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Afaf Al-Sagheir
Afaf Al-Sagheir
Medicine
Pediatrics
Ataxia
KCNJ10
Mutation
5
Papers
13
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Diagnosis and management of X-linked hypophosphatemia in children and adolescent in the Gulf Cooperation Council countries.
2021
Archives of Osteoporosis
Fahad Al Juraibah
Elham Al Amiri
Mohammed S. Al Dubayee
Jamal Al-Jubeh
Hessa Al-Kandari
Afaf Al-Sagheir
Adnan Al Shaikh
Salem A Beshyah
Asma Deeb
Abdelhadi M. Habeb
Manal Mustafa
Hanaa Zidan
M. Zulf Mughal
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Citations (2)
A Case Study of X-linked Hypophosphataemia: The Effect of Conventional Therapy from Childhood to Adulthood in Saudi Arabia
2019
Afaf Al-Sagheir
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Clinical, Endocrine, and Molecular Genetic Analysis of a Large Cohort of Saudi Arabian Patients with Laron Syndrome
2017
Hormone Research in Paediatrics
Abdullah A. Al-Ashwal
Afaf Al-Sagheir
Khushnooda Ramzan
Mohammed Al-Owain
Rabab Allam
Alya Qari
Nouf S. Al-Numair
Faiqa Imtiaz
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Lethal digenic mutations in the K+ channels Kir4.1 (KCNJ10) and SLACK (KCNT1) associated with severe-disabling seizures and neurodevelopmental delay
2017
American Journal of Physiology-heart and Circulatory Physiology
Sonia Hasan
Ameera Balobaid
Alessandro Grottesi
Omar Dabbagh
Marta Cenciarini
Rifaat Rawashdeh
Afaf Al-Sagheir
Cecilia Bove
Lara Macchioni
Mauro Pessia
Mohammed Al-Owain
Maria Cristina DAdamo
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Lethal digenic mutations in the K+ channels Kir4.1 (KCNJ10) and SLACK (KCNT1) associated with severe-disabling seizures and neurodevelopmental delay
2017
Journal of Neurophysiology
Sonia M. Hasan
Ameera Balobaid
Alessandro Grottesi
Omar Dabbagh
Marta Cenciarini
Rifaat Rawashdeh
Afaf Al-Sagheir
Cecilia Bove
Lara Macchioni
Mauro Pessia
Mohammed Al-Owain
Maria Cristina D'Adamo
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Citations (10)
1