Fahad Mushbb N Alqathani

Publication Activity (10 Years)

Years Active: 2024-2024
Publications (10 Years): 4

Top Topics

Top Venues

The American journal of case reports

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

Publications

Mohammed Shahab Uddin, AlZahra Y Alradhi, Fahad Mushbb N Alqathani, Othman Saleh Alessa, Ahmed Nawfal M Alshammari, Ratna Tripathy, Mohammed Ahmed Alomari
A Rare Case of Neonatal Hypomagnesemia with Secondary Hypocalcemia Caused by a Novel Homozygous TRPM6 Gene Variant. The American journal of case reports 25 (2024)
Mohammed Shahab Uddin, AlZahra Y Alradhi, Fahad Mushbb N Alqathani, Othman Saleh Alessa, Ahmed Nawfal M Alshammari, Ratna Tripathy, Mohammed Ahmed Alomari
A Rare Case of Neonatal Hypomagnesemia with Secondary Hypocalcemia Caused by a Novel Homozygous TRPM6 Gene Variant. The American journal of case reports 25 (2024)
Mohammed Shahab Uddin, AlZahra Y Alradhi, Fahad Mushbb N Alqathani, Othman Saleh Alessa, Ahmed Nawfal M Alshammari, Ratna Tripathy, Mohammed Ahmed Alomari
A Rare Case of Neonatal Hypomagnesemia with Secondary Hypocalcemia Caused by a Novel Homozygous TRPM6 Gene Variant. The American journal of case reports 25 (2024)
Mohammed Shahab Uddin, AlZahra Y Alradhi, Fahad Mushbb N Alqathani, Othman Saleh Alessa, Ahmed Nawfal M Alshammari, Ratna Tripathy, Mohammed Ahmed Alomari
A Rare Case of Neonatal Hypomagnesemia with Secondary Hypocalcemia Caused by a Novel Homozygous TRPM6 Gene Variant. The American journal of case reports 25 (2024)