These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

113 related articles for article (PubMed ID: 9364346)

  • 21. IGHD II: A Novel GH-1 Gene Mutation (GH-L76P) Severely Affects GH Folding, Stability, and Secretion.
    Miletta MC; Eblé A; Janner M; Parween S; Pandey AV; Flück CE; Mullis PE
    J Clin Endocrinol Metab; 2015 Dec; 100(12):E1575-83. PubMed ID: 26485222
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Growth hormone deficiency type IB caused by cryptic splicing of the GH-1 gene.
    Abdul-Latif H; Leiberman E; Brown MR; Carmi R; Parks JS
    J Pediatr Endocrinol Metab; 2000 Jan; 13(1):21-8. PubMed ID: 10689634
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Mutations in intron 3 of GH-1 gene associated with isolated GH deficiency type II in three Japanese families.
    Kamijo T; Hayashi Y; Shimatsu A; Kinoshita E; Yoshimoto M; Ogawa M; Seo H
    Clin Endocrinol (Oxf); 1999 Sep; 51(3):355-60. PubMed ID: 10469016
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Variability of isolated autosomal dominant GH deficiency (IGHD II): impact of the P89L GH mutation on clinical follow-up and GH secretion.
    Salemi S; Yousefi S; Baltensperger K; Robinson IC; Eblé A; Simon D; Czernichow P; Binder G; Sonnet E; Mullis PE
    Eur J Endocrinol; 2005 Dec; 153(6):791-802. PubMed ID: 16322384
    [TBL] [Abstract][Full Text] [Related]  

  • 25. A novel GH1 mutation in a family with isolated growth hormone deficiency type II.
    Gucev Z; Tasic V; Saranac L; Stobbe H; Kratzsch J; Klammt J; Pfäffle R
    Horm Res Paediatr; 2012; 77(3):200-4. PubMed ID: 22188748
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Clinical and molecular characterization of Brazilian patients with growth hormone gene deletions.
    Arnhold IJ; Osorio MG; Oliveira SB; Estefan V; Kamijo T; Krishnamani MR; Cogan JD; Phillips JA; Mendonca BB
    Braz J Med Biol Res; 1998 Apr; 31(4):491-7. PubMed ID: 9698799
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Type IA isolated growth hormone deficiency (IGHD) consistent with compound heterozygous deletions of 6.7 and 7.6 Kb at the GH1 gene locus.
    Keselman A; Scaglia PA; Rodríguez Prieto MS; Ballerini MG; Rodríguez ME; Ropelato MG; Bergadá I; Jasper HG; Domené HM
    Arq Bras Endocrinol Metabol; 2012 Nov; 56(8):558-63. PubMed ID: 23295298
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Isolated growth hormone deficiency and the GH-1 gene: update 2002.
    Binder G
    Horm Res; 2002; 58 Suppl 3():2-6. PubMed ID: 12435888
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Molecular diagnosis and endocrine evaluation of a patient with a homozygous 7.0 kb deletion of the growth hormone (GH) gene cluster: response to biosynthetic GH therapy.
    Pérez Jurado LA; Argente J; Barrios V; Pozo J; Muñoz MT; Hernández M; Francke U
    J Pediatr Endocrinol Metab; 1997; 10(2):185-90. PubMed ID: 9364351
    [TBL] [Abstract][Full Text] [Related]  

  • 30. De novo mutations of the growth hormone gene: an important cause of congenital isolated growth hormone deficiency?
    Massa GG; Binder G; Oostdijk W; Ranke MB; Wit JM
    Eur J Pediatr; 1998 Apr; 157(4):272-5. PubMed ID: 9578959
    [TBL] [Abstract][Full Text] [Related]  

  • 31. GH1 gene deletions and IGHD type 1A.
    Cogan JD; Phillips JA
    Pediatr Endocrinol Rev; 2006 Aug; 3 Suppl 3():480-8. PubMed ID: 17551470
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Characterization of GH-1 mutations in children with isolated growth hormone deficiency in the Turkish population.
    Coker A; Cetinkaya E; Dundar B; Siklar Z; Buyukgebiz A; Arman A
    J Pediatr Endocrinol Metab; 2009 Oct; 22(10):937-46. PubMed ID: 20020582
    [TBL] [Abstract][Full Text] [Related]  

  • 33. A novel frame shift mutation in the GHRH receptor gene in familial isolated GH deficiency: early occurrence of anterior pituitary hypoplasia.
    Shohreh R; Sherafat-Kazemzadeh R; Jee YH; Blitz A; Salvatori R
    J Clin Endocrinol Metab; 2011 Oct; 96(10):2982-6. PubMed ID: 21816782
    [TBL] [Abstract][Full Text] [Related]  

  • 34. A novel deletion in the GH1 gene including the IVS3 branch site responsible for autosomal dominant isolated growth hormone deficiency.
    Vivenza D; Guazzarotti L; Godi M; Frasca D; di Natale B; Momigliano-Richiardi P; Bona G; Giordano M
    J Clin Endocrinol Metab; 2006 Mar; 91(3):980-6. PubMed ID: 16368751
    [TBL] [Abstract][Full Text] [Related]  

  • 35. A novel gross indel in the growth hormone releasing hormone receptor gene of Indian IGHD patients.
    Kale S; Budyal S; Kasaliwal R; Shivane V; Raghavan V; Lila A; Bandgar T; Shah N
    Growth Horm IGF Res; 2014 Dec; 24(6):227-32. PubMed ID: 25153028
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Isolated GH deficiency with dominant inheritance: new mutations, new insights.
    Binder G; Keller E; Mix M; Massa GG; Stokvis-Brantsma WH; Wit JM; Ranke MB
    J Clin Endocrinol Metab; 2001 Aug; 86(8):3877-81. PubMed ID: 11502827
    [TBL] [Abstract][Full Text] [Related]  

  • 37. A functional common polymorphism in the vitamin D-responsive element of the GH1 promoter contributes to isolated growth hormone deficiency.
    Giordano M; Godi M; Mellone S; Petri A; Vivenza D; Tiradani L; Carlomagno Y; Ferrante D; Arrigo T; Corneli G; Bellone S; Giacopelli F; Santoro C; Bona G; Momigliano-Richiardi P
    J Clin Endocrinol Metab; 2008 Mar; 93(3):1005-12. PubMed ID: 18160466
    [TBL] [Abstract][Full Text] [Related]  

  • 38. New GH-1 gene mutations: expanding the spectrum of causes of isolated growth hormone deficiency.
    Mullis PE; Deladoëy J; Dannies PS
    J Pediatr Endocrinol Metab; 2002 Dec; 15 Suppl 5():1301-10. PubMed ID: 12510984
    [TBL] [Abstract][Full Text] [Related]  

  • 39. A Turkish family with 6.7 Kb deletion associated with isolated growth hormone deficiency type 1A.
    Korkmaz KS; Sercan OH; Yazicioğlu MV; Sakizli M; Darcan S; Büyükgebiz A
    Turk J Pediatr; 1997; 39(1):99-104. PubMed ID: 10868200
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Allelic variations in the human growth hormone-1 gene promoter of growth hormone-deficient patients and normal controls.
    Wagner JK; Eblé A; Cogan JD; Prince MA; Phillips JA; Mullis PE
    Eur J Endocrinol; 1997 Nov; 137(5):474-81. PubMed ID: 9405026
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 6.