135 related articles for article (PubMed ID: 12914740)
1. DNA testing in patients with GH deficiency at the time of transition.
Dattani MT
Growth Horm IGF Res; 2003 Aug; 13 Suppl A():S122-9. PubMed ID: 12914740
[TBL] [Abstract][Full Text] [Related]
2. Genetic causes of isolated and combined pituitary hormone deficiency.
Giordano M
Best Pract Res Clin Endocrinol Metab; 2016 Dec; 30(6):679-691. PubMed ID: 27974184
[TBL] [Abstract][Full Text] [Related]
3. Hypopituitarism oddities: congenital causes.
Kelberman D; Dattani MT
Horm Res; 2007; 68 Suppl 5():138-44. PubMed ID: 18174732
[TBL] [Abstract][Full Text] [Related]
4. Genetic spectrum and predictors of mutations in four known genes in Asian Indian patients with growth hormone deficiency and orthotopic posterior pituitary: an emphasis on regional genetic diversity.
Kale S; Gada JV; Jadhav S; Lila AR; Sarathi V; Budyal S; Patt H; Goroshi MR; Thadani PM; Arya S; Kamble AA; Patil VA; Acharya S; Sankhe S; Shivane V; Raghavan V; Bandgar TR; Shah NS
Pituitary; 2020 Dec; 23(6):701-715. PubMed ID: 32894409
[TBL] [Abstract][Full Text] [Related]
5. PROP1, HESX1, POU1F1, LHX3 and LHX4 mutation and deletion screening and GH1 P89L and IVS3+1/+2 mutation screening in a Dutch nationwide cohort of patients with combined pituitary hormone deficiency.
de Graaff LC; Argente J; Veenma DC; Drent ML; Uitterlinden AG; Hokken-Koelega AC
Horm Res Paediatr; 2010; 73(5):363-71. PubMed ID: 20389107
[TBL] [Abstract][Full Text] [Related]
6. Rare Frequency of Mutations in Pituitary Transcription Factor Genes in Combined Pituitary Hormone or Isolated Growth Hormone Deficiencies in Korea.
Choi JH; Jung CW; Kang E; Kim YM; Heo SH; Lee BH; Kim GH; Yoo HW
Yonsei Med J; 2017 May; 58(3):527-532. PubMed ID: 28332357
[TBL] [Abstract][Full Text] [Related]
7. [Genetic aspects of growth hormone deficiency].
Reynaud R; Castinetti F; Galon-Faure N; Albarel-Loy F; Saveanu A; Quentien MH; Jullien N; Khammar A; Enjalbert A; Barlier A; Brue T
Arch Pediatr; 2011 Jun; 18(6):696-706. PubMed ID: 21497494
[TBL] [Abstract][Full Text] [Related]
8. Growth hormone deficiency and combined pituitary hormone deficiency: does the genotype matter?
Dattani MT
Clin Endocrinol (Oxf); 2005 Aug; 63(2):121-30. PubMed ID: 16060904
[TBL] [Abstract][Full Text] [Related]
9. Combined pituitary hormone deficiency in Australian children: clinical and genetic correlates.
McLennan K; Jeske Y; Cotterill A; Cowley D; Penfold J; Jones T; Howard N; Thomsett M; Choong C
Clin Endocrinol (Oxf); 2003 Jun; 58(6):785-94. PubMed ID: 12780757
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. Long-Term Outcomes, Genetics, and Pituitary Morphology in Patients with Isolated Growth Hormone Deficiency and Multiple Pituitary Hormone Deficiencies: A Single-Centre Experience of Four Decades of Growth Hormone Replacement.
Rohayem J; Drechsel H; Tittel B; Hahn G; Pfaeffle R; Huebner A
Horm Res Paediatr; 2016; 86(2):106-116. PubMed ID: 27487097
[TBL] [Abstract][Full Text] [Related]
12. Identification of Novel PROP1 and POU1F1 Mutations in Patients with Combined Pituitary Hormone Deficiency.
Birla S; Khadgawat R; Jyotsna VP; Jain V; Garg MK; Bhalla AS; Sharma A
Horm Metab Res; 2016 Dec; 48(12):822-827. PubMed ID: 27756091
[TBL] [Abstract][Full Text] [Related]
13. HESX1 mutations in patients with congenital hypopituitarism: variable phenotypes with the same genotype.
Fang Q; Benedetti AF; Ma Q; Gregory L; Li JZ; Dattani M; Sadeghi-Nejad A; Arnhold IJ; Mendonca BB; Camper SA; Carvalho LR
Clin Endocrinol (Oxf); 2016 Sep; 85(3):408-14. PubMed ID: 27000987
[TBL] [Abstract][Full Text] [Related]
14. Novel insights into the aetiology and pathogenesis of hypopituitarism.
Dattani MT
Horm Res; 2004; 62 Suppl 3():1-13. PubMed ID: 15539793
[TBL] [Abstract][Full Text] [Related]
15. Mutation analysis of POUF-1, PROP-1 and HESX-1 show low frequency of mutations in children with sporadic forms of combined pituitary hormone deficiency and septo-optic dysplasia.
Rainbow LA; Rees SA; Shaikh MG; Shaw NJ; Cole T; Barrett TG; Kirk JM
Clin Endocrinol (Oxf); 2005 Feb; 62(2):163-8. PubMed ID: 15670191
[TBL] [Abstract][Full Text] [Related]
16. Molecular screening of a large cohort of Moroccan patients with congenital hypopituitarism.
Fritez N; Sobrier ML; Iraqi H; Vié-Luton MP; Netchine I; El Annas A; Pantel J; Collot N; Rose S; Piterboth W; Legendre M; Chraibi A; Amselem S; Kadiri A; Hilal L
Clin Endocrinol (Oxf); 2015 Jun; 82(6):876-84. PubMed ID: 25557026
[TBL] [Abstract][Full Text] [Related]
17. Adrenocorticotrope deficiency with clinical evidence for late onset in combined pituitary hormone deficiency caused by a homozygous 301-302delAG mutation of the PROP1 gene.
Lamesch C; Neumann S; Pfäffle R; Kiess W; Paschke R
Pituitary; 2002; 5(3):163-8. PubMed ID: 12812307
[TBL] [Abstract][Full Text] [Related]
18. A novel OTX2 mutation in a patient with combined pituitary hormone deficiency, pituitary malformation, and an underdeveloped left optic nerve.
Gorbenko Del Blanco D; Romero CJ; Diaczok D; de Graaff LC; Radovick S; Hokken-Koelega AC
Eur J Endocrinol; 2012 Sep; 167(3):441-52. PubMed ID: 22715480
[TBL] [Abstract][Full Text] [Related]
19. Genetic screening of combined pituitary hormone deficiency: experience in 195 patients.
Reynaud R; Gueydan M; Saveanu A; Vallette-Kasic S; Enjalbert A; Brue T; Barlier A
J Clin Endocrinol Metab; 2006 Sep; 91(9):3329-36. PubMed ID: 16735499
[TBL] [Abstract][Full Text] [Related]
20. Molecular basis of familial growth hormone deficiency.
Pérez Jurado LA; Argente J
Horm Res; 1994; 42(4-5):189-97. PubMed ID: 7868072
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
