Mustafa A M Salih
Overview
Explore the profile of Mustafa A M Salih including associated specialties, affiliations and a list of published articles.
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25
Citations
1192
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Recent Articles
1.
Elsayed L, Mohammed I, Hamed A, Elseed M, Salih M, Yahia A, et al.
Front Neurol
. 2020 Nov;
11:569996.
PMID: 33193012
Arginases catalyze the last step in the urea cycle. Hyperargininemia, a rare autosomal-recessive disorder of the urea cycle, presents after the first year of age with regression of milestones and...
2.
Elsayed L, Mohammed I, Hamed A, Elseed M, Salih M, Yahia A, et al.
BMC Med Genet
. 2018 May;
19(1):72.
PMID: 29739362
Background: Infantile neuroaxonal dystrophy (INAD) is a rare hereditary neurological disorder caused by mutations in PLA2G6. The disease commonly affects children below 3 years of age and presents with delay...
3.
Elsayed L, Mohammed I, Hamed A, Elseed M, Johnson A, Mairey M, et al.
Eur J Hum Genet
. 2016 Sep;
25(1):100-110.
PMID: 27601211
Hereditary spastic paraplegias (HSP) are the second most common type of motor neuron disease recognized worldwide. We investigated a total of 25 consanguineous families from Sudan. We used next-generation sequencing...
4.
Salih M, Murshid W, Mohamed A, Ignacio L, de Jesus J, Baabbad R, et al.
Sudan J Paediatr
. 2016 Aug;
14(2):49-60.
PMID: 27493405
Both genetic and non-genetic environmental factors are involved in the etiology of neural tube defects (NTD) which affect 0.5-2/1000 pregnancies worldwide. This study aimed to explore the risk factors for...
5.
Suliman O, Salih M, Karrar Z, Mohammed A, Helsing C
Sudan J Paediatr
. 2016 Aug;
11(2):32-42.
PMID: 27493317
A hospital-based case control study was carried out to determine the pattern of infections and immunoblobulin levels in Sudanese children with severe protein energy malnutrition (PEM). The pre-dietary rehabilitation levels...
6.
Suliman O, Salih M, Karrar Z, Mohammed A, Helsing C
Sudan J Paediatr
. 2016 Aug;
11(1):48-59.
PMID: 27493306
The pre-dietary rehabilitation levels of acute phase proteins (APP) namely, alpha-1-antitrypsin (AAT), orosomucoid (ORO), haptoglobin (HAP), fibrinogen (FIB) and C-reactive protein (CRP) in the plasma of Sudanese children with severe...
7.
Elsayed L, Drouet V, Usenko T, Mohammed I, Hamed A, Elseed M, et al.
Ann Neurol
. 2015 Dec;
79(2):335-7.
PMID: 26703368
No abstract available.
8.
Mohamed S, Osman A, Al Jurayyan N, Al Nemri A, Salih M
BMC Res Notes
. 2014 Mar;
7:184.
PMID: 24674575
Background: Congenital toxoplasmosis has a wide range of presentation at birth varying from severe neurological features such as hydrocephalus and chorioretinitis to a well appearing baby, who may develop complications...
9.
Tesson C, Nawara M, Salih M, Rossignol R, Zaki M, Al Balwi M, et al.
Am J Hum Genet
. 2012 Nov;
91(6):1051-64.
PMID: 23176821
Hereditary spastic paraplegia (HSP) is considered one of the most heterogeneous groups of neurological disorders, both clinically and genetically. The disease comprises pure and complex forms that clinically include slowly...
10.
Abu-Amero K, Kondkar A, Salih M, Alorainy I, Khan A, Oystreck D, et al.
Ophthalmic Genet
. 2012 Sep;
34(1-2):90-6.
PMID: 22950449
Purpose: To evaluate possible monogenic and chromosomal anomalies in a patient with bilateral Duane retraction syndrome and hearing impairment resulting in a phenotype resembling the HOXA1 spectrum disorder. Methods: Sequencing...