Results 11 to 20 of about 12,239 (244)

Pterostichus melas subsp. melas melas (Creutzer 1799 [PDF]

, 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

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

Pathology of mitochondria in MELAS syndrome: an ultrastructural study [PDF]

, 2017
Ultrastructural changes in skeletal muscle biopsy in a 24-year-old female patient with clinically suspected mitochondrial encephalomyopathy lactic acidosis and stroke-like episodes (MELAS) syndrome are presented.
Eliza Lewandowska, Elżbieta Pasennik, Tomasz Stępień, Monika Ołdak, Urszula Lechowicz, Agnieszka Pollak, Paulina Felczak, Iwona Stępniak, Teresa Wierzba-Bobrowicz   +8 more
core   +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

Malaria Panel Assay versus PCR: detection of naturally infected Anopheles melas in a coastal village of Equatorial Guinea. [PDF]

, 2004
BACKGROUND: A study was carried out in a village of the mainland region of Equatorial Guinea in order to ascertain a) which members of Anopheles gambiae complex could be involved in malaria transmission and b) the rate of infectivity for Anopheles melas ...
Ochando, Jordi, Buatiche, Jesús N, Bobuakasi, Leonardo, Micha, Francisco, Benito Agustín, Cano, Jorge, Marta Moreno, Bobuakasi Leonardo, Jesús N Buatiche, Moreno, Marta, Moreno Marta, Ondo, Melchor, Agustín Benito, Leonardo Bobuakasi, Ondo Melchor, Sisinio Nzambo, Melchor Ondo, Nzambo, Sisinio, Micha Francisco, Nzambo Sisinio, Cano Jorge, Benito, Agustín, Francisco Micha, Buatiche Jesús N, Jorge Cano   +24 more
core   +1 more source

Patent foramen ovale leading to mismanagement in a mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke‐like episodes patient

Clinical Case Reports, 2023
Key Clinical Message The stroke‐like episodes and brain MRI lesions in MELAS usually have a nonischemic pattern, are resolved over time, and have a migrating pattern that helps us distinguish them from ischemic cerebral infarcts. Nevertheless, conditions
Mehri Salari, Masoud Etemadifar, Ronak Rashedi, Romina Rashedi   +3 more
doaj   +1 more source