An asymptomatic boy, aged 1.5 years, was referred with presumed liver disease because of persistently increased transaminase. Ultimately Pompe disease was confirmed, without specific abnormalities in muscle biopsy. This case demonstrates that increased transaminases do not always suggest liver disease. It is hard to determine prognosis and to decide whether enzyme replacement therapy should be started in asymptomatic patients with Pompe disease.</p
Background: Pompe's disease is an inherited metabolic myopathy caused by acid \u3b1-glucosidase defi...
The aim of this study was to call the attention to the often disregarded message that hypertransamin...
Commonly used in clinical practice, glutamic oxalacetic (GOT) and glutamic piruvic (GPT) transaminas...
An asymptomatic boy, aged 1.5 years, was referred with presumed liver disease because of persistentl...
Pompe disease or type II glycogen storage disease is a rare autosomal hereditary disease. The preval...
Pompe disease or type II glycogen storage disease is a rare autosomal hereditary disease. The preval...
Introduction Elevated transaminases and/or creatine phosphokinase can indicate underlying muscle dis...
An asymptomatic 4.5 years-old Saudi girl was referred to the pediatric hepatology service with presu...
Twenty-one patients with incidental hypertransaminasaemia who were eventually diagnosed as muscular ...
The article discusses a clinical case of late-onset Pompe disease in a 15-year and 6-month-old adole...
Abstract: Aminotransferases increase in serum is generally considered indicative of liver cell injur...
Many physicians believe that muscle disease leads either to sole elevation of aspartate aminotransfe...
Background. Analysis of Pompe disease (PD) clinical features in children in order to determine its m...
The aim of this studywas to call the attention to the often disregarded message that hypertransamina...
Pompe disease is a metabolic myopathy. Since the first description of the disease in 1932 by J.C. P...
Background: Pompe's disease is an inherited metabolic myopathy caused by acid \u3b1-glucosidase defi...
The aim of this study was to call the attention to the often disregarded message that hypertransamin...
Commonly used in clinical practice, glutamic oxalacetic (GOT) and glutamic piruvic (GPT) transaminas...
An asymptomatic boy, aged 1.5 years, was referred with presumed liver disease because of persistentl...
Pompe disease or type II glycogen storage disease is a rare autosomal hereditary disease. The preval...
Pompe disease or type II glycogen storage disease is a rare autosomal hereditary disease. The preval...
Introduction Elevated transaminases and/or creatine phosphokinase can indicate underlying muscle dis...
An asymptomatic 4.5 years-old Saudi girl was referred to the pediatric hepatology service with presu...
Twenty-one patients with incidental hypertransaminasaemia who were eventually diagnosed as muscular ...
The article discusses a clinical case of late-onset Pompe disease in a 15-year and 6-month-old adole...
Abstract: Aminotransferases increase in serum is generally considered indicative of liver cell injur...
Many physicians believe that muscle disease leads either to sole elevation of aspartate aminotransfe...
Background. Analysis of Pompe disease (PD) clinical features in children in order to determine its m...
The aim of this studywas to call the attention to the often disregarded message that hypertransamina...
Pompe disease is a metabolic myopathy. Since the first description of the disease in 1932 by J.C. P...
Background: Pompe's disease is an inherited metabolic myopathy caused by acid \u3b1-glucosidase defi...
The aim of this study was to call the attention to the often disregarded message that hypertransamin...
Commonly used in clinical practice, glutamic oxalacetic (GOT) and glutamic piruvic (GPT) transaminas...