Salih MA - Search Results

1

Accelerating novel candidate gene discovery in neurogenetic disorders via whole-exome sequencing of prescreened multiplex consanguineous families.

Alazami AM, Patel N, Shamseldin HE, Anazi S, Al-Dosari MS, Alzahrani F, Hijazi H, Alshammari M, Aldahmesh MA, Salih MA, Faqeih E, Alhashem A, Bashiri FA, Al-Owain M, Kentab AY, Sogaty S, Al Tala S, Temsah MH, Tulbah M, Aljelaify RF, Alshahwan SA, Seidahmed MZ, Alhadid AA, Aldhalaan H, AlQallaf F, Kurdi W, Alfadhel M, Babay Z, Alsogheer M, Kaya N, Al-Hassnan ZN, Abdel-Salam GM, Al-Sannaa N, Al Mutairi F, El Khashab HY, Bohlega S, Jia X, Nguyen HC, Hammami R, Adly N, Mohamed JY, Abdulwahab F, Ibrahim N, Naim EA, Al-Younes B, Meyer BF, Hashem M, Shaheen R, Xiong Y, Abouelhoda M, Aldeeri AA, Monies DM, Alkuraya FS. Alazami AM, et al. Among authors: salih ma. Cell Rep. 2015 Jan 13;10(2):148-61. doi: 10.1016/j.celrep.2014.12.015. Epub 2014 Dec 31. Cell Rep. 2015. PMID: 25558065 Free article.

2

Lethal congenital muscular dystrophy in two sibs with arthrogryposis multiplex: new entity or variant of cobblestone lissencephaly syndrome?

Seidahmed MZ, Sunada Y, Ozo CO, Hamid F, Campbell KP, Salih MA. Seidahmed MZ, et al. Among authors: salih ma. Neuropediatrics. 1996 Dec;27(6):305-10. doi: 10.1055/s-2007-973799. Neuropediatrics. 1996. PMID: 9050048

3

Case of partial trisomy 2q3 with clinical manifestations of Marshall-Smith syndrome.

Seidahmed MZ, Rooney DE, Salih MA, Basit OB, Shaheed MM, Abdullah MA, Abomelha A. Seidahmed MZ, et al. Among authors: salih ma. Am J Med Genet. 1999 Jul 16;85(2):185-8. doi: 10.1002/(sici)1096-8628(19990716)85:2<185::aid-ajmg16>3.0.co;2-w. Am J Med Genet. 1999. PMID: 10406675 Review.

4

Determination of urinary S-sulphocysteine, xanthine and hypoxanthine by liquid chromatography-electrospray tandem mass spectrometry.

Rashed MS, Saadallah AA, Rahbeeni Z, Eyaid W, Seidahmed MZ, Al-Shahwan S, Salih MA, Osman ME, Al-Amoudi M, Al-Ahaidib L, Jacob M. Rashed MS, et al. Among authors: salih ma. Biomed Chromatogr. 2005 Apr;19(3):223-30. doi: 10.1002/bmc.439. Biomed Chromatogr. 2005. PMID: 15558695

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

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

7

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

8

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

9

Perinatal stroke in Saudi children. Clinical features and risk factors.

Salih MA, Abdel-Gader AG, Al-Jarallah AA, Kentab AY, Alorainy IA, Hassan HH, Al-Nasser MN. Salih MA, et al. Saudi Med J. 2006 Mar;27 Suppl 1:S35-40. Saudi Med J. 2006. PMID: 16532129

10

Infectious and inflammatory disorders of the circulatory system as risk factors for stroke in Saudi children.

Salih MA, Abdel-Gader AG, Al-Jarallah AA, Kentab AY, Gadelrab MO, Alorainy IA, Hassan HH, Zahraa JN. Salih MA, et al. Saudi Med J. 2006 Mar;27 Suppl 1:S41-52. Saudi Med J. 2006. PMID: 16532131

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