158 related articles for article (PubMed ID: 17356054)
21. Lack of evidence of premature atherosclerosis in untreated severe isolated growth hormone (GH) deficiency due to a GH-releasing hormone receptor mutation.
Menezes Oliveira JL; Marques-Santos C; Barreto-Filho JA; Ximenes Filho R; de Oliveira Britto AV; Oliveira Souza AH; Prado CM; Pereira Oliveira CR; Pereira RM; Ribeiro Vicente Tde A; Farias CT; Aguiar-Oliveira MH; Salvatori R
J Clin Endocrinol Metab; 2006 Jun; 91(6):2093-9. PubMed ID: 16522693
[TBL] [Abstract][Full Text] [Related]
22. 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]
23. Molecular and clinical aspects of GHRH receptor mutations.
Corazzini V; Salvatori R
Endocr Dev; 2013; 24():106-17. PubMed ID: 23392099
[TBL] [Abstract][Full Text] [Related]
24. Effect of severe growth hormone (GH) deficiency due to a mutation in the GH-releasing hormone receptor on insulin-like growth factors (IGFs), IGF-binding proteins, and ternary complex formation throughout life.
Aguiar-Oliveira MH; Gill MS; de A Barretto ES; Alcântara MR; Miraki-Moud F; Menezes CA; Souza AH; Martinelli CE; Pereira FA; Salvatori R; Levine MA; Shalet SM; Camacho-Hubner C; Clayton PE
J Clin Endocrinol Metab; 1999 Nov; 84(11):4118-26. PubMed ID: 10566659
[TBL] [Abstract][Full Text] [Related]
25. Contribution of human growth hormone-releasing hormone receptor (GHRHR) gene sequence variation to isolated severe growth hormone deficiency (ISGHD) and normal adult height.
Camats N; Fernández-Cancio M; Carrascosa A; Andaluz P; Albisu MÁ; Clemente M; Gussinyé M; Yeste D; Audí L
Clin Endocrinol (Oxf); 2012 Oct; 77(4):564-74. PubMed ID: 22489751
[TBL] [Abstract][Full Text] [Related]
26. Disruption of the GHRH receptor and its impact on children and adults: The Itabaianinha syndrome.
Aguiar-Oliveira MH; Salvatori R
Rev Endocr Metab Disord; 2021 Mar; 22(1):81-89. PubMed ID: 32935264
[TBL] [Abstract][Full Text] [Related]
27. [Growth or somatotrophic hormone: new perspectives in isolated GH deficiency after description of the mutation in the GHRH receptor gene in individuals of Itabaianinha County, Brazil].
Souza AH; Salvatori R; Martinelli CE; Carvalho WM; Menezes CA; Barretto ES; Barreto Filho JA; Alcântara MR; Oliveira CR; Alcântara PR; Ramalho RJ; Oliveira HA; Lima IB; Carneiro JN; Santos MM; Gill MS; Clayton PE; Oliveira MH
Arq Bras Endocrinol Metabol; 2004 Jun; 48(3):406-13. PubMed ID: 15640904
[TBL] [Abstract][Full Text] [Related]
28. Novel compound heterozygous mutations of the growth hormone-releasing hormone receptor gene in a case of isolated growth hormone deficiency.
Soneda A; Adachi M; Muroya K; Asakura Y; Takagi M; Hasegawa T; Inoue H; Itakura M
Growth Horm IGF Res; 2013 Aug; 23(4):89-97. PubMed ID: 23602557
[TBL] [Abstract][Full Text] [Related]
29. 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]
30. 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]
31. Ocular findings in adult subjects with an inactivating mutation in GH releasing hormone receptor gene.
Faro ACN; Pereira-Gurgel VM; Salvatori R; Campos VC; Melo GB; Oliveira FT; Oliveira-Santos AA; Oliveira CRP; Pereira FA; Hellström A; Oliveira-Neto LA; Valença EHO; Aguiar-Oliveira MH
Growth Horm IGF Res; 2017 Jun; 34():8-12. PubMed ID: 28456063
[TBL] [Abstract][Full Text] [Related]
32. Phenotypic analysis and growth response to different growth hormone treatment schedules in two siblings with an inactivating mutation in the growth hormone-releasing hormone receptor gene.
Espigares R; Martín de Lara I; Ruiz-Cabello F; Ortega L; Ferrández Longás A; Argente J; Salvatori R
J Pediatr Endocrinol Metab; 2004 May; 17(5):793-800. PubMed ID: 15237716
[TBL] [Abstract][Full Text] [Related]
33. Longevity in untreated congenital growth hormone deficiency due to a homozygous mutation in the GHRH receptor gene.
Aguiar-Oliveira MH; Oliveira FT; Pereira RM; Oliveira CR; Blackford A; Valenca EH; Santos EG; Gois-Junior MB; Meneguz-Moreno RA; Araujo VP; Oliveira-Neto LA; Almeida RP; Santos MA; Farias NT; Silveira DC; Cabral GW; Calazans FR; Seabra JD; Lopes TF; Rodrigues EO; Porto LA; Oliveira IP; Melo EV; Martari M; Salvatori R
J Clin Endocrinol Metab; 2010 Feb; 95(2):714-21. PubMed ID: 19965916
[TBL] [Abstract][Full Text] [Related]
34. 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]
35. Extensive phenotypic analysis of a family with growth hormone (GH) deficiency caused by a mutation in the GH-releasing hormone receptor gene.
Netchine I; Talon P; Dastot F; Vitaux F; Goossens M; Amselem S
J Clin Endocrinol Metab; 1998 Feb; 83(2):432-6. PubMed ID: 9467553
[TBL] [Abstract][Full Text] [Related]
36. 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]
37. Extended haplotypes in the growth hormone releasing hormone receptor gene (GHRHR) are associated with normal variation in height.
Johansson A; Jonasson I; Gyllensten U
PLoS One; 2009; 4(2):e4464. PubMed ID: 19209235
[TBL] [Abstract][Full Text] [Related]
38. Macrophages From Subjects With Isolated GH/IGF-I Deficiency Due to a GHRH Receptor Gene Mutation Are Less Prone to Infection by
Barrios MR; Campos VC; Peres NTA; de Oliveira LL; Cazzaniga RA; Santos MB; Aires MB; Silva RLL; Barreto A; Goto H; Almeida RP; Salvatori R; Aguiar-Oliveira MH; Jesus AMR
Front Cell Infect Microbiol; 2019; 9():311. PubMed ID: 31544067
[TBL] [Abstract][Full Text] [Related]
39. Identification and functional analysis of novel human growth hormone-releasing hormone receptor (GHRHR) gene mutations in Japanese subjects with short stature.
Inoue H; Kangawa N; Kinouchi A; Sakamoto Y; Kimura C; Horikawa R; Shigematsu Y; Itakura M; Ogata T; Fujieda K;
Clin Endocrinol (Oxf); 2011 Feb; 74(2):223-33. PubMed ID: 21044116
[TBL] [Abstract][Full Text] [Related]
40. Decreased expression of the GHRH receptor gene due to a mutation in a Pit-1 binding site.
Salvatori R; Fan X; Mullis PE; Haile A; Levine MA
Mol Endocrinol; 2002 Mar; 16(3):450-8. PubMed ID: 11875102
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
