Establishment of (JUCTCi007-A) iPSC line from a patient with congenital myasthenic syndrome (CMS) carrying a homozygous mutation p.Arg331Trp (c.991C > T) in the CHRNE gene

by Nidaa A. Ababneh, Ban Al-Kurdi, Dema Ali, Duaa Abuarqoub, Raghda Barham, Abdee T. Ryalat, Abdalla Awidi
Published 2020-08-01

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

by Nosaiba Tawfik Al-Ryalat, Saif Aldeen Saleh AlRyalat, Walid Sulaiman Mahafza, Osama Ahmad Samara, Abdee Tawfiq Ryalat, Azmy Mohammad Al-Hadidy
Published 2017-03-01

Establishment of a human induced pluripotent stem cell line, JUCTCi012-A, from multiple symmetric lipomatosis (MSL) patient carrying a homozygous Arg707Trp (c.2119C > T) mutation i...

by Nidaa A. Ababneh, Dema Ali, Raghda Barham, Ban Al-Kurdi, Nour Sharar, Sabal Al Hadidi, Omar Qanno', Abdee T. Ryalat, Bareqa Salah, Abdalla Awidi
Published 2020-10-01

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

by Nidaa A Ababneh, Dema Ali, Ban Al-Kurdi, Malik Sallam, Abdulla M Alzibdeh, Bareqa Salah, Abdee T Ryalat, Belal Azab, Basil Sharrack, Abdalla Awidi
Published 2020-01-01

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 m...

by Nidaa A. Ababneh, Ban Al-Kurdi, Dema Ali, Duaa Abuarqoub, Raghda Barham, Abdulla M. Alzibdeh, Asim N. Khanfar, Ahmad M. Altantawi, Abdee T. Ryalat, Basil Sharrack, Abdalla Awidi
Published 2020-10-01