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Optimised power harvesting by controlling the pressure applied to molecular junctions.

Wang X, Ismael A, Almutlg A, Alshammari M, Al-Jobory A, Alshehab A, Bennett TLR, Wilkinson LA, Cohen LF, Long NJ, Robinson BJ, Lambert C. Wang X, et al. Among authors: alshehab a. Chem Sci. 2021 Mar 4;12(14):5230-5235. doi: 10.1039/d1sc00672j. Chem Sci. 2021. PMID: 34163759 Free PMC article.

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Determining the knowledge of primary healthcare (PHC) physicians and factors influencing practices in the implementation of the catch-up vaccination program in PHC clinics in Dammam, Saudi Arabia.

AlFaraj RS, ALShehab A, Latif SA, Al Fraihi KJ. AlFaraj RS, et al. Among authors: alshehab a. Saudi Med J. 2020 Jun;41(6):645-651. doi: 10.15537/smj.2020.6.25116. Saudi Med J. 2020. PMID: 32518933 Free PMC article.

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Multiple sclerosis in Arabs in Jordan.

al-Din AS, el-Khateeb M, Kurdi A, Mubaidin A, Wriekat A, al-Shehab A, Khalil RW. al-Din AS, et al. J Neurol Sci. 1995 Aug;131(2):144-9. doi: 10.1016/0022-510x(95)00092-g. J Neurol Sci. 1995. PMID: 7595639

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Chromosome 17p-linked myasthenias stem from defects in the acetylcholine receptor epsilon-subunit gene.

Middleton L, Ohno K, Christodoulou K, Brengman J, Milone M, Neocleous V, Serdaroğlu P, Deymeer F, Ozdemir C, Mubaidin A, Horany K, Al-Shehab A, Mavromatis I, Mylonas I, Tsingis M, Zamba E, Pantzaris M, Kyriallis K, Engel AG. Middleton L, et al. Neurology. 1999 Sep 22;53(5):1076-82. doi: 10.1212/wnl.53.5.1076. Neurology. 1999. PMID: 10496269

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A study on intrabody communication for personal healthcare monitoring system.

Alshehab A, Kobayashi N, Ruiz J, Kikuchi R, Shimamoto S, Ishibashi H. Alshehab A, et al. Telemed J E Health. 2008 Oct;14(8):851-7. doi: 10.1089/tmj.2008.0102. Telemed J E Health. 2008. PMID: 18954257

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Effect of bristle stiffness of manual toothbrushes on normal and demineralized human enamel-An in vitro profilometric study.

AlShehab AH, AlHazoom AA, Alowa MH, AlAli HA, Abdulmohsen AA, Farooq I. AlShehab AH, et al. Int J Dent Hyg. 2018 May;16(2):e128-e132. doi: 10.1111/idh.12332. Epub 2018 Feb 19. Int J Dent Hyg. 2018. PMID: 29457353

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Mapping of the familial infantile myasthenia (congenital myasthenic syndrome type Ia) gene to chromosome 17p with evidence of genetic homogeneity.

Christodoulou K, Tsingis M, Deymeer F, Serdaroglu P, Ozdemir C, Al-Shehab A, Bairactaris C, Mavromatis I, Mylonas I, Evoli A, Kyriallis K, Middleton LT. Christodoulou K, et al. Hum Mol Genet. 1997 Apr;6(4):635-40. doi: 10.1093/hmg/6.4.635. Hum Mol Genet. 1997. PMID: 9097970

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Hyperexcitability of cutaneous afferents during the supernormal period. Relevance to paraesthesiae.

Ng A, Burke D, Al-Shehab A. Ng A, et al. Brain. 1987 Aug;110 ( Pt 4):1015-31. doi: 10.1093/brain/110.4.1015. Brain. 1987. PMID: 3651792

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Congenital myasthenic syndrome. (CMS) type Ia. Clinical and genetic diversity.

Middleton LT, Christodoulou K, Deymeer F, Serdaroglu P, Ozdemir C, al-Qudah AK, al-Shehab A, Mavromatis I, Mylonas I, Evoli A, Tsingis M, Zamba E, Kyriallis K. Middleton LT, et al. Ann N Y Acad Sci. 1998 May 13;841:157-66. doi: 10.1111/j.1749-6632.1998.tb10922.x. Ann N Y Acad Sci. 1998. PMID: 9668234 No abstract available.

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