Brown MR - Search Results

1

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

2

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

3

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

4

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

5

Characterization of a noncontiguous gene deletion of the growth hormone receptor in Laron's syndrome.

Meacham LR, Brown MR, Murphy TL, Keret R, Silbergeld A, Laron Z, Parks JS. Meacham LR, et al. Among authors: brown mr. J Clin Endocrinol Metab. 1993 Nov;77(5):1379-83. doi: 10.1210/jcem.77.5.8077336. J Clin Endocrinol Metab. 1993. PMID: 8077336

6

The spectrum of growth-hormone insensitivity.

Parks JS, Brown MR, Faase ME. Parks JS, et al. Among authors: brown mr. J Pediatr. 1997 Jul;131(1 Pt 2):S45-50. doi: 10.1016/s0022-3476(97)70011-8. J Pediatr. 1997. PMID: 9255228 Review.

7

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.

8

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.

9

Pituitary adenomas: screening for G alpha q mutations.

Oyesiku NM, Evans CO, Brown MR, Blevins LS, Tindall GT, Parks JS. Oyesiku NM, et al. Among authors: brown mr. J Clin Endocrinol Metab. 1997 Dec;82(12):4184-8. doi: 10.1210/jcem.82.12.4436. J Clin Endocrinol Metab. 1997. PMID: 9398737

10

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

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