Manahel Mahmood Alsabbagh

Publication Activity (10 Years)

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

Top Topics

Newly Diagnosed

Multiple Sclerosis

Mitochondrial Dna

Top Venues

Fetal and pediatric pathology

Pediatric dermatology

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

Publications

Manahel Mahmood Alsabbagh
Congenital Ichthyosis: Current Approaches to Prenatal Diagnoses. Fetal and pediatric pathology 43 (2) (2024)
Manahel Mahmood Alsabbagh
Congenital Ichthyosis: Current Approaches to Prenatal Diagnoses. Fetal and pediatric pathology (2024)
Manahel Mahmood Alsabbagh
Congenital Ichthyosis: Current Approaches to Prenatal Diagnoses. Fetal and pediatric pathology 43 (2) (2024)
Manahel Mahmood Alsabbagh
Keratitis-ichthyosis-deafness syndrome: A comprehensive review of cutaneous and systemic manifestations. Pediatric dermatology (2022)
Ghada Al-Kafaji, Materah Salem Alwehaidah, Manahel Mahmood Alsabbagh, Maram A Alharbi, Moiz Bakhiet
Mitochondrial DNA haplogroup analysis in Saudi Arab patients with multiple sclerosis. PloS one 17 (12) (2022)
Ghada Al-Kafaji, Materah Salem Alwehaidah, Manahel Mahmood Alsabbagh, Maram A Alharbi, Moiz Bakhiet
Mitochondrial DNA haplogroup analysis in Saudi Arab patients with multiple sclerosis. PloS one 17 (12) (2022)
Ghada Al-Kafaji, Materah Salem Alwehaidah, Manahel Mahmood Alsabbagh, Maram A Alharbi, Moiz Bakhiet
Mitochondrial DNA haplogroup analysis in Saudi Arab patients with multiple sclerosis. PloS one 17 (12) (2022)
Ghada Al-Kafaji, Materah Salem Alwehaidah, Manahel Mahmood Alsabbagh, Maram A Alharbi, Moiz Bakhiet
Mitochondrial DNA haplogroup analysis in Saudi Arab patients with multiple sclerosis. PloS one 17 (12) (2022)
Ghada Al-Kafaji, Materah Salem Alwehaidah, Manahel Mahmood Alsabbagh, Maram A Alharbi, Moiz Bakhiet
Mitochondrial DNA haplogroup analysis in Saudi Arab patients with multiple sclerosis. PloS one 17 (12) (2022)
Ghada Al-Kafaji, Halla F Bakheit, Faisal AlAli, Mina Fattah, Saad Alhajeri, Maram A Alharbi, Abdulqader Daif, Manahel Mahmood Alsabbagh, Materah Salem Alwehaidah, Moiz Bakhiet
Next-generation sequencing of the whole mitochondrial genome identifies functionally deleterious mutations in patients with multiple sclerosis. PloS one 17 (2) (2022)