نتایج جستجو برای: pompe disease

تعداد نتایج: 1490290  

2012
Dawn Phillips Angela E. Rosenberg

Purpose: To examine the responsiveness of the PDMS-2 in children diagnosed with Pompe disease who had different levels of functional mobility. To examine the concurrent validity between the PDMS-2 and the Alberta Infant Motor Scale (AIMS), the Pediatric Evaluation of Disability Inventory (PEDI) and the Pompe PEDI (PPEDI) in children diagnosed with Pompe disease. Methods: A secondary analysis wa...

Journal: :Molecular genetics and metabolism 2010
Priya S Kishnani Paula C Goldenberg Stephanie L DeArmey James Heller Danny Benjamin Sarah Young Deeksha Bali Sue Ann Smith Jennifer S Li Hanna Mandel Dwight Koeberl Amy Rosenberg Y-T Chen

Deficiency of acid alpha glucosidase (GAA) causes Pompe disease, which is usually fatal if onset occurs in infancy. Patients synthesize a non-functional form of GAA or are unable to form native enzyme. Enzyme replacement therapy with recombinant human GAA (rhGAA) prolongs survival in infantile Pompe patients but may be less effective in cross-reactive immunologic material (CRIM)-negative patien...

Journal: :The Canadian journal of neurological sciences. Le journal canadien des sciences neurologiques 2016
Mark Tarnopolsky Hans Katzberg Basil J Petrof Sandra Sirrs Harvey B Sarnat Kimberley Myers Nicolas Dupré Dubravka Dodig Angela Genge Shannon L Venance Lawrence Korngut Julian Raiman Aneal Khan

Pompe disease is a lysosomal storage disorder caused by a deficiency of the enzyme acid alpha-glucosidase. Patients have skeletal muscle and respiratory weakness with or without cardiomyopathy. The objective of our review was to systematically evaluate the quality of evidence from the literature to formulate evidence-based guidelines for the diagnosis and management of patients with Pompe disea...

Journal: :Current gene therapy 2009
Dwight D Koeberl Priya S Kishnani

Significant advances in therapy for lysosomal storage disorders have occurred with an accelerating pace over the past decade. Although enzyme replacement therapy has improved the outcome of lysosomal storage disorders, antibody responses have occurred and sometimes prevented efficacy, especially in cross-reacting immune material negative patients with Pompe disease. Preclinical gene therapy exp...

2009
Michael Beck

Pompe disease is a lysosomal storage disorder characterized by muscle weakness and cardiomyopathy. It shows a broad variability regarding the clinical severity as well as the age of onset. In the past, two different recombinant enzyme preparations have been developed for the treatment of Pompe patients: alpha-glucosidase, produced in rabbit milk, and alpha-glucosidase, produced in Chinese hamst...

2016
Fatemeh Bahreini Massoud Houshmand Mohammad Hossein Modaresi Hassan Tonekaboni Shahriar Nafissi Ferdoss Nazari Seyed Mohammad Akrami

OBJECTIVE Pompe disease is a rare neuromuscular genetic disorder and is classified into two forms of early and late-onset. Over the past two decades, mitochondrial abnor- malities have been recognized as an important contributor to an array of neuromuscular diseases. We therefore aimed to compare mitochondrial copy number and mitochondrial displacement-loop sequence variation in infantile and a...

Journal: :Journal of Neuromuscular Diseases 2015

Journal: :BMC Musculoskeletal Disorders 2013

Journal: :Case Reports in Neurological Medicine 2018

Journal: :The European respiratory journal 2012
Hélène Prigent David Orlikowski Pascal Laforêt Nadège Letilly Line Falaize Nadine Pellegrini Djillali Annane Jean-Claude Raphael Frédéric Lofaso

The onset of the adult form of Pompe disease, also known as acid maltase deficiency or glycogen storage disease type II, is a slow progressive muscular disorder in which little correlation exists between respiratory function and locomotor function [1]. The greater degree of respiratory dysfunction, compared with mobility loss, is mainly ascribable to the predominant and progressive involvement ...

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