1984 Apr; 41(6):421-3. PubMed ID: 6091586
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  • 17. [Fructose-1,6-diphosphatase deficiency. Clinical aspects and diagnosis based on a case report].
    Lohrer R, Ibel H, Holzapfel P, Gerg S.
    Monatsschr Kinderheilkd; 1987 Feb; 135(2):112-3. PubMed ID: 3033476
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  • 18. [Hypoglycemia. 3. Hypoglycemias caused by defined metabolic defects; hormonal regulation of blood glucose concentration and its disorders].
    Förster H.
    Fortschr Med; 1976 Feb 12; 94(5):269-76. PubMed ID: 176098
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  • 19. [Baker-Winegrad disease (hepatomegaly, hypoglycemia during fasting, hyperlactacidemic metabolic acidosis, hepatic fructose-1-6-diphosphatase deficiency). Presentation of the 1st Italian case and pathogenetic hypothesis].
    De Prà M, Laudanna E.
    Minerva Pediatr; 1978 Dec 31; 30(24):1973-86. PubMed ID: 224299
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  • 20. [Lactic acidosis, hypoglycemia and hepatomegaly due to hereditary defect in hepatic fructose-1, 6-diphosphatase].
    Saudubray JM, Dreyfus JC, Cepanec C, Le Lo'ch H, Trung PH, Mozziconacci P.
    Arch Fr Pediatr; 1973 Dec 31; 30(6):609-32. PubMed ID: 4156164
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