Search Results - "epilepsy"

Reelin-Related Neurological Disorders and Animal Models by Laura Lossi

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Purinergic Signaling in Health and Disease

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Identification of Missense <i>ADGRV1</i> Mutation as a Candidate Genetic Cause of Familial Febrile Seizure 4 by Ji Yoon Han, Hyun Joo Lee, Young-Mock Lee, Joonhong Park

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Pediatric Stroke in Southern Iran; Clinical Presentations, Etiologies and Outcomes: A Case-Series and Review of Literature by Soroor Inaloo, Zahra Foroughiniya, Saeedeh Haghbin, Tahereh Farkhondeh

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Case Report: resolution of refractory seizures after neurosurgical intervention in newborns with cerebral extra-axial hemorrhages by C. Rohaert, J. K. H. Spoor, M. Dremmen, A. M. van Hengel-Jacobs, L. S. Smit, L. S. Smit, R. Knol

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Profile of children with cerebral palsy at a tertiary hospital in eastern Nepal by Shipra Chaudhary, Nisha Keshary Bhatta, Prakash Poudel, Jyoti Agrawal, Rosan Prasad Shah Kalawar, Jitendra Prasad Jayswal

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Joint use of population pharmacokinetics and machine learning for optimizing antiepileptic treatment in pediatric population by Ivana Damnjanović, Nastia Tsyplakova, Nikola Stefanović, Tatjana Tošić, Aleksandra Catić-Đorđević, Vangelis Karalis

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Development of a novel glucose‐dendrimer based therapeutic targeting hyperexcitable neurons in neurological disorders by Anjali Sharma, Nirnath Sah, Rishi Sharma, Preeti Vyas, Wathsala Liyanage, Sujatha Kannan, Rangaramanujam M. Kannan

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Case Report and Review of the Literature: A New and a Recurrent Variant in the VARS2 Gene Are Associated With Isolated Lethal Hypertrophic Cardiomyopathy, Hyperlactatemia, and Pulm... by Katarína Kušíková, René Günther Feichtinger, Bernhard Csillag, Ognian Kostadinov Kalev, Serge Weis, Hans-Christoph Duba, Johannes Adalbert Mayr, Denisa Weis

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Wolf-Hirschhorn Syndrome: Clinical and Genetic Study of 7 New Cases, and Mini Review by Eva-Cristiana Gavril, Alina Costina Luca, Alexandrina-Stefania Curpan, Roxana Popescu, Irina Resmerita, Monica Cristina Panzaru, Lacramioara Ionela Butnariu, Eusebiu Vlad Gorduza, Mihaela Gramescu, Cristina Rusu

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Human taeniasis: current insights into prevention and management strategies in endemic countries by Okello A, Thomas LF

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Clinical management of tuberous sclerosis complex over the lifetime of a patient by Frost M, Hulbert J

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Novel mutation in XPNPEP3 in a patient with heart failure without nephronophthisis-like nephropathy (NPHPL1): case report and literature review by Zhen Zhen, Ziyan Dong, Lu Gao, Qin Wang, Xi Chen, Jia Na, Yue Yuan

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Family inherited, prenatal and perinatal risk factors in Cuban children with primary autism by Daniel Quintana Hernández, Paulina Araceli Lantigua Cruz, Teddy Osmin Tamargo Barbeito, Yohandra Calixto Robert, Nancy Hernández Hernández

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A rare case of dysembryoplastic neuroepithelial tumor combined with encephalocraniocutaneous lipomatosis and intractable seizures by Jee-Yeon Han, Mi-Sun Yum, Eun-Hee Kim, Seokho Hong, Tae-Sung Ko

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Comprehensive evaluation of the child with global developmental delays or intellectual disability by Abdullah Nasser Aldosari, T. Saeed Aldosari

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Benefícios e riscos da prática de atividade física recreativa e/ou esportiva por pessoas com epilepsia by Rodrigo Luiz Vancini, Claudio Andre Barbosa de Lira, Fúlvio Alexandre Scorza, Ricardo Mario Arida

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Cost burden and net monetary benefit loss of neonatal hypoglycaemia by Matthew J. Glasgow, Richard Edlin, Jane E. Harding

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Anxiolytic and sedative effects of sodium valproate with different experimental paradigms in male and female rats by María de losÁngeles Cintado, Luis Gonzalo De la Casa, Gabriel González

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Novel compound heterozygous TARS2 variants in a Chinese family with mitochondrial encephalomyopathy: a case report by Xiaojing Li, Bingwei Peng, Chi Hou, Jinliang Li, Yiru Zeng, Wenxiao Wu, Yinting Liao, Yang Tian, Wen-Xiong Chen

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