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References from Quantitative super-resolution imaging with deep learning segmentation reveals early mitochondrial network remodeling and altered mitochondria-lysosome interactions in Pompe disease muscle. Local targets link to admitted publications; unresolved targets remain external evidence.
Unresolved reference
2002 · External reference
Unresolved reference
2009 · External reference
α-Glucosidase deficiency in generalized glycogen-storage disease (Pompe’s disease)
10.1042/bj0860011 · 1963 · External reference
Pompe’s disease
10.1016/s0140-6736(08)61555-x · 2008 · External reference
The Natural Course of Infantile Pompe’s Disease: 20 Original Cases Compared With 133 Cases From the Literature
10.1542/peds.112.2.332 · 2003 · External reference
Pompe disease: Design, methodology, and early findings from the Pompe Registry
10.1016/j.ymgme.2011.02.004 · 2011 · External reference
Pompe disease diagnosis and management guideline
2006 · External reference
Characterization of pre- and post-treatment pathology after enzyme replacement therapy for pompe disease
10.1038/labinvest.3700484 · 2006 · External reference
Dysfunction of endocytic and autophagic pathways in a lysosomal storage disease
10.1002/ana.20807 · 2006 · External reference
Role of autophagy in the pathogenesis of Pompe disease
2006 · External reference
Lysosomal dysfunction in muscle with special reference to glycogen storage disease type II
10.1016/s0925-4439(02)00229-6 · 2003 · External reference
Satellite cells fail to contribute to muscle repair but are functional in Pompe disease (glycogenosis type II)
10.1186/s40478-018-0609-y · 2018 · External reference
Impact of capillary and sarcolemmal proximity on mitochondrial structure and energetic function in skeletal muscle
10.1113/jp286246 · 2024 · External reference
Power Grid Protection of the Muscle Mitochondrial Reticulum
10.1016/j.celrep.2017.03.063 · 2017 · External reference
Mitochondrial morphology and function: two for the price of one!
10.1111/jmi.12891 · 2020 · External reference
Pathology of skeletal muscle cells in adult-onset glycogenosis type II (Pompe disease): ultrastructural study
2008 · External reference
Raben, N. Defects in calcium homeostasis and mitochondria can be reversed in Pompe disease
10.1080/15548627.2015.1009779 · 2015 · External reference
Adult glycogenosis II with paracrystalline mitochondrial inclusions and Hirano bodies in skeletal muscle
10.1016/s0960-8966(98)00117-5 · 1999 · External reference
Autophagy and mitochondria in Pompe disease: Nothing is so new as what has long been forgotten
10.1002/ajmg.c.31317 · 2012 · External reference
Super-resolution microscopy demystified
10.1038/s41556-018-0251-8 · 2019 · External reference
Unresolved reference
2022 · External reference
W. STED microscopy with a supercontinuum laser source
10.1364/oe.16.009614 · 2008 · External reference
W. STED with wavelengths closer to the emission maximum
10.1364/oe.20.005225 · 2012 · External reference
Mosaic dysfunction of mitophagy in mitochondrial muscle disease
10.1016/j.cmet.2021.12.017 · 2022 · External reference
Single-molecule localization microscopy
10.1038/s43586-021-00038-x · 2021 · External reference
A pipeline for multidimensional confocal analysis of mitochondrial morphology, function, and dynamics in pancreatic β-cells
10.1152/ajpendo.00457.2019 · 2020 · External reference
A. A simple ImageJ macro tool for analyzing mitochondrial network morphology in mammalian cell culture
10.1016/j.acthis.2017.03.001 · 2017 · External reference
E. R. SKELETAL MUSCLE FIBER TYPES IN C57BL6J MICE
2004 · External reference
Scaling of muscle architecture and fiber types in the rat hindlimb
10.1242/jeb.017640 · 2008 · External reference
Mitochondria–lysosome contacts regulate mitochondrial fission via RAB7 GTP hydrolysis
10.1038/nature25486 · 2018 · External reference
Unresolved reference
2020 · External reference
Mitochondria – the CEO of the cell
10.1242/jcs.263403 · 2025 · External reference
Mitochondrial Dysfunction in Lysosomal Storage Disorders
10.3390/diseases4040031 · 2016 · External reference
Interplay between mitochondrial dysfunction and lysosomal storage: challenges in genetic metabolic muscle diseases with a focus on infantile onset Pompe disease
10.3389/fcvm.2024.1367108 · 2024 · External reference
Autophagy and Mistargeting of Therapeutic Enzyme in Skeletal Muscle in Pompe Disease
10.1016/j.ymthe.2006.08.009 · 2006 · External reference
A pilot study on using rapamycin-carrying synthetic vaccine particles (SVP) in conjunction with enzyme replacement therapy to induce immune tolerance in Pompe disease
2017 · External reference
