Zobrazeno 1 - 6 of 6 pro vyhledávání: '"Lieve, Claes"'
1
Non-fragrance allergens in specific cosmetic products
Autor: J Drieghe, An Goossens, Lieve Claes, Ana Rita Travassos, Lies Boey
Publikováno v: Contact Dermatitis. 65:276-285
Background. Together with preservative agents, fragrance components are the most important sensitizing culprits in cosmetic products. Objectives. To identify the nature of the fragrance ingredients responsible for allergic contact dermatitis (ACD) fr
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::325180742771f6bcf76c754787fadd80
https://doi.org/10.1111/j.1600-0536.2011.01968.x
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2
16p11.2 600 kb Duplications confer risk for typical and atypical Rolandic epilepsy
Autor: Eva M. Reinthaler, Dennis Lal, Sebastien Lebon, Michael S. Hildebrand, Hans-Henrik M. Dahl, Brigid M. Regan, Martha Feucht, Hannelore Steinböck, Birgit Neophytou, Gabriel M. Ronen, Laurian Roche, Ursula Gruber-Sedlmayr, Julia Geldner, Edda Haberlandt, Per Hoffmann, Stefan Herms, Christian Gieger, Melanie Waldenberger, Andre Franke, Michael Wittig, Susanne Schoch, Albert J. Becker, Andreas Hahn, Katrin Männik, Mohammad R. Toliat, Georg Winterer, Holger Lerche, Peter Nürnberg, Heather Mefford, Ingrid E. Scheffer, Samuel F. Berkovic, Jacques S. Beckmann, Thomas Sander, Sebastien Jacquemont, Alexandre Reymond, Fritz Zimprich, Bernd A. Neubauer, Bernd Neubauer, Martina Mörzinger, Arvid Suls, Sarah Weckhuysen, Lieve Claes, Liesbet Deprez, Katrien Smets, Tine Van Dyck, Tine Deconinck, Peter De Jonghe, Rikke S Møller, Laura L. Klitten, Helle Hjalgrim, Kiel Campus, Ingo Helbig, Hiltrud Muhle, Philipp Ostertag, Sarah von Spiczak, Ulrich Stephani, Holger Trucks, Christian E. Elger, Ailing A. Kleefuß-Lie, Wolfram S. Kunz, Rainer Surges, Verena Gaus, Dieter Janz, Bettina Schmitz, Felix Rosenow, Karl Martin Klein, Philipp S. Reif, Wolfgang H. Oertel, Hajo M. Hamer, Felicitas Becker, Yvonne Weber, Bobby P.C. Koeleman, Carolien de Kovel, Dick Lindhout, Agnès Ameil, Joris Andrieux, Sonia Bouquillon, Odile Boute, Jeanne de Flandre, Jean Marie Cuisset, Jean-Christophe Cuvellier, Roger Salengro, Albert David, Bert de Vries, Marie-Ange Delrue, Martine Doco-Fenzy, Bridget A. Fernandez, Delphine Heron, Boris Keren, Robert Lebel, Bruno Leheup, Suzanne Lewis, Maria Antonietta Mencarelli, Cyril Mignot, Jean-Claude Minet, Alexandre Moerman, Fanny Morice-Picard, Mafalda Mucciolo, Katrin Ounap, Laurent Pasquier, Florence Petit, Francesca Ragona, Evica Rajcan-Separovic, Alessandra Renieri, Claudine Rieubland, Damien Sanlaville, Elisabeth Sarrazin, Yiping Shen, Mieke van Haelst, Anneke Vulto-van Silfhout
Publikováno v: 16p11.2 European Consortium, EPICURE Consortium, The EuroEPINOMICS Consortium & Møller, R S 2014, ' 16p11.2 600 kb Duplications confer risk for typical and atypical Rolandic epilepsy ', Human Molecular Genetics, vol. 23, no. 22, pp. 6069-6080 . https://doi.org/10.1093/hmg/ddu306
Human Molecular Genetics, vol. 23, no. 22, pp. 6069-6080
Human molecular genetics, 23(22), 6069-6080. Oxford University Press
Human molecular genetics
Hum. Mol. Genet. 23, 6069-6080 (2014)
HUMAN MOLECULAR GENETICS
Reinthaler, Eva M; Lal, Dennis; Lebon, Sebastien; Hildebrand, Michael S; Dahl, Hans-Henrik M; Regan, Brigid M; Feucht, Martha; Steinböck, Hannelore; Neophytou, Birgit; Ronen, Gabriel M; Roche, Laurian; Gruber-Sedlmayr, Ursula; Geldner, Julia; Haberlandt, Edda; Hoffmann, Per; Herms, Stefan; Gieger, Christian; Waldenberger, Melanie; Franke, Andre; Wittig, Michael; ... (2014). 16p11.2 600 kb Duplications confer risk for typical and atypical Rolandic epilepsy. Human molecular genetics, 23(22), pp. 6069-6080. Oxford University Press 10.1093/hmg/ddu306
Rolandic epilepsy (RE) is the most common idiopathic focal childhood epilepsy. Its molecular basis is largely unknown and a complex genetic etiology is assumed in the majority of affected individuals. The present study tested whether six large recurr
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::780d31edaa034478bbfc1c48d66221a6
http://hdl.handle.net/11365/975064
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3
Fragrance allergens in 'specific' cosmetic products
Autor: Andrea Nardelli, Jacques Drieghe, Lieve Claes, Lies Boey, An Goossens
Publikováno v: Contact dermatitis. 64(4)
Together with preservative agents, fragrance components are the most important sensitizing culprits in cosmetic products.To identify the nature of the fragrance ingredients responsible for allergic contact dermatitis (ACD) from specific cosmetic prod
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ae423939ef82d1c2f31d494a5ad12c93
https://pubmed.ncbi.nlm.nih.gov/21392029
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4
[Clinical and genetic diagnosis of Dravet syndrome: report of 20 cases]
Autor: Zsuzsa, Siegler, Magdolna, Neuwirth, Márta, Hegyi, Eva, Paraicz, Beatrix, Pálmafy, Andrea, Tegzes, Péter, Barsi, Veronika, Karcagi, Lieve, Claes, Peter, De Jonghe, Agnes, Herczegfalvi, András, Fogarasi
Publikováno v: Ideggyogyaszati szemle. 61(11-12)
Severe myoclonic epilepsy in infancy (SMEI; Dravet's syndrome) is a malignant epilepsy syndrome characterized by prolonged febrile hemiconvulsions or generalized seizures starting in the first year of life. Later on myoclonic, atypical absence, and c
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::f6aca8a19a6d47420e3bdcfa26aa8f45
https://pubmed.ncbi.nlm.nih.gov/19070316
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5
De novo SCN1A mutations are a major cause of severe myoclonic epilepsy of infancy
Autor: Lieve, Claes, Berten, Ceulemans, Dominique, Audenaert, Katrien, Smets, Ann, Löfgren, Jurgen, Del-Favero, Sirpa, Ala-Mello, Lina, Basel-Vanagaite, Barbara, Plecko, Salmo, Raskin, Paul, Thiry, Nicole I, Wolf, Christine, Van Broeckhoven, Peter, De Jonghe
Publikováno v: Human mutation. 21(6)
Severe myoclonic epilepsy of infancy (SMEI or Dravet syndrome) is a rare disorder occurring in young children often without a family history of a similar disorder. The earliest disease manifestations are usually fever-associated seizures. Later in li
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::480da2da422be130d7d6f55b6a84eae0
https://pubmed.ncbi.nlm.nih.gov/12754708
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