De Leener A - Search Results

1

AMH mutations with reduced in vitro bioactivity are related to premature ovarian insufficiency.

Alvaro Mercadal B, Imbert R, Demeestere I, Gervy C, De Leener A, Englert Y, Costagliola S, Delbaere A. Alvaro Mercadal B, et al. Among authors: de leener a. Hum Reprod. 2015 May;30(5):1196-202. doi: 10.1093/humrep/dev042. Epub 2015 Mar 6. Hum Reprod. 2015. PMID: 25750103

2

Variants of the BMP15 gene in a cohort of patients with premature ovarian failure.

Tiotiu D, Alvaro Mercadal B, Imbert R, Verbist J, Demeestere I, De Leener A, Englert Y, Vassart G, Costagliola S, Delbaere A. Tiotiu D, et al. Among authors: de leener a. Hum Reprod. 2010 Jun;25(6):1581-7. doi: 10.1093/humrep/deq073. Epub 2010 Apr 3. Hum Reprod. 2010. PMID: 20364024

3

Understanding ovarian hyperstimulation syndrome.

Delbaere A, Smits G, De Leener A, Costagliola S, Vassart G. Delbaere A, et al. Among authors: de leener a. Endocrine. 2005 Apr;26(3):285-90. doi: 10.1385/ENDO:26:3:285. Endocrine. 2005. PMID: 16034183 Review.

4

[Molecular mechanisms selected by evolution m primates for self-protection against human chorionic gonadotropin].

Costagliola S, De Leener A. Costagliola S, et al. Among authors: de leener a. Bull Mem Acad R Med Belg. 2008;163(10-12):481-4; discussion 484-5. Bull Mem Acad R Med Belg. 2008. PMID: 20120254 French.

5

Identification of the first germline mutation in the extracellular domain of the follitropin receptor responsible for spontaneous ovarian hyperstimulation syndrome.

De Leener A, Caltabiano G, Erkan S, Idil M, Vassart G, Pardo L, Costagliola S. De Leener A, et al. Hum Mutat. 2008 Jan;29(1):91-8. doi: 10.1002/humu.20604. Hum Mutat. 2008. PMID: 17721928

6

Presence and absence of follicle-stimulating hormone receptor mutations provide some insights into spontaneous ovarian hyperstimulation syndrome physiopathology.

De Leener A, Montanelli L, Van Durme J, Chae H, Smits G, Vassart G, Costagliola S. De Leener A, et al. J Clin Endocrinol Metab. 2006 Feb;91(2):555-62. doi: 10.1210/jc.2005-1580. Epub 2005 Nov 8. J Clin Endocrinol Metab. 2006. PMID: 16278261

7

Metabolic characteristics of women who developed ovarian hyperstimulation syndrome.

Delvigne A, Kostyla K, De Leener A, Lejeune B, Cantiniaux B, Bergmann P, Rozenberg S. Delvigne A, et al. Among authors: de leener a. Hum Reprod. 2002 Aug;17(8):1994-6. doi: 10.1093/humrep/17.8.1994. Hum Reprod. 2002. PMID: 12151426

8

The specificity of binding of glycoprotein hormones to their receptors.

Caltabiano G, Campillo M, De Leener A, Smits G, Vassart G, Costagliola S, Pardo L. Caltabiano G, et al. Among authors: de leener a. Cell Mol Life Sci. 2008 Aug;65(16):2484-92. doi: 10.1007/s00018-008-8002-9. Cell Mol Life Sci. 2008. PMID: 18438608 Free PMC article. Review.

9

A familial heterozygous null mutation of MET in autism spectrum disorder.

Lambert N, Wermenbol V, Pichon B, Acosta S, van den Ameele J, Perazzolo C, Messina D, Musumeci MF, Dessars B, De Leener A, Abramowicz M, Vilain C. Lambert N, et al. Among authors: de leener a. Autism Res. 2014 Oct;7(5):617-22. doi: 10.1002/aur.1396. Epub 2014 Jun 6. Autism Res. 2014. PMID: 24909855

10

A family with a novel TSH receptor activating germline mutation (p.Ala485Val).

Akcurin S, Turkkahraman D, Tysoe C, Ellard S, De Leener A, Vassart G, Costagliola S. Akcurin S, et al. Among authors: de leener a. Eur J Pediatr. 2008 Nov;167(11):1231-7. doi: 10.1007/s00431-007-0659-9. Epub 2008 Jan 4. Eur J Pediatr. 2008. PMID: 18175146

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