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Lancet Infectious Diseases, The, ISSN 1473-3099, 2017, Volume 17, Issue 5, pp. 510 - 519
Summary Background Listeriosis is a severe foodborne infection and a notifiable disease in France. We did a nationwide prospective study to characterise its... 
Infectious Disease | MORTALITY | MENINGITIS | INFECTIOUS DISEASES | MONOCYTOGENES | RISK-FACTORS | MANAGEMENT | GUIDELINES | SURVEILLANCE | PREGNANCY | Foodborne Diseases - microbiology | Infant, Newborn, Diseases - epidemiology | Prognosis | Prospective Studies | Humans | Listeriosis - diagnosis | Bacteremia - mortality | Male | Infant, Newborn, Diseases - microbiology | Listeriosis - epidemiology | Mandatory Reporting | Listeria monocytogenes - classification | Adult | Female | Pregnancy Complications, Infectious - microbiology | Infant, Newborn | Meningoencephalitis - epidemiology | France - epidemiology | Meningoencephalitis - mortality | Pregnancy Complications, Infectious - epidemiology | Risk Factors | Listeria monocytogenes - isolation & purification | Hospitalization | Infectious Disease Transmission, Vertical | Pregnancy | Meningoencephalitis - microbiology | Bacteremia - epidemiology | Listeriosis - microbiology | Aged | Population Surveillance | Listeriosis | Neonates | Food-borne diseases | Disease | Brain stem | Clinical trials | Infections | Genomes | Gestation | Epidemiology | Risk factors | Windows (intervals) | Listeria | Meningitis | Public health | Food | Dexamethasone | Bacterial infections | Mortality | Fetuses | Regression analysis | Clustering | Patients | Bacteremia | Meningoencephalitis | Studies | Surveillance | Medical prognosis | Health risk assessment | Cancer | Life Sciences
Journal Article
Human Molecular Genetics, ISSN 0964-6906, 2014, Volume 23, Issue 9, pp. 2279 - 2289
Journal Article
1979, Bibliothèque des lettres québécoises, ISBN 2760604217, xxxv, 348 p., [2] leaves of plates
Book
Journal Article
by Oosterloo, Mayke and Bijlsma, Emilia K and van Kuijk, Sander MJ and Minkels, Floor and de Die-Smulders, Christine EM and Bachoud-Lévi, Anne-Catherine and Bentivoglio, Anna-Rita and Bentivoglio, Anna Rita and Biunno, Ida and Bonelli, Raphael M and Bronzova, Juliana and Burgunder, Jean-Marc and Dunnett, Stephen and Dunnett, Stephen B and Ferreira, Joaquim J and Frich, Jan C and Frich, Jan and Giuliano, Joe and Handley, Olivia J and Heiberg, Arvid and Illarioshkin, Sergey and Illmann, Torsten and Klempir, Jiri and Landwehrmeyer, Bernhard and Landwehrmeyer, G. Bernhard and Levey, Jamie and McLean, Tim and Nielsen, Jørgen and Nielsen, Jørgen E and Koivisto, Susana Pro and Päivärinta, Markku and Pålhagen, Sven and Quarrell, Oliver and Ramos-Arroyo, Maria and Ramos-Arroyo, Maria Antonia and Roos, Raymund A.C and Roos, Raymund AC and Roos, Peter and Saft, Carsten and Sebastián, Ana Rojo and Tabrizi, Sarah and Tabrizi, Sarah J and Vandenberghe, Wim and Verellen-Dumoulin, Christine and Uhrova, Tereza and Wahlström+, Jan and Zaremba, Jacek and (formerly Rödig, Verena Baake and Barth, Katrin and Garde, Monica Bascuñana and Becanovic, Kristina and Bernard, Tomáš and Betz, Sabrina and Bos, Reineke and Come, Adrien and Guedes, Leonor Correia and Callaghan, Jenny and Capodarca, Selene and Charpentier, Sébastien and Vieira da Silva, Wildson and Di Renzo, Martina and Ecker, Daniel and Finisterra, Ana Maria and Fullam, Ruth and Genoves, Camille and Gilling, Mette and Horta, Andrea and Hvalstedt, Carina and Held, Christine and Hussain, Hasina and Koppers, Kerstin and Lamanna, Claudia and Laurà, Matilde and Descals, Asunción Martínez and Martinez-Horta, Saul and Mestre, Tiago and Minster, Sara and Monza, Daniela and Münkel, Kristina and Mütze, Lisanne and Oehmen, Martin and Padieu, Helene and Paterski, Laurent and Peppa, Nadia and Rindal, Beate and Rogers, Dawn and Røren (formerly Heinonen), Niini and Salgueiro, Ana and Šašinková, Pavla and Seliverstov, Yury and Taylor, Catherine and Taylor, Cat and Taylor, Rachel and Taylor, Anne-Marie and Timewell, Erika and Townhill, Jenny and Cubillo, Patricia Trigo and van Walsem, Marleen R and van Walsem, Marleen and Witjes-Ané, Marie-Noelle and ... and EHDN's associate site in Singapore and REGISTRY Investigators of the European Huntington's Disease Network and Registry Steering committee and Language coordinators
Parkinsonism and Related Disorders, ISSN 1353-8020, 04/2019, Volume 61, pp. 101 - 105
The frequency of late-onset Huntington's disease (>59 years) is assumed to be low and the clinical course milder. However, previous literature on late-onset... 
Age of onset | Huntington's disease | Late-onset Huntington's disease | CLINICAL NEUROLOGY | AGE | FEATURES | Genetic research
Journal Article