E-LIB Suche - Ergebnisse für: Hamad, Muddathir H

1

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/..

2

Virtual Objective Structured Clinical Examination (OSCE) Tr..:

Saeed, Elshazaly ; Hamad, Muddathir H ; Alhuzaimi, Abdullah N...
Cureus. , 2024

Link: https://doi.org/10.7759/..

3

Prevalence of DDC genotypes in patients with aromatic L-ami..:

Himmelreich, Nastassja ; Bertoldi, Mariarita ; Alfadhel, Majid...
Molecular Genetics and Metabolism. 139 (2023) 3 - p. 107624 , 2023

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

4

Genotype–Phenotype Analysis of Children with Epilepsy Refer..:

Bashiri, Fahad A. ; AlSheikh, Rawan ; Hamad, Muddathir H....
Children. 10 (2023) 8 - p. 1334 , 2023

Link: https://doi.org/10.3390/..

5

Developmental and/or epileptic encephalopathy with spike-an..:

Alsini, Hanin ; Alghamdi, Abdulaziz ; Alshafi, Shatha...
Seizure: European Journal of Epilepsy. 107 (2023) - p. 146-154 , 2023

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

6

Corrigendum to: Prevalence of DDC genotypes in patients wit..:

Himmelreich, Nastassja ; Bertoldi, Mariarita ; Alfadhel, Majid...
Molecular Genetics and Metabolism. 139 (2023) 4 - p. 107647 , 2023

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

7

Case report: A late and isolated presentation of meningoenc..:

Alosaimi, Mohammed F. ; Hamad, Muddathir H. ; AlShammari, Muneera J...
Frontiers in Pediatrics. 11 (2023) - p. , 2023

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

8

Prevalence and Related Risk Factors of Vitamin D Deficiency..:

Al Khalifah, Reem ; Hamad, Muddathir H. ; Hudairi, Abrar...
Children. 9 (2022) 11 - p. 1696 , 2022

Link: https://doi.org/10.3390/..

9

International alliance and AGREE-ment of 71 clinical practi..:

Amer, Yasser S. ; Titi, Maher A. ; Godah, Mohammad W....
Journal of Clinical Epidemiology. 142 (2022) - p. 333-370 , 2022

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

10

Pattern and etiology of early childhood epilepsy: An Experi..:

Kentab, Amal Y. ; Al Bulayhi, Shumukh ; Hamad, Muddathir H...
Neurosciences. 27 (2022) 4 - p. 244-250 , 2022

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

11

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/..

12

Genomic, Proteomic, and Phenotypic Spectrum of Novel O-Sial..:

Ali Alghamdi, Malak ; Benabdelkamel, Hicham ; Masood, Afshan...
Frontiers in Genetics. 13 (2022) - p. , 2022

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

13

Hypermanganesemia with Dystonia Type 2: A Potentially Treat..:

Alhasan, Khalid A. ; Alshuaibi, Walaa ; Hamad, Muddathir H....
Children. 9 (2022) 9 - p. 1335 , 2022

Link: https://doi.org/10.3390/..

14

Adapting evidence-based clinical practice guidelines for pe..:

Bashiri, Fahad A. ; Albatti, Turki H. ; Hamad, Muddathir H....
Child and Adolescent Psychiatry and Mental Health. 15 (2021) 1 - p. , 2021

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

15

An identical‐by‐descent novel splice‐donor variant inPRUNE1..:

Koko, Mahmoud ; Yahia, Ashraf ; Elsayed, Liena E....
Annals of Human Genetics. 85 (2021) 5 - p. 186-195 , 2021

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