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PUBMED FOR HANDHELDS

Journal Abstract Search


391 related items for PubMed ID: 27329029

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  • 3. Molecular Genetics, Clinical Characteristics, and Treatment Outcomes of KATP-Channel Neonatal Diabetes Mellitus in Vietnam National Children's Hospital.
    Ngoc CTB, Dien TM, De Franco E, Ellard S, Houghton JAL, Lan NN, Thao BP, Khanh NN, Flanagan SE, Craig ME, Dung VC.
    Front Endocrinol (Lausanne); 2021; 12():727083. PubMed ID: 34566892
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  • 5. Sulfonylurea in the treatment of neonatal diabetes mellitus children with heterogeneous genetic backgrounds.
    Zhang M, Chen X, Shen S, Li T, Chen L, Hu M, Cao L, Cheng R, Zhao Z, Luo F.
    J Pediatr Endocrinol Metab; 2015 Jul; 28(7-8):877-84. PubMed ID: 25781672
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  • 7. Case report: Better late than never, but sooner is better: switch from CSII to sulfonylureas in two patients with neonatal diabetes due to KCNJ11 variants.
    Mancioppi V, Pozzi E, Zanetta S, Missineo A, Savastio S, Barbetti F, Mellone S, Giordano M, Rabbone I.
    Front Endocrinol (Lausanne); 2023 Jul; 14():1143736. PubMed ID: 37251668
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  • 8. Personalized precision medicine in extreme preterm infants with transient neonatal diabetes mellitus.
    Kylat RI, Senguttuvan R, Bader MY.
    J Pediatr Endocrinol Metab; 2017 May 01; 30(5):593-596. PubMed ID: 28350539
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  • 12. Successful transition to sulfonylurea therapy in two Iraqi siblings with neonatal diabetes mellitus and iDEND syndrome due to ABCC8 mutation.
    Ozsu E, Giri D, Seymen Karabulut G, Senniappan S.
    J Pediatr Endocrinol Metab; 2016 Dec 01; 29(12):1403-1406. PubMed ID: 27849623
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  • 13. A successful transition to sulfonylurea treatment in male infant with neonatal diabetes caused by the novel abcc8 gene mutation and three years follow-up.
    Katanic D, Vorgučin I, Hattersley A, Ellard S, Houghton JAL, Obreht D, Knežević Pogančev M, Vlaški J, Pavkov D.
    Diabetes Res Clin Pract; 2017 Jul 01; 129():59-61. PubMed ID: 28511139
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  • 14. Clinical and Molecular Characterization of Children with Neonatal Diabetes Mellitus at a Tertiary Care Center in Northern India.
    Jain V, Satapathy A, Yadav J, Sharma R, Radha V, Mohan V, De Franco E, Ellard S.
    Indian Pediatr; 2017 Jun 15; 54(6):467-471. PubMed ID: 28667717
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  • 15. Neonatal diabetes due to potassium channel mutation: Response to sulfonylurea according to the genotype.
    Garcin L, Mericq V, Fauret-Amsellem AL, Cave H, Polak M, Beltrand J.
    Pediatr Diabetes; 2020 Sep 15; 21(6):932-941. PubMed ID: 32418263
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  • 16. Differences between transient neonatal diabetes mellitus subtypes can guide diagnosis and therapy.
    Bonfanti R, Iafusco D, Rabbone I, Diedenhofen G, Bizzarri C, Patera PI, Reinstadler P, Costantino F, Calcaterra V, Iughetti L, Savastio S, Favia A, Cardella F, Lo Presti D, Girtler Y, Rabbiosi S, D'Annunzio G, Zanfardino A, Piscopo A, Casaburo F, Pintomalli L, Russo L, Grasso V, Minuto N, Mucciolo M, Novelli A, Marucci A, Piccini B, Toni S, Silvestri F, Carrera P, Rigamonti A, Frontino G, Trada M, Tinti D, Delvecchio M, Rapini N, Schiaffini R, Mammì C, Barbetti F, Diabetes Study Group of ISPED.
    Eur J Endocrinol; 2021 Apr 15; 184(4):575-585. PubMed ID: 33606663
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  • 19. Neonatal diabetes mellitus: a disease linked to multiple mechanisms.
    Polak M, Cavé H.
    Orphanet J Rare Dis; 2007 Mar 09; 2():12. PubMed ID: 17349054
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