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Record W2890882905 · doi:10.1186/s13023-018-0889-0

Eight years after an international workshop on myotonic dystrophy patient registries: case study of a global collaboration for a rare disease

2018· article· en· W2890882905 on OpenAlexafffund
Libby Wood, Guillaume Bassez, Corinne Bleyenheuft, Craig Campbell, Louise Cossette, Cecilia Jimenez‐Moreno, Yi Dai, Hugh Dawkins, Jorge Alberto Diaz Manera, Céline Dogan, Rasha El Sherif, Barbara Fossati, Caroline Graham, James E. Hilbert, Kristina Kastreva, En Kimura, Lawrence Korngut, Anna Kostera‐Pruszczyk, Christopher Lindberg, Björn Lindvall, Elizabeth Luebbe, Anna Łusakowska, Radim Mazanec, Giovani Meola, Liannna Orlando, Masanori Takahashi, Stojan Perić, Jack Puymirat, Vidosava Rakočević-Stojanović, Miriam Rodrigues, Richard Roxburgh, Benedikt Schoser, Sonia Segovia, Andriy Shatillo, Simone Thiele, Ivailo Tournev, Baziel G.M. van Engelen, Stanislav Voháňka, Hanns Lochmüller

Bibliographic record

VenueOrphanet Journal of Rare Diseases · 2018
Typearticle
Languageen
FieldNeuroscience
TopicGenetic Neurodegenerative Diseases
Canadian institutionsUniversity of CalgaryCentre hospitalier de l'Université LavalWestern University
FundersNational Institute of Neurological Disorders and StrokeSanofi GenzymeMaryland Sea Grant, University of MarylandMinistarstvo Prosvete, Nauke i Tehnološkog RazvojaNational Center of Neurology and PsychiatryNational Institutes of HealthNewcastle UniversityMinistero della SaluteMuscular Dystrophy UKMedical Research CouncilBiogenALS Society of CanadaDeutsche Gesellschaft für MuskelkrankeUniversity of RochesterSanofi
KeywordsMyotonic dystrophyMedicineDiseaseFamily medicineVariety (cybernetics)Muscular dystrophyNeuromuscular diseasePediatricsPathology

Abstract

fetched live from OpenAlex

BACKGROUND: Myotonic Dystrophy is the most common form of muscular dystrophy in adults, affecting an estimated 10 per 100,000 people. It is a multisystemic disorder affecting multiple generations with increasing severity. There are currently no licenced therapies to reverse, slow down or cure its symptoms. In 2009 TREAT-NMD (a global alliance with the mission of improving trial readiness for neuromuscular diseases) and the Marigold Foundation held a workshop of key opinion leaders to agree a minimal dataset for patient registries in myotonic dystrophy. Eight years after this workshop, we surveyed 22 registries collecting information on myotonic dystrophy patients to assess the proliferation and utility the dataset agreed in 2009. These registries represent over 10,000 myotonic dystrophy patients worldwide (Europe, North America, Asia and Oceania). RESULTS: The registries use a variety of data collection methods (e.g. online patient surveys or clinician led) and have a variety of budgets (from being run by volunteers to annual budgets over €200,000). All registries collect at least some of the originally agreed data items, and a number of additional items have been suggested in particular items on cognitive impact. CONCLUSIONS: The community should consider how to maximise this collective resource in future therapeutic programmes.

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)0.001
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 score0.167
Threshold uncertainty score0.901

Codex and Gemma teacher scores by category

CategoryCodexGemma
Metaresearch0.0000.001
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 head0.022
GPT teacher head0.305
Teacher spread0.283 · 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".

Quick stats

Citations26
Published2018
Admission routes2
Has abstractyes

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