Causal relation between alpha-synuclein gene duplication and familial Parkinson's disease von Ibáñez, P, Bonnet, A-M, Débarges, B, Lohmann, E, Tison, F, Pollak, P, Agid, Y, Dürr, A, Brice, A

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Grading of a positive sputum smear and the risk of Mycobacterium tuberculosis transmission von Lohmann, E. M., Koster, B. F. P. J., le Cessie, S., Kamst-van Agterveld, M. P., van Soolingen, D., Arend, S. M.

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Diabetes, metformin and breast cancer: a tangled web von Lohmann, A.E., Goodwin, P.J.

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Genome-wide association study confirms BST1 and suggests a locus on 12q24 as the risk loci for Parkinson's disease in the European population von SAAD, Mohamad, LESAGE, Suzanne, POLLAK, Pierre, DAMIER, Philippe, TISON, François, SILBURN, Peter A, TZOURIO, Christophe, FORIANI, Sylvie, LORIOT, Marie-Anne, GIROUD, Maurice, HELMER, Catherine, PORTET, Florence, SAINT-PIERRE, Aude, AMOUYEL, Philippe, LATHROP, Mark, ELBAZ, Alexis, DURR, Alexandra, MARTINEZ, Maria, BRICE, Alexis, CORVOL, Jean-Christophe, ZELENIKA, Diana, LAMBERT, Jean-Charles, VIDAILHET, Marie, MELLICK, George D, LOHMANN, Ebba, DURIF, Franck

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Sexual health in long-term breast cancer survivors von Soldera, Sara V., Ennis, Marguerite, Lohmann, Ana E., Goodwin, Pamela J.

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A multidisciplinary study of patients with early-onset PD with and without parkin mutations von LOHMANN, E, THOBOIS, S, POLLAK, P, AGID, Y, BRICE, A, LESAGE, S, BROUSSOLLE, E, TEZENAS DU MONTCEL, S, RIBEIRO, M.-J, REMY, P, PELISSOLO, A, DUBOIS, B, MALLET, L

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Parkinson's disease-related LRRK2 G2019S mutation results from independent mutational events in humans von Lesage, Suzanne, Patin, Etienne, Condroyer, Christel, Leutenegger, Anne-Louise, Lohmann, Ebba, Giladi, Nir, Bar-Shira, Anat, Belarbi, Soraya, Hecham, Nassima, Pollak, Pierre, Ouvrard-Hernandez, Anne-Marie, Bardien, Soraya, Carr, Jonathan, Benhassine, Traki, Tomiyama, Hiroyuki, Pirkevi, Caroline, Hamadouche, Tarik, Cazeneuve, Cécile, Basak, A. Nazli, Hattori, Nobutaka, Dürr, Alexandra, Tazir, Meriem, Orr-Urtreger, Avi, Quintana-Murci, Lluis, Brice, Alexis

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Prognostic associations of plasma hepcidin in women with early breast cancer von Jerzak, Katarzyna J., Lohmann, Ana E., Ennis, Marguerite, Nemeth, Elizabeta, Ganz, Tomas, Goodwin, Pamela J.

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A unifying model for matrix-based pairing situations von Tejada, O., Borm, P., Lohmann, E.

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Molecular analyses of the LRRK2 gene in European and North African autosomal dominant Parkinson’s disease von Lesage, S, Condroyer, C, Lannuzel, A, Lohmann, E, Troiano, A, Tison, F, Damier, P, Thobois, S, Ouvrard-Hernandez, A-M, Rivaud-Péchoux, S, Brefel-Courbon, C, Destée, A, Tranchant, C, Romana, M, Leclere, L, Dürr, A, Brice, A

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Genetic bases and phenotypes of autosomal recessive Parkinson disease in a Turkish population von Lohmann, E., Dursun, B., Lesage, S., Hanagasi, H. A., Sevinc, G., Honore, A., Bilgic, B., Gürvit, H., Dogu, O., Kaleagası, H., Babacan, G., Yazici, J., Erginel-Unaltuna, N., Brice, A., Emre, M.

