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Alajlan, Huda
14
results:
Search for persons
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Format
Online (14)
Mediatypes
Articles (Online) (9)
OpenAccess-fulltext (5)
Sorted by: Relevance
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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
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/..
?
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
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/..
?
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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