Salih MA - Search Results

1

Clinical characterization of the HOXA1 syndrome BSAS variant.

Bosley TM, Salih MA, Alorainy IA, Oystreck DT, Nester M, Abu-Amero KK, Tischfield MA, Engle EC. Bosley TM, et al. Among authors: salih ma. Neurology. 2007 Sep 18;69(12):1245-53. doi: 10.1212/01.wnl.0000276947.59704.cf. Neurology. 2007. PMID: 17875913 Free PMC article.

2

Clinical and molecular pathological features of severe childhood autosomal recessive muscular dystrophy in Saudi Arabia.

Salih MA, Mahdi AH, al-Rikabi AC, al-Bunyan M, Roberds SL, Anderson RD, Campbell KP. Salih MA, et al. Dev Med Child Neurol. 1996 Mar;38(3):262-70. doi: 10.1111/j.1469-8749.1996.tb15089.x. Dev Med Child Neurol. 1996. PMID: 8631523

3

Familial horizontal gaze palsy with progressive scoliosis maps to chromosome 11q23-25.

Jen J, Coulin CJ, Bosley TM, Salih MA, Sabatti C, Nelson SF, Baloh RW. Jen J, et al. Among authors: salih ma. Neurology. 2002 Aug 13;59(3):432-5. doi: 10.1212/wnl.59.3.432. Neurology. 2002. PMID: 12177379

4

Mutations in a human ROBO gene disrupt hindbrain axon pathway crossing and morphogenesis.

Jen JC, Chan WM, Bosley TM, Wan J, Carr JR, Rüb U, Shattuck D, Salamon G, Kudo LC, Ou J, Lin DD, Salih MA, Kansu T, Al Dhalaan H, Al Zayed Z, MacDonald DB, Stigsby B, Plaitakis A, Dretakis EK, Gottlob I, Pieh C, Traboulsi EI, Wang Q, Wang L, Andrews C, Yamada K, Demer JL, Karim S, Alger JR, Geschwind DH, Deller T, Sicotte NL, Nelson SF, Baloh RW, Engle EC. Jen JC, et al. Among authors: salih ma. Science. 2004 Jun 4;304(5676):1509-13. doi: 10.1126/science.1096437. Epub 2004 Apr 22. Science. 2004. PMID: 15105459 Free PMC article.

5

Neurologic features of horizontal gaze palsy and progressive scoliosis with mutations in ROBO3.

Bosley TM, Salih MA, Jen JC, Lin DD, Oystreck D, Abu-Amero KK, MacDonald DB, al Zayed Z, al Dhalaan H, Kansu T, Stigsby B, Baloh RW. Bosley TM, et al. Among authors: salih ma. Neurology. 2005 Apr 12;64(7):1196-203. doi: 10.1212/01.WNL.0000156349.01765.2B. Neurology. 2005. PMID: 15824346

6

Homozygous HOXA1 mutations disrupt human brainstem, inner ear, cardiovascular and cognitive development.

Tischfield MA, Bosley TM, Salih MA, Alorainy IA, Sener EC, Nester MJ, Oystreck DT, Chan WM, Andrews C, Erickson RP, Engle EC. Tischfield MA, et al. Among authors: salih ma. Nat Genet. 2005 Oct;37(10):1035-7. doi: 10.1038/ng1636. Epub 2005 Sep 11. Nat Genet. 2005. PMID: 16155570

7

Brain stem and cerebellar findings in Joubert syndrome.

Alorainy IA, Sabir S, Seidahmed MZ, Farooqu HA, Salih MA. Alorainy IA, et al. Among authors: salih ma. J Comput Assist Tomogr. 2006 Jan-Feb;30(1):116-21. doi: 10.1097/01.rct.0000191681.05473.13. J Comput Assist Tomogr. 2006. PMID: 16365585

8

Stroke from cervicocephalic arterial dissection in Saudi children.

Salih MA, Al-Jarallah AA, Al-Salman MM, Alorainy IA, Hassan HH. Salih MA, et al. Saudi Med J. 2006 Mar;27 Suppl 1:S103-7. Saudi Med J. 2006. PMID: 16532124

9

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

10

Hematologic risk factors for stroke in Saudi children.

Salih MA, Abdel-Gader AG, Al-Jarallah AA, Kentab AY, Alorainy IA, Hassan HH, Bahakim HM, Kurbaan KM, Zahraa JN, Murshid WR, El-Hazmi MA, Khoja WA. Salih MA, et al. Saudi Med J. 2006 Mar;27 Suppl 1:S21-34. Saudi Med J. 2006. PMID: 16532128

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