225 related articles for article (PubMed ID: 9439906)
1. GH and TSH deficiency.
Pfäffle RW; Martinez R; Kim C; Frisch H; Lebl J; Otten B; Heimann G
Exp Clin Endocrinol Diabetes; 1997; 105 Suppl 4():1-5. PubMed ID: 9439906
[TBL] [Abstract][Full Text] [Related]
2. GH transcription factors.
Pfaffle RW; Kim C; Blankenstein O; Kentrup H
J Pediatr Endocrinol Metab; 1999 Apr; 12 Suppl 1():311-7. PubMed ID: 10698595
[TBL] [Abstract][Full Text] [Related]
3. Cellular determination in the anterior pituitary gland: PIT-1 and PROP-1 mutations as causes of human combined pituitary hormone deficiency.
Rodriguez R; Andersen B
Minerva Endocrinol; 2003 Jun; 28(2):123-33. PubMed ID: 12717343
[TBL] [Abstract][Full Text] [Related]
4. Mutations in PROP1 cause familial combined pituitary hormone deficiency.
Wu W; Cogan JD; Pfäffle RW; Dasen JS; Frisch H; O'Connell SM; Flynn SE; Brown MR; Mullis PE; Parks JS; Phillips JA; Rosenfeld MG
Nat Genet; 1998 Feb; 18(2):147-9. PubMed ID: 9462743
[TBL] [Abstract][Full Text] [Related]
5. The de novo Q167K mutation in the POU1F1 gene leads to combined pituitary hormone deficiency in an Italian patient.
Malvagia S; Poggi GM; Pasquini E; Donati MA; Pela I; Morrone A; Zammarchi E
Pediatr Res; 2003 Nov; 54(5):635-40. PubMed ID: 12904605
[TBL] [Abstract][Full Text] [Related]
6. [The pituitary specific transcription factor Pit-1/GHF-1 and PIT1 abnormality].
Tatsumi K; Amino N
Rinsho Byori; 1997 Jul; 45(7):656-9. PubMed ID: 9256012
[TBL] [Abstract][Full Text] [Related]
7. [Molecular pathology of congenital pituitary hypothyroidism--discovery of new clinical entities].
Tatsumi K; Amino N; Miyai K
Rinsho Byori; 1993 May; 41(5):533-40. PubMed ID: 8350517
[TBL] [Abstract][Full Text] [Related]
8. [Pituitary specific transcription factor Pit-1/GHF-1 and combined pituitary hormone deficiency].
Tatsumi K
Nihon Rinsho; 1994 Apr; 52(4):957-61. PubMed ID: 8196186
[TBL] [Abstract][Full Text] [Related]
9. Thyrotropin (TSH) beta-subunit gene expression--an example for the complex regulation of pituitary hormone genes.
Steinfelder HJ; Wondisford FE
Exp Clin Endocrinol Diabetes; 1997; 105(4):196-203. PubMed ID: 9285205
[TBL] [Abstract][Full Text] [Related]
10. Autosomal recessive deficiency of combined pituitary hormones (except ACTH) in a consanguineous Brazilian kindred.
Nogueira CR; Leite CC; Chedid EP; Liberman B; Pimentel-Filho FR; Kopp P; Medeiros-Neto GA
J Endocrinol Invest; 1997 Nov; 20(10):629-33. PubMed ID: 9438923
[TBL] [Abstract][Full Text] [Related]
11. Combined pituitary hormone deficiency and pituitary hypoplasia due to a mutation of the Pit-1 gene.
Frisch H; Kim C; Häusler G; Pfäffle R
Clin Endocrinol (Oxf); 2000 May; 52(5):661-5. PubMed ID: 10792348
[TBL] [Abstract][Full Text] [Related]
12. Description of a Brazilian patient bearing the R271W Pit-1 gene mutation.
Rodrigues Martineli AM; Braga M; De Lacerda L; Raskin S; Graf H
Thyroid; 1998 Apr; 8(4):299-304. PubMed ID: 9588494
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. Induction of GH, PRL, and TSH beta mRNA by transfection of Pit-1 in a human pituitary adenoma-derived cell line.
Miyai S; Yoshimura S; Iwasaki Y; Takekoshi S; Lloyd RV; Osamura RY
Cell Tissue Res; 2005 Nov; 322(2):269-77. PubMed ID: 16133148
[TBL] [Abstract][Full Text] [Related]
15. A novel germline mutation, IVS4+1G>A, of the POU1F1 gene underlying combined pituitary hormone deficiency.
Snabboon T; Plengpanich W; Buranasupkajorn P; Khwanjaipanich R; Vasinanukorn P; Suwanwalaikorn S; Khovidhunkit W; Shotelersuk V
Horm Res; 2008; 69(1):60-4. PubMed ID: 18059085
[TBL] [Abstract][Full Text] [Related]
16. A "hot spot" in the Pit-1 gene responsible for combined pituitary hormone deficiency: clinical and molecular correlates.
Cohen LE; Wondisford FE; Salvatoni A; Maghnie M; Brucker-Davis F; Weintraub BD; Radovick S
J Clin Endocrinol Metab; 1995 Feb; 80(2):679-84. PubMed ID: 7852536
[TBL] [Abstract][Full Text] [Related]
17. Pro239Ser: a novel recessive mutation of the Pit-1 gene in seven Middle Eastern children with growth hormone, prolactin, and thyrotropin deficiency.
Pernasetti F; Milner RD; al Ashwal AA; de Zegher F; Chavez VM; Muller M; Martial JA
J Clin Endocrinol Metab; 1998 Jun; 83(6):2079-83. PubMed ID: 9626142
[TBL] [Abstract][Full Text] [Related]
18. Cretinism with combined hormone deficiency caused by a mutation in the PIT1 gene.
Tatsumi K; Miyai K; Notomi T; Kaibe K; Amino N; Mizuno Y; Kohno H
Nat Genet; 1992 Apr; 1(1):56-8. PubMed ID: 1302000
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. Central hypothyroidism reveals compound heterozygous mutations in the Pit-1 gene.
Brown MR; Parks JS; Adess ME; Rich BH; Rosenthal IM; Voss TC; VanderHeyden TC; Hurley DL
Horm Res; 1998; 49(2):98-102. PubMed ID: 9485179
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
