BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

156 related articles for article (PubMed ID: 34680961)

  • 21. Novel Hypoglycemia Phenotype in Congenital Hyperinsulinism Due to Dominant Mutations of Uncoupling Protein 2.
    Ferrara CT; Boodhansingh KE; Paradies E; Fiermonte G; Steinkrauss LJ; Topor LS; Quintos JB; Ganguly A; De Leon DD; Palmieri F; Stanley CA
    J Clin Endocrinol Metab; 2017 Mar; 102(3):942-949. PubMed ID: 27967291
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Glucokinase mutations in pediatric patients with impaired fasting glucose.
    Aloi C; Salina A; Minuto N; Tallone R; Lugani F; Mascagni A; Mazza O; Cassanello M; Maghnie M; d'Annunzio G
    Acta Diabetol; 2017 Oct; 54(10):913-923. PubMed ID: 28726111
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Phenotype variability and neonatal diabetes in a large family with heterozygous mutation of the glucokinase gene.
    Borowiec M; Mysliwiec M; Fendler W; Antosik K; Brandt A; Malecki M; Mlynarski W
    Acta Diabetol; 2011 Sep; 48(3):203-8. PubMed ID: 21437567
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Insights into the structure and regulation of glucokinase from a novel mutation (V62M), which causes maturity-onset diabetes of the young.
    Gloyn AL; Odili S; Zelent D; Buettger C; Castleden HA; Steele AM; Stride A; Shiota C; Magnuson MA; Lorini R; d'Annunzio G; Stanley CA; Kwagh J; van Schaftingen E; Veiga-da-Cunha M; Barbetti F; Dunten P; Han Y; Grimsby J; Taub R; Ellard S; Hattersley AT; Matschinsky FM
    J Biol Chem; 2005 Apr; 280(14):14105-13. PubMed ID: 15677479
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Case Report: Hypoglycemia Due to a Novel Activating Glucokinase Variant in an Adult - a Molecular Approach.
    Koneshamoorthy A; Seniveratne-Epa D; Calder G; Sawyer M; Kay TWH; Farrell S; Loudovaris T; Mariana L; McCarthy D; Lyu R; Liu X; Thorn P; Tong J; Chin LK; Zacharin M; Trainer A; Taylor S; MacIsaac RJ; Sachithanandan N; Thomas HE; Krishnamurthy B
    Front Endocrinol (Lausanne); 2022; 13():842937. PubMed ID: 35370948
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Persistent hyperinsulinemic hypoglycemia of infancy due to homozygous KCNJ11 (T294M) mutation.
    Ilamaran V; Venkatesh C; Manish K; Adhisivam B
    Indian J Pediatr; 2010 Jul; 77(7):803-4. PubMed ID: 20589481
    [TBL] [Abstract][Full Text] [Related]  

  • 27. A novel syndrome of autosomal-dominant hyperinsulinemic hypoglycemia linked to a mutation in the human insulin receptor gene.
    Højlund K; Hansen T; Lajer M; Henriksen JE; Levin K; Lindholm J; Pedersen O; Beck-Nielsen H
    Diabetes; 2004 Jun; 53(6):1592-8. PubMed ID: 15161766
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Case report: A particularly rare case of endogenous hyperinsulinemic hypoglycemia complicated with pregnancy treated with short-acting somatostatin analog injections.
    Barsi Á; Beke A; Sármán B
    Front Endocrinol (Lausanne); 2022; 13():964481. PubMed ID: 36187120
    [TBL] [Abstract][Full Text] [Related]  

