Results 71 to 80 of about 4,757 (204)

Late and Severe Myopathy in a Patient With Glycogenosis VII Worsened by Cyclosporine and Amiodarone

open access: yesFrontiers in Neurology, 2019
Glycogenosis VII (GSD VII) is a rare autosomal recessive glycogen storage disorder caused by mutations in the PFKM gene encoding the phosphofructokinase (PFK) enzyme.
Massimiliano Filosto   +11 more
doaj   +1 more source

Equine paralytic myoglobinuria: etiology, pathogenesis, diagnosis and treatment

open access: yes, 2016
Examined the horse paralytic myoglobinuria, disease etiology, pathogenesis, diagnosis and treatment. described the main diagnostic method aminotransferaze and creatinkinaze research in horses, females and males.
Jakubėnaitė, Dalia
core  

Muscle cell membrane damage by very low serum sodium [PDF]

open access: yesThe Pan African Medical Journal, 2009
A 63-year-old male was admitted with complaints of upper gastrointestinal symptoms with fatigue and myalgia. Investigations revealed severe hyponatremia with elevated creatine phosphokinase levels.
Prem Nair   +4 more
doaj  

Rhabdomyolysis and compartment syndrome in a bodybuilder undergoing minimally invasive cardiac surgery

open access: yesAnnals of Cardiac Anaesthesia, 2017
Rhabdomyolysis is the result of skeletal muscle tissue injury and is characterized by elevated creatine kinase levels, muscle pain, and myoglobinuria. It is caused by crush injuries, hyperthermia, drugs, toxins, and abnormal metabolic states.
Sebastian John Baxter   +2 more
doaj   +1 more source

Association between rapid serum sodium correction and rhabdomyolysis in water intoxication: a retrospective cohort study

open access: yesJournal of Intensive Care, 2017
Background Patients with water intoxication may develop rhabdomyolysis. Existing studies suggest a relationship between the serum sodium correction rate and rhabdomyolysis.
Masahiro Kashiura   +2 more
doaj   +1 more source

LPIN-1 gene variant in Egyptian children: acute recurrent myoglobinuria

open access: yesJournal of Rare Diseases
Background Children with LPIN-1 gene variant have recurrent acute myoglobinuria, rose-colored urine, general weakness, and fatigue. Treatment for this gene variant remains ameliorative and supportive. Here, we report the clinical data of three cases from
Tarek M. A. Abdallah   +4 more
doaj   +1 more source

Rhabdomyolisys as a Cause of Acute Renal Injury

open access: yesActa Medica Bulgarica, 2018
Rhabdomyolysis (RM) is defined as striate muscle-cell damage with disintegration of skeletal muscles and release of intracellular constituents to the circulation, with or without subsequent kidney injury.
Nikolova M.   +17 more
doaj   +1 more source

Rhabdomyolysis in Dak-Bum devotees: A case series

open access: yesJournal of Family Medicine and Primary Care, 2016
Introduction: India is a land of culture and heritage always known for its rituals. The devotees offer their prayers in the form of fasting, sacrifices and many other difficult ways to please Almighty!
Sonia Singh, Pankaj Hans
doaj   +1 more source

A Call for sting treatment protocol: Case report of a 3 year old with massive bee sting resulting in acute kidney injury

open access: yesNigerian Journal of Paediatrics
Acute Kidney Injury in children following bee sting envenomation is rare and survival is hinged on early recognition and prompt appropriate management. This report is aimed at raising awareness among healthcare workers, of one of the systemic effects of ...
Jimoh AO, Akuse RM, Bugaje MA , Mayaki S
doaj  

Atypical myoglobinuria : a new disease ?

open access: yes, 2003
Communication présentée lors des Journées AEEMA-AESA, 22-23 mai 2003National audienceIn autumn 2002 (between 17 October and 31 November), 66 grazing horses (located in 34 french area) suffered a prostrating illness caused by a myopathy and died (56/66 ...
Bernadac, Michel   +5 more
core  

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