Search research articles
Contact Us
Filters
Showing results (1-10 of 18) with videos related to
Page
of 2
Sort By:
Cureus
|
November 8, 2023
Rhinolith Misdiagnosed as Fungal Mucin
Nuha Alrayes, Abdulrahman Alhumaizi, Alanoud Alomair, et al.
The Journal of Gene Medicine
|
November 22, 2019
Novel missense alteration in LRP4 gene underlies Cenani-Lenz syndactyly syndrome in a consanguineous family
Nuha Alrayes, Abdul Aziz, Farman Ullah, et al.
JPMA. the Journal of the Pakistan Medical Association
|
February 14, 2025
Correlation of anti-oxidant and pro-oxidant enzymes with insulin resistance in diabetic nephropathy
Turky Alamri, Hamed Khouja, Nuha Alrayes, et al.
International Journal of Endocrinology
|
April 3, 2026
TGF-β1 Gene Polymorphisms in Saudi Patients With Type 2 Diabetes With or Without Diabetic Nephropathy
Amani Alhozali, Suad Muthaffar, Samar Sultan, et al.
Saudi Medical Journal
|
June 3, 2024
Prevalence of CEA, CA 125, and CA 15-3 serum tumour markers in different regions of Saudi Arabia
Abrar Ashi, Marwan Al-Hajeili, Sarah Almaghrabi, et al.
Plos One
|
October 4, 2022
Integrative weighted molecular network construction from transcriptomics and genome wide association data to identify shared genetic biomarkers for COPD and lung cancer
Babajan Banaganapalli, Bayan Mallah, Kawthar Saad Alghamdi, et al.
BMC Research Notes
|
June 27, 2015
Truncating mutation in intracellular phospholipase A₁ gene (DDHD2) in hereditary spastic paraplegia with intellectual disability (SPG54)
Nuha Alrayes, Hussein Sheikh Ali Mohamoud, Musharraf Jelani, et al.
Frontiers in Psychology
|
April 27, 2026
Maternal experiences and family dynamics following Down syndrome diagnosis in Saudi Arabia
Nuha Alrayes, Reem Alyoubi, Anas Alyazidi, et al.
Scientific Reports
|
February 3, 2018
A missense mutation in TRAPPC6A leads to build-up of the protein, in patients with a neurodevelopmental syndrome and dysmorphic features
Hussein Sheikh Mohamoud, Saleem Ahmed, Musharraf Jelani, et al.
Saudi Journal of Biological Sciences
|
July 18, 2022
Identifying significant genes and functionally enriched pathways in familial hypercholesterolemia using integrated gene co-expression network analysis
Zuhier Awan, Nuha Alrayes, Zeenath Khan, et al.
Page
of 2
Search research articles
Search
Showing results (1-10 of 18) with videos related to
Sort By:
Page
of 2
Cureus
|
November 8, 2023
Rhinolith Misdiagnosed as Fungal Mucin
Nuha Alrayes, Abdulrahman Alhumaizi, Alanoud Alomair, et al.
The Journal of Gene Medicine
|
November 22, 2019
Novel missense alteration in LRP4 gene underlies Cenani-Lenz syndactyly syndrome in a consanguineous family
Nuha Alrayes, Abdul Aziz, Farman Ullah, et al.
JPMA. the Journal of the Pakistan Medical Association
|
February 14, 2025
Correlation of anti-oxidant and pro-oxidant enzymes with insulin resistance in diabetic nephropathy
Turky Alamri, Hamed Khouja, Nuha Alrayes, et al.
International Journal of Endocrinology
|
April 3, 2026
TGF-β1 Gene Polymorphisms in Saudi Patients With Type 2 Diabetes With or Without Diabetic Nephropathy
Amani Alhozali, Suad Muthaffar, Samar Sultan, et al.
Saudi Medical Journal
|
June 3, 2024
Prevalence of CEA, CA 125, and CA 15-3 serum tumour markers in different regions of Saudi Arabia
Abrar Ashi, Marwan Al-Hajeili, Sarah Almaghrabi, et al.
Plos One
|
October 4, 2022
Integrative weighted molecular network construction from transcriptomics and genome wide association data to identify shared genetic biomarkers for COPD and lung cancer
Babajan Banaganapalli, Bayan Mallah, Kawthar Saad Alghamdi, et al.
BMC Research Notes
|
June 27, 2015
Truncating mutation in intracellular phospholipase A₁ gene (DDHD2) in hereditary spastic paraplegia with intellectual disability (SPG54)
Nuha Alrayes, Hussein Sheikh Ali Mohamoud, Musharraf Jelani, et al.
Frontiers in Psychology
|
April 27, 2026
Maternal experiences and family dynamics following Down syndrome diagnosis in Saudi Arabia
Nuha Alrayes, Reem Alyoubi, Anas Alyazidi, et al.
Scientific Reports
|
February 3, 2018
A missense mutation in TRAPPC6A leads to build-up of the protein, in patients with a neurodevelopmental syndrome and dysmorphic features
Hussein Sheikh Mohamoud, Saleem Ahmed, Musharraf Jelani, et al.
Saudi Journal of Biological Sciences
|
July 18, 2022
Identifying significant genes and functionally enriched pathways in familial hypercholesterolemia using integrated gene co-expression network analysis
Zuhier Awan, Nuha Alrayes, Zeenath Khan, et al.
Page
of 2