Zobrazeno 1 - 10
of 85
pro vyhledávání: '"Felicitas Becker"'
Publikováno v:
Epilepsy & Behavior Reports, Vol 27, Iss , Pp 100697- (2024)
A 24-year-old female patient with pre-existing refractory epilepsy caused by tuberous sclerosis (TSC) and electroclinical features of Lennox-Gastaut syndrome (LGS) was referred to our hospital from an external clinic. Upon arrival, she presented with
Externí odkaz:
https://doaj.org/article/9c2aa7e982df4b3790c9997bf764a45c
Autor:
Katri Silvennoinen, Nikola deLange, Sara Zagaglia, Simona Balestrini, Ganna Androsova, Merel Wassenaar, Pauls Auce, Andreja Avbersek, Felicitas Becker, Bianca Berghuis, Ellen Campbell, Antonietta Coppola, Ben Francis, Stefan Wolking, Gianpiero L. Cavalleri, John Craig, Norman Delanty, Michael R. Johnson, Bobby P. C. Koeleman, Wolfram S. Kunz, Holger Lerche, Anthony G. Marson, Terence J. O’Brien, Josemir W. Sander, Graeme J. Sills, Pasquale Striano, Federico Zara, Job van derPalen, Roland Krause, Chantal Depondt, Sanjay M. Sisodiya, the EpiPGX Consortium
Publikováno v:
Epilepsia Open, Vol 4, Iss 3, Pp 420-430 (2019)
Abstract Objective To study the effectiveness and tolerability of antiepileptic drugs (AEDs) commonly used in juvenile myoclonic epilepsy (JME). Methods People with JME were identified from a large database of individuals with epilepsy, which include
Externí odkaz:
https://doaj.org/article/7e0bae26f0854a818290ffd6aefbb5da
Autor:
Dennis Lal, Eva M Reinthaler, Borislav Dejanovic, Patrick May, Holger Thiele, Anna-Elina Lehesjoki, Günter Schwarz, Erik Riesch, M Arfan Ikram, Cornelia M van Duijn, Andre G Uitterlinden, Albert Hofman, Hannelore Steinböck, Ursula Gruber-Sedlmayr, Birgit Neophytou, Federico Zara, Andreas Hahn, Genetic Commission of the Italian League against Epilepsy, EuroEPINOMICS CoGIE Consortium, Padhraig Gormley, Felicitas Becker, Yvonne G Weber, Maria Roberta Cilio, Wolfram S Kunz, Roland Krause, Fritz Zimprich, Johannes R Lemke, Peter Nürnberg, Thomas Sander, Holger Lerche, Bernd A Neubauer
Publikováno v:
PLoS ONE, Vol 11, Iss 3, p e0150426 (2016)
ObjectiveThe SCN1A gene, coding for the voltage-gated Na+ channel alpha subunit NaV1.1, is the clinically most relevant epilepsy gene. With the advent of high-throughput next-generation sequencing, clinical laboratories are generating an ever-increas
Externí odkaz:
https://doaj.org/article/57fdd972a5f4468aab854329d85979d2
In recent years, anthropologists, historians, and others have been drawn to study the profuse and creative usages of digital media by religious movements. At the same time, scholars of Christian Africa have long been concerned with the history of tex
Autor:
Felicitas Becker, Wenzel Geissler
This volume explores how AIDS is understood, confronted and lived with through religious ideas and practices, and how these, in turn, are reinterpreted and changed by the experience of AIDS. Examining the social production, and productivity, of AIDS
Autor:
Felicitas Becker, Salvatory S. Nyanto, James Giblin, Ann McDougall, Alexander Meckelburg, Lotte Pelckmans
Publikováno v:
Becker, F, Nyanto, S S, Giblin, J, McDougall, A, Meckelburg, A & Pelckmans, L 2023, ' Researching the Aftermath of Slavery in Mainland East Africa: Methodological, Ethical, and Practical Challenges ', Slavery & abolition, vol. ahead-of-print, no. ahead-of-print, pp. 1-26 .
