Levine MA - Search Results

1

Paternally inherited inactivating mutations of the GNAS1 gene in progressive osseous heteroplasia.

Shore EM, Ahn J, Jan de Beur S, Li M, Xu M, Gardner RJ, Zasloff MA, Whyte MP, Levine MA, Kaplan FS. Shore EM, et al. Among authors: levine ma. N Engl J Med. 2002 Jan 10;346(2):99-106. doi: 10.1056/NEJMoa011262. N Engl J Med. 2002. PMID: 11784876 Free article.

2

Mutation in the gene encoding the stimulatory G protein of adenylate cyclase in Albright's hereditary osteodystrophy.

Patten JL, Johns DR, Valle D, Eil C, Gruppuso PA, Steele G, Smallwood PM, Levine MA. Patten JL, et al. Among authors: levine ma. N Engl J Med. 1990 May 17;322(20):1412-9. doi: 10.1056/NEJM199005173222002. N Engl J Med. 1990. PMID: 2109828 Free article.

3

Hypercalcemia.

Jan de Beur SM, Levine MA. Jan de Beur SM, et al. Among authors: levine ma. Curr Ther Endocrinol Metab. 1997;6:551-6. Curr Ther Endocrinol Metab. 1997. PMID: 9174805 Review. No abstract available.

4

Pseudohypoparathyroidism 1b: exclusion of parathyroid hormone and its receptors as candidate disease genes.

Jan de Beur SM, Ding CL, LaBuda MC, Usdin TB, Levine MA. Jan de Beur SM, et al. Among authors: levine ma. J Clin Endocrinol Metab. 2000 Jun;85(6):2239-46. doi: 10.1210/jcem.85.6.6620. J Clin Endocrinol Metab. 2000. PMID: 10852457

5

Deficiency of the alpha-subunit of the stimulatory G protein and severe extraskeletal ossification.

Eddy MC, Jan De Beur SM, Yandow SM, McAlister WH, Shore EM, Kaplan FS, Whyte MP, Levine MA. Eddy MC, et al. Among authors: levine ma. J Bone Miner Res. 2000 Nov;15(11):2074-83. doi: 10.1359/jbmr.2000.15.11.2074. J Bone Miner Res. 2000. PMID: 11092390 Free article.

6

Molecular pathogenesis of hypophosphatemic rickets.

Jan de Beur SM, Levine MA. Jan de Beur SM, et al. Among authors: levine ma. J Clin Endocrinol Metab. 2002 Jun;87(6):2467-73. doi: 10.1210/jcem.87.6.8688. J Clin Endocrinol Metab. 2002. PMID: 12050201 Review. No abstract available.

7

The pseudohypoparathyroidism type lb locus is linked to a region including GNAS1 at 20q13.3.

Jan De Beur SM, O'Connell JR, Peila R, Cho J, Deng Z, Kam S, Levine MA. Jan De Beur SM, et al. Among authors: levine ma. J Bone Miner Res. 2003 Mar;18(3):424-33. doi: 10.1359/jbmr.2003.18.3.424. J Bone Miner Res. 2003. PMID: 12619926 Free article.

8

Discordance between genetic and epigenetic defects in pseudohypoparathyroidism type 1b revealed by inconsistent loss of maternal imprinting at GNAS1.

Jan de Beur S, Ding C, Germain-Lee E, Cho J, Maret A, Levine MA. Jan de Beur S, et al. Among authors: levine ma. Am J Hum Genet. 2003 Aug;73(2):314-22. doi: 10.1086/377136. Epub 2003 Jul 11. Am J Hum Genet. 2003. PMID: 12858292 Free PMC article.

9

Growth hormone deficiency in pseudohypoparathyroidism type 1a: another manifestation of multihormone resistance.

Germain-Lee EL, Groman J, Crane JL, Jan de Beur SM, Levine MA. Germain-Lee EL, et al. Among authors: levine ma. J Clin Endocrinol Metab. 2003 Sep;88(9):4059-69. doi: 10.1210/jc.2003-030028. J Clin Endocrinol Metab. 2003. PMID: 12970262

10

Genetic basis for resistance to parathyroid hormone.

Levine MA, Germain-Lee E, Jan de Beur S. Levine MA, et al. Horm Res. 2003;60 Suppl 3:87-95. doi: 10.1159/000074508. Horm Res. 2003. PMID: 14671404 Review.

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 Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

542 results

Search Page

Filters