Levine MA - Search Results

1

Body mass index differences in pseudohypoparathyroidism type 1a versus pseudopseudohypoparathyroidism may implicate paternal imprinting of Galpha(s) in the development of human obesity.

Long DN, McGuire S, Levine MA, Weinstein LS, Germain-Lee EL. Long DN, et al. Among authors: levine ma. J Clin Endocrinol Metab. 2007 Mar;92(3):1073-9. doi: 10.1210/jc.2006-1497. Epub 2006 Dec 12. J Clin Endocrinol Metab. 2007. PMID: 17164301

2

Hypocalcemia in nonwhite breast-fed infants. Vitamin D deficiency revisited.

Chang YT, Germain-Lee EL, Doran TF, Migeon CJ, Levine MA, Berkovitz GD. Chang YT, et al. Among authors: levine ma. Clin Pediatr (Phila). 1992 Nov;31(11):695-8. doi: 10.1177/000992289203101111. Clin Pediatr (Phila). 1992. PMID: 1424401 No abstract available.

3

Immunochemical analysis of the alpha-subunit of the stimulatory G-protein of adenylyl cyclase in patients with Albright's hereditary osteodystrophy.

Patten JL, Levine MA. Patten JL, et al. Among authors: levine ma. J Clin Endocrinol Metab. 1990 Nov;71(5):1208-14. doi: 10.1210/jcem-71-5-1208. J Clin Endocrinol Metab. 1990. PMID: 2121768

4

Activity of the stimulatory guanine nucleotide-binding protein is reduced in erythrocytes from patients with pseudohypoparathyroidism and pseudopseudohypoparathyroidism: biochemical, endocrine, and genetic analysis of Albright's hereditary osteodystrophy in six kindreds.

Levine MA, Jap TS, Mauseth RS, Downs RW, Spiegel AM. Levine MA, et al. J Clin Endocrinol Metab. 1986 Mar;62(3):497-502. doi: 10.1210/jcem-62-3-497. J Clin Endocrinol Metab. 1986. PMID: 3003142

5

Characterization of Albright hereditary osteodystrophy and related disorders.

Koo BB, Schwindinger WF, Levine MA. Koo BB, et al. Among authors: levine ma. Zhonghua Min Guo Xiao Er Ke Yi Xue Hui Za Zhi. 1995 Jan-Feb;36(1):3-13. Zhonghua Min Guo Xiao Er Ke Yi Xue Hui Za Zhi. 1995. PMID: 7778442 Review.

6

Heterogeneous mutations in the gene encoding the alpha-subunit of the stimulatory G protein of adenylyl cyclase in Albright hereditary osteodystrophy.

Miric A, Vechio JD, Levine MA. Miric A, et al. Among authors: levine ma. J Clin Endocrinol Metab. 1993 Jun;76(6):1560-8. doi: 10.1210/jcem.76.6.8388883. J Clin Endocrinol Metab. 1993. PMID: 8388883

7

Urinary cyclic adenosine 3',5'-monophosphate response in McCune-Albright syndrome: clinical evidence for altered renal adenylate cyclase activity.

Zung A, Chalew SA, Schwindinger WF, Levine MA, Phillip M, Jara A, Counts DR, Kowarski AA. Zung A, et al. Among authors: levine ma. J Clin Endocrinol Metab. 1995 Dec;80(12):3576-81. doi: 10.1210/jcem.80.12.8530601. J Clin Endocrinol Metab. 1995. PMID: 8530601

8

Olfactory dysfunction in type I pseudohypoparathyroidism: dissociation from Gs alpha protein deficiency.

Doty RL, Fernandez AD, Levine MA, Moses A, McKeown DA. Doty RL, et al. Among authors: levine ma. J Clin Endocrinol Metab. 1997 Jan;82(1):247-50. doi: 10.1210/jcem.82.1.3713. J Clin Endocrinol Metab. 1997. PMID: 8989268

9

Thyroid-specific expression of cholera toxin A1 subunit causes thyroid hyperplasia and hyperthyroidism in transgenic mice.

Zeiger MA, Saji M, Gusev Y, Westra WH, Takiyama Y, Dooley WC, Kohn LD, Levine MA. Zeiger MA, et al. Among authors: levine ma. Endocrinology. 1997 Aug;138(8):3133-40. doi: 10.1210/endo.138.8.5347. Endocrinology. 1997. PMID: 9231760

10

Targeted disruption of Gnas in embryonic stem cells.

Schwindinger WF, Reese KJ, Lawler AM, Gearhart JD, Levine MA. Schwindinger WF, et al. Among authors: levine ma. Endocrinology. 1997 Oct;138(10):4058-63. doi: 10.1210/endo.138.10.5439. Endocrinology. 1997. PMID: 9322912

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

531 results

Search Page