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

Biodegradation of feather waste by keratinase produced from newly isolated Bacillus licheniformis ALW1

por Abdel-Fattah, Azza M., El-Gamal, Mamdouh S., Ismail, Siham A., Emran, Mohamed A., Hashem, Amal M.
Publicado 2018

Multiplexed Integrating Plasmids for Engineering of the Erythromycin Gene Cluster for Expression in Streptomyces spp. and Combinatorial Biosynthesis

por Fayed, Bahgat, Ashford, David A., Hashem, Amal M., Amin, Magdy A., El Gazayerly, Omaima N., Gregory, Matthew A., Smith, Margaret C. M.
Publicado 2015

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