A novel variant in ATM gene causes ataxia telangiectasia revealed by whole-exome sequencing

por Alonazi, Noufa A., Hundallah, Khalid J., Al Hashem, Amal M., Mohamed, Sarar
Publicado 2018

Neurological expression of an inherited translocation of chromosomal 1 and 7

por AlMajhad, Nabil A., AlHashem, Amal M., Bouhjar, Inesse A., Tabarki, Brahim M.
Publicado 2017

Neuroregression, coarse features, and oligosaccharides in urines

por BoAli, Ahmed Y., Tlili-Graiess, Kalthoum, AlHashem, Amal M., Tabarki, Brahim M.
Publicado 2017

Patterns of folic acid use in pregnant Saudi women and prevalence of neural tube defects — Results from a nested case–control study()

por Al Rakaf, Maha S., Kurdi, Ahmed M., Ammari, Amer N., Al Hashem, Amal M., Shoukri, Mohamed M., Garne, Ester, Majeed-Saidan, Muhammad Ali
Publicado 2015

Congenital anomalies and associated risk factors in a Saudi population: a cohort study from pregnancy to age 2 years

por Kurdi, Ahmed M, Majeed-Saidan, Muhammad Ali, Al Rakaf, Maha S, AlHashem, Amal M, Botto, Lorenzo D, Baaqeel, Hassan S, Ammari, Amer N
Publicado 2019

Epilepsy, neuropsychiatric phenotypes, neuroimaging findings, and genotype-neurophenotype correlation in 22q11.2 deletion syndrome

por AlKalaf, Heeba Y., AlHashem, Amal M., AlSaleh, Norah S., AlJohar, Norah M., Abo Thneen, Aliyah M., ElGhezal, Hatem M., Bouhjar, Inesse B., Tlili-Graiess, Kalthoum, Sahari, Atif H., Tabarki, Brahim M.
Publicado 2020