نتایج جستجو برای: mitochondrial myopathies

تعداد نتایج: 134607  

Journal: :Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease 1995

Journal: :Biophysical journal 2013
Salil P Desai Sangeeta N Bhatia Mehmet Toner Daniel Irimia

During cancer cell invasion, faster moving cancer cells play a dominant role by invading further and metastasizing earlier. Despite the importance of these outlier cells, the source of heterogeneity in their migratory behavior remains poorly understood. Here, we show that anterior localization of mitochondria, in between the nucleus and the leading edge of migrating epithelial cancer cells, cor...

2017
Qiang Zheng Penghui Wei Jinfeng Zhou Haipeng Zhou Fucheng Ji Wenxi Tang Jianjun Li

BACKGROUND Mitochondrial myopathies represent a group of disorders caused by mitochondrial defects that disrupt energy production. Most patients have issues from infancy to early childhood. Pregnancy in women with mitochondrial myopathy is uncommon and the management for these parturients is full of challenges. CASE PRESENTATION A 36-year-old woman with mitochondrial myopathy was scheduled fo...

Journal: :Canadian journal of anaesthesia = Journal canadien d'anesthesie 1996
O P Rosaeg S Morrison J P MacLeod

PURPOSE We describe the anaesthetic management for Caesarean section in a parturient with a defect in complex III of the respiratory chain who had increased lactate concentrations at rest and with exercise. CLINICAL FEATURES We administered effective epidural anaesthesia with lidocaine for Caesarean delivery. The serum lactate concentration was less than the preoperative value both during and...

2013
Sally Spendiff Mojgan Reza Julie L. Murphy Grainne Gorman Emma L. Blakely Robert W. Taylor Rita Horvath Georgia Campbell Jane Newman Hanns Lochmüller Doug M. Turnbull

Progressive myopathy is a major clinical feature of patients with mitochondrial DNA (mtDNA) disease. There is limited treatment available for these patients although exercise and other approaches to activate muscle stem cells (satellite cells) have been proposed. The majority of mtDNA defects are heteroplasmic (a mixture of mutated and wild-type mtDNA present within the muscle) with high levels...

2014
Maurizio Moggio Irene Colombo Lorenzo Peverelli Luisa Villa Rubjona Xhani Silvia Testolin Salvatore Di Mauro Monica Sciacco

Mitochondrial diseases are a heterogeneous group of progressive, genetically transmitted, multisystem disorders caused by impaired mitochondrial function. The disease course for individuals with mitochondrial myopathies varies greatly from patient to patient because disease progression largely depends on the type of disease and on the degree of involvement of various organs which makes the prog...

2016
Ossama K. Abou Hassan Mohamad Karnib Riyad El-Khoury Georges Nemer Mamdouha Ahdab-Barmada Pierre BouKhalil

The recent rise in the use of linezolid to treat a variety of resistant pathogens has uncovered many side effects. Some patients develop lactic acidosis, myelosuppression, optic or peripheral neuropathies, and myopathies. We evaluated an elderly patient who presented to the Emergency Room with linezolid toxicity and a novel neurologic complication characterized by bilateral globi pallidi necros...

Journal: :Nucleic acids research 1989
I J Holt A E Harding J A Morgan-Hughes

Forty per cent of patients with mitochondrial myopathies, a diverse group of multisystem diseases predominantly affecting skeletal muscle and the brain, have large deletions of a proportion of muscle mitochondrial DNA (mt DNA). These appeared to be identical in 13 of 28 cases, contained within the region 8286-13595 bp. Analysis of the deletion junction in two cases showed a 13 nucleotide sequen...

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