Debray FG - Search Results

1

Kaux JF, Le Goff C, Debray FG, Crielaard JM, Reginster JY. Kaux JF, et al. Among authors: debray fg. Rev Med Liege. 2009 Jan;64(1):11-5. Rev Med Liege. 2009. PMID: 19317096 Free article. French.

2

[How to explore ... congenital isolated hypogonadotrophic hypogonadism].

Valdes-Socin H, Debray FG, Parent AS, Lebrethon MC, Bourguignon JP, Bours V, Beckers A. Valdes-Socin H, et al. Among authors: debray fg. Rev Med Liege. 2010 Nov;65(11):634-41. Rev Med Liege. 2010. PMID: 21189530 Free article. Review. French.

3

[Current and new therapeutic options in inborn errors of metabolism].

Debray FG, Weekers L, Dadoumont C, Grandjean C, Deberg M, Boemer F, Bours V. Debray FG, et al. Rev Med Liege. 2020 May;75(5-6):420-425. Rev Med Liege. 2020. PMID: 32496691 Free article. French.

4

Early infantile cardiomyopathy and liver disease: a multisystemic disorder caused by congenital lipodystrophy.

Debray FG, Baguette C, Colinet S, Van Maldergem L, Verellen-Dumouin C. Debray FG, et al. Mol Genet Metab. 2013 Jun;109(2):227-9. doi: 10.1016/j.ymgme.2013.04.011. Epub 2013 Apr 23. Mol Genet Metab. 2013. PMID: 23647707

5

Temple-Baraitser syndrome: a rare and possibly unrecognized condition.

Jacquinet A, Gérard M, Gabbett MT, Rausin L, Misson JP, Menten B, Mortier G, Van Maldergem L, Verloes A, Debray FG. Jacquinet A, et al. Among authors: debray fg. Am J Med Genet A. 2010 Sep;152A(9):2322-6. doi: 10.1002/ajmg.a.33574. Am J Med Genet A. 2010. PMID: 20683999

6

Reproduction, smell, and neurodevelopmental disorders: genetic defects in different hypogonadotropic hypogonadal syndromes.

Valdes-Socin H, Rubio Almanza M, Tomé Fernández-Ladreda M, Debray FG, Bours V, Beckers A. Valdes-Socin H, et al. Among authors: debray fg. Front Endocrinol (Lausanne). 2014 Jul 9;5:109. doi: 10.3389/fendo.2014.00109. eCollection 2014. Front Endocrinol (Lausanne). 2014. PMID: 25071724 Free PMC article. Review.

7

How to recognize Cowden syndrome: A novel PTEN mutation description.

Delannoy P, Debray FG, Verloes A, Beckers A, Valdes-Socin H. Delannoy P, et al. Among authors: debray fg. Ann Endocrinol (Paris). 2017 Jul;78(3):188-190. doi: 10.1016/j.ando.2017.01.001. Epub 2017 Mar 2. Ann Endocrinol (Paris). 2017. PMID: 28262255 No abstract available.

8

A next-generation newborn screening pilot study: NGS on dried blood spots detects causal mutations in patients with inherited metabolic diseases.

Boemer F, Fasquelle C, d'Otreppe S, Josse C, Dideberg V, Segers K, Guissard V, Capraro V, Debray FG, Bours V. Boemer F, et al. Among authors: debray fg. Sci Rep. 2017 Dec 15;7(1):17641. doi: 10.1038/s41598-017-18038-x. Sci Rep. 2017. PMID: 29247206 Free PMC article.

9

Mutation of the iron-sulfur cluster assembly gene IBA57 causes fatal infantile leukodystrophy.

Debray FG, Stümpfig C, Vanlander AV, Dideberg V, Josse C, Caberg JH, Boemer F, Bours V, Stevens R, Seneca S, Smet J, Lill R, van Coster R. Debray FG, et al. J Inherit Metab Dis. 2015 Nov;38(6):1147-53. doi: 10.1007/s10545-015-9857-1. Epub 2015 May 14. J Inherit Metab Dis. 2015. PMID: 25971455

10

[Diagnosis and monitoring of phenylketonuria by LC-MS-MS in Morocco].

Meiouet F, Kabbaj SE, Debray FG, Boemer F. Meiouet F, et al. Among authors: debray fg. Ann Biol Clin (Paris). 2021 Feb 1;79(1):49-55. doi: 10.1684/abc.2021.1619. Ann Biol Clin (Paris). 2021. PMID: 33570037 Free article. French.

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

72 results

Search Page

Filters