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184 related items for PubMed ID: 24351577

  • 1. Delayed presentation of prolonged hyperinsulinaemic hypoglycaemia in a preterm small-for-gestational age neonate.
    Chong JH, Chandran S, Agarwal P, Rajadurai VS.
    BMJ Case Rep; 2013 Dec 18; 2013():. PubMed ID: 24351577
    [Abstract] [Full Text] [Related]

  • 2. Clinical and molecular characterisation of hyperinsulinaemic hypoglycaemia in infants born small-for-gestational age.
    Arya VB, Flanagan SE, Kumaran A, Shield JP, Ellard S, Hussain K, Kapoor RR.
    Arch Dis Child Fetal Neonatal Ed; 2013 Jul 18; 98(4):F356-8. PubMed ID: 23362136
    [Abstract] [Full Text] [Related]

  • 3. Ten years' experience of persistent hyperinsulinaemic hypoglycaemia of infancy.
    Tyrrell VJ, Ambler GR, Yeow WH, Cowell CT, Silink M.
    J Paediatr Child Health; 2001 Oct 18; 37(5):483-8. PubMed ID: 11885714
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  • 4. Randomised controlled trial of diazoxide for small for gestational age neonates with hyperinsulinaemic hypoglycaemia provided early hypoglycaemic control without adverse effects.
    Balachandran B, Mukhopadhyay K, Sachdeva N, Walia R, Attri SV.
    Acta Paediatr; 2018 Jun 18; 107(6):990-995. PubMed ID: 29385640
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  • 6. Heterogeneity of persistent hyperinsulinaemic hypoglycaemia. A series of 175 cases.
    de Lonlay P, Fournet JC, Touati G, Groos MS, Martin D, Sevin C, Delagne V, Mayaud C, Chigot V, Sempoux C, Brusset MC, Laborde K, Bellane-Chantelot C, Vassault A, Rahier J, Junien C, Brunelle F, Nihoul-Fékété C, Saudubray JM, Robert JJ.
    Eur J Pediatr; 2002 Jan 18; 161(1):37-48. PubMed ID: 11808879
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  • 8. Paradoxical hypoglycaemia associated with diazoxide therapy for hyperinsulinaemic hypoglycaemia.
    Ponmani C, Gannon H, Hussain K, Senniappan S.
    Horm Res Paediatr; 2013 Jan 18; 80(2):129-33. PubMed ID: 23886961
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  • 10. Genotype and phenotype correlations in Iranian patients with hyperinsulinaemic hypoglycaemia.
    Senniappan S, Sadeghizadeh A, Flanagan SE, Ellard S, Hashemipour M, Hosseinzadeh M, Salehi M, Hussain K.
    BMC Res Notes; 2015 Aug 13; 8():350. PubMed ID: 26268944
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  • 11. [Pitfalls in the diagnosis of congenital hyperinsulinism: a case report and review of the literature].
    Fernandez Alvarez JR, Rabe H, Wilichowski E, Pekrun A.
    Klin Padiatr; 2006 Aug 13; 218(4):233-6. PubMed ID: 16819706
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  • 13. Clinical and genetic heterogeneity of HNF4A/HNF1A mutations in a multicentre paediatric cohort with hyperinsulinaemic hypoglycaemia.
    McGlacken-Byrne SM, Mohammad JK, Conlon N, Gubaeva D, Siersbæk J, Schou AJ, Demirbilek H, Dastamani A, Houghton JAL, Brusgaard K, Melikyan M, Christesen H, Flanagan SE, Murphy NP, Shah P.
    Eur J Endocrinol; 2022 Feb 22; 186(4):417-427. PubMed ID: 35089870
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  • 14. Partial diazoxide responsiveness in a neonate with hyperinsulinism due to homozygous ABCC8 mutation.
    Kiff S, Babb C, Guemes M, Dastamani A, Gilbert C, Flanagan SE, Ellard S, Barton J, Dattani M, Shah P.
    Endocrinol Diabetes Metab Case Rep; 2019 Feb 11; 2019():. PubMed ID: 30753133
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  • 15. The evolving course of HNF4A hyperinsulinaemic hypoglycaemia--a case series.
    McGlacken-Byrne SM, Hawkes CP, Flanagan SE, Ellard S, McDonnell CM, Murphy NP.
    Diabet Med; 2014 Jan 11; 31(1):e1-5. PubMed ID: 23796040
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  • 16. Update on neonatal hypoglycemia.
    Rozance PJ.
    Curr Opin Endocrinol Diabetes Obes; 2014 Feb 11; 21(1):45-50. PubMed ID: 24275620
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  • 17. Prematurity, macrosomia, hyperinsulinaemic hypoglycaemia and a dominant ABCC8 gene mutation.
    Khoriati D, Arya VB, Flanagan SE, Ellard S, Hussain K.
    BMJ Case Rep; 2013 Apr 05; 2013():. PubMed ID: 23563683
    [Abstract] [Full Text] [Related]

  • 18. Diazoxide-unresponsive Hyperinsulinemic Hypoglycaemia in a Preterm Infant with Heterozygous Insulin Receptor Gene Mutation.
    Poon SW, Chung BH, Wong MS, Tsang AM.
    J Clin Res Pediatr Endocrinol; 2023 Apr 19. PubMed ID: 37074094
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  • 19. The hyperinsulinaemic hypoglycaemias in infancy: a study of six cases.
    Amendt P, Kohnert KD, Kunz J.
    Eur J Pediatr; 1988 Nov 19; 148(2):107-12. PubMed ID: 2906871
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  • 20. Prolonged episodes of hypoglycaemia in HNF4A-MODY mutation carriers with IGT. Evidence of persistent hyperinsulinism into early adulthood.
    Bacon S, Kyithar MP, Condron EM, Vizzard N, Burke M, Byrne MM.
    Acta Diabetol; 2016 Dec 19; 53(6):965-972. PubMed ID: 27552834
    [Abstract] [Full Text] [Related]

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