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 *

155 related articles for article (PubMed ID: 25226297)

  • 1. Familial isolated growth hormone deficiency due to a novel homozygous missense mutation in the growth hormone releasing hormone receptor gene: clinical presentation with hypoglycemia.
    Demirbilek H; Tahir S; Baran RT; Sherif M; Shah P; Ozbek MN; Hatipoglu N; Baran A; Arya VB; Hussain K
    J Clin Endocrinol Metab; 2014 Dec; 99(12):E2730-4. PubMed ID: 25226297
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. Three new mutations in the gene for the growth hormone (gh)-releasing hormone receptor in familial isolated gh deficiency type ib.
    Salvatori R; Fan X; Phillips JA; Espigares-Martin R; Martin De Lara I; Freeman KL; Plotnick L; Al-Ashwal A; Levine MA
    J Clin Endocrinol Metab; 2001 Jan; 86(1):273-9. PubMed ID: 11232012
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. Variability in anterior pituitary size within members of a family with GH deficiency due to a new splice mutation in the GHRH receptor gene.
    Alba M; Hall CM; Whatmore AJ; Clayton PE; Price DA; Salvatori R
    Clin Endocrinol (Oxf); 2004 Apr; 60(4):470-5. PubMed ID: 15049962
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Growth hormone releasing hormone receptor (GHRH-r) gene mutation in Indian children with familial isolated growth hormone deficiency: a study from western India.
    Desai MP; Upadhye PS; Kamijo T; Yamamoto M; Ogawa M; Hayashi Y; Seo H; Nair SR
    J Pediatr Endocrinol Metab; 2005 Oct; 18(10):955-73. PubMed ID: 16355809
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A new missense mutation in the growth hormone-releasing hormone receptor gene in familial isolated GH deficiency.
    Carakushansky M; Whatmore AJ; Clayton PE; Shalet SM; Gleeson HK; Price DA; Levine MA; Salvatori R
    Eur J Endocrinol; 2003 Jan; 148(1):25-30. PubMed ID: 12534354
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Identification of novel GHRHR and GH1 mutations in patients with isolated growth hormone deficiency.
    Birla S; Khadgawat R; Jyotsna VP; Jain V; Garg MK; Bhalla AS; Sharma A
    Growth Horm IGF Res; 2016 Aug; 29():50-56. PubMed ID: 27114065
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Magnetic resonance imaging study of pituitary morphology in subjects homozygous and heterozygous for a null mutation of the GHRH receptor gene.
    Oliveira HA; Salvatori R; Krauss MP; Oliveira CR; Silva PR; Aguiar-Oliveira MH
    Eur J Endocrinol; 2003 Apr; 148(4):427-32. PubMed ID: 12656663
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Expanding the spectrum of mutations in GH1 and GHRHR: genetic screening in a large cohort of patients with congenital isolated growth hormone deficiency.
    Alatzoglou KS; Turton JP; Kelberman D; Clayton PE; Mehta A; Buchanan C; Aylwin S; Crowne EC; Christesen HT; Hertel NT; Trainer PJ; Savage MO; Raza J; Banerjee K; Sinha SK; Ten S; Mushtaq T; Brauner R; Cheetham TD; Hindmarsh PC; Mullis PE; Dattani MT
    J Clin Endocrinol Metab; 2009 Sep; 94(9):3191-9. PubMed ID: 19567534
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A recurrent signal peptide mutation in the growth hormone releasing hormone receptor with defective translocation to the cell surface and isolated growth hormone deficiency.
    Godi M; Mellone S; Petri A; Arrigo T; Bardelli C; Corrado L; Bellone S; Prodam F; Momigliano-Richiardi P; Bona G; Giordano M
    J Clin Endocrinol Metab; 2009 Oct; 94(10):3939-47. PubMed ID: 19622623
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Pathogenic and likely pathogenic genetic alterations and polymorphisms in growth hormone gene (GH1) and growth hormone releasing hormone receptor gene (GHRHR) in a cohort of isolated growth hormone deficient (IGHD) children in Sri Lanka.
    Sundralingam T; Tennekoon KH; de Silva S; De Silva S; Hewage AS
    Growth Horm IGF Res; 2017 Oct; 36():22-29. PubMed ID: 28910730
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Two siblings with isolated GH deficiency due to loss-of-function mutation in the GHRHR gene: successful treatment with growth hormone despite late admission and severe growth retardation.
    Sıklar Z; Berberoğlu M; Legendre M; Amselem S; Evliyaoğlu O; Hacıhamdioğlu B; Savaş Erdeve S; Oçal G
    J Clin Res Pediatr Endocrinol; 2010; 2(4):164-7. PubMed ID: 21274317
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Unusual phenotypic features in a patient with a novel splice mutation in the GHRHR gene.
    Hilal L; Hajaji Y; Vie-Luton MP; Ajaltouni Z; Benazzouz B; Chana M; Chraïbi A; Kadiri A; Amselem S; Sobrier ML
    Mol Med; 2008; 14(5-6):286-92. PubMed ID: 18297129
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Contribution of functionally assessed GHRHR mutations to idiopathic isolated growth hormone deficiency in patients without GH1 mutations.
    Cohen E; Belkacem S; Fedala S; Collot N; Khallouf E; Dastot F; Polak M; Duquesnoy P; Brioude F; Rose S; Viot G; Soleyan A; Carel JC; Sobrier ML; Chanson P; Gatelais F; Heinrichs C; Kaffel N; Coutant R; Savaş Erdeve Ş; Kurnaz E; Aycan Z; Thalassinos C; Lyonnet S; Şıklar Z; Berberoglu M; Brachet C; Amselem S; Legendre M
    Hum Mutat; 2019 Nov; 40(11):2033-2043. PubMed ID: 31231873
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Genetic screening of a Dutch population with isolated GH deficiency (IGHD).
    de Graaff LC; Argente J; Veenma DC; Herrebout MA; Friesema EC; Uitterlinden AG; Drent ML; Campos-Barros A; Hokken-Koelega AC
    Clin Endocrinol (Oxf); 2009 May; 70(5):742-50. PubMed ID: 18785993
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Novel growth hormone-releasing hormone receptor gene mutations in Turkish children with isolated growth hormone deficiency.
    Arman A; Dündar BN; Çetinkaya E; Erzaim N; Büyükgebiz A
    J Clin Res Pediatr Endocrinol; 2014 Dec; 6(4):202-8. PubMed ID: 25541890
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Familial dwarfism due to a novel mutation of the growth hormone-releasing hormone receptor gene.
    Salvatori R; Hayashida CY; Aguiar-Oliveira MH; Phillips JA; Souza AH; Gondo RG; Toledo SP; Conceicão MM; Prince M; Maheshwari HG; Baumann G; Levine MA
    J Clin Endocrinol Metab; 1999 Mar; 84(3):917-23. PubMed ID: 10084571
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Partial Loss of Function of the GHRH Receptor Leads to Mild Growth Hormone Deficiency.
    Gregory LC; Alatzoglou KS; McCabe MJ; Hindmarsh PC; Saldanha JW; Romano N; Le Tissier P; Dattani MT
    J Clin Endocrinol Metab; 2016 Oct; 101(10):3608-3615. PubMed ID: 27501283
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A GHRHR founder mutation causes isolated growth hormone deficiency type IV in a consanguineous Pakistani family.
    Ahmad S; Ali MZ; Abbasi SW; Abbas S; Ahmed I; Abbas S; Nawaz S; Ziab M; Ahmed I; Fakhro KA; Khan MA; Akil AA
    Front Endocrinol (Lausanne); 2023; 14():1066182. PubMed ID: 36960394
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.