1/Lesage Rare heterozygous parkin variants in French early ...
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by S Lesage · · Cited by 71 — Suzanne Lesage, Ebba Lohmann, François Tison, Franck Durif, Alexandra Dürr, Alexis. Brice, for the French Parkinson's Disease Genetics Study ... › early › jmg full.pdf
www.taylorfrancis.com › booksParkinson's Disease | Genetics and Pathogenesis | Taylor ...
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Clinical and Genetic Features of PARKIN-Related Parkinson's Disease. ByEbba Lohmann, Alexis Brice, Alexandra Durr, Merle Ruberg.
Frequency of the LRRK2 G2019S mutation in siblings with ...
pubmed.ncbi.nlm.nih.gov
by S Lesage · · Cited by 14 — Suzanne Lesage , Laurence Leclere, Ebba Lohmann, Michel Borg, Merle Ruberg, Alexandra Dürr, Alexis Brice, French Parkinson's Disease Genetics Study Group ... by NE Mencacci · · Cited by 110 — ... Robert Kleta,6 Miryam Carecchio,15,16 Giovanna Zorzi,15 Nardo Nardocci,15 Barbara Garavaglia,16Ebba Lohmann,7 Anne Weissbach,17 Christine Klein,17 John ... › ... › articles › PMC
Characterization of Recessive Parkinson Disease in a Large ...
pubmed.ncbi.nlm.nih.gov
by S Lesage · · Cited by 10 — ... Chokri Mhiri , Ebba Lohmann , Andrew Singleton , Jean-Christophe Corvol , Alexis Brice , French Parkinson Disease Genetics Study Group ... by S Lesage · · Cited by 14 — Suzanne Lesage , Laurence Leclere, Ebba Lohmann, Michel Borg, Merle Ruberg, Alexandra Dürr, Alexis Brice, French Parkinson's Disease Genetics Study Group ... › ...
Ebba Lohmann's Research | CureHunter
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Login. Send password reminder... Ebba Lohmann Selected Research. Ebba Lohmann Research Topics. Disease. 10, Parkinson Disease (Parkinson's Disease)
Table of contents for Parkinson's disease
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Table of Contents for Parkinson's disease : genetics and pathogenesis / [edited by] Ted M. Dawson, available from the Library of Congress.
All web results to the name "Ebba Lohmann"
EIF4G1 in familial Parkinson's disease: pathogenic mutations ...
europepmc.org
by S Lesage · · Cited by 41 — ... Filter current search by 'Stephan Klebe' · Klebe S ,. Ebba Lohmann. More. Find articles by 'Ebba Lohmann' · Filter current search by 'Ebba Lohmann'. › article › med
LRRK2 G2019S as a cause of Parkinson's Read by QxMD
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LRRK2 G2019S as a cause of Parkinson's disease in North African Arabs. Suzanne Lesage, Alexandra Dürr, Meriem Tazir, Ebba Lohmann, Anne-Louise Leutenegger, ... › read
Parkinson's disease-related LRRK2 G2019S mutation results ...
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by S Lesage · · Cited by 55 — Suzanne Lesage 1 Etienne Patin 2 Christel Condroyer 1 Anne-Louise Leutenegger 3Ebba Lohmann 1 Nir Giladi 4, 5 Anat Bar-Shira 6 Soraya Belarbi 7 Nassima ... › RIIP_PARIS
Clinical and Genetic Features of PARKIN-Related Parkinson's ...
www.taylorfrancis.com
by E Lohmann · — ByEbba Lohmann, Alexis Brice, Alexandra Durr, Merle Ruberg. BookParkinson's Disease. Click here to navigate to parent product. Edition 1st Edition. › chapters › edit › clinica...
hal.archives-ouvertes.fr › inserm Parkinson's disease-related LRRK2 G2019S mutation results ...
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Suzanne Lesage, Etienne Patin, Christel Condroyer, Anne-Louise Leutenegger, Ebba Lohmann, et al.. Parkinson's disease-related LRRK2 G2019S mutation ...
Archive ouverte HAL - LRRK2 G2019S as a cause of Parkinson's disease...
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Suzanne Lesage, Alexandra Dürr, Meriem Tazir, Ebba Lohmann, Anne-Louise Leutenegger, et al.. LRRK2 G2019S as a cause of Parkinson's disease in North ...
Late Breaking Science Abstracts LBS.001 Efficacy and Safety ...
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Suzanne Lesage, Pablo Ibanez, Ebba Lohmann, et al. Parkinson's Disease is Frequent and its Penetrance is Age-Dependant: LBS › content › full.pdf
Inserm - EIF4G1 in familial Parkinson's disease: pathogenic mutations...
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auteur(s) : Suzanne Lesage 1, Christel Condroyer 1, Stephan Klebe 1, 2, 3, 4, Ebba Lohmann 1, Franck Durif 5, Philippe Damier 6, François ...
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