Koka M

References (6)

Title : Congenital myasthenic syndromes a rare case of AGRN mutation - Parrey_2025_Am.J.Neurodegener.Dis_14_108
Author(s) : Parrey AH , Koka M , Ismail M , Dar A
Ref : Am J Neurodegener Dis , 14 :108 , 2025
Abstract :
PubMedSearch : Parrey_2025_Am.J.Neurodegener.Dis_14_108
PubMedID: 41280347

Title : Congenital myasthenic syndromes a rare case of AGRN mutation - Parrey_2025_Am.J.Neurodegener.Dis_14_108
Author(s) : Parrey AH , Koka M , Ismail M , Dar A
Ref : Am J Neurodegener Dis , 14 :108 , 2025
Abstract :
PubMedSearch : Parrey_2025_Am.J.Neurodegener.Dis_14_108
PubMedID: 41280347

Title : Congenital myasthenic syndromes a rare case of AGRN mutation - Parrey_2025_Am.J.Neurodegener.Dis_14_108
Author(s) : Parrey AH , Koka M , Ismail M , Dar A
Ref : Am J Neurodegener Dis , 14 :108 , 2025
Abstract :
PubMedSearch : Parrey_2025_Am.J.Neurodegener.Dis_14_108
PubMedID: 41280347

Title : Early Markers in Severe Organophosphorus Poisoning and Their Association with Mortality - Parrey_2024_J.Emerg.Med__
Author(s) : Parrey AH , Koka M , Ismail M , Ashraf M , Lone H
Ref : J Emerg Med , : , 2024
Abstract :
PubMedSearch : Parrey_2024_J.Emerg.Med__
PubMedID: 40340161

Title : Early Markers in Severe Organophosphorus Poisoning and Their Association with Mortality - Parrey_2024_J.Emerg.Med__
Author(s) : Parrey AH , Koka M , Ismail M , Ashraf M , Lone H
Ref : J Emerg Med , : , 2024
Abstract :
PubMedSearch : Parrey_2024_J.Emerg.Med__
PubMedID: 40340161

Title : Early Markers in Severe Organophosphorus Poisoning and Their Association with Mortality - Parrey_2024_J.Emerg.Med__
Author(s) : Parrey AH , Koka M , Ismail M , Ashraf M , Lone H
Ref : J Emerg Med , : , 2024
Abstract :
PubMedSearch : Parrey_2024_J.Emerg.Med__
PubMedID: 40340161