Dobbelaere D - Search Results

1

Citrin deficiency: Does the reactivation of liver aralar-1 come into play and promote HCC development?

Mention K, Joncquel Chevalier Curt M, Dessein AF, Douillard C, Dobbelaere D, Vamecq J. Mention K, et al. Among authors: dobbelaere d. Biochimie. 2021 Nov;190:20-23. doi: 10.1016/j.biochi.2021.06.018. Epub 2021 Jul 3. Biochimie. 2021. PMID: 34228977 Review.

2

Neonatal severe intractable diarrhoea as the presenting manifestation of an unclassified congenital disorder of glycosylation (CDG-x).

Mention K, Michaud L, Dobbelaere D, Guimber D, Gottrand F, Turck D. Mention K, et al. Among authors: dobbelaere d. Arch Dis Child Fetal Neonatal Ed. 2001 Nov;85(3):F217-9. doi: 10.1136/fn.85.3.f217. Arch Dis Child Fetal Neonatal Ed. 2001. PMID: 11668168 Free PMC article. Review.

3

[Diagnostic approach and treatment of neonates and children cholestasis].

Mention K, Dobbelaere D, Gottrand F. Mention K, et al. Among authors: dobbelaere d. Arch Pediatr. 2007 Jun;14(6):569-72. doi: 10.1016/j.arcped.2007.03.021. Epub 2007 Apr 18. Arch Pediatr. 2007. PMID: 17446052 French. No abstract available.

4

Doctor, my son is so tired... about a case of hereditary fructose intolerance.

Guery MJ, Douillard C, Marcelli-Tourvieille S, Dobbelaere D, Wemeau JL, Vantyghem MC. Guery MJ, et al. Among authors: dobbelaere d. Ann Endocrinol (Paris). 2007 Dec;68(6):456-9. doi: 10.1016/j.ando.2007.09.002. Epub 2007 Nov 26. Ann Endocrinol (Paris). 2007. PMID: 18035330

5

Spectrum of movement disorders associated with glutaric aciduria type 1: a study of 16 patients.

Gitiaux C, Roze E, Kinugawa K, Flamand-Rouvière C, Boddaert N, Apartis E, Valayannopoulos V, Touati G, Motte J, Devos D, Mention K, Dobbelaere D, Rodriguez D, Roubertie A, Chabrol B, Feillet F, Vidailhet M, Bahi-Buisson N. Gitiaux C, et al. Among authors: dobbelaere d. Mov Disord. 2008 Dec 15;23(16):2392-7. doi: 10.1002/mds.22313. Mov Disord. 2008. PMID: 18823014

6

[Hypoglycemia and endocrine effects of adults' inborn errors of metabolism].

Vantyghem MC, Mention C, Dobbelaere D, Douillard C. Vantyghem MC, et al. Among authors: dobbelaere d. Ann Endocrinol (Paris). 2009 Mar;70(1):25-42. doi: 10.1016/j.ando.2008.12.007. Epub 2009 Feb 10. Ann Endocrinol (Paris). 2009. PMID: 19211097 French.

7

Deuterated palmitate-driven acylcarnitine formation by whole-blood samples for a rapid diagnostic exploration of mitochondrial fatty acid oxidation disorders.

Dessein AF, Fontaine M, Dobbelaere D, Mention-Mulliez K, Martin-Ponthieu A, Briand G, Vamecq J. Dessein AF, et al. Among authors: dobbelaere d. Clin Chim Acta. 2009 Aug;406(1-2):23-6. doi: 10.1016/j.cca.2009.04.026. Epub 2009 May 5. Clin Chim Acta. 2009. PMID: 19422814

8

A novel mutation of the ACADM gene (c.145C>G) associated with the common c.985A>G mutation on the other ACADM allele causes mild MCAD deficiency: a case report.

Dessein AF, Fontaine M, Andresen BS, Gregersen N, Brivet M, Rabier D, Napuri-Gouel S, Dobbelaere D, Mention-Mulliez K, Martin-Ponthieu A, Briand G, Millington DS, Vianey-Saban C, Wanders RJ, Vamecq J. Dessein AF, et al. Among authors: dobbelaere d. Orphanet J Rare Dis. 2010 Oct 5;5:26. doi: 10.1186/1750-1172-5-26. Orphanet J Rare Dis. 2010. PMID: 20923556 Free PMC article.

9

Rise in brain GABA to further stress the metabolic link between valproate and creatine.

Vamecq J, Joncquel-Chevalier Curt M, Mention-Mulliez K, Dobbelaere D, Briand G. Vamecq J, et al. Among authors: dobbelaere d. Mol Genet Metab. 2011 Feb;102(2):232-4. doi: 10.1016/j.ymgme.2010.10.006. Epub 2010 Oct 14. Mol Genet Metab. 2011. PMID: 21056934 No abstract available.

10

Heterogeneity of follow-up procedures in French and Belgian patients with treated hereditary tyrosinemia type 1: results of a questionnaire and proposed guidelines.

Schiff M, Broue P, Chabrol B, De Laet C, Habes D, Mention K, Sarles J, Spraul A, Valayannopoulos V, Ogier de Baulny H; French-Belgian study group for HT-1. Schiff M, et al. J Inherit Metab Dis. 2012 Sep;35(5):823-9. doi: 10.1007/s10545-011-9429-y. Epub 2011 Dec 14. J Inherit Metab Dis. 2012. PMID: 22167277

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