Heterogeneity in ALSFRS-R decline and survival: a population-based study in Italy. - Wikidata - wikimedia - TriplyDB

Heterogeneity in ALSFRS-R decline and survival: a population-based study in Italy.

Heterogeneity in ALSFRS-R decline and survival: a population-based study in Italy.

http://www.wikidata.org/entity/Q41553914

about

Assessment of the factorial validity and reliability of the ALSFRS-R: a revision of its measurement model.The ALSFRS as an outcome measure in therapeutic trials and its relationship to symptom onset Patients with ALS show highly correlated progression rates in left and right limb muscles.Imaging muscle as a potential biomarker of denervation in motor neuron disease.Changes in routine laboratory tests and survival in amyotrophic lateral sclerosis.A retrospective investigation of the relationship between baseline covariates and rate of ALSFRS-R decline in ALS clinical trials.Using an onset-anchored Bayesian hierarchical model to improve predictions for amyotrophic lateral sclerosis disease progression.Unraveling the Complexity of Amyotrophic Lateral Sclerosis Survival Prediction.

P2860

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P2860

Heterogeneity in ALSFRS-R decline and survival: a population-based study in Italy.

http://www.wikidata.org/entity/Q41553914

description

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2015年论文

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2015年论文

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name

Heterogeneity in ALSFRS-R decline and survival: a population-based study in Italy.

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Heterogeneity in ALSFRS-R decline and survival: a population-based study in Italy.

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Heterogeneity in ALSFRS-R decline and survival: a population-based study in Italy.

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Neurological Sciences

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Heterogeneity in ALSFRS-R decline and survival: a population-based study in Italy.

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Alessandro Ravasio

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Annamaria Borghi

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Antonio Fasano

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Carlo Guidi

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ERRALS Group

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Eleni Georgoulopoulou

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Elisabetta Chierici

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Elisabetta Sette

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Emilio Terlizzi

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Fabrizio Salvi

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P2860

Clinical significance in the change of decline in ALSFRS-R

Phenotypic heterogeneity of amyotrophic lateral sclerosis: a population based study

El Escorial revisited: revised criteria for the diagnosis of amyotrophic lateral sclerosis

Amyotrophic lateral sclerosis disease progression model.

Prognostic factors for the course of functional status of patients with ALS: a systematic review.

Clinical diagnosis and management of amyotrophic lateral sclerosis.

Late-onset patients with sporadic amyotrophic lateral sclerosis in Japan have a higher progression rate of ALSFRS-R at the time of diagnosis.

Disease progression in amyotrophic lateral sclerosis: predictors of survival.

Measuring function in advanced ALS: validation of ALSFRS-EX extension items.

The ALSFRSr predicts survival time in an ALS clinic population.

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Enrico Granieri

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