Guidelines, “minimal requirements” and standard of care in glioblastoma around the Mediterranean Area: A report from the AROME (Association of Radiotherapy and Oncology of the Mediterranean arEa) Neuro-Oncology working party

Autor: Belkacemi, Y., Bolle, S., Bourdeaut, F., Collin, P., Cornu, P., Delatre, J.-Y., Dhermain, F., Doz, F., Habrand, J.-L., Hoang-Xuan, K., Idbaih, A., Mammar, H., Martin-Duverneuil, N., Mokhtari, K., Roujeau, T., Acharqui, A., Atit Benali, S., Bakhti, S., Bena, F., Bendjaafar, N., Benider, A., Bouaouina, N., Bounedjar, A., Boussen, H., Bouyoucef, K., Bouzid, K., Chougai, Z., Daoud, J., Errihani, H., Essoudaigui, F., Gachi, F., Harif, M., Hilmani, S., Hsissen, L., Idali, B., Karkouri, M., Kerboua, E., Ouahabi, A., Sahraoui, S., Sadki, O., Sami, A., Samlali, R, Terkmani, F.

Publikováno v: In Critical Reviews in Oncology / Hematology February 2016 98:189-199

Pretransplant HLA mistyping in diagnostic samples of acute myeloid leukemia patients due to acquired uniparental disomy.

Autor: Dubois, V¹, Sloan-Béna, F², Cesbron, A³, Hepkema, B G⁴, Gagne, K⁵, Gimelli, S², Heim, D⁶, Tichelli, A⁶, Delaunay, J⁷, Drouet, M⁸, Jendly, S⁹, Villard, J⁹, Tiercy, J-M⁹

Publikováno v: Leukemia (08876924). Sep2012, Vol. 26 Issue 9, p2079-2085. 7p. 1 Color Photograph, 1 Diagram, 3 Charts, 1 Graph.

The 16p11.2 locus modulates brain structures common to autism, schizophrenia and obesity

Autor: Maillard, Am, Ruef, A, Pizzagalli, F, Migliavacca, E, Hippolyte, L, Adaszewski, S, Dukart, J, Ferrari, C, Conus, P, Männik, K, Zazhytska, M, Siffredi, V, Maeder, P, Kutalik, Z, Kherif, F, Hadjikhani, N, Beckmann, Js, Reymond, A, Draganski, B, Jacquemont, S, 2 European Consortium including Addor MC, 1. 6. p. 1. 1., Andrieux, J, Arveiler, B, Baujat, G, Béna, F, Bouquillon, S, Boute, O, Brusco, Alfredo, Campion, D, David, A, Delrue, Ma, Doco Fenzy, M, Fagerberg, C, Faivre, L, Forzano, F, Giachino, Daniela Francesca, Guichet, A, Guillin, O, Héron, D, Isidor, B, Jacquette, A, Journel, H, Keren, B, Lacombe, D, Le Caignec, C, Lespinasse, J, Mandrile, Giorgia, Mathieu Dramard, M, Mignot, C, Petit, F, Plessis, G, Prieur, F, Sanlaville, D, Van Haelst, M, Van Maldergem, L.

Publikováno v: Molecular Psychiatry
MOLECULAR PSYCHIATRY
Molecular Psychiatry, vol. 20, no. 1, pp. 140-147
Molecular psychiatry, 20(1), 140-147. Nature Publishing Group
Molecular psychiatry

Anatomical structures and mechanisms linking genes to neuropsychiatric disorders are not deciphered. Reciprocal copy number variants at the 16p11.2 BP4-BP5 locus offer a unique opportunity to study the intermediate phenotypes in carriers at high risk

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::daf4d6c0c2411b2a6b84ffb5aab79eba
https://hdl.handle.net/21.11116/0000-0001-B87A-711858/00-001M-0000-0029-AC39-6

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Diagnostic Exome Sequencing to Elucidate the Genetic Basis of Likely Recessive Disorders in Consanguineous Families

Autor: Makrythanasis, P. Nelis, M. Santoni, F.A. Guipponi, M. Vannier, A. Béna, F. Gimelli, S. Stathaki, E. Temtamy, S. Mégarbané, A. Masri, A. Aglan, M.S. Zaki, M.S. Bottani, A. Fokstuen, S. Gwanmesia, L. Aliferis, K. Bustamante Eduardo, M. Stamoulis, G. Psoni, S. Kitsiou-Tzeli, S. Fryssira, H. Kanavakis, E. Al-Allawi, N. Sefiani, A. Al Hait, S. Elalaoui, S.C. Jalkh, N. Al-Gazali, L. Al-Jasmi, F. Bouhamed, H.C. Abdalla, E. Cooper, D.N. Hamamy, H. Antonarakis, S.E.

Rare, atypical, and undiagnosed autosomal-recessive disorders frequently occur in the offspring of consanguineous couples. Current routine diagnostic genetic tests fail to establish a diagnosis in many cases. We employed exome sequencing to identify

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od______2127::de6e50fbe034d3c9fa0a7dfd96ababda
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3087744