Ahmed M Almatrafi (Ahmad Almatrafi, Ahmad M Almatrafi)

Publication Activity (10 Years)

Years Active: 2019-2024
Publications (10 Years): 8

Top Topics

Botulinum Toxin

Candida Albicans

Top Venues

Journal of clinical medicine

Annals of dermatology

International journal of developmental neuroscience : the official journal of the International Society for Developmental Neuroscience

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

Publications

Ahmed M Almatrafi, Abdulfatah M Alayoubi, Majed M Alluqmani, Jamil A Hashmi, Sulman Basit
Exome Sequence Analysis to Characterize Undiagnosed Family Segregating Motor Impairment and Dystonia. Journal of clinical medicine 13 (14) (2024)
Ahmed M Almatrafi, Abdulfatah M Alayoubi, Majed M Alluqmani, Jamil A Hashmi, Sulman Basit
Exome Sequence Analysis to Characterize Undiagnosed Family Segregating Motor Impairment and Dystonia. Journal of clinical medicine 13 (14) (2024)
Ahmed M Almatrafi, Abdulfatah M Alayoubi, Majed M Alluqmani, Jamil A Hashmi, Sulman Basit
Exome Sequence Analysis to Characterize Undiagnosed Family Segregating Motor Impairment and Dystonia. Journal of clinical medicine 13 (14) (2024)
Ahmed M Almatrafi, Ali M Hibshi, Sulman Basit
Exome Sequencing to Identify Novel Variants Associated with Secondary Amenorrhea and Premature Ovarian Insufficiency (POI) in Saudi Women. Biomedicines 12 (4) (2024)
Ahmed M Almatrafi, Ali M Hibshi, Sulman Basit
Exome Sequencing to Identify Novel Variants Associated with Secondary Amenorrhea and Premature Ovarian Insufficiency (POI) in Saudi Women. Biomedicines 12 (4) (2024)
Ahmed M Almatrafi, Majed M Alluqmani, Sulman Basit
Homozygous Duplication in the CHRNE in a Family with Congenital Myasthenic Syndrome 4C: 18-Year Follow Up. Biomedicines 11 (11) (2023)
Asmat Ullah, Abid Ali Shah, Majed Alluqmani, Nighat Haider, Hasan Aman, Fatima Alfadhli, Ahmed M Almatrafi, Alia M Albalawi, Jai Krishin, Fati Ullah Khan, Bilal Ali Anjam, null Abdullah, Elionora Peña Lozano, Abdus Samad, Wasim Ahmad, Torben Hansen, Kun Xia, Sulman Basit
Clinical and genetic characterization of patients segregating variants in KPTN, MINPP1, NGLY1, AP4B1, and SON underlying neurodevelopmental disorders: Genetic and phenotypic expansion. International journal of developmental neuroscience : the official journal of the International Society for Developmental Neuroscience 82 (8) (2022)
Alia M Albalawi, Jamil A Hashmi, Fatima Alfadhli, Ahmed M Almatrafi, Khushnooda Ramzan, Sulman Basit
Missense Mutations in the CTSC Gene in Saudi Families Segregating Papillon-Lefèvre Syndrome. Annals of dermatology 32 (1) (2019)