125 related articles for article (PubMed ID: 30764079)
1. Hypothalamic-pituitary magnetic resonance imaging in growth hormone deficiency.
Maghnie M; Rossi A; di Iorgi N; Gastaldi R; Tortori-Donati P; Lorini R
Expert Rev Endocrinol Metab; 2006 May; 1(3):413-423. PubMed ID: 30764079
[TBL] [Abstract][Full Text] [Related]
2. Classical and non-classical causes of GH deficiency in the paediatric age.
Di Iorgi N; Morana G; Allegri AE; Napoli F; Gastaldi R; Calcagno A; Patti G; Loche S; Maghnie M
Best Pract Res Clin Endocrinol Metab; 2016 Dec; 30(6):705-736. PubMed ID: 27974186
[TBL] [Abstract][Full Text] [Related]
3. Pituitary gland imaging and outcome.
Di Iorgi N; Morana G; Gallizia AL; Maghnie M
Endocr Dev; 2012; 23():16-29. PubMed ID: 23182817
[TBL] [Abstract][Full Text] [Related]
4. [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]
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. Clinical characteristics and molecular analysis of PIT1, PROP1,LHX3, and HESX1 in combined pituitary hormone deficiency patients with abnormal pituitary MR imaging.
Kim SS; Kim Y; Shin YL; Kim GH; Kim TU; Yoo HW
Horm Res; 2003; 60(6):277-83. PubMed ID: 14646405
[TBL] [Abstract][Full Text] [Related]
7. The use of neuroimaging for assessing disorders of pituitary development.
Di Iorgi N; Allegri AE; Napoli F; Bertelli E; Olivieri I; Rossi A; Maghnie M
Clin Endocrinol (Oxf); 2012 Feb; 76(2):161-76. PubMed ID: 21955099
[TBL] [Abstract][Full Text] [Related]
8. Molecular and Clinical Findings in Patients with LHX4 and OTX2 Mutations.
Tajima T; Ishizu K; Nakamura A
Clin Pediatr Endocrinol; 2013 Apr; 22(2):15-23. PubMed ID: 23990694
[TBL] [Abstract][Full Text] [Related]
9. Clinical lessons learned in constitutional hypopituitarism from two decades of experience in a large international cohort.
Jullien N; Saveanu A; Vergier J; Marquant E; Quentien MH; Castinetti F; Galon-Faure N; Brauner R; Marrakchi Turki Z; Tauber M; El Kholy M; Linglart A; Rodien P; Fedala NS; Bergada I; Cortet-Rudelli C; Polak M; Nicolino M; Stuckens C; Barlier A; Brue T; Reynaud R;
Clin Endocrinol (Oxf); 2021 Feb; 94(2):277-289. PubMed ID: 33098107
[TBL] [Abstract][Full Text] [Related]
10. LHX3 and LHX4 transcription factors in pituitary development and disease.
Colvin SC; Mullen RD; Pfaeffle RW; Rhodes SJ
Pediatr Endocrinol Rev; 2009 Jan; 6 Suppl 2():283-90. PubMed ID: 19337183
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. Congenital Hypopituitarism During the Neonatal Period: Epidemiology, Pathogenesis, Therapeutic Options, and Outcome.
Bosch I Ara L; Katugampola H; Dattani MT
Front Pediatr; 2020; 8():600962. PubMed ID: 33634051
[No Abstract] [Full Text] [Related]
13. Gradual loss of ACTH due to a novel mutation in LHX4: comprehensive mutation screening in Japanese patients with congenital hypopituitarism.
Takagi M; Ishii T; Inokuchi M; Amano N; Narumi S; Asakura Y; Muroya K; Hasegawa Y; Adachi M; Hasegawa T
PLoS One; 2012; 7(9):e46008. PubMed ID: 23029363
[TBL] [Abstract][Full Text] [Related]
14. Hormonal, pituitary magnetic resonance, LHX4 and HESX1 evaluation in patients with hypopituitarism and ectopic posterior pituitary lobe.
Melo ME; Marui S; Carvalho LR; Arnhold IJ; Leite CC; Mendonça BB; Knoepfelmacher M
Clin Endocrinol (Oxf); 2007 Jan; 66(1):95-102. PubMed ID: 17201807
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. 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]
17. Two coexisting heterozygous frameshift mutations in PROP1 are responsible for a different phenotype of combined pituitary hormone deficiency.
Ziemnicka K; Budny B; Drobnik K; Baszko-Błaszyk D; Stajgis M; Katulska K; Waśko R; Wrotkowska E; Słomski R; Ruchała M
J Appl Genet; 2016 Aug; 57(3):373-81. PubMed ID: 26608600
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. [Clinical and genetic aspects of combined pituitary hormone deficiencies].
Castinetti F; Reynaud R; Saveanu A; Quentien MH; Albarel F; Barlier A; Enjalbert A; Brue T
Ann Endocrinol (Paris); 2008 Feb; 69(1):7-17. PubMed ID: 18291347
[TBL] [Abstract][Full Text] [Related]
20. Growth hormone deficiency (GHD) and small for gestational age (SGA): genetic alterations.
Jancevska A; Gucev ZS; Tasic V; Pop-Jordanova N
Prilozi; 2009 Dec; 30(2):33-55. PubMed ID: 20087248
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]