Search Results - "EEG"

Interhemispheric Functional Connectivity in Childhood Absence Epilepsy by J Gordon Millichap

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Interregional research and practical conference with international attendance "Epilepsy and Paroxysmal Conditions as an Interdisciplinary Problem"(19 February 2020) by D. A. Petrenko

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A Dysmorphic Child with a Pericentric Inversion of Chromosome 8 by Venkateshwari Ananthapur, Srilekha Avvari, Sujatha Madireddi, Pratibha Nallari, Jyothy Akka

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2017 AHA Heart Science Forum Innovation Challenge Award 1st Place Winner and the 1st Annual Samsung Digital Health Summit Technology Pitch Contest Award 1st Place Winner by Joseph T Shen, Raffi B Shen

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Management of Children with Speech Disorders via Transcranial Magnetic Stimulation: Non-Randomized Controlled Study by Julia V. Nesterova, George A. Karkashadze, Leonid M. Yatsik, Leyla S. Namazova-Baranova, Elena A. Vishneva, Elena V. Kaytukova, Kamilla E. Efendieva, Daria A. Bushueva, Tinatin Yu. Gogberashvili, Tatiana A. Konstantinidi, Natalia E. Sergeeva, Safarbegim H. Sadilloeva, Marina A. Kurakina, Julia E. Kazanceva, Inessa A. Povalyaeva, Nadezhda A. Ulkina, Tatiana A. Salimgareeva, Natalia S. Sergienko, Oksana D. Mescheryakova, Viktor V. Altunin, Elizaveta V. Leonova, Elena S. Zibrova

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Spasmele epileptice la copii: aspecte clinico-electroencefalografice. by Ludmila Feghiu, Svetlana Hadjiu, Cornelia Călcîi, Ludmila Cuzneț, Corina Grîu, Stanislav Groppa

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Epilepsiile la copilul cu paralizie cerebrală spastică by Ludmila Cuzneț, Svetlana Hadjiu, Cornelia Călcîi, Ludmila Feghiu, Corina Grîu, Ninel Revenco

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Safety and efficacy of topiramate in neonates with hypoxic ischemic encephalopathy treated with hypothermia (NeoNATI) by Filippi Luca, Fiorini Patrizio, Daniotti Marta, Catarzi Serena, Savelli Sara, Fonda Claudio, Bartalena Laura, Boldrini Antonio, Giampietri Matteo, Scaramuzzo Rosa, Papoff Paola, Del Balzo Francesca, Spalice Alberto, la Marca Giancarlo, Malvagia Sabrina, Della Bona Maria, Donzelli Gianpaolo, Tinelli Francesca, Cioni Giovanni, Pisano Tiziana, Falchi Melania, Guerrini Renzo

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GENETIC EPILEPTIC AND DEVELOPMENTAL ENCEPHALOPATHIES OF THE EARLY AGE: FROM SYMPTOMS GENETIC TESTING TO DIAGNOSIS by Л. Кирилова, О. Юзва, О. Мірошников, Н. Бондаренко, О. Берегела

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Bone Health in Rats With Temporal Lobe Epilepsy in the Absence of Anti-Epileptic Drugs by Rhys D. Brady, Rhys D. Brady, Ker Rui Wong, Dale L. Robinson, Richelle Mychasiuk, Stuart J. McDonald, Stuart J. McDonald, Ryan A. D'Cunha, Glenn R. Yamakawa, Mujun Sun, John D. Wark, Peter Vee Sin Lee, Terence J. O'Brien, Terence J. O'Brien, Pablo M. Casillas-Espinosa, Pablo M. Casillas-Espinosa, Sandy R. Shultz, Sandy R. Shultz

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Ocena stopnia poinformowania oraz wiedzy pacjentów na temat badania elektroencefalograficznego = Evaluation level of information and knowledge of patients about the study electroe... by Justyna Zych, Joanna Skonieczna, Dominik Olejniczak, Karolina Zakrzewska

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Ocena stopnia poinformowania oraz wiedzy pacjentów na temat badania elektroencefalograficznego = Evaluation level of information and knowledge of patients about the study electroe... by Justyna Zych, Joanna Skonieczna, Dominik Olejniczak, Karolina Zakrzewska

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Biomedical Signal and Image Processing by Najarian, Kayvan

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Ein Ansatz zur Bewertung klimapolitischer Instrumente am Beispiel der Metallerzeugung und -verarbeitung by Breun, Patrick

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Impact of acute cardiovascular collapse on cerebral electrical activity: importance of heart-brain interaction by Kristin L. Riley, Heidi M. Harmon, Brady A. Thomas, Adrianne R. Bischoff, Regan E. Giesinger, Patrick J. McNamara

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Delirium: a common preventable medical disorder in elderly patients by Afaf Hemeda

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The Impact of Preterm Birth on Sleep through Infancy, Childhood and Adolescence and Its Implications by Jayne Trickett, Catherine Hill, Topun Austin, Samantha Johnson

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Clinical case of focal epilepsy due to non-traumatic intracranial hemorrhage by Alina A. Seryogina, Artem E. Khmelevsky

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Magnetoencephalography: an emerging neuroimaging tool for studying normal and abnormal human brain development by Patricia Ellen Grant

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Novel ANKRD11 gene mutation in an individual with a mild phenotype of KBG syndrome associated to a GEFS+ phenotypic spectrum: a case report by Rita Maria Alves, Paolo Uva, Marielza F. Veiga, Manuela Oppo, Fabiana C. R. Zschaber, Giampiero Porcu, Henrique P. Porto, Ivana Persico, Stefano Onano, Gianmauro Cuccuru, Rossano Atzeni, Lauro C. N. Vieira, Marcos V. A. Pires, Francesco Cucca, Maria Betânia P. Toralles, Andrea Angius, Laura Crisponi

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