Causal relation between alpha-synuclein gene duplication and familial Parkinson's disease
Ibáñez, P, Bonnet, A-M, Débarges, B, Lohmann, E, Tison, F, Pollak, P, Agid, Y, Dürr, A, Brice, A
Published in The Lancet (British edition) (25.09.2004)
Published in The Lancet (British edition) (25.09.2004)
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Journal Article
Grading of a positive sputum smear and the risk of Mycobacterium tuberculosis transmission
Lohmann, E. M., Koster, B. F. P. J., le Cessie, S., Kamst-van Agterveld, M. P., van Soolingen, D., Arend, S. M.
Published in The international journal of tuberculosis and lung disease (01.11.2012)
Published in The international journal of tuberculosis and lung disease (01.11.2012)
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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
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
Published in Human molecular genetics (01.02.2011)
Published in Human molecular genetics (01.02.2011)
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Journal Article
A multidisciplinary study of patients with early-onset PD with and without parkin mutations
Lohmann, E, Thobois, S, Lesage, S, Broussolle, E, du Montcel, S Tezenas, Ribeiro, M-J, Remy, P, Pelissolo, A, Dubois, B, Mallet, L, Pollak, P, Agid, Y, Brice, A
Published in Neurology (13.01.2009)
Published in Neurology (13.01.2009)
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Parkinson's disease-related LRRK2 G2019S mutation results from independent mutational events in humans
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
Published in Human molecular genetics (15.05.2010)
Published in Human molecular genetics (15.05.2010)
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Journal Article
Genetic bases and phenotypes of autosomal recessive Parkinson disease in a Turkish population
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.
Published in European journal of neurology (01.05.2012)
Published in European journal of neurology (01.05.2012)
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Journal Article
Molecular analyses of the LRRK2 gene in European and North African autosomal dominant Parkinson’s disease
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
Published in Journal of medical genetics (01.07.2009)
Published in Journal of medical genetics (01.07.2009)
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Journal Article
Sexual health in long-term breast cancer survivors
Soldera, Sara V., Ennis, Marguerite, Lohmann, Ana E., Goodwin, Pamela J.
Published in Breast cancer research and treatment (01.11.2018)
Published in Breast cancer research and treatment (01.11.2018)
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Journal Article
Low disease risk in relatives of north african lrrk2 Parkinson disease patients
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
Published in Neurology (21.09.2010)
Published in Neurology (21.09.2010)
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Journal Article
LRRK2 mutations are uncommon in Turkey
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.
Published in European journal of neurology (01.10.2011)
Published in European journal of neurology (01.10.2011)
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Journal Article
Rare heterozygous parkin variants in French early-onset Parkinson disease patients and controls
Lesage, S, Lohmann, E, Tison, F, Durif, F, Dürr, A, Brice, A
Published in Journal of medical genetics (01.01.2008)
Published in Journal of medical genetics (01.01.2008)
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Journal Article
Screening for DJ-1 mutations in early onset autosomal recessive parkinsonism
Ibáñez, P, De Michele, G, Bonifati, V, Lohmann, E, Thobois, S, Pollak, P, Agid, Y, Heutink, P, Dürr, A, Brice, A
Published in Neurology (25.11.2003)
Published in Neurology (25.11.2003)
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Journal Article
New parkin mutations and atypical phenotypes in families with autosomal recessive parkinsonism
Rawal, N, Periquet, M, Lohmann, E, Lücking, C B, Teive, H A, Ambrosio, G, Raskin, S, Lincoln, S, Hattori, N, Guimaraes, J, Horstink, M W I M, Dos Santos Bele, W, Brousolle, E, Destée, A, Mizuno, Y, Farrer, M, Deleuze, J-F, De Michele, G, Agid, Y, Dürr, A, Brice, A
Published in Neurology (22.04.2003)
Published in Neurology (22.04.2003)
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Journal Article
Absence of NR4A2 exon 1 mutations in 108 families with autosomal dominant Parkinson disease
Ibáñez, P, Lohmann, E, Pollak, P, Durif, F, Tranchant, C, Agid, Y, Dürr, A, Brice, A
Published in Neurology (08.06.2004)
Published in Neurology (08.06.2004)
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Journal Article
TREM2 mutations implicated in neurodegeneration impair cell surface transport and phagocytosis
Kleinberger, Gernot, Yamanishi, Yoshinori, Suárez-Calvet, Marc, Czirr, Eva, Lohmann, Ebba, Cuyvers, Elise, Struyfs, Hanne, Pettkus, Nadine, Wenninger-Weinzierl, Andrea, Mazaheri, Fargol, Tahirovic, Sabina, Lleó, Alberto, Alcolea, Daniel, Fortea, Juan, Willem, Michael, Lammich, Sven, Molinuevo, José L, Sánchez-Valle, Raquel, Antonell, Anna, Ramirez, Alfredo, Heneka, Michael T, Sleegers, Kristel, van der Zee, Julie, Martin, Jean-Jacques, Engelborghs, Sebastiaan, Demirtas-Tatlidede, Asli, Zetterberg, Henrik, Van Broeckhoven, Christine, Gurvit, Hakan, Wyss-Coray, Tony, Hardy, John, Colonna, Marco, Haass, Christian
Published in Science translational medicine (02.07.2014)
Published in Science translational medicine (02.07.2014)
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Journal Article
Large-scale screening of the Gaucher's disease-related glucocerebrosidase gene in Europeans with Parkinson's disease
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
Published in Human molecular genetics (2011)
Published in Human molecular genetics (2011)
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