Fuad Al Mutairi (Fuad Almutairi)

ORCID

Publication Activity (10 Years)

Years Active: 2017-2024
Publications (10 Years): 6

Top Venues

Journal of child neurology

BMC pulmonary medicine

Journal of central nervous system disease

American journal of medical genetics. Part A

King Saud bin Abdulaziz University for Health Sciences College of Medicine

This page only lists publications with an associated author ORCID identifier.

Affiliation History

King Saud bin Abdulaziz University for Health Sciences College of Medicine Jun 15 2015

Saudi Arabia

Assistant Professor :: Prdiatrics

King Abdulaziz Medical City Oct 12 2014

Saudi Arabia

Consultant Medical Genetics :: Department of Prdiatrics

Publications

Muhammad Talal Alrifai, Yousof Alrumayyan, Duaa Baarmah, Ahmed Alrumayyan, Waleed Altuwaijri, Mohammed AlMuqbil, Wafaa Eyaid, Abdulrahman Swaid, Fuad Al Mutairi, Majid Alfadhel
Genetic Microcephaly in a Saudi Population: Unique Spectrum of Affected Genes Including a Novel One. Journal of child neurology (2024)
Muhammad Talal Alrifai, Yousof Alrumayyan, Duaa Baarmah, Ahmed Alrumayyan, Waleed Altuwaijri, Mohammed AlMuqbil, Wafaa Eyaid, Abdulrahman Swaid, Fuad Al Mutairi, Majid Alfadhel
Genetic Microcephaly in a Saudi Population: Unique Spectrum of Affected Genes Including a Novel One. Journal of child neurology 39 (5-6) (2024)
Fuad Al Mutairi, Randa Alkhalaf, Abdullah Alkhorayyef, Fayhan Alroqi, Alyafee Yusra, Muhammad Umair, Fetaini Nouf, Amjad Khan, Alharbi Meshael, Aleidi Hamad, Alaujan Monira, Abdulaziz Asiri, Kheloud M Alhamoudi, Majid Alfadhel
Homozygous truncating NEK10 mutation, associated with primary ciliary dyskinesia: a case report. BMC pulmonary medicine 20 (1) (2020)
Meshal Almutairi, Sultan Al-Khenaizan, Fahd Al Sufiani, Mohammed Al Balwi, Fuad Al Mutairi
Peeling of skin as presenting manifestation in congenital disorders of glycosylation. The Journal of dermatology 47 (9) (2020)
Fuad Al Mutairi
Hyperhomocysteinemia: Clinical Insights. Journal of central nervous system disease 12 (2020)
Ahmed Alfares, Sultan Al-Khenaizan, Fuad Al Mutairi
Peeling skin syndrome associated with novel variant in FLG2 gene. American journal of medical genetics. Part A 173 (12) (2017)

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Publication Activity (10 Years)

Top Topics

Top Venues

Fuad Al Mutairi (Fuad Almutairi)