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A Bashiri

Showing results (41-50 of 107) with videos related to

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Sudanese Journal of Paediatrics|August 6, 2016
Sturge-Weber syndrome: Continued vigilance is neededSaeed Hassan, Amir Babiker, Fahad A Bashiri, et al.
European Journal of Obstetrics, Gynecology, and Reproductive Biology|December 10, 1998
Meconium stained amniotic fluid in preterm delivery is an independent risk factor for perinatal complicationsM Mazor, R Hershkovitz, A Bashiri, et al.
Brain & Development|December 12, 2024
The correlation of intracranial parenchymal calcium score and the severity of neurological clinical presentation in carbonic anhydrase deficiency type 2Basma AlFaris, Fahad B AlBader, Rawan AlSheikh, et al.
European Journal of Medical Genetics|January 19, 2020
Expanding the phenotype and the genotype of Stromme syndrome: A novel variant of the CENPF gene and literature reviewMalak Alghamdi, Waleed H Alkhamis, Fahad A Bashiri, et al.
Sudanese Journal of Paediatrics|February 26, 2019
Drowning in the desert: family denial of brain deathMohamad-Hani Temsah, Fahad Alsohaim, Ayman Al-Eyadhy, et al.
European Journal of Obstetrics, Gynecology, and Reproductive Biology|February 13, 2001
Indomethacin activity in the fetal vasculature of normal and meconium exposed human placentaeG Holcberg, O Sapir, M Huleihel, et al.
Human Genetics|May 11, 2015
ARL6IP6, a susceptibility locus for ischemic stroke, is mutated in a patient with syndromic Cutis Marmorata Telangiectatica CongenitaIman S Abumansour, Hadia Hijazi, Anas Alazmi, et al.
Children (Basel, Switzerland)|August 26, 2023
Genotype-Phenotype Analysis of Children with Epilepsy Referred for Whole-Exome Sequencing at a Tertiary Care University HospitalFahad A Bashiri, Rawan AlSheikh, Muddathir H Hamad, et al.
Neurosciences (Riyadh, Saudi Arabia)|January 18, 2021
Erratum: A consensus statement on spinal muscular atrophy management in Saudi Arabia in the context of COVID-19Fouad Alghamdi, Nahla Alshaikh, Ahmed K Bamaga, et al.
Clinical Genetics|September 5, 2020
Phenotypic and molecular spectrum of pyridoxamine-5'-phosphate oxidase deficiency: A scoping review of 87 cases of pyridoxamine-5'-phosphate oxidase deficiencyMalak Alghamdi, Fahad A Bashiri, Marwa Abdelhakim, et al.
Pageof 11

Showing results (41-50 of 107) with videos related to

Sort By:
Pageof 11
Sudanese Journal of Paediatrics|August 6, 2016
Sturge-Weber syndrome: Continued vigilance is neededSaeed Hassan, Amir Babiker, Fahad A Bashiri, et al.
European Journal of Obstetrics, Gynecology, and Reproductive Biology|December 10, 1998
Meconium stained amniotic fluid in preterm delivery is an independent risk factor for perinatal complicationsM Mazor, R Hershkovitz, A Bashiri, et al.
Brain & Development|December 12, 2024
The correlation of intracranial parenchymal calcium score and the severity of neurological clinical presentation in carbonic anhydrase deficiency type 2Basma AlFaris, Fahad B AlBader, Rawan AlSheikh, et al.
European Journal of Medical Genetics|January 19, 2020
Expanding the phenotype and the genotype of Stromme syndrome: A novel variant of the CENPF gene and literature reviewMalak Alghamdi, Waleed H Alkhamis, Fahad A Bashiri, et al.
Sudanese Journal of Paediatrics|February 26, 2019
Drowning in the desert: family denial of brain deathMohamad-Hani Temsah, Fahad Alsohaim, Ayman Al-Eyadhy, et al.
European Journal of Obstetrics, Gynecology, and Reproductive Biology|February 13, 2001
Indomethacin activity in the fetal vasculature of normal and meconium exposed human placentaeG Holcberg, O Sapir, M Huleihel, et al.
Human Genetics|May 11, 2015
ARL6IP6, a susceptibility locus for ischemic stroke, is mutated in a patient with syndromic Cutis Marmorata Telangiectatica CongenitaIman S Abumansour, Hadia Hijazi, Anas Alazmi, et al.
Children (Basel, Switzerland)|August 26, 2023
Genotype-Phenotype Analysis of Children with Epilepsy Referred for Whole-Exome Sequencing at a Tertiary Care University HospitalFahad A Bashiri, Rawan AlSheikh, Muddathir H Hamad, et al.
Neurosciences (Riyadh, Saudi Arabia)|January 18, 2021
Erratum: A consensus statement on spinal muscular atrophy management in Saudi Arabia in the context of COVID-19Fouad Alghamdi, Nahla Alshaikh, Ahmed K Bamaga, et al.
Clinical Genetics|September 5, 2020
Phenotypic and molecular spectrum of pyridoxamine-5'-phosphate oxidase deficiency: A scoping review of 87 cases of pyridoxamine-5'-phosphate oxidase deficiencyMalak Alghamdi, Fahad A Bashiri, Marwa Abdelhakim, et al.
Pageof 11