Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Hadeer Abdel Ghaffar"'
Publikováno v:
The Egyptian Journal of Neurology, Psychiatry and Neurosurgery, Vol 54, Iss 1, Pp 1-6 (2018)
Abstract Background Carnitine deficiency is relatively common in epileptic patients. The risk factors reported include the combination of valproic acid with other antiepileptic drugs (AEDs), young age, multiple neurologic disabilities, non-ambulatory
Externí odkaz:
https://doaj.org/article/d4b829c80f654b8da2ab4fff5c906960
Autor:
Hoiyda A. Abdel-Rasol, Hadeer Abdel Ghaffar, Marwa S. Mohamed, Rosa W. Jad, Omayma O. Abelaleem, Noha K. Abdelghaffar
Publikováno v:
Neurological Research. :1-8
Publikováno v:
Fayoum University Medical Journal. 2:79-88
Publikováno v:
Middle East Journal of Medical Genetics. 6:70-74
Publikováno v:
The Egyptian Journal of Laboratory Medicine. 32:1
Background Epilepsy is one of the most common serious neurological disorders, affecting more than 4% of all children. One of the most common conditions leading to epilepsy is hypoxic ischemic encephalopathy (HIE), which is a condition that occurs whe
Publikováno v:
The Egyptian Journal of Neurology, Psychiatry and Neurosurgery
The Egyptian Journal of Neurology, Psychiatry and Neurosurgery, Vol 54, Iss 1, Pp 1-6 (2018)
The Egyptian Journal of Neurology, Psychiatry and Neurosurgery, Vol 54, Iss 1, Pp 1-6 (2018)
Background Carnitine deficiency is relatively common in epileptic patients. The risk factors reported include the combination of valproic acid with other antiepileptic drugs (AEDs), young age, multiple neurologic disabilities, non-ambulatory status,
Autor:
Hadeer Abdel Ghaffar, Heba El-Awady, Rabab M Abdel Moktader, Nashwa M Samra, Mohamed R Soltan
Publikováno v:
Autism-Open Access.
Background: Epilepsy is strongly associated with Autism Spectrum Disorders (ASD). This high rate of epilepsy suggests that ASD and epilepsy might share a common pathophysiological basis. Objective: To study the characteristics of EEG findings and epi
Autor:
Wael S. Ragab, Khaled Eid, Somaya Elgawhary, Magy Abdel Wahab, Hadeer Abdel Ghaffar, Wael F. Saleh
Publikováno v:
Egyptian Journal of Medical Human Genetics; Vol 14, No 4 (2013); 361-366
Objective: To use chorionic villi sampling (CVS) and amniocentesis to determine the genotyping of Gaucher Disease (GD) of fetuses of pregnant mothers who had a previous child affected by GD. Methods: The study was conducted between January 2009 and D
Publikováno v:
European Journal of Paediatric Neurology. 15:131-137
Background and objectives Tuberous sclerosis complex (TSC) is a multi-systemic disorder that involves primarily CNS, skin, kidney and heart. The aim of this study is to determine whether seizures type, interictal EEGs and tubers burden in MRI are cor
Febrile seizures (FSs) are the most common form of childhood seizures. The higher levels of pro-inflammatory cytokines in children may induce seizures, and alternatively, higher levels of anti-inflammatory cytokines may act as a defense mechanism aga
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0cb56e66437d2ae0ee8fa8bc7e76f0d1
http://hdl.handle.net/11562/944255
http://hdl.handle.net/11562/944255