Jan de Beur SM - Search Results

1

Localisation of mesenchymal tumours by somatostatin receptor imaging.

Jan de Beur SM, Streeten EA, Civelek AC, McCarthy EF, Uribe L, Marx SJ, Onobrakpeya O, Raisz LG, Watts NB, Sharon M, Levine MA. Jan de Beur SM, et al. Lancet. 2002 Mar 2;359(9308):761-3. doi: 10.1016/s0140-6736(02)07846-7. Lancet. 2002. PMID: 11888589

2

Global guidance for the recognition, diagnosis, and management of tumor-induced osteomalacia.

Jan de Beur SM, Minisola S, Xia WB, Abrahamsen B, Body JJ, Brandi ML, Clifton-Bligh R, Collins M, Florenzano P, Houillier P, Imanishi Y, Imel EA, Khan AA, Zillikens MC, Fukumoto S. Jan de Beur SM, et al. J Intern Med. 2023 Mar;293(3):309-328. doi: 10.1111/joim.13593. Epub 2022 Dec 13. J Intern Med. 2023. PMID: 36511653 Free PMC article. Review.

3

Hypercalcemia.

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

4

Molecular pathogenesis of hypophosphatemic rickets.

Jan de Beur SM, Levine MA. Jan de Beur SM, et al. 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.

5

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.

6

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. J Clin Endocrinol Metab. 2000 Jun;85(6):2239-46. doi: 10.1210/jcem.85.6.6620. J Clin Endocrinol Metab. 2000. PMID: 10852457

7

FGF-23 inhibits renal tubular phosphate transport and is a PHEX substrate.

Bowe AE, Finnegan R, Jan de Beur SM, Cho J, Levine MA, Kumar R, Schiavi SC. Bowe AE, et al. Among authors: jan de beur sm. Biochem Biophys Res Commun. 2001 Jun 22;284(4):977-81. doi: 10.1006/bbrc.2001.5084. Biochem Biophys Res Commun. 2001. PMID: 11409890

8

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. N Engl J Med. 2002 Jan 10;346(2):99-106. doi: 10.1056/NEJMoa011262. N Engl J Med. 2002. PMID: 11784876 Free article.

9

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. 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.

10

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. 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.

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

49 results

Search Page

Filters