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G51D α-synuclein mutation causes a novel Parkinsonian-pyramidal syndrome von Lesage, Suzanne, Anheim, Mathieu, Letournel, Franck, Bousset, Luc, Honoré, Aurélie, Rozas, Nelly, Pieri, Laura, Madiona, Karine, Dürr, Alexandra, Melki, Ronald, Verny, Christophe, Brice, Alexis

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Low disease risk in relatives of north african lrrk2 Parkinson disease patients von Troiano, A R, Elbaz, A, Lohmann, E, Belarbi, S, Vidailhet, M, Bonnet, A-M, Lesage, S, Pollak, P, Cazeneuve, C, Borg, M, Feingold, J, Dürr, A, Tazir, M, Brice, A

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Large-scale screening of the Gaucher's disease-related glucocerebrosidase gene in Europeans with Parkinson's disease von LESAGE, Suzanne, ANHEIM, Mathieu, RIVAUD, Sophie, VIDAILHET, Marie, DÜRR, Alexandra, BRICE, Alexis, CONDROYER, Christel, POLLAK, Pierre, DURIF, Franck, DUPUITS, Céline, VIALLET, François, LOHMANN, Ebba, CORVOL, Jean-Christophe, HONORE, Aurélie

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LRRK2 mutations are uncommon in Turkey von Hanagasi, H. A., Lohmann, E., Dursun, B., Honoré, A., Lesage, S., Dogu, O., Kaleagasi, H., Aydın, O., Gürvit, H., Erginel-Unaltuna, N., Brice, A., Emre, M.

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Minimal exact balancedness von Lohmann, E., Borm, P., Herings, P.J.J.

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Rare heterozygous parkin variants in French early-onset Parkinson disease patients and controls von Lesage, S, Lohmann, E, Tison, F, Durif, F, Dürr, A, Brice, A

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LRRK2 G2019S as a Cause of Parkinson's Disease in North African Arabs von Tazir, Meriem, Pollak, Pierre, Lesage, Suzanne, Lohmann, Ebba, Brice, Alexis, Dürr, Alexandra, Leutenegger, Anne-Louise, Janin, Sabine

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Association of LRRK2 exonic variants with susceptibility to Parkinson's disease: a case–control study von Ross, Owen A, Dr, Soto-Ortolaza, Alexandra I, BSc, Heckman, Michael G, MS, Aasly, Jan O, Prof, Abahuni, Nadine, MD, Annesi, Grazia, Prof, Bacon, Justin A, BSc, Bardien, Soraya, PhD, Bozi, Maria, MD, Brice, Alexis, Prof, Brighina, Laura, MD, Van Broeckhoven, Christine, Prof, Carr, Jonathan, Prof, Chartier-Harlin, Marie-Christine, Prof, Dardiotis, Efthimios, MD, Dickson, Dennis W, Prof, Diehl, Nancy N, BS, Elbaz, Alexis, Prof, Ferrarese, Carlo, Prof, Ferraris, Alessandro, MD, Fiske, Brian, PhD, Gibson, J Mark, Prof, Gibson, Rachel, PhD, Hadjigeorgiou, Georgios M, MD, Hattori, Nobutaka, Prof, Ioannidis, John PA, Prof, Jasinska-Myga, Barbara, MD, Jeon, Beom S, Prof, Kim, Yun Joong, Prof, Klein, Christine, Prof, Kruger, Rejko, MD, Kyratzi, Elli, MD, Lesage, Suzanne, PhD, Lin, Chin-Hsien, MD, Lynch, Timothy, Prof, Maraganore, Demetrius M, Prof, Mellick, George D, PhD, Mutez, Eugénie, MD, Nilsson, Christer, Prof, Opala, Grzegorz, Prof, Park, Sung Sup, Prof, Puschmann, Andreas, MD, Quattrone, Aldo, Prof, Sharma, Manu, PhD, Silburn, Peter A, Prof, Sohn, Young Ho, Prof, Stefanis, Leonidas, MD, Tadic, Vera, MD, Theuns, Jessie, PhD, Tomiyama, Hiroyuki, MD, Uitti, Ryan J, Prof, Valente, Enza Maria, Prof, van de Loo, Simone, PhD, Vassilatis, Demetrios K, PhD, Vilariño-Güell, Carles, PhD, White, Linda R, Prof, Wirdefeldt, Karin, MD, Wszolek, Zbigniew K, Prof, Wu, Ruey-Meei, Prof, Farrer, Matthew J, Prof

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For All. 1906 R.6 nr12

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