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Record W338315497

I-1History of Myology in Italy and its internationalcollections

2011· article· en· W338315497 on OpenAlexaboutno aff
C. Angelini

Bibliographic record

VenuePubMed Central · 2011
Typearticle
Languageen
FieldBiochemistry, Genetics and Molecular Biology
TopicMuscle Physiology and Disorders
Canadian institutionsnot available
Fundersnot available
KeywordsMyologyMedicineLibrary scienceClassicsHistoryAnatomy
DOInot available

Abstract

fetched live from OpenAlex

The history of Myology in Italy begins in 16th century with muscle anatomy pictures by Vesalius and Canani while in the 19th century the Neapolitan physician Gaetano Conte described Duchenne muscular dystrophy on clinical basis (1). Myology reached a major development in the 20th century with the establishment of the CNR center in Padova (professor Massimiliano Aloisi) a cardiomyological and genetic center in Naples (professor Giovanni Nigro) and a neurological center in Milan (professor Guglielmo Scarlato). In the 60th prof. Aloisi and Federico Milcovich, a myodystrophic patient, started the Italian Muscular Dystrophy patients association (UILDM) with contacts with MDA (2). The first congress in Neuromuscular diseases took place in Milan in 1969 by the organization of professor Scarlato, Aloisi, Canal and was attended by several outstanding international muscle researchers such as AG Engel, WK Engel, LP Rowland, M.Fardeau and I.Hausmanowa-Petrusewicz. Eleven meetings in many countries followed this, up to the last XII international Congress on Neuromuscular Diseases in Naples in 2010. Several laboratories arose in the country especially in Neurological Institutes; several researchers emigrated permanently or went for a stage to improve their myological skills especially in USA, UK, Canada, France both in basic and/or pathological, clinical research (Table 1). The laboratory of Columbia in New York, lead by professor Di Mauro was a common place of training especially in the field of mitochondrial myopathies. Table 1. The main international connections. As in other developed countries, the basis of neuromuscular research and diagnosis were expanded on immunohistochemical, biochemical and molecular grounds, during the 20th and the beginning of the 21st century. Enzo Ferrari – a race car factory engineer – was a support to research in muscular dystrophy in Milan, Padova and Modena. Telethon has contributed to support in neuromuscular disorders. Myology with the enlargement of scientific basis in the molecular era began to split in subspecialities i.e. genetics, physiopathology etc. and a spectrum of knowledge was accumulated both for diagnostic and therapeutic purposes. In the field of metabolic diseases and limb-girdle myopathies several Italian laboratories described new entities. A number of treatments, beside the treatment of inflammatory myopathies and myasthenia gravis, were found and applied in metabolic myopathies: i.e. carnitine, Coenzyme Q, enzyme replacement in glycogenosis type II. The continuous challenge of the treatment of the primary muscular dystrophy remains for the future since so far there are only emerging molecular therapies: antisense oligonucleotides in DMD, adenoviral therapy in sarcoglycanopathies, cell therapy might contribute to answer to a promises for muscular patients. In the translation area many laboratories and Italian groups continue with new researchers and they have contributed to meetings of European Neuromuscular Center and to the Foundation and organisation of the World Muscle Society with meetings in Italy (Naples, Taormina), and to the Treat – NMD and Eurobiobank networks.

Fetched live from OpenAlex and de-inverted. Abstracts are not stored in this database: the inverted indexes are 8.6 GB of the frame’s 9.3 GB of text, and the host has 13 GB free.

How this classification was reachedexpand

Full frame distilled prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. Learned from the 10,348 direct Codex labels and 10,348 direct Gemma labels. Candidate is the union of thresholded teacher heads; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels or direct frontier model labels.

metaresearch head score (Codex)0.000
metaresearch head score (Gemma)0.000
Version: codex-gemma-dda1882f352aValidation status: machine_predicted_unvalidated
Candidate categoriesnone
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Observational · Consensus signal: Observational
GenreCandidate signal: Empirical · Consensus signal: Empirical
Teacher disagreement score0.264
Threshold uncertainty score0.184

Codex and Gemma teacher scores by category

CategoryCodexGemma
Metaresearch0.0000.000
Meta-epidemiology (narrow)0.0000.000
Meta-epidemiology (broad)0.0000.000
Bibliometrics0.0000.000
Science and technology studies0.0000.000
Scholarly communication0.0000.000
Open science0.0000.000
Research integrity0.0000.000
Insufficient payload (model declined to judge)0.0000.000

Machine scores (provisional)

The two teacher heads of the student model, read on this work. A score orders the frame for review; it never asserts a category, and the validation status ships verbatim with every row.

Baseline scores from an immature model (maturity gate not passed, 7 training rounds). Scores rank; they never assert a category.

Opus teacher head0.017
GPT teacher head0.206
Teacher spread0.189 · how far apart the two teachers sit on this one work
Validation statusscore_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from it

Classification

machine, unvalidated

Machine predicted; a candidate call from one teacher head, not a consensus.

The models applied no category: nothing in the taxonomy fit this work.
Study designObservational
Domainnot available
GenreEmpirical

How this classification was reached, model by model and score by score, is at the end of the page under "How this classification was reached".

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Citations0
Published2011
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