Výsledky vyhledávání - "Jafri M Abdullah"

Subthalamic Nucleus (STN)-Deep Brain Stimulation Reduces the Power of Mu and Beta Rhythms and Enhances Synchrony at the Motor Cortices in Parkinson's Disease: A Report of Two Cases

Autor: Zaitun Zakaria, Zamzuri Idris, Sanihah Abdul Halim, Abdul Rahman Izaini Ghani, Jafri M Abdullah

Publikováno v: Cureus.

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::4e6d5396f55935e95af76be13f40d7d2
https://doi.org/10.7759/cureus.35057

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Reverse Cervical Lordosis Caused by Giant Vertebral Artery Aneurysm in von Recklinghausen Disease

Autor: Umaira Saleh, Muhammad Ihfaz Ismail, Nur Asma Sapiai, Kok Beng Loh, Nasser Abd Wahab, Jafri M Abdullah

Publikováno v: Cureus.

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::7279530e3f23927dde4472795d43fb2b
https://doi.org/10.7759/cureus.29795

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Development of a Brain Glutamate Microbiosensor

Autor: Kartika S. Hamdan, Zainiharyati M. Zain, Halim, Mohamed I. A., Jafri M. Abdullah, O'Neill, Robert D.

This work attempts to improve the permselectivity of poly-ortho-phenylenediamine (PPD) coating for glutamate biosensor applications on Pt microelectrode, using constant potential amperometry and cyclic voltammetry. Percentage permeability of the modi

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::244c96345dad88e525ddd62652afad4b

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Platelet alloantigen polymorphism and migraine headaches

Autor: Shalini, Bhaskar, Jafri M, Abdullah

Publikováno v: Neurosciences (Riyadh, Saudi Arabia). 18(2)

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::24acea87f6c0bdcd5c7b8feb592b2ace
https://pubmed.ncbi.nlm.nih.gov/23545624

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Coexistence of CACNA1A, ATP1A2, and KCNN3 gene mutation in migraine patients with human platelet polymorphism

Autor: Shalini, Bhaskar, Jafri M, Abdullah, Mazira M, Ghazali

Publikováno v: Neurosciences (Riyadh, Saudi Arabia). 13(4)

To look for any possible coexistence of CACNA1A, ATP1A2, and KCNN3 gene mutations in migraine patients who had human platelet HPA-1a/1b polymorphism, which is also known as PlA1/A2 polymorphism.The study was carried out at the Neurology Clinic, Hospi

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::e33b6e4ad260e74e284eb1e9479218b7
https://pubmed.ncbi.nlm.nih.gov/21063360

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