Fatal intracranial haemorrhage in acute promyelocytic leukemia patients with short isoform of PML-RARα: Review of molecular and radiological data

por Abudawood, Manal, Alorini, Hanan, Samman, Manar A., Bashir, Salman M., AlSwayed, Azizah, Binhassan, Sarah, Peer-Zada, Abdul Ali
Publicado 2023

Favorable outcome of PML‐RARα short isoform and FLT3‐ITD mutation in a patient with several adverse prognostic markers: A case report

por Bafail, Mohammed A., AlTahan, Rahaf, Samman, Manar A., Tashkandi, Suha A., Motabi, Ibraheem H., Peer‐Zada, Abdul Ali
Publicado 2023

Reclassifying variations of unknown significance in diseases affecting Saudi Arabia’s population reveal new associations

por Al Eissa, Mariam M., Alotibi, Raniah S., Alhaddad, Bader, Aloraini, Taghrid, Samman, Manar S., AlAsiri, Abdulrahman, Abouelhoda, Mohamed, AlQahtani, Amerh S.
Publicado 2023

Progressive Ataxia and Neurologic Regression in RFXANK-Associated Bare Lymphocyte Syndrome

por Alharby, Essa, Obaid, Mona, Elamin, Mohammed A.O., Almuntashri, Makki, Bakhsh, Ismail, Samman, Manar, Peake, Roy W.A., Alasmari, Ali, Almontashiri, Naif A.M.
Publicado 2021

A GRM7 mutation associated with developmental delay reduces mGlu(7) expression and produces neurological phenotypes

por Fisher, Nicole M., AlHashim, Aqeela, Buch, Aditi B., Badivuku, Hana, Samman, Manar M., Weiss, Kelly M., Cestero, Gabriela I., Does, Mark D., Rook, Jerri M., Lindsley, Craig W., Conn, P. Jeffrey, Gogliotti, Rocco G., Niswender, Colleen M.
Publicado 2021