Zuhair Al Hassnan (Zuhair N Al-Hassnan, Zuhair Al-Hassnan)

Publication Activity (10 Years)

Years Active: 2021-2023
Publications (10 Years): 4

Top Topics

Prognostic Factors

Palliative Care

Top Venues

Orphanet journal of rare diseases

American journal of medical genetics. Part A

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

Publications

Zuhair Al Hassnan, Nadia Al Hashmi, Nawal Makhseed, Tawfeg Ben Omran, Fatma Al Jasmi, Amal Al Teneiji
Correction: Expert Group Consensus on early diagnosis and management of infantile-onset pompe disease in the Gulf Region. Orphanet journal of rare diseases 18 (1) (2023)
Sahar Tulbah, Nadiah Alruwaili, Amal M Alhashem, Arwa Aljohany, Faten Alhadeq, Dimpna C Albert Brotons, Abdullah Alwadai, Zuhair Al Hassnan
Variable phenotype of a null PPP1R13L allele in children with dilated cardiomyopathy. American journal of medical genetics. Part A (2023)
Zuhair Al Hassnan, Nadia Al Hashmi, Nawal Makhseed, Tawfeg Ben Omran, Fatma Al Jasmi, Amal Al Teneiji
Expert Group Consensus on early diagnosis and management of infantile-onset pompe disease in the Gulf Region. Orphanet journal of rare diseases 17 (1) (2022)
Malak A Alghamdi, Mohammed Tohary, Hamad Alzaidan, Faiqa Imtiaz, Zuhair Al Hassnan
Clinical variability and outcome of succinyl-CoA:3-ketoacid CoA transferase deficiency caused by a single OXCT1 mutation: Report of 17 cases. JIMD reports 62 (1) (2021)