Brown MR - Search Results

1

Clinical and biochemical phenotype of familial anterior hypopituitarism from mutation of the PROP1 gene.

Rosenbloom AL, Almonte AS, Brown MR, Fisher DA, Baumbach L, Parks JS. Rosenbloom AL, et al. Among authors: brown mr. J Clin Endocrinol Metab. 1999 Jan;84(1):50-7. doi: 10.1210/jcem.84.1.5366. J Clin Endocrinol Metab. 1999. PMID: 9920061

2

The spectrum of hypopituitarism caused by PROP1 mutations.

Mody S, Brown MR, Parks JS. Mody S, et al. Among authors: brown mr. Best Pract Res Clin Endocrinol Metab. 2002 Sep;16(3):421-31. doi: 10.1053/beem.2002.0218. Best Pract Res Clin Endocrinol Metab. 2002. PMID: 12464226 Review.

3

Heritable disorders of pituitary development.

Parks JS, Brown MR, Hurley DL, Phelps CJ, Wajnrajch MP. Parks JS, et al. Among authors: brown mr. J Clin Endocrinol Metab. 1999 Dec;84(12):4362-70. doi: 10.1210/jcem.84.12.6209. J Clin Endocrinol Metab. 1999. PMID: 10599689 Review.

4

Clinical, biochemical, and molecular investigations of a genetic isolate of growth hormone insensitivity (Laron's syndrome).

Baumbach L, Schiavi A, Bartlett R, Perera E, Day J, Brown MR, Stein S, Eidson M, Parks JS, Cleveland W. Baumbach L, et al. Among authors: brown mr. J Clin Endocrinol Metab. 1997 Feb;82(2):444-51. doi: 10.1210/jcem.82.2.3784. J Clin Endocrinol Metab. 1997. PMID: 9024234

5

Mechanisms responsible for dominant expression of human growth hormone gene mutations.

Binder G, Brown M, Parks JS. Binder G, et al. J Clin Endocrinol Metab. 1996 Nov;81(11):4047-50. doi: 10.1210/jcem.81.11.8923859. J Clin Endocrinol Metab. 1996. PMID: 8923859

6

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. Brown MR, et al. Horm Res. 1998;49(2):98-102. doi: 10.1159/000023134. Horm Res. 1998. PMID: 9485179

7

Compound heterozygous deletion of the PROP-1 gene in children with combined pituitary hormone deficiency.

Fofanova O, Takamura N, Kinoshita E, Parks JS, Brown MR, Peterkova VA, Evgrafov OV, Goncharov NP, Bulatov AA, Dedov II, Yamashita S. Fofanova O, et al. Among authors: brown mr. J Clin Endocrinol Metab. 1998 Jul;83(7):2601-4. doi: 10.1210/jcem.83.7.5094. J Clin Endocrinol Metab. 1998. PMID: 9661653 Clinical Trial.

8

Clinical and molecular characterization of a Brazilian patient with Pit-1 deficiency.

Arnhold IJ, Nery M, Brown MR, Voss TC, VanderHeyden TC, Adess ME, Hurley DL, Wajchenberg BL, Parks JS. Arnhold IJ, et al. Among authors: brown mr. J Pediatr Endocrinol Metab. 1998 Sep-Oct;11(5):623-30. doi: 10.1515/jpem.1998.11.5.623. J Pediatr Endocrinol Metab. 1998. PMID: 9829213

9

Growth hormone deficiency type IB caused by cryptic splicing of the GH-1 gene.

Abdul-Latif H, Leiberman E, Brown MR, Carmi R, Parks JS. Abdul-Latif H, et al. Among authors: brown mr. J Pediatr Endocrinol Metab. 2000 Jan;13(1):21-8. doi: 10.1515/jpem.2000.13.1.21. J Pediatr Endocrinol Metab. 2000. PMID: 10689634

10

A mutational hot spot in the Prop-1 gene in Russian children with combined pituitary hormone deficiency.

Fofanova OV, Takamura N, Kinoshita E, Parks JS, Brown MR, Peterkova VA, Evgrafov OV, Goncharov NP, Bulatov AA, Dedov II, Yamashita S. Fofanova OV, et al. Among authors: brown mr. Pituitary. 1998 Apr;1(1):45-9. doi: 10.1023/a:1009918924945. Pituitary. 1998. PMID: 11081182

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