E-LIB Suche - Ergebnisse für: Alrifai, Muhammad Talal

1

Genetic Microcephaly in a Saudi Population: Unique Spectrum..:

Alrifai, Muhammad Talal ; Alrumayyan, Yousof ; Baarmah, Duaa...
Journal of Child Neurology. 39 (2024) 5-6 - p. 209-217 , 2024

Link: https://doi.org/10.1177/..

2

Effectiveness of intra-thecal methotrexate in refractory An..:

Hommady, Raid ; Alsohibani, Abdullah ; Alayed, Ruba...
BMC Neurology. 23 (2023) 1 - p. , 2023

Link: https://doi.org/10.1186/..

3

Clinical Characteristics and Risk Factors of Neonatal Hypox..:

AlMuqbil, Mohammed ; Alanazi, Jawaher ; Alsaif, Nada...
International Journal of General Medicine. 16 (2023) - p. 525-536 , 2023

Link: https://doi.org/10.2147/..

4

Congenital disorder of glycosylation with defective fucosyl..:

Al Tuwaijri, Abeer ; Alyafee, Yusra ; Umair, Muhammad...
Molecular Genetics & Genomic Medicine. 11 (2022) 4 - p. , 2022

Link: https://doi.org/10.1002/..

5

The Leukodystrophy Spectrum in Saudi Arabia: Epidemiologica..:

Alfadhel, Majid ; Almuqbil, Mohammed ; Al Mutairi, Fuad...
Frontiers in Pediatrics. 9 (2021) - p. , 2021

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

6

Pediatrics COVID-19 and neurological manifestations: Single..:

Aljomah, Lama ; Almedlej, Sara ; Baarmah, Duaa...
eNeurologicalSci. 24 (2021) - p. 100355 , 2021

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

7

Biallelic loss-of-function variants in NEMF cause central n..:

Ahmed, Ashfaque ; Wang, Meng ; Bergant, Gaber...
Human Genetics. 140 (2020) 4 - p. 579-592 , 2020

Link: https://doi.org/10.1007/..

8

EMC10 homozygous variant identified in a family with global..:

Umair, Muhammad ; Ballow, Mariam ; Asiri, Abdulaziz...
Clinical Genetics. 98 (2020) 6 - p. 555-561 , 2020

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

9

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/..

10

Genomic testing and counseling: The contribution of next‐ge..:

Alsubaie, Lamia ; Aloraini, Taghrid ; Amoudi, Manal...
Annals of Human Genetics. 84 (2020) 6 - p. 431-436 , 2020

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

11

The comorbidity of headaches in pediatric epilepsy patients..:

Al-Gethami, Hanin ; Alrifai Muhammad, Talal ; AlRumayyan, Ahmed..
Neurosciences. 24 (2019) 4 - p. 284-289 , 2019

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

12

Epilepsy in Propionic Acidemia: Case Series of 14 Saudi Pat..:

AlGhamdi, Afnan ; Alrifai, Muhammad Talal ; Al Hammad, Abdullah I....
Journal of Child Neurology. 33 (2018) 11 - p. 713-717 , 2018

Link: https://doi.org/10.1177/..

13

Further Delineation of the Clinical Phenotype of Cerebellar..:

Alsahli, Saud ; Alrifai, Muhammad Talal ; Al Tala, Saeed..
Journal of Central Nervous System Disease. 10 (2018) - p. 117957351875968 , 2018

Link: https://doi.org/10.1177/..

14

Further delineation of the phenotypic spectrum ofISCA2 defe..:

Alfadhel, Majid ; Nashabat, Marwan ; Alrifai, Muhammad Talal...
European Journal of Paediatric Neurology. 22 (2018) 1 - p. 46-55 , 2018

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

15

Mutation in SLC6A9 encoding a glycine transporter causes a ..:

Alfadhel, Majid ; Nashabat, Marwan ; Qahtani, Hanan Al...
Human Genetics. 135 (2016) 11 - p. 1263-1268 , 2016

Link: https://doi.org/10.1007/..