221 related articles for article (PubMed ID: 1967179)
21. [Diagnosis by DNA analysis in familial isolated growth hormone deficiency type I-A].
Campos JL; Hierro FR; Monfar M; Boronat A; Rivera F; Casamitjana R; Ferrer A; Cruz M
Med Clin (Barc); 1989 Feb; 92(7):261-3. PubMed ID: 2716409
[TBL] [Abstract][Full Text] [Related]
22. A novel mutation at the donor splice site of intron 3 of the GH-I gene in a patient with isolated growth hormone deficiency.
Hayashi Y; Kamijo T; Yamamoto M; Ohmori S; Phillips JA; Ogawa M; Igarashi Y; Seo H
Growth Horm IGF Res; 1999 Dec; 9(6):434-7. PubMed ID: 10629163
[TBL] [Abstract][Full Text] [Related]
23. Molecular basis for familial isolated growth hormone deficiency.
Phillips JA; Hjelle BL; Seeburg PH; Zachmann M
Proc Natl Acad Sci U S A; 1981 Oct; 78(10):6372-5. PubMed ID: 6273867
[TBL] [Abstract][Full Text] [Related]
24. Isolated growth hormone deficiency type 2: from gene to therapy.
Miletta MC; Lochmatter D; Pektovic V; Mullis PE
Endocr Dev; 2012; 23():109-20. PubMed ID: 23182825
[TBL] [Abstract][Full Text] [Related]
25. Familial growth hormone deficiency resulting from a 7.6 kb deletion within the growth hormone gene cluster.
Braga S; Phillips JA; Joss E; Schwarz H; Zuppinger K
Am J Med Genet; 1986 Nov; 25(3):443-52. PubMed ID: 3024485
[TBL] [Abstract][Full Text] [Related]
26. Genetic polymorphisms in the locus control region and promoter of GH1 are related to serum IGF-I levels and height in patients with isolated growth hormone deficiency and healthy controls.
de Graaff LC; Argente J; van Meurs JB; Uitterlinden AG; Hokken-Koelega AC
Horm Res Paediatr; 2010; 73(1):25-34. PubMed ID: 20190537
[TBL] [Abstract][Full Text] [Related]
27. Growth, development, puberty and adult height before and during treatment in children with congenital isolated growth hormone deficiency.
Smuel K; Kauli R; Lilos P; Laron Z
Growth Horm IGF Res; 2015 Aug; 25(4):182-8. PubMed ID: 26077773
[TBL] [Abstract][Full Text] [Related]
28. 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]
29. Growth hormone (GH-1) gene deletions in children with isolated growth hormone deficiency (IGHD).
Desai MP; Mithbawkar SM; Upadhye PS; Shalia KK
Indian J Pediatr; 2012 Jul; 79(7):875-83. PubMed ID: 22016154
[TBL] [Abstract][Full Text] [Related]
30. Clinical characteristics, etiologies and pathophysiology of patients with severe short stature with severe GH deficiency: questionnaire study on the data registered with the foundation for growth science, Japan.
Hanew K; Tachibana K; Yokoya S; Fujieda K; Tanaka T; Igarashi Y; Shimatsu A; Tanaka H; Tanizawa T; Teramoto A; Nishi Y; Hasegawa Y; Hizuka N; Hirano T; Fujita K
Endocr J; 2006 Apr; 53(2):259-65. PubMed ID: 16618986
[TBL] [Abstract][Full Text] [Related]
31. 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]
32. Isolated growth hormone deficiency: testing the little mouse hypothesis in man and exclusion of mutations within the extracellular domain of the growth hormone-releasing hormone receptor.
Cao Y; Wagner JK; Hindmarsh PC; Eblé A; Mullis PE
Pediatr Res; 1995 Dec; 38(6):962-6. PubMed ID: 8618801
[TBL] [Abstract][Full Text] [Related]
33. Screening for growth hormone (GH) gene splice-site mutations in sporadic cases with severe isolated GH deficiency using ectopic transcript analysis.
Binder G; Ranke MB
J Clin Endocrinol Metab; 1995 Apr; 80(4):1247-52. PubMed ID: 7714096
[TBL] [Abstract][Full Text] [Related]
34. Growth hormone (GH) treatment in short normal children: absence of influence of time of injection and resistance to GH autofeedback.
Chanoine JP; Vanderschueren-Lodeweyckx M; Maes M; Thiry-Counson G; Craen M; Van Vliet G
J Clin Endocrinol Metab; 1991 Dec; 73(6):1269-75. PubMed ID: 1955508
[TBL] [Abstract][Full Text] [Related]
35. Growth hormone (GH) pharmacogenetics: influence of GH receptor exon 3 retention or deletion on first-year growth response and final height in patients with severe GH deficiency.
Jorge AA; Marchisotti FG; Montenegro LR; Carvalho LR; Mendonca BB; Arnhold IJ
J Clin Endocrinol Metab; 2006 Mar; 91(3):1076-80. PubMed ID: 16291702
[TBL] [Abstract][Full Text] [Related]
36. Catch-up growth in autosomal dominant isolated growth hormone deficiency (IGHD type II).
Binder G; Iliev DI; Mullis PE; Ranke MB
Growth Horm IGF Res; 2007 Jun; 17(3):242-8. PubMed ID: 17360215
[TBL] [Abstract][Full Text] [Related]
37. Short stature in carriers of recessive mutation causing familial isolated growth hormone deficiency.
Leiberman E; Pesler D; Parvari R; Elbedour K; Abdul-Latif H; Brown MR; Parks JS; Carmi R
Am J Med Genet; 2000 Jan; 90(3):188-92. PubMed ID: 10678654
[TBL] [Abstract][Full Text] [Related]
38. [Behavior of growth hormone after stimulation with growth hormone releasing hormone (GHRH) in children with disorders of the hypothalamo-hypophyseal axis and girls with Turner syndrome].
Schmitt K; Schober E; Birnbacher R; Frisch H
Klin Padiatr; 1996; 208(1):29-34. PubMed ID: 8851324
[TBL] [Abstract][Full Text] [Related]
39. Role of magnetic resonance imaging in the diagnosis and prognosis of growth hormone deficiency.
Bozzola M; Adamsbaum C; Biscaldi I; Zecca M; Cisternino M; Genovese E; Richard I; Kalifa G; Chaussain JL
Clin Endocrinol (Oxf); 1996 Jul; 45(1):21-6. PubMed ID: 8796134
[TBL] [Abstract][Full Text] [Related]
40. Autosomal-dominant isolated growth hormone deficiency (IGHD type II) with normal GH-1 gene.
Fintini D; Salvatori R; Salemi S; Otten B; Ubertini G; Cambiaso P; Mullis PE
Horm Res; 2006; 65(2):76-82. PubMed ID: 16424673
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]