Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Nebiyu Bekele"'
Autor:
Ephrem Fantu, Workagegnehu Hailu, Nebiyu Bekele, Tewodros Tsegaye, Melaku Tadesse, Mezgebu Silamsaw Asres
Publikováno v:
BMC Neurology, Vol 22, Iss 1, Pp 1-8 (2022)
Abstract Background Stroke is one of the most common causes of disability among adults. Post-stroke depression (PSD) is a frequent neuropsychiatric complication in stroke patients. Despite the increasing prevalence of stroke, there is a paucity of da
Externí odkaz:
https://doaj.org/article/076d47d9ab8346a89395920f105eaace
Autor:
Negalgn Byadgie Gelaw, Achenef Asmamaw Muche, Adugnaw Zeleke Alem, Nebiyu Bekele Gebi, Yazachew Moges Chekol, Tigabu Kidie Tesfie, Tsion Mulat Tebeje
Publikováno v:
PLoS ONE, Vol 18, Iss 8, p e0276472 (2023)
BackgroundDiabetic neuropathy is the most common complication in both Type-1 and Type-2 DM patients with more than one half of all patients developing nerve dysfunction in their lifetime. Although, risk prediction model was developed for diabetic neu
Externí odkaz:
https://doaj.org/article/ba3163136a514fc09869b1989fd33efc
Publikováno v:
SAGE Open Medicine, Vol 10 (2022)
Background: Epilepsy is characterized by two or more unprovoked recurrent seizures, which often respond to available antiseizure medications. However, seizure control among epileptic patients in the developing world is low. Factors determining seizur
Externí odkaz:
https://doaj.org/article/305b2be3f286489399bf27ddefd7f947
Publikováno v:
Advances in Hematology, Vol 2021 (2021)
Introduction. Warfarin is a widely used oral anticoagulant in clinical practice. It has variable intraindividual and interindividual dose response and a narrow therapeutic index. Therefore, it requires frequent and regular international normalized ra
Externí odkaz:
https://doaj.org/article/b0e47cc1257a4569aa28b2fb526d80fd
Publikováno v:
Case Reports in Medicine, Vol 2020 (2020)
Background. Wilson’s disease is an inherited autosomal recessive disorder of copper metabolism. Clinical signs, biochemical parameters, histologic findings, and/or ATP7B genetic testing are required to diagnose Wilson’s disease. Case Presentation
Externí odkaz:
https://doaj.org/article/b84a1f7fccae44a6a59bd5fcd75adf32
Autor:
Chekol, Yazachew Moges, Merid, Mehari Woldemariam, Tesema, Getayeneh Antehunegn, Tesfie, Tigabu Kidie, Tebeje, Tsion Mulat, Gelaw, Negalegn Byadgie, Gebi, Nebiyu Bekele, Seretew, Wullo Sisay
Publikováno v:
Degenerative Neurological & Neuromuscular Disease; Dec2023, Vol. 13, p89-110, 22p
Publikováno v:
International Medical Case Reports Journal
Background Neuromyelitis optica spectrum disorder is an autoimmune, astrocytopathic CNS disease, mainly involving the optic nerves, spinal cord, and brain stem regions. The “International Panel for NMOSD Diagnosis (IPND) Diagnostic Criteria” was
Autor:
Negalgn Byadgie Gelaw, Achenef Asmamaw Muche, Adugnaw Zeleke Alem, Nebiyu Bekele Gebi, Yazachew Moges Chekol, Tigabu Kidie Tesfie, Tsion Mulat Tebeje
BackgroundDiabetic neuropathy is the most common complication in both Type-1 and Type-2 DM patients with more than one half of all patients developing nerve dysfunction in their lifetime. Although, risk prediction model was developed for diabetic neu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d0e238883cde4a9e15d8033c1efae20c
https://doi.org/10.1101/2022.10.10.22280924
https://doi.org/10.1101/2022.10.10.22280924
Autor:
Gelaw, Negalgn Byadgie, Muche, Achenef Asmamaw, Alem, Adugnaw Zeleke, Gebi, Nebiyu Bekele, Chekol, Yazachew Moges, Tesfie, Tigabu Kidie, Tebeje, Tsion Mulat
Publikováno v:
PLoS ONE; 8/29/2023, Vol. 18 Issue 8, p1-30, 30p
Publikováno v:
International Medical Case Reports Journal. 13:591-595
Background Paroxysmal sympathetic hyperactivity (PSH) is a neurologic syndrome characterized by paroxysmal and simultaneous occurrence of hypertension, hyperpyrexia, tachycardia, tachypnea, diaphoresis and dystonic posturing due to surge in sympathet