Anomalous coronary artery anatomy with a single coronary ostium arising from the right coronary: a case report and literature review

por Abdulshakour, Bothaina Mohammed, Saeed, Muhammad, Taher, Mohiuddin M
Publicado 2019

Arterial Tortuosity Syndrome in a Newborn: A Case Report With Literature Review

por Al-Blushi, Sania, Bantan, Najwa Abdalkabeer A, Al-Abdullatif, Saad, Taher, Mohiuddin M
Publicado 2022

Correction: Arterial Tortuosity Syndrome in a Newborn: A Case Report With Literature Review

por Al-Blushi, Sania, Bantan, Najwa Abdalkabeer A, Al-Abdullatif, Saad, Taher, Mohiuddin M
Publicado 2023

Effects of mineral trioxide aggregate, calcium hydroxide, biodentine and Emdogain on osteogenesis, Odontogenesis, angiogenesis and cell viability of dental pulp stem cells

por Youssef, Abdel-Rahman, Emara, Ramy, Taher, Mohiuddin M., Al-Allaf, Faisal A., Almalki, Majed, Almasri, Mazen A., Siddiqui, Shahid S.
Publicado 2019

Primary Anorectal Amelanotic Melanoma: The First Case Report from Saudi Arabia

por Baniyaseen, Khaled Ali, Saeed, Muhammad, Albonni, Ahmed Omar, Abdulshakour, Bothaina Mohammed, Dairi, Ghida, Al-Allaf, Faisal A., Taher, Mohiuddin M.
Publicado 2019

Supratentorial Sporadic Hemangioblastoma: A Case Report With Mutation Profiling Using Next-Generation DNA Sequencing

por Taher, Mohiuddin M, Bantan, Najwa A, Alwalily, Mustafa H, Saeed, Muhammad, Taher, Nuha M, Bouzidi, Meriem, Jastania, Raid A, Balkhoyour, Kamal B
Publicado 2023

Evidence of Trem2 Variant Associated with Triple Risk of Alzheimer’s Disease

por Abduljaleel, Zainularifeen, Al-Allaf, Faisal A., Khan, Wajahatullah, Athar, Mohammad, Shahzad, Naiyer, Taher, Mohiuddin M., Elrobh, Mohamed, Alanazi, Mohammed S., El-Huneidi, Waseem
Publicado 2014

Molecular Analysis of Factor VIII and Factor IX Genes in Hemophilia Patients: Identification of Novel Mutations and Molecular Dynamics Studies

por Al-Allaf, Faisal A., Taher, Mohiuddin M., Abduljaleel, Zainularifeen, Bouazzaoui, Abdellatif, Athar, Mohammed, Bogari, Neda M., Abalkhail, Halah A., Owaidah, Tarek MA.
Publicado 2017

Mutation profiling of anaplastic ependymoma grade III by Ion Proton next generation DNA sequencing

por Butt, Ejaz, Alyami, Sabra, Nageeti, Tahani, Saeed, Muhammad, AlQuthami, Khalid, Bouazzaoui, Abdellatif, Athar, Mohammad, Abduljaleel, Zainularifeen, Al-Allaf, Faisal, Taher, Mohiuddin
Publicado 2020

Adamantinomatous Craniopharyngioma in an Adult: A Case Report with NGS Analysis

por Jastania, Raid A, Saeed, Muhammad, Al-Khalidi, Hisham, AlQuthami, Khalid, Nageeti, Tahani H, Al-Allaf, Faisal A, Valerie, Kristoffer, Taher, Mohiuddin M
Publicado 2020

Profile of Male Breast Cancer in Makkah Region of Saudi Arabia: A 4-Year Retrospective Analysis of Radiology and Histopathology

por Saeed, Muhammad, Abdulshakour, Bothaina Mohammed, Bantan, Najwa Abdalkabeer A., Falemban, Afnan Hisham, Abdulla, Munir, Melibary, Ehab M., Mufti, Ahmad H., Taher, Mohiuddin M.
Publicado 2022

