Creatine biosynthesis and transport in health and disease.

Autor: Joncquel-Chevalier Curt M; Biochemistry and Molecular Biology, Hormonology-Metabolism-Nutrition & Oncology (HMNO), Center of Biology & Pathology (CBP) Pierre-Marie Degand, CHRU Lille, 59037 Lille, France; RADEME Research Team for Rare Metabolic and Developmental Diseases, EA 7364, Université Lille 2, Lille, France., Voicu PM; Clinical Chemistry Laboratory, Dr Schaffner Hospital of Lens, 62307 Lens, France., Fontaine M; Biochemistry and Molecular Biology, Hormonology-Metabolism-Nutrition & Oncology (HMNO), Center of Biology & Pathology (CBP) Pierre-Marie Degand, CHRU Lille, 59037 Lille, France; RADEME Research Team for Rare Metabolic and Developmental Diseases, EA 7364, Université Lille 2, Lille, France., Dessein AF; Biochemistry and Molecular Biology, Hormonology-Metabolism-Nutrition & Oncology (HMNO), Center of Biology & Pathology (CBP) Pierre-Marie Degand, CHRU Lille, 59037 Lille, France., Porchet N; Biochemistry and Molecular Biology, Hormonology-Metabolism-Nutrition & Oncology (HMNO), Center of Biology & Pathology (CBP) Pierre-Marie Degand, CHRU Lille, 59037 Lille, France; Inserm, Lille, France., Mention-Mulliez K; RADEME Research Team for Rare Metabolic and Developmental Diseases, EA 7364, Université Lille 2, Lille, France; Medical Reference Center for Inherited Metabolic Diseases, Jeanne de Flandres Hospital, CHRU Lille, 59037 Lille, France., Dobbelaere D; RADEME Research Team for Rare Metabolic and Developmental Diseases, EA 7364, Université Lille 2, Lille, France; Medical Reference Center for Inherited Metabolic Diseases, Jeanne de Flandres Hospital, CHRU Lille, 59037 Lille, France., Soto-Ares G; Department of Neuroradiology, Roger Salengro Hospital, CHRU Lille, 59037 Lille, France., Cheillan D; Hospices Civils de Lyon, Service Maladies Héréditaires du Métabolisme et Dépistage Néonatal, Groupement Hospitalier Est, 69677 Bron, France; Lyon University, INSERM U1060, CarMeN Laboratory, University Lyon-1, INSA-Lyon, F-69600 Oullins, France., Vamecq J; Biochemistry and Molecular Biology, Hormonology-Metabolism-Nutrition & Oncology (HMNO), Center of Biology & Pathology (CBP) Pierre-Marie Degand, CHRU Lille, 59037 Lille, France; RADEME Research Team for Rare Metabolic and Developmental Diseases, EA 7364, Université Lille 2, Lille, France; Inserm, Lille, France. Electronic address: joseph.vamecq@inserm.fr.

Publikováno v: Biochimie [Biochimie] 2015 Dec; Vol. 119, pp. 146-65. Date of Electronic Publication: 2015 Nov 02.

Prevalence of HFE (hemochromatosis) gene mutations C282Y and H63D in a Romanian population.

Autor: Voicu PM, Cojocariu C, Petrescu-Danila E, Covic M, Stanciu C, Rusu M

Publikováno v: Blood cells, molecules & diseases [Blood Cells Mol Dis] 2009 Jan-Feb; Vol. 42 (1), pp. 14-5. Date of Electronic Publication: 2008 Oct 07.

Method for protein tagging in Schizosaccharomyces pombe.

Autor: Petrescu-Dănilă E; Gr. T. Popa University of Medicine and Pharmacy Iaşi, School of Medicine, Biochemesttry Department., Voicu PM, Poiţelea M, Stoica B, Stănescu R, Rusu M

Publikováno v: Revista medico-chirurgicala a Societatii de Medici si Naturalisti din Iasi [Rev Med Chir Soc Med Nat Iasi] 2006 Apr-Jun; Vol. 110 (2), pp. 403-8.

[Method for the molecular diagnosis of lipoprotein lipase genetic deficiency].

Autor: Ionescu CR; Disciplina de Biologie Celulară si Moleculară, Facultatea de Medicina, Universitatea de Medicină si Farmacie 'Gr. T. Popa', Iaşi., Petrescu-Dănilă E, Voicu PM, Durbală I, Botnariu G, Graur M, Petrovanu R, Dimofte I

Publikováno v: Revista medico-chirurgicala a Societatii de Medici si Naturalisti din Iasi [Rev Med Chir Soc Med Nat Iasi] 2005 Oct-Dec; Vol. 109 (4), pp. 848-53.