- A novel mutation in the DNMT1 gene in a patient presenting with pure cerebellar ataxia
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Algahtani , Shirah B
- KMID: 2401809
- J Genet Med.
- 2017 Dec;14(2):71-74.
- doi: 10.5734/JGM.2017.14.2.71
Mutations in the DNA methyltransferase 1 gene (DNMT1) were reported to cause two phenotypes: OMIM 604121 and OMIM 614116. The first phenotype includes autosomal dominant cerebellar ataxia, deafness, and narcolepsy,... -
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- Thromboprophylaxis after bariatric surgery
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Almarshad , Almegren M, Alshuaibi , Alobaodi N, Almutawa A, Basunbl H, AlGahtani , Al Rawahi
- KMID: 2472007
- Blood Res.
- 2020 Mar;55(1):44-48.
- doi: 10.5045/br.2020.55.1.44
BACKGROUND: Venous thromboembolism (VTE), which includes deep vein thrombosis (DVT) and pulmonary embolism (PE), is a known cause of morbidity and mortality after bariatric surgery. However, the data concerning appropriate... -
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- Neurological Manifestations of Acute Posterior Multifocal Placoid Pigment Epitheliopathy
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Algahtani , Alkhotani , Shirah B
- KMID: 2385111
- J Clin Neurol.
- 2016 Oct;12(4):460-467.
- doi: 10.3988/jcn.2016.12.4.460
BACKGROUND AND PURPOSE: Acute posterior multifocal placoid pigment epitheliopathy (APMPPE) is an immune-mediated chorioretinal disease that causes acute visual symptoms with characteristic ophthalmoscopic findings. Neurological complications are rarely reported in... -
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