Case report: First case report of an Emirati child with a novel gene variant causing aromatic L-amino acid decarboxylase deficiency

por Babiker, Mohamed O. E., Kurian, Manju A., Suleiman, Jehan
Publicado 2022

A novel de novo mutation in DYNC1H1 gene underlying malformation of cortical development and cataract

por Hertecant, Jozef, Komara, Makanko, Nagi, Aslam, Suleiman, Jehan, Al-Gazali, Lihadh, Ali, Bassam R.
Publicado 2016

17q23.2q23.3 de novo duplication in association with speech and language disorder, learning difficulties, incoordination, motor skill impairment, and behavioral disturbances: a cas...

por Wessel, Karen, Suleiman, Jehan, Khalaf, Tamam E., Kishore, Shivendra, Rolfs, Arndt, El-Hattab, Ayman W.
Publicado 2017

Correction to: Aromatic L-amino acid decarboxylase deficiency in countries in the Middle East: a case series and literature review

por Abukhaled, Musaad, Al Muqbil, Mohammed, Alghamdi, Malak Ali, Hundallah, Khalid, Suleiman, Jehan, Ben-Omran, Tawfeg, Alfadhel, Majid, Almannai, Mohammed, Alsaleh, Rehab, Tabarki, Brahim
Publicado 2023

Aromatic L-amino acid decarboxylase deficiency in countries in the Middle East: a case series and literature review

por Abukhaled, Musaad, Al Muqbil, Mohammed, Alghamdi, Malak Ali, Hundallah, Khalid, Suleiman, Jehan, Ben-Omran, Tawfeg, Alfadhel, Majid, Almannai, Mohammed, Alsaleh, Rehab, Tabarki, Brahim
Publicado 2023

Compound heterozygous variants in the multiple PDZ domain protein (MPDZ) cause a case of mild non-progressive communicating hydrocephalus

por Al-Jezawi, Nesreen K., Al-Shamsi, Aisha M., Suleiman, Jehan, Ben-Salem, Salma, John, Anne, Vijayan, Ranjit, Ali, Bassam R., Al-Gazali, Lihadh
Publicado 2018