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Adel A H Mahmoud

Showing results (1-10 of 6) with videos related to

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Pediatric Neurology|October 8, 2013
Limbic encephalitis in a child: an atypical presentationAdel A H Mahmoud, Fouad A S Al Ghamdi, Michael V Johnston
American Journal of Medical Genetics|July 19, 2002
Cockayne syndrome in three sisters with varying clinical presentationAdel A H Mahmoud, George M Yousef, Ibrahim Al-Hifzi, et al.
Epilepsia|September 3, 2011
Incidence of kidney stones with topiramate treatment in pediatric patientsAdel A H Mahmoud, Tamer Rizk, Nahid K El-Bakri, et al.
Journal of Pediatric Neurosciences|January 8, 2020
Anti-<i>N</i>-methyl-d-aspartate Receptor Encephalitis: A Case Series and Review of the LiteratureCheri M John, Deepa E Mathew, Maysara Abdelaziz, et al.
Brain : a Journal of Neurology|September 26, 2020
Defining the clinical, molecular and imaging spectrum of adaptor protein complex 4-associated hereditary spastic paraplegiaDarius Ebrahimi-Fakhari, Julian Teinert, Robert Behne, et al.
Nature Communications|February 1, 2020
Loss-of-function mutations in UDP-Glucose 6-Dehydrogenase cause recessive developmental epileptic encephalopathyHolger Hengel, Célia Bosso-Lefèvre, George Grady, et al.
Pageof 1

Showing results (1-10 of 6) with videos related to

Sort By:
Pageof 1
Pediatric Neurology|October 8, 2013
Limbic encephalitis in a child: an atypical presentationAdel A H Mahmoud, Fouad A S Al Ghamdi, Michael V Johnston
American Journal of Medical Genetics|July 19, 2002
Cockayne syndrome in three sisters with varying clinical presentationAdel A H Mahmoud, George M Yousef, Ibrahim Al-Hifzi, et al.
Epilepsia|September 3, 2011
Incidence of kidney stones with topiramate treatment in pediatric patientsAdel A H Mahmoud, Tamer Rizk, Nahid K El-Bakri, et al.
Journal of Pediatric Neurosciences|January 8, 2020
Anti-<i>N</i>-methyl-d-aspartate Receptor Encephalitis: A Case Series and Review of the LiteratureCheri M John, Deepa E Mathew, Maysara Abdelaziz, et al.
Brain : a Journal of Neurology|September 26, 2020
Defining the clinical, molecular and imaging spectrum of adaptor protein complex 4-associated hereditary spastic paraplegiaDarius Ebrahimi-Fakhari, Julian Teinert, Robert Behne, et al.
Nature Communications|February 1, 2020
Loss-of-function mutations in UDP-Glucose 6-Dehydrogenase cause recessive developmental epileptic encephalopathyHolger Hengel, Célia Bosso-Lefèvre, George Grady, et al.
Pageof 1