Pelckmans, L 2023, ' Researching the Aftermath of Slavery in Mainland East Africa : Methodological, Ethical, and Practical Challenges ', Slavery and Abolition, vol. 44, no. 1, pp. 131-156 . https://doi.org/10.1080/0144039X.2022.2121888
SLAVERY & ABOLITION
Pelckmans, L 2023, ' Researching the Aftermath of Slavery in Mainland East Africa : Methodological, Ethical, and Practical Challenges ', Slavery and Abolition, vol. 44, no. 1, pp. 131-156 . https://doi.org/10.1080/0144039X.2022.2121888
SLAVERY & ABOLITION
This article examines ethical, practical, and methodological challenges in researching the aftermath of slavery in continental East Africa away from the coastal plantation belt. Interest in post-slavery there is recent and inspired by the apparent co
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f6257e61b815aa8ccc26c63f921ed2c8
https://pure.au.dk/portal/da/publications/researching-the-aftermath-of-slavery-in-mainland-east-africa-methodological-ethical-and-practical-challenges(83f46e5e-e615-40a6-a7d4-5a30e80e3771).html
https://pure.au.dk/portal/da/publications/researching-the-aftermath-of-slavery-in-mainland-east-africa-methodological-ethical-and-practical-challenges(83f46e5e-e615-40a6-a7d4-5a30e80e3771).html
Autor:
Felicitas Becker
Publikováno v:
Current History. 120:189-195
For a time, Tanzania enjoyed a reputation for mostly free elections and public debate. But after President John Magufuli was elected in 2015, he introduced measures to stifle the media and tilt the electoral playing field in favor of the longtime rul
Autor:
Felicitas Becker
Publikováno v:
JOURNAL OF AFRICAN DIASPORA ARCHAEOLOGY AND HERITAGE
This article traces the history of slavery and of post-slavery struggles for livelihood and status in the layout, the physical structures, and the social lives of three towns on the southern Swahili Coast: Kilwa, Mikindani, and Lindi. These towns wer
Autor:
G. Dulini C. Mendis, Gina E. Elsen, Snezana Maljevic, Melissa Castillo-Lizardo, Filip Rosa, Betuel Uysal, Felicitas Becker, Stephan Mueller, Ashutosh Dhingra, Claire E Cuddy, Christopher A. Reid, Peter Heutink, Steven Petrou, Holger Lerche, Heidi Loeffler, Niklas Schwarz
Publikováno v:
Stem cell reports 15(1), 22-37 (2020). doi:10.1016/j.stemcr.2020.05.015
Stem Cell Reports
Stem Cell Reports
Summary Neurons differentiated from induced pluripotent stem cells (iPSCs) typically show regular spiking and synaptic activity but lack more complex network activity critical for brain development, such as periodic depolarizations including simultan
Bi-allelic GAD1 variants cause a neonatal onset syndromic developmental and epileptic encephalopathy
Autor:
Eudeline Alix, Anne-Lise Poulat, Nilay Güneş, Yvonne G. Weber, Maryam Najafi, José M. Serratosa, Ehsan Ghayoor Karimiani, Kaya Bilguvar, Tarek Omar, Katia Hardies, Dana Craiu, Hande Caglayan, Stéphanie Baulac, Fernando Kok, Reza Maroofian, Gaetan Lesca, Heba Morsy, Damien Sanlaville, Carla Marini, Renzo Guerrini, Nina Barišić, Luiza Ramos, Sarah von Spiczak, Miriam Schmidts, Patrick May, Karl Martin Klein, Beyhan Tüysüz, Audrey Labalme, Sarah Weckhuysen, Dilek Uludağ Alkaya, Julitta de Bellescize, Felix Rosenow, Farah Ashrafzadeh, Rudi Balling, Homa Tajsharghi, Amira Nabil, Katalin Sterbova, Felicitas Becker, Nicolas Chatron, Ali-Reza Moslemi, Holger Lerche, Hiltrud Muhle, Ingo Helbig, Haytham Hussien, Sandra Roselli
Publikováno v:
Brain
Brain, 143, pp. 1447-1461
Brain, 143, 1447-1461
Brain, 143, pp. 1447-1461
Brain, 143, 1447-1461
Chatron et al. describe a novel syndrome caused by bi-allelic loss-of-function mutations in GAD1, the gene encoding the GABA synthetic enzyme GAD67. The syndrome is characterized by the unique association of developmental and epileptic encephalopathy