Neural tube defects: Challenging, yet preventable

por Salih, Mustafa A.
Publicado 2014

Message from the Guest Editor

por Salih, Mustafa A.
Publicado 2014

Classification, clinical features, and genetics of neural tube defects

por Salih, Mustafa A., Murshid, Waleed R., Seidahmed, Mohammed Z.
Publicado 2014

Epidemiology, prenatal management, and prevention of neural tube defects

por Salih, Mustafa A., Murshid, Waleed R., Seidahmed, Mohammed Z.
Publicado 2014

Glutaric aciduria type 1 as a cause of dystonic cerebral palsy

por Mohamed, Sarar, Hamad, Muddathir H., Hassan, Hamdy H., Salih, Mustafa A.
Publicado 2015

Sirenomelia and severe caudal regression syndrome

por Seidahmed, Mohammed Z., Abdelbasit, Omer B., Alhussein, Khalid A., Miqdad, Abeer M., Khalil, Mohammed I., Salih, Mustafa A.
Publicado 2014

A de novo marker chromosome derived from 9p in a patient with 9p partial duplication syndrome and autism features: genotype-phenotype correlation

por Abu-Amero, Khaled K, Hellani, Ali M, Salih, Mustafa A, Seidahmed, Mohammad Z, Elmalik, Tageldin S, Zidan, Ghassan, Bosley, Thomas M
Publicado 2010

Agenesis of the corpus callosum associated with spinal open neural tube defect

por Elgamal, Essam A., Elwatidy, Sherif M., Alhabib, Amro F., Jamjoom, Zain B., Murshid, Waleed R., Hassan, Hamdy H., Salih, Mustafa A.
Publicado 2014

Neurodevelopmental and epilepsy outcomes of patients with infantile spasms treated in a tertiary care center

por Bashiri, Fahad A., Al-Sehemi, Matar A., Hamad, Muddathir H., Alshammari, Nawaf R., Aljumah, Mujtaba A, Kentab, Amal, Salih, Mustafa A.
Publicado 2021

Split cord malformation associated with spinal open neural tube defect

por Elgamal, Essam A., Hassan, Hamdy H., Elwatidy, Sherif M., Altwijri, Ikhllas, Alhabib, Amro F., Jamjoom, Zain B., Murshid, Waleed R., Salih, Mustafa A.
Publicado 2014

Epidemiology of neural tube defects

por Seidahmed, Mohammed Z., Abdelbasit, Omar B., Shaheed, Meeralebbae M., Alhussein, Khalid A., Miqdad, Abeer M., Khalil, Mohamed I., Al-Enazy, Naif M., Salih, Mustafa A.
Publicado 2014

The natural history of infantile neuroaxonal dystrophy

por Altuame, Fadie D., Foskett, Gretchen, Atwal, Paldeep S., Endemann, Sarah, Midei, Mark, Milner, Peter, Salih, Mustafa A., Hamad, Muddathir, Al-Muhaizea, Mohammad, Hashem, Mais, Alkuraya, Fowzan S.
Publicado 2020

Genetic, chromosomal, and syndromic causes of neural tube defects

por Seidahmed, Mohammed Z., Abdelbasit, Omer B., Shaheed, Meeralebbae M., Alhussein, Khalid A., Miqdad, Abeer M., Samadi, Abdulmohsen S., Khalil, Mohammed I., Al-Mardawi, Elham, Salih, Mustafa A.
Publicado 2014

A novel syndrome of lethal familial hyperekplexia associated with brain malformation

por Seidahmed, Mohammed Zein, Salih, Mustafa A, Abdulbasit, Omer B, Shaheed, Meeralebbae, Al Hussein, Khalid, Miqdad, Abeer M, Al Rasheed, Abdullah K, Alazami, Anas M, Alorainy, Ibrahim A, Alkuraya, Fowzan S
Publicado 2012

Ancient founder mutation in RUBCN: a second unrelated family confirms Salih ataxia (SCAR15)

por Seidahmed, Mohammed Z., Hamad, Muddathir H., AlBakheet, Albandary, Elmalik, Salah A., AlDrees, Abdulmajeed, Al-Sufayan, Jumanah, Alorainy, Ibrahim, Ghozzi, Ibrahim M., Colak, Dilek, Salih, Mustafa A., Kaya, Namik
Publicado 2020

A heterozygous mutation in the CCDC88C gene likely causes early-onset pure hereditary spastic paraplegia: a case report

por Yahia, Ashraf, Chen, Zhefan Stephen, Ahmed, Ammar E., Emad, Sara, Adil, Rawaa, Abubaker, Rayan, Taha, Shaimaa Omer M. A., Salih, Mustafa A., Elsayed, Liena, Chan, Ho Yin Edwin, Stevanin, Giovanni
Publicado 2021

Hyperekplexia, microcephaly and simplified gyral pattern caused by novel ASNS mutations, case report

por Seidahmed, Mohammed Zain, Salih, Mustafa A., Abdulbasit, Omer B., Samadi, Abdulmohsen, Al Hussien, Khalid, Miqdad, Abeer M., Biary, Maha S., Alazami, Anas M., Alorainy, Ibrahim A., Kabiraj, Mohammad M., Shaheen, Ranad, Alkuraya, Fowzan S.
Publicado 2016

First report of two successive deletions on chromosome 15q13 cytogenetic bands in a boy and girl: additional data to 15q13.3 syndrome with a report of high IQ patient

por Alsagob, Maysoon, Salih, Mustafa A., Hamad, Muddathir H. A., Al-Yafee, Yusra, Al-Zahrani, Jawaher, Al-Bakheet, Albandary, Nester, Michael, Sakati, Nadia, Wakil, Salma M., AlOdaib, Ali, Colak, Dilek, Kaya, Namik
Publicado 2019

Molecular and neurological characterizations of three Saudi families with lipoid proteinosis

por Salih, Mustafa A, Abu-Amero, Khaled K, Alrasheed, Saleh, Alorainy, Ibrahim A, Liu, Lu, McGrath, John A, Van Maldergem, Lionel, Al-Fakey, Yasser H, AlSuhaibani, Adel H, Oystreck, Darren T, Bosley, Thomas M
Publicado 2011

Mutation in GM2A Leads to a Progressive Chorea-dementia Syndrome

por Salih, Mustafa A., Seidahmed, Mohammed Z., El Khashab, Heba Y., Hamad, Muddathir H. A., Bosley, Thomas M., Burn, Sabrina, Myers, Angela, Landsverk, Megan L., Crotwell, Patricia L., Bilguvar, Kaya, Mane, Shrikant, Kruer, Michael C.
Publicado 2015