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Citation: P. De Lonlay et al., Hyperinsulinism and hyperammonemia syndrome: Report of twelve unrelated patients, PEDIAT RES, 50(3), 2001, pp. 353-357

Authors: Aral, B

Citation: B. Aral, Dispensing with tradition? Turkish politics and international society during the Ozal decade, 1983-93, MIDDLE E ST, 37(1), 2001, pp. 72-88

Authors: Baumgartner, MR Hu, CAA Almashanu, S Steel, G Obie, C Aral, B Rabier, D Kamoun, P Saudubray, JM Valle, D

Citation: Mr. Baumgartner et al., Hyperammonemia with reduced ornithine, citrulline, arginine and proline: anew inborn error caused by a mutation in the gene encoding Delta(1)-pyrroline-5-carboxylate synthase, HUM MOL GEN, 9(19), 2000, pp. 2853-2858

Authors: Rouillac, C Aral, B Fouque, F Marchant, D Saudubray, JM Dumez, Y Lindsay, G Abitbol, M Dufier, JL Marsac, C Benelli, C

Citation: C. Rouillac et al., First prenatal diagnosis of defects in the HsPDX1 gene encoding protein X,an additional lipoyl-containing subunit of the human pyruvate dehydrogenase complex, PRENAT DIAG, 19(12), 1999, pp. 1160-1164

Authors: Chappuis, P Aral, B Ceballos-Picot, I

Citation: P. Chappuis et al., Copper related diseases, MET ION BIO, 5, 1998, pp. 729-736