Sedel F - Search Results

1

A French experience of type 3 Gaucher disease: Phenotypic diversity and neurological outcome of 10 patients.

Kraoua I, Sedel F, Caillaud C, Froissart R, Stirnemann J, Chaurand G, Flodrops H, Tari S, Gourfinkel-An I, Mathieu S, Belmatoug N, Billette de Villemeur T, Mignot C. Kraoua I, et al. Among authors: sedel f. Brain Dev. 2011 Feb;33(2):131-9. doi: 10.1016/j.braindev.2010.02.005. Epub 2010 Mar 21. Brain Dev. 2011. PMID: 20307947

2

Parkinsonism in Gaucher's disease type 1: ten new cases and a review of the literature.

Kraoua I, Stirnemann J, Ribeiro MJ, Rouaud T, Verin M, Annic A, Rose C, Defebvre L, Réménieras L, Schüpbach M, Belmatoug N, Vidailhet M, Sedel F. Kraoua I, et al. Among authors: sedel f. Mov Disord. 2009 Jul 30;24(10):1524-30. doi: 10.1002/mds.22593. Mov Disord. 2009. PMID: 19513999 Review.

3

The French Gaucher's disease registry: clinical characteristics, complications and treatment of 562 patients.

Stirnemann J, Vigan M, Hamroun D, Heraoui D, Rossi-Semerano L, Berger MG, Rose C, Camou F, de Roux-Serratrice C, Grosbois B, Kaminsky P, Robert A, Caillaud C, Froissart R, Levade T, Masseau A, Mignot C, Sedel F, Dobbelaere D, Vanier MT, Valayanopoulos V, Fain O, Fantin B, de Villemeur TB, Mentré F, Belmatoug N. Stirnemann J, et al. Among authors: sedel f. Orphanet J Rare Dis. 2012 Oct 9;7:77. doi: 10.1186/1750-1172-7-77. Orphanet J Rare Dis. 2012. PMID: 23046562 Free PMC article.

4

[Neurological manifestations of type 1 Gaucher's disease: Is a revision of disease classification needed?].

Chérin P, Sedel F, Mignot C, Schupbach M, Gourfinkel-An I, Verny M, Baumann N. Chérin P, et al. Among authors: sedel f. Rev Neurol (Paris). 2006 Nov;162(11):1076-83. doi: 10.1016/s0035-3787(06)75120-7. Rev Neurol (Paris). 2006. PMID: 17086144 French.

5

Krabbe disease in adults: phenotypic and genotypic update from a series of 11 cases and a review.

Debs R, Froissart R, Aubourg P, Papeix C, Douillard C, Degos B, Fontaine B, Audoin B, Lacour A, Said G, Vanier MT, Sedel F. Debs R, et al. Among authors: sedel f. J Inherit Metab Dis. 2013 Sep;36(5):859-68. doi: 10.1007/s10545-012-9560-4. Epub 2012 Nov 30. J Inherit Metab Dis. 2013. PMID: 23197103

6

Epilepsy and inborn errors of metabolism in adults: a diagnostic approach.

Sedel F, Gourfinkel-An I, Lyon-Caen O, Baulac M, Saudubray JM, Navarro V. Sedel F, et al. J Inherit Metab Dis. 2007 Nov;30(6):846-54. doi: 10.1007/s10545-007-0723-7. Epub 2007 Oct 22. J Inherit Metab Dis. 2007. PMID: 17957491 Review.

7

24 month-treatment with miglustat of three patients with Niemann-Pick disease type C: follow up using brain spectroscopy.

Galanaud D, Tourbah A, Lehéricy S, Leveque N, Heron B, Billette de Villemeur T, Guffon N, Feillet F, Baumann N, Vanier MT, Sedel F. Galanaud D, et al. Among authors: sedel f. Mol Genet Metab. 2009 Feb;96(2):55-8. doi: 10.1016/j.ymgme.2008.10.002. Epub 2008 Nov 13. Mol Genet Metab. 2009. PMID: 19013089

8

Aseptic meningitis and ischaemic stroke in Fabry disease.

Lidove O, Chauveheid MP, Caillaud C, Froissart R, Benoist L, Alamowitch S, Doan S, Szalat R, Baumann N, Alexandra JF, Lavallée P, Klein I, Vuillemet F, Sedel F, Sacré K, Samson Y, Roullet E, Papo T. Lidove O, et al. Among authors: sedel f. Int J Clin Pract. 2009 Nov;63(11):1663-7. doi: 10.1111/j.1742-1241.2009.02115.x. Int J Clin Pract. 2009. PMID: 19832823

9

Cirrhosis and liver failure: expanding phenotype of Acid sphingomyelinase-deficient niemann-pick disease in adulthood.

Lidove O, Sedel F, Charlotte F, Froissart R, Vanier MT. Lidove O, et al. Among authors: sedel f. JIMD Rep. 2015;15:117-21. doi: 10.1007/8904_2014_306. Epub 2014 Apr 10. JIMD Rep. 2015. PMID: 24718843 Free PMC article.

10

Acute but transient neurological deterioration revealing adult polyglucosan body disease.

Billot S, Hervé D, Akman HO, Froissart R, Baussan C, Claeys KG, Piraud M, Sedel F, Mochel F, Laforêt P. Billot S, et al. Among authors: sedel f. J Neurol Sci. 2013 Jan 15;324(1-2):179-82. doi: 10.1016/j.jns.2012.10.015. Epub 2012 Nov 10. J Neurol Sci. 2013. PMID: 23146612

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