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Amal M Alhashem

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Cureus|February 4, 2020
Intellectual Disability in Two Brothers Caused by De Novo Novel Unbalanced Translocation (13;18) (q34,q23) and De Novo Microdeletion 6q25 SyndromeAmal M Alhashem, Manal S Almohaid, Lina Alanazi, et al.
Neurosciences (Riyadh, Saudi Arabia)|January 9, 2017
Neurological expression of an inherited translocation of chromosomal 1 and 7Nabil A AlMajhad, Amal M AlHashem, Inesse A Bouhjar, et al.
Saudi Medical Journal|January 10, 2020
Peripheral venous route for administration of ammonul infusion for treatment of acute hyperammonemia. An experience from a tertiary center in Saudi ArabiaAmal M Alhashem, Rihab M Salih, Aida I Al-Aqeel, et al.
Saudi Medical Journal|February 6, 2020
Fructose-1,6-bisphosphatase deficiency with confirmed molecular diagnosis. An important cause of hypoglycemia in childrenRihab M Salih, Esraa A Mohammed, Amal M Alhashem, et al.
American Journal of Medical Genetics. Part A|May 8, 2021
The genotypic and phenotypic spectrum of pycnodysostosis in Saudi Arabia: Novel variants and clinical findingsAziza M Mushiba, Eissa Faqeih, Mohammed A Saleh, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|November 4, 2014
Effect of consanguinity on birth defects in Saudi women: results from a nested case-control studyMuhammad Ali Majeed-Saidan, Amer N Ammari, Amal M AlHashem, et al.
BMJ Open|September 8, 2019
Congenital anomalies and associated risk factors in a Saudi population: a cohort study from pregnancy to age 2 yearsAhmed M Kurdi, Muhammad Ali Majeed-Saidan, Maha S Al Rakaf, et al.
Saudi Medical Journal|July 1, 2020
Incidence of newborn screening disorders among 56632 infants in Central Saudi Arabia. A 6-year studySarar Mohamed, Wafa Elsheikh, Aida I Al-Aqeel, et al.
American Journal of Medical Genetics. Part A|January 26, 2016
Crisponi/CISS1 syndrome: A case seriesAmal M Alhashem, Muhammad Ali Majeed-Saidan, Amer N Ammari, et al.
Neurosciences (Riyadh, Saudi Arabia)|November 1, 2020
Epilepsy, neuropsychiatric phenotypes, neuroimaging findings, and genotype-neurophenotype correlation in 22q11.2 deletion syndromeHeeba Y AlKalaf, Amal M AlHashem, Norah S AlSaleh, et al.
Pageof 2

Showing results (1-10 of 16) with videos related to

Sort By:
Pageof 2
Cureus|February 4, 2020
Intellectual Disability in Two Brothers Caused by De Novo Novel Unbalanced Translocation (13;18) (q34,q23) and De Novo Microdeletion 6q25 SyndromeAmal M Alhashem, Manal S Almohaid, Lina Alanazi, et al.
Neurosciences (Riyadh, Saudi Arabia)|January 9, 2017
Neurological expression of an inherited translocation of chromosomal 1 and 7Nabil A AlMajhad, Amal M AlHashem, Inesse A Bouhjar, et al.
Saudi Medical Journal|January 10, 2020
Peripheral venous route for administration of ammonul infusion for treatment of acute hyperammonemia. An experience from a tertiary center in Saudi ArabiaAmal M Alhashem, Rihab M Salih, Aida I Al-Aqeel, et al.
Saudi Medical Journal|February 6, 2020
Fructose-1,6-bisphosphatase deficiency with confirmed molecular diagnosis. An important cause of hypoglycemia in childrenRihab M Salih, Esraa A Mohammed, Amal M Alhashem, et al.
American Journal of Medical Genetics. Part A|May 8, 2021
The genotypic and phenotypic spectrum of pycnodysostosis in Saudi Arabia: Novel variants and clinical findingsAziza M Mushiba, Eissa Faqeih, Mohammed A Saleh, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|November 4, 2014
Effect of consanguinity on birth defects in Saudi women: results from a nested case-control studyMuhammad Ali Majeed-Saidan, Amer N Ammari, Amal M AlHashem, et al.
BMJ Open|September 8, 2019
Congenital anomalies and associated risk factors in a Saudi population: a cohort study from pregnancy to age 2 yearsAhmed M Kurdi, Muhammad Ali Majeed-Saidan, Maha S Al Rakaf, et al.
Saudi Medical Journal|July 1, 2020
Incidence of newborn screening disorders among 56632 infants in Central Saudi Arabia. A 6-year studySarar Mohamed, Wafa Elsheikh, Aida I Al-Aqeel, et al.
American Journal of Medical Genetics. Part A|January 26, 2016
Crisponi/CISS1 syndrome: A case seriesAmal M Alhashem, Muhammad Ali Majeed-Saidan, Amer N Ammari, et al.
Neurosciences (Riyadh, Saudi Arabia)|November 1, 2020
Epilepsy, neuropsychiatric phenotypes, neuroimaging findings, and genotype-neurophenotype correlation in 22q11.2 deletion syndromeHeeba Y AlKalaf, Amal M AlHashem, Norah S AlSaleh, et al.
Pageof 2