History of international connections of myology in Europe

Over the past centuries, myology as a basic and clinical science has passed through three major stages of development: the classical period, the modern nosographic stage, and the molecular era. The classical period spans the sixteenth century up to the earlier parts of the twentieth century. During...

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Main Author: Corrado Angelini
Format: Article
Language:English
Published: PAGEPress Publications 2023-07-01
Series:European Journal of Translational Myology
Subjects:
Online Access:https://www.pagepressjournals.org/index.php/bam/article/view/11439
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author Corrado Angelini
author_facet Corrado Angelini
author_sort Corrado Angelini
collection DOAJ
description Over the past centuries, myology as a basic and clinical science has passed through three major stages of development: the classical period, the modern nosographic stage, and the molecular era. The classical period spans the sixteenth century up to the earlier parts of the twentieth century. During this time, several major muscle diseases were clinically and pathologically characterized, including Duchenne muscular dystrophy (DMD), myotonic dystrophy, and facio-scapulo-humeral dystrophy, by master clinicians such as Duchenne, Erb, Becker, Steinert, Landouzy, Dejerine, Meryon, and others. These accomplishments laid solid foundations for the following modern era with nosographic classification and the following molecular era. European clinicians and scientists were major contributors to the modern era in the second half of the twentieth century, which is characterized by three major discoveries. First, it was observed that substantial elevation of the serum activity of creatine kinase indicates muscle damage or destruction. Then, the adaptation of modern histo-and cytochemical techniques to the study of muscle biopsies markedly improved the diagnostic accuracy and made possible the identification of new changes and structures. Thirdly, the advent of modern biochemical techniques permitted the identification of various enzyme defects/storage diseases such as Pompe disease, McArdle's disease, and carnitine deficiency states. The molecular era was made possible by the strikingly fast development of molecular biology and its application to muscle diseases. This permitted the identification of gene defects in many inherited diseases, leading to an accurate and specific diagnosis. The growth of international collaboration in Europe was achieved through the exchange of international scientists and collaborative networks.
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spelling doaj.art-53b7d20440324cd2b4ffa626c2f329892023-07-10T22:51:56ZengPAGEPress PublicationsEuropean Journal of Translational Myology2037-74522037-74602023-07-0110.4081/ejtm.2023.11439History of international connections of myology in EuropeCorrado Angelini0Department of Neuroscience, University of Padova, Padua Over the past centuries, myology as a basic and clinical science has passed through three major stages of development: the classical period, the modern nosographic stage, and the molecular era. The classical period spans the sixteenth century up to the earlier parts of the twentieth century. During this time, several major muscle diseases were clinically and pathologically characterized, including Duchenne muscular dystrophy (DMD), myotonic dystrophy, and facio-scapulo-humeral dystrophy, by master clinicians such as Duchenne, Erb, Becker, Steinert, Landouzy, Dejerine, Meryon, and others. These accomplishments laid solid foundations for the following modern era with nosographic classification and the following molecular era. European clinicians and scientists were major contributors to the modern era in the second half of the twentieth century, which is characterized by three major discoveries. First, it was observed that substantial elevation of the serum activity of creatine kinase indicates muscle damage or destruction. Then, the adaptation of modern histo-and cytochemical techniques to the study of muscle biopsies markedly improved the diagnostic accuracy and made possible the identification of new changes and structures. Thirdly, the advent of modern biochemical techniques permitted the identification of various enzyme defects/storage diseases such as Pompe disease, McArdle's disease, and carnitine deficiency states. The molecular era was made possible by the strikingly fast development of molecular biology and its application to muscle diseases. This permitted the identification of gene defects in many inherited diseases, leading to an accurate and specific diagnosis. The growth of international collaboration in Europe was achieved through the exchange of international scientists and collaborative networks. https://www.pagepressjournals.org/index.php/bam/article/view/11439muscle dystrophymitochondrial disorderslimb-girdle dystrophyfacio-scapulo-humeral dystrophymetabolic myopathies
spellingShingle Corrado Angelini
History of international connections of myology in Europe
European Journal of Translational Myology
muscle dystrophy
mitochondrial disorders
limb-girdle dystrophy
facio-scapulo-humeral dystrophy
metabolic myopathies
title History of international connections of myology in Europe
title_full History of international connections of myology in Europe
title_fullStr History of international connections of myology in Europe
title_full_unstemmed History of international connections of myology in Europe
title_short History of international connections of myology in Europe
title_sort history of international connections of myology in europe
topic muscle dystrophy
mitochondrial disorders
limb-girdle dystrophy
facio-scapulo-humeral dystrophy
metabolic myopathies
url https://www.pagepressjournals.org/index.php/bam/article/view/11439
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