Zobrazeno 1 - 10
of 222
pro vyhledávání: '"Lactic Acidosis and Stroke-like Episodes"'
Publikováno v:
Journal of Diabetology, Vol 14, Iss 3, Pp 173-176 (2023)
Maternally inherited diabetes and deafness (MIDD) is a rare subtype of diabetes with a prevalence of up to 1% globally but often missed if not suspected. We present a case of MIDD and a thorough review of the literature related to it. The phenotypic
Externí odkaz:
https://doaj.org/article/a0e8144bf36a4277b26145b94a5ef64a
Publikováno v:
American Journal of Ophthalmology Case Reports, Vol 26, Iss , Pp 101411- (2022)
Retro-mode illumination imaging can provide good visualization of chorio-retinal atrophy and of the retinal pigment epithelial alterations occurring in m.3243A > G associated retinopathy.
Externí odkaz:
https://doaj.org/article/678670f2d2734495bbe5ce1a4e24867a
Publikováno v:
Frontiers in Neurology, Vol 13 (2022)
Mitochondrial myopathy encephalopathy lactic acidosis and stroke-like episodes (MELAS) is an important cause of stroke-mimicking diseases that predominantly affect patients before 40 years of age. MELAS results from gene mutations in either mitochond
Externí odkaz:
https://doaj.org/article/873eccf7fc9647299572fa43e40df6da
General anesthesia with remimazolam in a patient with mitochondrial encephalomyopathy: a case report
Publikováno v:
JA Clinical Reports, Vol 7, Iss 1, Pp 1-3 (2021)
Abstract Background Systemic anesthetic management of patients with mitochondrial disease requires careful preoperative preparation to administer adequate anesthesia and address potential disease-related complications. The appropriate general anesthe
Externí odkaz:
https://doaj.org/article/7a9c7d29c4fb42c5b91a8d7ec86e38dc
Autor:
Mai Fukuda, Yoshiro Nagao
Publikováno v:
Journal of Medical Case Reports, Vol 13, Iss 1, Pp 1-7 (2019)
Abstract Background Maternally inherited diabetes and deafness, and mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes are examples of mitochondrial diseases that are relatively common in the adult population. Mitochond
Externí odkaz:
https://doaj.org/article/be01e598b7a5478a82221107781546e1
Autor:
Durjoy Lahiri, Vishal Madhukar Sawale, Subhadeep Banerjee, Souvik Dubey, Biman Kanti Roy, Shyamal Kumar Das
Publikováno v:
Journal of Medical Case Reports, Vol 13, Iss 1, Pp 1-5 (2019)
Abstract Background Mitochondrial encephalopathy, lactic acidosis, and stroke-like episodes, the most common maternally inherited mitochondrial disease, can present with a wide range of neurological manifestations including both central and periphera
Externí odkaz:
https://doaj.org/article/bb4b471c846e48f5bed3feb5dbde6e61
Publikováno v:
Clinical Interventions in Aging, Vol Volume 13, Pp 2421-2424 (2018)
Gao-Li Fang,1 Yang Zheng,2 Yin-Xi Zhang2 1Department of Neurology, Hangzhou Red Cross Hospital, Hangzhou, China; 2Department of Neurology, Second Affiliated Hospital, School of Medicine, Zhejiang University, Hangzhou, China Abstract: Few cases of mit
Externí odkaz:
https://doaj.org/article/c3ffd80792d146e7ab960778ac8f26ec
Akademický článek
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Autor:
Olukorede, Opeoluwa
Mitochondrial diseases are caused by gene mutations in either mitochondrial DNA (mtDNA) or nuclear DNA (nDNA) and they are among one of the most common forms of inherited disorders. It is estimated that 1 out of every 5000 individuals will develop a
Externí odkaz:
https://hdl.handle.net/2144/47456
Publikováno v:
Frontiers in Neurology, Vol 9 (2018)
Background: Analysis of serum biomarkers and magnetic resonance spectroscopy (MRS) are useful for monitoring disease progression in patients with mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes (MELAS). We evaluated the cor
Externí odkaz:
https://doaj.org/article/bd583646388640938f10a2aadde0912c