Salih MA - Search Results

1

Hemiconvulsion-hemiplegia-epilepsy syndrome. A clinical, electroencephalographic and neuroradiological study.

Salih MA, Kabiraj M, Al-Jarallah AS, El Desouki M, Othman S, Palkar VA. Salih MA, et al. Childs Nerv Syst. 1997 May;13(5):257-63. doi: 10.1007/s003810050079. Childs Nerv Syst. 1997. PMID: 9224914

2

Childhood neuromuscular disorders: a decade's experience in Saudi Arabia.

Salih MA, Mahdi AH, al-Jarallah AA, al Jarallah AS, al-Saadi M, Hafeez MA, Aziz SA. Salih MA, et al. Ann Trop Paediatr. 1996 Dec;16(4):271-80. doi: 10.1080/02724936.1996.11747838. Ann Trop Paediatr. 1996. PMID: 8985523

3

Autosomal recessive hereditary neuropathy with focally folded myelin sheaths and linked to chromosome 11q23: a distinct and homogeneous entity.

Salih MA, Maisonobe T, Kabiraj M, al Rayess M, al-Turaiki MH, Akbar M, Tahan A, Urtizberea JA, Grid D, Hamadouche T, Guilbot A, Brice A, Leguern E. Salih MA, et al. Neuromuscul Disord. 2000 Jan;10(1):10-5. doi: 10.1016/s0960-8966(99)00057-7. Neuromuscul Disord. 2000. PMID: 10677858

4

Stroke in Saudi children. Epidemiology, clinical features and risk factors.

Salih MA, Abdel-Gader AG, Al-Jarallah AA, Kentab AY, Alorainy IA, Hassan HH, Bahakim HM, Kurbaan KM, Zahraa JN, Al-Nasser MN, Nasir AA, Khoja WA, Kabiraj MM. Salih MA, et al. Saudi Med J. 2006 Mar;27 Suppl 1:S12-20. Saudi Med J. 2006. PMID: 16532126

5

Cardiac diseases as a risk factor for stroke in Saudi children.

Salih MA, Al-Jarallah AS, Abdel-Gader AG, Al-Jarallah AA, Al-Saadi MM, Kentab AY, Alorainy IA, Hassan HH. Salih MA, et al. Saudi Med J. 2006 Mar;27 Suppl 1:S61-8. Saudi Med J. 2006. PMID: 16532133

6

Moyamoya syndrome as a risk factor for stroke in Saudi children. Novel and usual associations.

Salih MA, Murshid WR, Al-Salman MM, Abdel-Gader AG, Al-Jarallah AA, Alorainy IA, Hassan HH, Kentab AY, Van Maldergem L, Othman SA, El-Desouki MI, Elgamal EA. Salih MA, et al. Saudi Med J. 2006 Mar;27 Suppl 1:S69-80. Saudi Med J. 2006. PMID: 16532134

7

Nonketotic hyperglycinemia: A life-threatening disorder in Saudi newborns.

Haider N, Salih MA, Al-Rasheed S, Al-Mofada S, Krahn PM, Kabiraj M. Haider N, et al. Among authors: salih ma. Ann Saudi Med. 1996 Jul;16(4):400-4. doi: 10.5144/0256-4947.1996.400. Ann Saudi Med. 1996. PMID: 17372475 Free article.

8

Congenital myasthenic syndrome due to homozygous CHRNE mutations: report of patients in Arabia.

Salih MA, Oystreck DT, Al-Faky YH, Kabiraj M, Omer MI, Subahi EM, Beeson D, Abu-Amero KK, Bosley TM. Salih MA, et al. J Neuroophthalmol. 2011 Mar;31(1):42-7. doi: 10.1097/WNO.0b013e3181f50bea. J Neuroophthalmol. 2011. PMID: 21150643

9

New findings in a global approach to dissect the whole phenotype of PLA2G6 gene mutations.

Salih MA, Mundwiller E, Khan AO, AlDrees A, Elmalik SA, Hassan HH, Al-Owain M, Alkhalidi HM, Katona I, Kabiraj MM, Chrast R, Kentab AY, Alzaidan H, Rodenburg RJ, Bosley TM, Weis J, Koenig M, Stevanin G, Azzedine H. Salih MA, et al. PLoS One. 2013 Oct 9;8(10):e76831. doi: 10.1371/journal.pone.0076831. eCollection 2013. PLoS One. 2013. PMID: 24130795 Free PMC article.

10

C19orf12 mutation leads to a pallido-pyramidal syndrome.

Kruer MC, Salih MA, Mooney C, Alzahrani J, Elmalik SA, Kabiraj MM, Khan AO, Paudel R, Houlden H, Azzedine H, Alkuraya F. Kruer MC, et al. Among authors: salih ma. Gene. 2014 Mar 10;537(2):352-6. doi: 10.1016/j.gene.2013.11.039. Epub 2013 Dec 17. Gene. 2014. PMID: 24361204 Free PMC article.

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