PubMed (OMIM) for id: 209236

Year	Number of Results
1953	1
1954	1
1964	1
1965	1
1967	2
1969	1
1974	1
1985	1
1990	1
1995	1
1996	3
1998	5
1999	4
2000	4
2001	4
2002	1
2003	1
2004	2
2024	0

1

A familial form of congenital hypopituitarism due to a PROP1 mutation in a large kindred: phenotypic and in vitro functional studies.

Reynaud R, Chadli-Chaieb M, Vallette-Kasic S, Barlier A, Sarles J, Pellegrini-Bouiller I, Enjalbert A, Chaieb L, Brue T. Reynaud R, et al. J Clin Endocrinol Metab. 2004 Nov;89(11):5779-86. doi: 10.1210/jc.2003-032124. J Clin Endocrinol Metab. 2004. PMID: 15531542

2

Pituitary magnetic resonance imaging in 15 patients with Prop1 gene mutations: pituitary enlargement may originate from the intermediate lobe.

Voutetakis A, Argyropoulou M, Sertedaki A, Livadas S, Xekouki P, Maniati-Christidi M, Bossis I, Thalassinos N, Patronas N, Dacou-Voutetakis C. Voutetakis A, et al. J Clin Endocrinol Metab. 2004 May;89(5):2200-6. doi: 10.1210/jc.2003-031765. J Clin Endocrinol Metab. 2004. PMID: 15126542

3

STUDIES IN ISOLATES.

FRASER GR. FRASER GR. J Genet Hum. 1964;13:32-46. J Genet Hum. 1964. PMID: 14192062 No abstract available.

4

[Clinical, hereditary and constitutional studies of primordial dwarfs].

KIRCHHOFF HW, LEHMANN W, SCHAEFER U. KIRCHHOFF HW, et al. Z Kinderheilkd. 1954;75(3):243-66. Z Kinderheilkd. 1954. PMID: 13227184 German. No abstract available.

5

[The role of hereditary factors in growth disorders].

HANHART E. HANHART E. Schweiz Med Wochenschr. 1953 Feb 21;83(8):198-203. Schweiz Med Wochenschr. 1953. PMID: 13076009 Undetermined Language. No abstract available.

6

Familial combined pituitary hormone deficiency due to a novel mutation R99Q in the hot spot region of Prophet of Pit-1 presenting as constitutional growth delay.

Vieira TC, Dias da Silva MR, Cerutti JM, Brunner E, Borges M, Arnaldi LT, Kopp P, Abucham J. Vieira TC, et al. J Clin Endocrinol Metab. 2003 Jan;88(1):38-44. doi: 10.1210/jc.2001-011872. J Clin Endocrinol Metab. 2003. PMID: 12519826

7

Pituitary magnetic resonance imaging and function in patients with growth hormone deficiency with and without mutations in GHRH-R, GH-1, or PROP-1 genes.

Osorio MG, Marui S, Jorge AA, Latronico AC, Lo LS, Leite CC, Estefan V, Mendonca BB, Arnhold IJ. Osorio MG, et al. J Clin Endocrinol Metab. 2002 Nov;87(11):5076-84. doi: 10.1210/jc.2001-011936. J Clin Endocrinol Metab. 2002. PMID: 12414875

8

A familial syndrome of isolated "aplasia" of the anterior pituitary. Diagnostic studies and treatment in the neonatal period.

Sadeghi-Nejad A, Senior B. Sadeghi-Nejad A, et al. J Pediatr. 1974 Jan;84(1):79-84. doi: 10.1016/s0022-3476(74)80557-3. J Pediatr. 1974. PMID: 12119961 Review.

9

Extending the lifespan of long-lived mice.

Bartke A, Wright JC, Mattison JA, Ingram DK, Miller RA, Roth GS. Bartke A, et al. Nature. 2001 Nov 22;414(6862):412. doi: 10.1038/35106646. Nature. 2001. PMID: 11719795 Free article. No abstract available.

10

PROP1 gene screening in patients with multiple pituitary hormone deficiency reveals two sites of hypermutability and a high incidence of corticotroph deficiency.

Vallette-Kasic S, Barlier A, Teinturier C, Diaz A, Manavela M, Berthezène F, Bouchard P, Chaussain JL, Brauner R, Pellegrini-Bouiller I, Jaquet P, Enjalbert A, Brue T. Vallette-Kasic S, et al. J Clin Endocrinol Metab. 2001 Sep;86(9):4529-35. doi: 10.1210/jcem.86.9.7811. J Clin Endocrinol Metab. 2001. PMID: 11549703

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