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1

Severe Combined Immunodeficiency from a Homozygous DNA Liga..:

Alajlan, Huda ; Raducanu, Vlad-Stefan ; Lopez de los Santos, Yossef...
Journal of Clinical Immunology. 44 (2024) 7 - p. , 2024

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

2

A unique STK4 mutation truncating only the C-terminal SARAH..:

Al-Saud, Bandar ; Alajlan, Huda ; Alruwaili, Hibah...
Frontiers in Immunology. 15 (2024) - p. , 2024

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

3

ZNFX1 Deficiency in a Child with Interstitial Pneumonitis a..:

Al-Saud, Bandar ; Al-Mogarri, Ibrahim ; Alajlan, Huda...
Journal of Clinical Immunology. 43 (2023) 7 - p. 1529-1532 , 2023

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

4

Phenotypic and Genotypic Characterization of Hereditary Ang..:

Sheikh, Farrukh ; Alajlan, Huda ; Albanyan, Maram...
Journal of Clinical Immunology. 43 (2022) 2 - p. 479-484 , 2022

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

5

Autosomal recessive ADCY5-Related dystonia and myoclonus: E..:

Bohlega, Saeed A. ; Abou-Al-Shaar, Hussam ; AlDakheel, Amaal...
Parkinsonism & Related Disorders. 64 (2019) - p. 145-149 , 2019

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

6

STK4 Deficiency in a Patient with Immune Complex Glomerulon..:

Al-Saud, Bandar ; Alajlan, Huda ; Sabar, Haneen...
Journal of Clinical Immunology. 39 (2019) 8 - p. 823-826 , 2019

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

7

Human interleukin-2 receptor β mutations associated with de..:

Zhang, Zinan ; Gothe, Florian ; Pennamen, Perrine...
Journal of Experimental Medicine. 216 (2019) 6 - p. 1311-1327 , 2019

Link: https://doi.org/10.1084/..

8

Novel CARMIL2 Mutations in Patients with Variable Clinical ..:

Alazami, Anas M. ; Al-Helale, Maryam ; Alhissi, Safa...
Frontiers in Immunology. 9 (2018) - p. , 2018

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

9

PAX1 is essential for development and function of the human..:

Yamazaki, Yasuhiro ; Urrutia, Raul ; Franco, Luis M...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7189207/. , 2020

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

10

DataSheet_1_A unique STK4 mutation truncating only the C-te..:

Bandar Al-Saud ; Huda Alajlan ; Hibah Alruwaili...
doi:10.3389/fimmu.2024.1329610.s001. , 2024

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

11

DataSheet_1_A unique STK4 mutation truncating only the C-te..:

Bandar Al-Saud ; Huda Alajlan ; Hibah Alruwaili...
doi:10.3389/fimmu.2024.1329610.s001. , 2024

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

12

Novel CARMIL2 Mutations in Patients with Variable Clinical ..:

Anas M. Alazami ; Maryam Al-Helale ; Safa Alhissi...
http://journal.frontiersin.org/article/10.3389/fimmu.2018.00203/full. , 2018

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

13

Mutation of fibulin-1 causes a novel syndrome involving the..:

Bohlega, Saeed ; Al-Ajlan, Huda ; Al-Saif, Amr
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3992572/. , 2014

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

14

A simulation study: Improved ratio-in-regression type varia..:

Ahmad, Sohaib ; Hussain, Sardar ; Ullah, Kalim...
PLOS ONE. 17 (2022) 11 - p. e0276540 , 2022

Link: https://doi.org/10.1371/..

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