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Ali Alghamdi, Malak
39
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1
Classical phenylketonuria presenting as maternal PKU syndro..:
Malak Ali Alghamdi
;
Anne O'Donnell‐Luria
;
Naif A. Almontashiri
...
https://doi.org/10.1002/jmd2.12384. , 2023
Link:
https://doi.org/10.1002/..
?
2
Adult ADHD Positive Screening and Sibship, Birth Order and ..:
AlOmar, Reem
;
AlShamlan, Nouf
;
Al-Johani, Wejdan M
...
info:eu-repo/semantics/altIdentifier/doi/10.2147/PRBM.S426715. , 2023
Link:
https://www.dovepress.co..
?
3
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..
?
4
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..
?
5
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..
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6
ACCEPTANCE OF PATIENTS FOR EXAMINATION OF ANAL DISEASES:
Masoud Ahmad Al-Ghamdi
;
Mohannad Adnan Munshi
;
Fahad Salih Aldhafeeri
...
doi:10.5281/zenodo.7533102. , 2022
Link:
https://zenodo.org/recor..
?
7
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/..
?
8
Bi-allelic variants in WNT7B disrupt the development of mul..:
Bouasker, Samir
;
Patel, Nisha
;
Greenlees, Rebecca
...
info:eu-repo/semantics/altIdentifier/doi/10.1136/jmedgenet-2022-108475. , 2022
Link:
https://u-paris.hal.scie..
?
9
Bi-allelic variants in WNT7B disrupt the development of mul..:
Bouasker, Samir
;
Patel, Nisha
;
Greenlees, Rebecca
...
info:eu-repo/semantics/altIdentifier/doi/10.1136/jmedgenet-2022-108475. , 2022
Link:
https://u-paris.hal.scie..
?
10
Bi-allelic variants in WNT7B disrupt the development of mul..:
Bouasker, Samir
;
Patel, Nisha
;
Greenlees, Rebecca
...
info:eu-repo/semantics/altIdentifier/doi/10.1136/jmedgenet-2022-108475. , 2022
Link:
https://u-paris.hal.scie..
?
11
Atypical presentation of pallister–Hall syndrome with centr..:
Hala Gasim Omer
;
Amal Ali Alhakami
;
Malak Ali Alghamdi
.
http://www.jnsmonline.org/article.asp?issn=2589-627X;year=2022;volume=5;issue=3;spage=309;epage=312;aulast=Omer. , 2022
Link:
https://doi.org/10.4103/..
?
12
Social anxiety disorder and its associated factors: a cross..:
Wejdan M. Al‑Johani
;
Nouf A. AlShamlan
;
Naheel A. AlAmer
...
https://doi.org/10.1186/s12888-022-04147-z. , 2022
Link:
https://doi.org/10.1186/..
?
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
Bi-allelic variants in WNT7B disrupt the development of mul..:
Bouasker, Samir
;
Patel, Nisha
;
Greenlees, Rebecca
...
info:eu-repo/semantics/altIdentifier/doi/10.1136/jmedgenet-2022-108475. , 2022
Link:
https://u-paris.hal.scie..
?
15
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/..
1-15