Abdelnaser Zalan

Publication Activity (10 Years)

Years Active: 2022-2024
Publications (10 Years): 5

Top Topics

Attention Deficit Hyperactivity Disorder

Duchenne Muscular Dystrophy

Intellectual Disability

Bioinformatics Analysis

Top Venues

Children (Basel, Switzerland)

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

Publications

Rajech Sharkia, Abdelnaser Zalan, Amit Kessel, Wasif Al-Shareef, Hazar Zahalka, Holger Hengel, Ludger Schöls, Abdussalam Azem, Muhammad Mahajnah
SCAPER -Related Autosomal Recessive Retinitis Pigmentosa with Intellectual Disability: Confirming and Extending the Phenotypic Spectrum and Bioinformatics Analyses. Genes 15 (6) (2024)
Rajech Sharkia, Abdelnaser Zalan, Amit Kessel, Wasif Al-Shareef, Hazar Zahalka, Holger Hengel, Ludger Schöls, Abdussalam Azem, Muhammad Mahajnah
SCAPER -Related Autosomal Recessive Retinitis Pigmentosa with Intellectual Disability: Confirming and Extending the Phenotypic Spectrum and Bioinformatics Analyses. Genes 15 (6) (2024)
Rajech Sharkia, Sahil Jain, Muhammad Mahajnah, Clair Habib, Abdussalam Azem, Wasif Al-Shareef, Abdelnaser Zalan
PTRH2 Gene Variants: Recent Review of the Phenotypic Features and Their Bioinformatics Analysis. Genes 14 (5) (2023)
Genizi Jacob, Lotan Berger, Muhammad Mahajnah, Yulia Shlonsky, Orit Golan-Shany, Azriel Romem, Ayelet Halevy, Keren Nathan, Rajech Sharkia, Abdelnaser Zalan, Aharon Kessel, Rony Cohen
High CCL2 Levels Detected in CSF of Patients with Pediatric Pseudotumor Cerebri Syndrome. Children (Basel, Switzerland) 10 (7) (2023)
Rajech Sharkia, Abdelnaser Zalan, Hazar Zahalka, Amit Kessel, Ayman Asaly, Wasif Al-Shareef, Muhammad Mahajnah
CLN8 Gene Compound Heterozygous Variants: A New Case and Protein Bioinformatics Analyses. Genes 13 (8) (2022)