  • 29. 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; 82(4):1192-4. PubMed ID: 9100595
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Hyperinsulinemic hypoglycemia evolving to gestational diabetes and diabetes mellitus in a family carrying the inactivating ABCC8 E1506K mutation.
    Vieira TC; Bergamin CS; Gurgel LC; Moisés RS
    Pediatr Diabetes; 2010 Nov; 11(7):505-8. PubMed ID: 20042013
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Congenital hyperinsulinism due to compound heterozygous mutations in ABCC8 responsive to diazoxide therapy.
    Taylor-Miller T; Houghton J; Munyard P; Kumar Y; Puvirajasinghe C; Giri D
    J Pediatr Endocrinol Metab; 2020 May; 33(5):671-674. PubMed ID: 32267248
    [TBL] [Abstract][Full Text] [Related]  

  • 32. The second activating glucokinase mutation (A456V): implications for glucose homeostasis and diabetes therapy.
    Christesen HB; Jacobsen BB; Odili S; Buettger C; Cuesta-Munoz A; Hansen T; Brusgaard K; Massa O; Magnuson MA; Shiota C; Matschinsky FM; Barbetti F
    Diabetes; 2002 Apr; 51(4):1240-6. PubMed ID: 11916951
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Nutrient sensing in pancreatic islets: lessons from congenital hyperinsulinism and monogenic diabetes.
    Lu M; Li C
    Ann N Y Acad Sci; 2018 Jan; 1411(1):65-82. PubMed ID: 29044608
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Impact of Type 2 diabetes on Glucokinase diabetes (GCK-MODY) phenotype in a Roma (Gypsy) family - case report.
    Stanik J; Kusekova M; Huckova M; Valentinova L; Masindova I; Stanikova D; Ferenczova J; Gasperikova D; Klimes I
    Endocr Regul; 2012 Apr; 46(2):99-105. PubMed ID: 22540858
    [TBL] [Abstract][Full Text] [Related]  

  • 35. [Hyperglycemia caused by mutation of GCK gene in 10 patients analysis of clinical and mutation characteristics].
    Zhang J; Yuan K; Ding SX; Kong YM; Zhu JF; Fang YL; Liang L; Fu JF; Wang CL
    Zhonghua Er Ke Za Zhi; 2019 Jun; 57(6):440-444. PubMed ID: 31216801
    [No Abstract]   [Full Text] [Related]  

  • 36. Mutations in PMM2 gene in four unrelated Spanish families with polycystic kidney disease and hyperinsulinemic hypoglycemia.
    Moreno Macián F; De Mingo Alemany C; León Cariñena S; Ortega López P; Rausell Felix D; Aparisi Navarro M; Martinez Matilla M; Cardona Gay C; Martinez Castellano F; Albiach Mesado V
    J Pediatr Endocrinol Metab; 2020 Aug; 33(10):1283-1288. PubMed ID: 32841164
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Caudal regression syndrome in a fetus of a glucokinase-maturity-onset diabetes of the young pregnancy.
    Taylor RAM; Mackie A; Mogra R; Pinner J; Rajendran S; Ross GP
    Diabet Med; 2019 Feb; 36(2):252-255. PubMed ID: 30362177
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Persistent hyperinsulinemic hypoglycemia and maturity-onset diabetes of the young due to heterozygous HNF4A mutations.
    Kapoor RR; Locke J; Colclough K; Wales J; Conn JJ; Hattersley AT; Ellard S; Hussain K
    Diabetes; 2008 Jun; 57(6):1659-63. PubMed ID: 18268044
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Clinical Management and Gene Mutation Analysis of Children with Congenital Hyperinsulinism in South China.
    Xu A; Cheng J; Sheng H; Wen Z; Lin Y; Zhou Z; Zeng C; Shao Y; Li C; Liu L; Li X
    J Clin Res Pediatr Endocrinol; 2019 Nov; 11(4):400-409. PubMed ID: 31208162
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Sirolimus therapy in infants with severe hyperinsulinemic hypoglycemia.
    Senniappan S; Alexandrescu S; Tatevian N; Shah P; Arya V; Flanagan S; Ellard S; Rampling D; Ashworth M; Brown RE; Hussain K
    N Engl J Med; 2014 Mar; 370(12):1131-7. PubMed ID: 24645945
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.