Neural tube defects: Challenging, yet preventable

Por Salih, Mustafa A.
Publicado no Saudi Med J (2014)

Message from the Guest Editor

Por Salih, Mustafa A.
Publicado no Saudi Med J (2014)

Classification, clinical features, and genetics of neural tube defects

Por Salih, Mustafa A., Murshid, Waleed R., Seidahmed, Mohammed Z.
Publicado no Saudi Med J (2014)

Epidemiology, prenatal management, and prevention of neural tube defects

Por Salih, Mustafa A., Murshid, Waleed R., Seidahmed, Mohammed Z.
Publicado no Saudi Med J (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 no Saudi Med J (2015)

Acute phase reactants in Sudanese children with severe protein-energy malnutrition*

Por Suliman, Omer S. M., Salih, Mustafa A. M., Karrar, Zein A., Mohammed, Abdelrahim O., Helsing, Chrestover
Publicado no Sudan J Paediatr (2011)

Infection and immunoglobulin levels in Sudanese children with severe protein-energy malnutrition*

Por Suliman, Omer S. M., Salih, Mustafa A. M., Karrar, Zein A., Mohammed, Abdelrahim O., Helsing, Chrestover
Publicado no Sudan J Paediatr (2011)

Sturge-Weber syndrome: Continued vigilance is needed

Por Hassan, Saeed, Babiker, Amir, Bashiri, Fahad A, Hassan, Hamdi H, Husseini, Maha El, Salih, Mustafa A
Publicado no Sudan J Paediatr (2015)

Acute poisoning in a child following topical treatment of head lice (pediculosis capitis) with an organophosphate pesticide

Por Hamad, Muddathir H, Adeel, Ahmed Awad, Alhaboob, Ali Abdu N, Ashri, Ahmed M, Salih, Mustafa A
Publicado no Sudan J Paediatr (2016)

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 no Saudi Med J (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 em 2010

Cerebral Iron Accumulation Is Not a Major Feature of FA2H/SPG35

Por Marelli, Cecilia, Salih, Mustafa A., Nguyen, Karine, Mallaret, Martial, Leboucq, Nicolas, Hassan, Hamdy H., Drouot, Nathalie, Labauge, Pierre, Koenig, Michel
Publicado no Mov Disord Clin Pract (2015)

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 no Saudi Med J (2014)

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 no Saudi Med J (2014)

Risk factors for neural tube defects in Riyadh City, Saudi Arabia: Case-control study

Por Salih, Mustafa A M, Murshid, Waleed R, Mohamed, Ashry Gad, Ignacio, Lena C, de Jesus, Julie E, Baabbad, Rubana, El Bushra, Hassan M
Publicado no Sudan J Paediatr (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 no Saudi Med J (2014)

Idiopathic intracranial hypertension in children: Diagnostic and management approach

Por Albakr, Abdulrahman, Hamad, Muddathir H, Alwadei, Ali H, Bashiri, Fahad A, Hassan, Hamdy H, Idris, Hiyam, Hassan, Saeed, Muayqil, Taim, Altweijri, Ikhlass, Salih, Mustafa A
Publicado no Sudan J Paediatr (2016)

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 no Saudi Med J (2014)

The Clinical Spectrum of Homozygous HOXA1 Mutations

Por Bosley, Thomas M., Alorainy, Ibrahim A., Salih, Mustafa A., Aldhalaan, Hesham M., Abu-Amero, Khaled K., Oystreck, Darren T., Tischfield, Max A, Engle, Elizabeth C., Erickson, Robert P.
Publicado em 2008

C19orf12 mutation leads to Karak pallido-pyramidal syndrome

Por Kruer, Michael C., Salih, Mustafa A., Mooney, Catherine, Alzahrani, Jawahir, Elmalik, Salah A., Kabiraj, Mohammad M., Khan, Arif O., Paudel, Reema, Houlden, Henry, Azzedine, Hamid, Alkuraya, Fowzan
Publicado no Gene (2013)