Zobrazeno 1 - 10
of 23
pro vyhledávání: '"Mohammed Ghiath Shamdeen"'
Autor:
Daniel Ebrahimi-Fakhari, Ulrich Dillmann, Marina Flotats-Bastardas, Martin Poryo, Hashim Abdul-Khaliq, Mohammed Ghiath Shamdeen, Bernhard Mischo, Michael Zemlin, Sascha Meyer
Publikováno v:
Frontiers in Pediatrics, Vol 7 (2019)
Externí odkaz:
https://doaj.org/article/ac1bff66f3e849a7a8d5bf9f1ef8c03c
Autor:
Daniel Ebrahimi-Fakhari, Ulrich Dillmann, Marina Flotats-Bastardas, Martin Poryo, Hashim Abdul-Khaliq, Mohammed Ghiath Shamdeen, Bernhard Mischo, Michael Zemlin, Sascha Meyer
Publikováno v:
Frontiers in Pediatrics, Vol 6 (2018)
About 15% of Duchenne muscular dystrophy (DMD) cases are caused by point mutations leading to premature stop codons and disrupted synthesis of the dystrophin protein. Stop codon read-through therapy is available with the drug Ataluren (Translarna® b
Externí odkaz:
https://doaj.org/article/405ae404fd94497e863379476b75ce6c
Autor:
Hashim Abdul-Khaliq, Daniel Ebrahimi-Fakhari, Michael Zemlin, Mohammed Ghiath Shamdeen, Ulrich Dillmann, Marina Flotats-Bastardas, Martin Poryo, Sascha Meyer, Bernhard Mischo
Publikováno v:
Frontiers in Pediatrics, Vol 7 (2019)
About 15% of Duchenne muscular dystrophy (DMD) cases are caused by point mutations leading to premature stop codons and disrupted synthesis of the dystrophin protein. Stop codon read-through therapy is available with the drug Ataluren (Translarna® b
Autor:
Martin Poryo, Ulrich Dillmann, Bernhard Mischo, Hashim Abdul-Khaliq, Daniel Ebrahimi-Fakhari, Marina Flotats-Bastardas, Sascha Meyer, Michael Zemlin, Mohammed Ghiath Shamdeen
Publikováno v:
Frontiers in Pediatrics
Frontiers in Pediatrics, Vol 6 (2018)
Frontiers in Pediatrics, Vol 6 (2018)
About 15% of Duchenne muscular dystrophy (DMD) cases are caused by point mutations leading to premature stop codons and disrupted synthesis of the dystrophin protein. Stop codon read-through therapy is available with the drug Ataluren (Translarna® b
Autor:
Ludwig Gortner, Sascha Meyer, Hans-Jochaim Schäfers, Hashim Abdul-Khaliq, Sven Gottschling, Mohammed Ghiath Shamdeen, Mohammed Shatat
Publikováno v:
Journal of Pediatric Intensive Care. :037-041
Neurological dysfunction may occur after corrective cardiac surgery using cardio-pulmonary bypass (CPB) with or without circulatory arrest. Different neurophysiological monitoring systems have been employed to detect neurological complications and po
Autor:
Tilman Polster, Joerg Klepper, Marion Traus, Thomas Bast, Hartmut Koch, Florian Heinen, Andreas Fiedler, Dietz Rating, Rudolf Korinthenberg, Martina Baethmann, Harald Bode, Moritz Tacke, Christiane Hikel, Joachim Opp, Soeren Heß, Hildegard Wendker-Magrabi, Gerhard Kluger, Hedwig Freitag, Katharina Vill, Elisabeth Tuschen-Hofstätter, Zeecam Hoovey, Peter Dahlem, Hiltrud Muhle, Evemarie Feldmann, Gabriele Weber, Johann Penzien, Hans-Georg Hoffmann, Gerhard Kurlemann, Peter Navratil, Walter Koch, Hans-Michael Straßburg, Friedrich Bosch, Mohammed Ghiath Shamdeen, Ulrich Brandl, Stephan Waltz, Markus Wolff, Bärbel Töpke, Ilona Krois, Klaus Reinhardt, Jan-Peter Ernst, Axel Quattländer, Matthias Kieslich, Michaela Bonfert, Hermann Kühne, Harald M Blank, Michael Gerigk, Christian Blank, Ingo Borggraefe, Ulrich Stephani, K. Brockmann, Ulrike Schara, Frank U Wien, Bernd A. Neubauer, Friedrich A. M. Baumeister, Lucia Gerstl, Ötzcam Sönmez, Ulrike Mause, Regina Trollmann, Michaela Mandl, Viola Prietsch, Karl Bentele, Andreas Sprinz
Publikováno v:
Seizure. 56
Purpose BECTS (benign childhood epilepsy with centrotemporal spikes) is associated with characteristic EEG findings. This study examines the influence of anti-convulsive treatment on the EEG. Methods In a randomized controlled trial including 43 chil
Autor:
Sascha Meyer, Mohammed Ghiath Shamdeen, Christine Vianey-Saban, Cécile Acquaviva, Dorothea Haas
Publikováno v:
Pediatric Neurology. 43:363-367
Nonketotic hyperglycinemia (OMIM #605899), also known as glycine encephalopathy, is an autosomal recessive disorder of glycine metabolism caused by a defect in the glycine cleavage system. A term neonate developed progressive lethargy, muscular hypot
Autor:
Sven Gottschling, Mohammed Ghiath Shamdeen, Matthias Strittmatter, Ludwig Gortner, Sascha Meyer
Publikováno v:
Journal of Paediatrics and Child Health. 47:326-331
Sudden unexpected death in epilepsy (SUPEP) is the commonest cause of seizure-related mortality in people with intractable epilepsy. The incidence of SUDEP varies in different epilepsy populations, with lower rates in population-based studies, higher
Autor:
Sascha Meyer, Ludwig Gortner, Mohammed Ghiath Shamdeen, Sven Gottschling, Mathias Hermann, Markus Klotz, Tobias Struffert, Jörg Wüllenweber
Publikováno v:
Wiener Medizinische Wochenschrift. 157:37-42
The high morbidity and mortality of tuberculous meningoencephalitis (TBM) warrants an early diagnosis and treatment. BCG vaccine has been proven to reduce the incidence of disseminated disease in children. We report on two siblings (2-year-old boy an
Autor:
U. Grundmann, Ludwig Gortner, S. Meyer, Sven Gottschling, T. Mencke, Mohammed Ghiath Shamdeen, B. Kegel
Publikováno v:
Anaesthesia. 61:1040-1047
Summary There is an ongoing debate as to whether propofol exhibits pro- or anticonvulsant effects, and whether it should be used in patients with epilepsy. We prospectively assessed the occurrence of seizure-like phenomena and the effects of intraven