Results 11 to 20 of about 14,094 (239)

Pterostichus melas subsp. melas melas (Creutzer 1799

, 2016
Published as part of Hoess, René, 2016, Interessante Neufunde von Laufkäfern (Coleoptera: Carabidae) aus der Schweiz, pp.
Hoess, René
openaire   +3 more sources

Diagnosis of adult-onset MELAS syndrome in a 63-year-old patient with suspected recurrent strokes – a case report [PDF]

BMC Neurology, 2019
Background Mitochondrial encephalomyopathy, lactic acidosis and stroke-like episodes (MELAS) is a mitochondrial cytopathy caused by mutations in mitochondrial DNA. Clinical manifestation is typically before the age of 40. Case presentation We present the
Tim Sinnecker, Michaela Andelova, Michael Mayr, Stephan Rüegg, Michael Sinnreich, Juergen Hench, Stephan Frank, André Schaller, Christoph Stippich, Jens Wuerfel, Leo H. Bonati   +10 more
doaj   +3 more sources

Based on a Single Case, Cardiopulmonary Training Cannot Be Recommended as Therapy for Hemiparesis in MELAS With Ischemic Stroke. [PDF]

Kaohsiung J Med Sci
The Kaohsiung Journal of Medical Sciences, EarlyView.
Mehri S, Finsterer J.
europepmc   +2 more sources

Labiaticola melas

, 2018
Published as part of Yunakov, Nikolai, Nazarenko, Vitalij, Filimonov, Rostislav & Volovnik, Semyon, 2018, A survey of the weevils of Ukraine (Coleoptera: Curculionoidea), pp.
Yunakov, Nikolai, Nazarenko, Vitalij, Filimonov, Rostislav, Volovnik, Semyon   +3 more
openaire   +3 more sources

Cardiopulmonary Exercise Testing (CPET) Guided Sub-Anaerobic Threshold Rehabilitation in MELAS Syndrome: A Case Report. [PDF]

Kaohsiung J Med Sci
The Kaohsiung Journal of Medical Sciences, EarlyView.
Tsai YL, Cheng KY, Lu YS, Lin KL.
europepmc   +2 more sources

Topological reorganization of brain functional networks in patients with mitochondrial encephalomyopathy with lactic acidosis and stroke‐like episodes

NeuroImage: Clinical, 2020
Mitochondrial encephalomyopathy with lactic acidosis and stroke‐like episodes (MELAS) is a rare maternally inherited genetic disease; however, little is known about its underlying brain basis. Furthermore, the topological organization of brain functional
Rong Wang, Jie Lin, Chong Sun, Bin Hu, Xueling Liu, Daoying Geng, Yuxin Li, Liqin Yang   +7 more
doaj   +1 more source

Stroke-like lesions in mitochondrial disease may resemble ischemic stroke

Journal of Family Medicine and Primary Care, 2021
The patient is a 73-y-male who was referred after a fall without losing consciousness or secessus. Clinical exam revealed disorientation, ophthalmoparesis, hemianopia to the left, left hemineglect, hypoacusis, quadruparesis, general wasting, generally ...
Josef Finsterer
doaj   +1 more source

Clinical Characteristics of Mitochondrial Encephalomyopathy, Lactic Acidosis, and Stroke-Like Episodes

Life, 2021
Mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes (MELAS) syndrome, a maternally inherited mitochondrial disorder, is characterized by its genetic, biochemical and clinical complexity.
Hueng-Chuen Fan, Hsiu-Fen Lee, Chen-Tang Yue, Ching-Shiang Chi   +3 more
doaj   +1 more source

A rare cause of mixed hypertrophic and dilated phenotype cardiomyopathy – the MELAS syndrome

Romanian Journal of Cardiology, 2023
MELAS is a systemic hereditary condition that can present as hypertrophic or mixed hypertrophic and dilated phenotype cardiomyopathy in young individuals, although a late-onset form is also described in the literature.
Casian Mihnea, Dragotoiu Nic, Onciul Sebastian, Popescu Bogdan A., Jurcuţ Ruxandra   +4 more
doaj   +1 more source

Progress in Diagnosing Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-like Episodes

Chinese Medical Journal, 2015
Objective: Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS) is a progressive, multisystem affected mitochondrial disease associated with a number of disease-related defective genes.
Ying-Xin Wang, Wei-Dong Le
doaj   +1 more source