Exome sequencing reveals a novel Moroccan founder mutation in SLC19A3 as a new cause of early-childhood fatal Leigh syndrome von GERARDS, Mike, KAMPS, Rick, RATBI, Ilham, COPPIETERS, Wouter, KARIM, Latifa, DE COO, René, VAN DEN BOSCH, Bianca, SMELTS, Hubert, VAN OEVELEN, Jo, BOESTEN, Iris, JONGEN, Eveline, DE KONING, Bart, SCHOLTE, Hans R, DE ANGST, Isabel, SCHOONDERWOERD, Kees, SEFIANI, Abdelaziz

Volltext

Impact of Two Functional Progesterone Receptor Polymorphisms (PRP): +331G/A and PROGINS on the Cancer Risks in Familial Breast/Ovarian Cancer von Romano, Andrea, Baars, Marleen, Martens, Herman, Brandao, Rita, Detisch, Yvonne, Jongen, Eveline, Blok, Marinus J., Lindsey, Patrick, Fischer, Dagmar-C., Gomez Garcia, Encarna B.

Volltext

Drug adherence and multidisciplinary care in patients with multiple sclerosis: protocol of a prospective, web-based, patient-centred, nation-wide, Dutch cohort study in glatiramer... von Jongen, Peter J, Hengstman, Gerald, Hupperts, Raymond, Schrijver, Hans, Gilhuis, Job, Vliegen, Joseph H, Hoogervorst, Erwin, van Huizen, Marc, van Munster, Eric, Samijn, Johnny, de Schryver, Els, Siepman, Theodora, Tonk, Martijn, Zandbergen, Eveline, ten Holter, Jacques, van der Kruijk, Ruud, Borm, George

Volltext