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

1

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

Himmelreich, Nastassja ; Bertoldi, Mariarita ; Alfadhel, Majid...
https://research-information.bris.ac.uk/en/publications/e124cba8-b376-4981-a0d4-a4fff9a86fab. , 2023

Link: https://hdl.handle.net/1..

2

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

Himmelreich, Nastassja ; Bertoldi, Mariarita ; Alfadhel, Majid...
https://discovery.ucl.ac.uk/id/eprint/10172442/1/Kurian_Prevalence%20of%20DDC%20genotypes%20in%20patients%20with%20aromatic%20L-amino%20acid%20decarboxylase%20%28AADC%29%20deficiency%20and%20in%20silico%20prediction%20of%20structural%20protein%20changes_VoR.pdf. , 2023

Link: https://discovery.ucl.ac..

3

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

Himmelreich, Nastassja ; Bertoldi, Mariarita ; Alfadhel, Majid...
info:eu-repo/semantics/altIdentifier/pmid/37348148. , 2023

Link: https://hdl.handle.net/1..

4

Loss of UGP2 in brain leads to a severe epileptic encephalo..:

Perenthaler, E. (Elena) ; Nikoncuk, A. (Anita) ; Yousefi, S. (Soheil)...
http://repub.eur.nl/pub/122932. , 2019

Link: http://repub.eur.nl/pub/..

5

Mutation in GM2A Leads to a Progressive Chorea-Dementia Syn..:

Salih, Mustafa A ; Seidahmed, Mohammed Z ; El Khashab, Heba Y...
https://doi.org/10.7916/D8GM86SD. , 2015

Link: https://doi.org/10.7916/..

6

Mutation in GM2A Leads to a Progressive Chorea-dementia Syn..:

Salih, Mustafa A ; Seidahmed, Mohammed Z ; El Khashab, Heba Y...
https://account.tremorjournal.org/index.php/up-j-tohm/article/view/246/343. ,

Link: https://account.tremorjo..

7

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

Fahad A. Bashiri ; Rawan AlSheikh ; Muddathir H. Hamad...
Child Neurology. , 2023

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

8

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

Mohammed F. Alosaimi ; Muddathir H. Hamad ; Muneera J. AlShammari..
https://www.frontiersin.org/articles/10.3389/fped.2023.1269396/full. , 2023

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

9

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

Fahad A. Bashiri ; Rawan AlSheikh ; Muddathir H. Hamad...
https://www.mdpi.com/2227-9067/10/8/1334. , 2023

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

10

DataSheet1_Genomic, Proteomic, and Phenotypic Spectrum of N..:

Malak Ali Alghamdi ; Hicham Benabdelkamel ; Afshan Masood...
doi:10.3389/fgene.2022.806190.s001. , 2022

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

11

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

Reem Al Khalifah ; Muddathir H. Hamad ; Abrar Hudairi...
Child Neurology. , 2022

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

12

Childhood absence epilepsy: Electro-clinical manifestations..:

Fahad A. Bashiri ; Abdullah Al dosari ; Muddathir H. Hamad..
http://www.sciencedirect.com/science/article/pii/S2352646721000922. , 2022

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

13

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

Malak Ali Alghamdi ; Hicham Benabdelkamel ; Afshan Masood...
https://www.frontiersin.org/articles/10.3389/fgene.2022.806190/full. , 2022

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

14

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

Khalid A. Alhasan ; Walaa Alshuaibi ; Muddathir H. Hamad...
https://www.mdpi.com/2227-9067/9/9/1335. , 2022

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

15

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

Reem Al Khalifah ; Muddathir H. Hamad ; Abrar Hudairi...
https://www.mdpi.com/2227-9067/9/11/1696. , 2022

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