E-LIB Suche - Ergebnisse für: Alwadei, Ali H

1

Clinical and Molecular Characteristics of Neuronal Ceroid L..:

Saleh, Mohammed M. ; Hamhom, Abdulrahim M. ; Al-Otaibi, Ali...
Pediatric Neurology. 155 (2024) - p. 149-155 , 2024

Link: https://doi.org/10.1016/..

2

Case Report: A rare treatable metabolic syndrome (Brown-Via..:

Kentab, Amal Y. ; Alsalloum, Yara ; Labani, Mai...
Frontiers in Pediatrics. 12 (2024) - p. , 2024

Link: https://doi.org/10.3389/..

3

SHQ1-associated neurodevelopmental disorder: Report of the ..:

AlHargan, Aljouhra ; AlMuhaizea, Mohammed A. ; Almass, Rawan...
Human Genome Variation. 10 (2023) 1 - p. , 2023

Link: https://doi.org/10.1038/..

4

Efficacy and safety of corpus callosotomy versus vagus nerv..:

Alanazi, Ghalib M. ; ALOsaimi, Turki F. ; Alwadei, Ali H....
Neurosciences. 27 (2022) 2 - p. 59-64 , 2022

Link: https://doi.org/10.17712..

5

Childhood absence epilepsy: Electro-clinical manifestations..:

Bashiri, Fahad A. ; Al dosari, Abdullah ; Hamad, Muddathir H...
International Journal of Pediatrics and Adolescent Medicine. 9 (2022) 2 - p. 131-135 , 2022

Link: https://doi.org/10.1016/..

6

Acute Necrotizing Encephalopathy of Childhood: A Multicente..:

Bashiri, Fahad A. ; Al Johani, Sultan ; Hamad, Muddathir H....
Frontiers in Pediatrics. 8 (2020) - p. , 2020

Link: https://doi.org/10.3389/..

7

Clinical, molecular, and biochemical delineation of asparag..:

Alharby, Essa ; Faqeih, Eissa A. ; Saleh, Mohammed...
Genetics in Medicine. 22 (2020) 12 - p. 2071-2080 , 2020

Link: https://doi.org/10.1038/..

8

Predicting future handedness and hemispheric dominance duri..:

Alwadei, Ali H. ; AlOsaimi, Turki F. ; Bayounis, Manar A...
Neurosciences. 25 (2020) 3 - p. 188-192 , 2020

Link: https://doi.org/10.17712..

9

Genomic and phenotypic delineation of congenital microcepha..:

Shaheen, Ranad ; Maddirevula, Sateesh ; Ewida, Nour...
Genetics in Medicine. 21 (2019) 3 - p. 545-552 , 2019

Link: https://doi.org/10.1038/..

10

Pediatric intracranial hypertension: Experience from 2 Tert..:

Bashiri, Fahad A. ; Al Abdulsalam, Hissah K. ; Hassan, Saeed M....
Neurosciences. 24 (2019) 4 - p. 257-263 , 2019

Link: https://doi.org/10.17712..

11

FARS2 deficiency; new cases, review of clinical, biochemica..:

Almannai, Mohammed ; Wang, Julia ; Dai, Hongzheng...
Molecular Genetics and Metabolism. 125 (2018) 3 - p. 281-291 , 2018

Link: https://doi.org/10.1016/..

12

Management of convulsive status epilepticus in children: an..:

Bashiri, Fahad A. ; Hamad, Muddathir H. ; Amer, Yasser S....
Neurosciences. 22 (2017) 2 - p. 146-155 , 2017

Link: https://doi.org/10.17712..

13

Loss-of-function mutation inRUSC2causes intellectual disabi..:

Alwadei, Ali H ; Benini, Ruba ; Mahmoud, Adel...
Developmental Medicine & Child Neurology. 58 (2016) 12 - p. 1317-1322 , 2016

Link: https://doi.org/10.1111/..

14

SHQ1-associated neurodevelopmental disorder: Report of the ..:

AlHargan, Aljouhra ; AlMuhaizea, Mohammed A ; AlMass, Rawan...
https://www.nature.com/articles/s41439-023-00234-z. , 2023

Link: http://hdl.handle.net/10..

15

SHQ1-associated neurodevelopmental disorder: Report of the ..:

AlHargan, Aljouhra ; AlMuhaizea, Mohammed A ; Almass, Rawan...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9944922/. , 2023

Link: http://www.ncbi.nlm.nih...