A. T. Ryalat

The utility of whole-exome sequencing in accurate diagnosis of neuromuscular disorders in consanguineous families in Jordan.

B. Sharrack, M. El-Khateeb, A. Awidi, 2021, Clinica chimica acta; international journal of clinical chemistry.

Identification of APTX disease-causing mutation in two unrelated Jordanian families with cerebellar ataxia and sensitivity to DNA damaging agents

B. Sharrack, Bareqa Salah, A. Awidi, 2020, PloS one.

Generation and characterization of induced pluripotent stem cell (iPSC) line (JUCTCi002-A) from a patient with ataxia with oculomotor apraxia type 1 (AOA1) harboring a homozygous mutation in the APTX gene.

B. Sharrack, D. Abuarqoub, A. Awidi, 2020, Stem cell research.

Approach to low back pain in conservative societies and developing countries

S. A. Alryalat, Nosaiba T. Al-Ryalat, A. T. Ryalat, 2017 .

Myelopathy associated with age-related cervical disc herniation: a retrospective review of magnetic resonance images

S. A. Alryalat, O. Samara, Nosaiba T. Al-Ryalat, 2017, Annals of Saudi medicine.