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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: heraoui d. 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.
[Gaucher disease].
Stirnemann J, de Villemeur TB, Heraoui D, Belmatoug N; Comité d'évaluation du traitement de la maladie de Gaucher. Stirnemann J, et al. Among authors: heraoui d. Rev Prat. 2011 Feb;61(2):165-8. Rev Prat. 2011. PMID: 21618759 French. No abstract available.
[Gaucher disease and pregnancy].
Belmatoug N, Heraoui D. Belmatoug N, et al. Among authors: heraoui d. Presse Med. 2009 Dec;38 Suppl 2:2S17-23. doi: 10.1016/S0755-4982(09)73663-2. Presse Med. 2009. PMID: 20304300 French. No abstract available.
The uptake of recombinant glucocerebrosidases by blood monocytes from type 1 Gaucher disease patients is variable.
Berger J, Stirnemann J, Bourgne C, Pereira B, Pigeon P, Heraoui D, Froissart R, Rapatel C, Rose C, Belmatoug N, Berger MG. Berger J, et al. Among authors: heraoui d. Br J Haematol. 2012 Apr;157(2):274-7. doi: 10.1111/j.1365-2141.2011.08989.x. Epub 2012 Jan 9. Br J Haematol. 2012. PMID: 22224474 Free article. Clinical Trial. No abstract available.