Pattern of Thyroid Lesions in Western Region of Saudi Arabia: A Retrospective Analysis and Literature Review

por Saeed, Muhammad I., Hassan, Amal Ali, Butt, Muhammad Ejaz, Baniyaseen, Khalid Ali, Siddiqui, Muhammad I., Bogari, Neda M., Al-Allaf, Faisal A., Taher, Mohiuddin M.
Publicado 2018

Next Generation Exome Sequencing of Pediatric Asthma Identifies Rare and Novel Variants in Candidate Genes

por Bogari, Neda M., Amin, Amr A., Rayes, Husni H., Abdelmotelb, Ahmed, Taher, Mohiuddin M., Al-Allaf, Faisal A., Bouazzaoui, Abdellatif, O'Gorman, Luke, Holloway, John W.
Publicado 2021

Compound A Increases Cell Infiltration in Target Organs of Acute Graft-versus-Host Disease (aGVHD) in a Mouse Model

por Bouazzaoui, Abdellatif, Abdellatif, Ahmed A. H., Al-Allaf, Faisal A., Bogari, Neda M., Taher, Mohiuddin M., Athar, Mohammad, Schubert, Thomas, Habeebullah, Turki M., Qari, Sameer H.
Publicado 2021

A unique case of multiple calvarial hemangiomas with one large symplastic hemangioma

por Bantan, Najwa Abdalkabeer A., Abouissa, Ahmed H., Saeed, Muhammad, Alwalily, Mustafa Hassan, Balkhoyour, Kamal Bakour, Ashour, Khalid Mohammad, Hassan, Amal Ali, Falemban, Afnan Hisham, Taher, Mohiuddin M.
Publicado 2021

The Co-existence of ADHD With Autism in Saudi Children: An Analysis Using Next-Generation DNA Sequencing

por Bogari, Neda M., Al-Allaf, Faisal A., Aljohani, Ashwag, Taher, Mohiuddin M., Qutub, Nermeen A., Alhelfawi, Suhair, Alobaidi, Amal, Alqudah, Derar M., Banni, Hussain, Dairi, Ghida, Amin, Amr A.
Publicado 2020

Association between HindIII (rs320) variant in the lipoprotein lipase gene and the presence of coronary artery disease and stroke among the Saudi population

por Bogari, Neda M., Aljohani, Ashwag, Dannoun, Anas, Elkhateeb, Osama, Porqueddu, Masimo, Amin, Amr A., Bogari, Dema N., Taher, Mohiuddin M., Buba, Faruk, Allam, Reem M., Bogari, Mustafa N., Alamanni, Francesco
Publicado 2020

EGFRvIII expression and isocitrate dehydrogenase mutations in patients with glioma

por Taher, Mohiuddin M., Dairi, Ghida, Butt, Ejaz Muhammad, Al-Quthami, Khalid, Al-Khalidi, Hisham, Jastania, Raid A., Nageeti, Tahani H., Bogari, Neda M., Athar, Mohammad, Al-Allaf, Faisal A., Valerie, Kristoffer
Publicado 2020

Identification of a novel nonsense variant c.1332dup, p.(D445*) in the LDLR gene that causes familial hypercholesterolemia

por Al-Allaf, Faisal A, Athar, Mohammad, Abduljaleel, Zainularifeen, Bouazzaoui, Abdellatif, Taher, Mohiuddin M, Own, Rakan, Al-Allaf, Ahmad F, AbuMansour, Iman, Azhar, Zohor, Ba-hammam, Faisal A, Abalkhail, Hala, Alashwal, Abdullah
Publicado 2014

Next generation DNA sequencing of atypical choroid plexus papilloma of brain: Identification of novel mutations in a female patient by Ion Proton

por Taher, Mohiuddin M., Hassan, Amal Ali, Saeed, Muhammad, Jastania, Raid A., Nageeti, Tahani H., Alkhalidi, Hisham, Dairi, Ghida, Abduljaleel, Zainularifeen, Athar, Mohammad, Bouazzaoui, Abdellatif, El-Bjeirami, Wafa M., Al-Allaf, Faisal A.
Publicado 2019