Functional changes in Duchenne muscular dystrophy: a 12-month longitudinal cohort study

E Mazzone; Gessica Vasco; Mp Sormani; Y Torrente; A Berardinelli; S Messina; Adele D'Amico; L Doglio; L Politano; Fabio Cavallaro; S Frosini; L Bello; S Bonfiglio; E Zucchini; R De Sanctis; M Scutifero; Flaviana Bianco; F Rossi; Mc Motta; Angela Sacco; Maria Benedetta Donati; T Mongini; A Pini; R Battini; E Pegoraro; Marika Pane; S Gasperini; S Previtali; S Napolitano; Danilo Martinelli; Cristina Bruno; G Vita; G Comi; E Bertini; Eugenio Maria Mercuri

doi:10.1212/WNL.0b013e318225ab2e

Functional changes in Duchenne muscular dystrophy: a 12-month longitudinal cohort study

E Mazzone
, Gessica Vasco
, Mp Sormani
, Y Torrente
, A Berardinelli
, S Messina
, Adele D'Amico
, L Doglio
, L Politano
, Fabio Cavallaro
, S Frosini
, L Bello
, S Bonfiglio
, E Zucchini
, R De Sanctis
, M Scutifero
, Flaviana Bianco
, F Rossi
, Mc Motta
, Angela Sacco

Maria Benedetta Donati, T Mongini, A Pini, R Battini, E Pegoraro, Marika Pane, S Gasperini, S Previtali, S Napolitano, Danilo Martinelli, Cristina Bruno, G Vita, G Comi, E Bertini, Eugenio Maria Mercuri

Risultato della ricerca: Contributo in rivista › Articolo

117 Citazioni (Scopus)

Abstract

The aim of the study was to assess different outcome measures in a cohort of ambulant boys with Duchenne muscular dystrophy (DMD) over 12 months in order to establish the spectrum of possible changes in relation to age and steroid treatment.

Lingua originale	Inglese
pagine (da-a)	250-256
Numero di pagine	7
Rivista	Neurology
Volume	77
DOI	https://doi.org/10.1212/WNL.0b013e318225ab2e
Stato di pubblicazione	Pubblicato - 2011

Keywords

Adolescent
Anti-Inflammatory Agents
Child
Child, Preschool
Cohort Studies
Cross-Sectional Studies
Disease Progression
Female
Humans
Male
Muscular Dystrophy, Duchenne
Prednisolone
Pregnenediones
Reproducibility of Results
Severity of Illness Index
Statistics as Topic
Walking

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10.1212/WNL.0b013e318225ab2e

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Mazzone, E., Vasco, G., Sormani, M., Torrente, Y., Berardinelli, A., Messina, S., D'Amico, A., Doglio, L., Politano, L., Cavallaro, F., Frosini, S., Bello, L., Bonfiglio, S., Zucchini, E., De Sanctis, R., Scutifero, M., Bianco, F., Rossi, F., Motta, M., ... Mercuri, E. M. (2011). Functional changes in Duchenne muscular dystrophy: a 12-month longitudinal cohort study. Neurology, 77, 250-256. https://doi.org/10.1212/WNL.0b013e318225ab2e

@article{c20ef296c7464b5e8f92ae80feb4484c,

title = "Functional changes in Duchenne muscular dystrophy: a 12-month longitudinal cohort study",

abstract = "The aim of the study was to assess different outcome measures in a cohort of ambulant boys with Duchenne muscular dystrophy (DMD) over 12 months in order to establish the spectrum of possible changes in relation to age and steroid treatment.",

keywords = "Adolescent, Anti-Inflammatory Agents, Child, Child, Preschool, Cohort Studies, Cross-Sectional Studies, Disease Progression, Female, Humans, Male, Muscular Dystrophy, Duchenne, Prednisolone, Pregnenediones, Reproducibility of Results, Severity of Illness Index, Statistics as Topic, Walking, Adolescent, Anti-Inflammatory Agents, Child, Child, Preschool, Cohort Studies, Cross-Sectional Studies, Disease Progression, Female, Humans, Male, Muscular Dystrophy, Duchenne, Prednisolone, Pregnenediones, Reproducibility of Results, Severity of Illness Index, Statistics as Topic, Walking",

author = "E Mazzone and Gessica Vasco and Mp Sormani and Y Torrente and A Berardinelli and S Messina and Adele D'Amico and L Doglio and L Politano and Fabio Cavallaro and S Frosini and L Bello and S Bonfiglio and E Zucchini and \{De Sanctis\}, R and M Scutifero and Flaviana Bianco and F Rossi and Mc Motta and Angela Sacco and Donati, \{Maria Benedetta\} and T Mongini and A Pini and R Battini and E Pegoraro and Marika Pane and S Gasperini and S Previtali and S Napolitano and Danilo Martinelli and Cristina Bruno and G Vita and G Comi and E Bertini and Mercuri, \{Eugenio Maria\}",

year = "2011",

doi = "10.1212/WNL.0b013e318225ab2e",

language = "English",

volume = "77",

pages = "250--256",

journal = "Neurology",

issn = "0028-3878",

publisher = "Lippincott Williams and Wilkins",

}

Mazzone, E, Vasco, G, Sormani, M, Torrente, Y, Berardinelli, A, Messina, S, D'Amico, A, Doglio, L, Politano, L, Cavallaro, F, Frosini, S, Bello, L, Bonfiglio, S, Zucchini, E, De Sanctis, R, Scutifero, M, Bianco, F, Rossi, F, Motta, M, Sacco, A, Donati, MB, Mongini, T, Pini, A, Battini, R, Pegoraro, E, Pane, M, Gasperini, S, Previtali, S, Napolitano, S, Martinelli, D, Bruno, C, Vita, G, Comi, G, Bertini, E & Mercuri, EM 2011, 'Functional changes in Duchenne muscular dystrophy: a 12-month longitudinal cohort study', Neurology, vol. 77, pagg. 250-256. https://doi.org/10.1212/WNL.0b013e318225ab2e

TY - JOUR

T1 - Functional changes in Duchenne muscular dystrophy: a 12-month longitudinal cohort study

AU - Mazzone, E

AU - Vasco, Gessica

AU - Sormani, Mp

AU - Torrente, Y

AU - Berardinelli, A

AU - Messina, S

AU - D'Amico, Adele

AU - Doglio, L

AU - Politano, L

AU - Cavallaro, Fabio

AU - Frosini, S

AU - Bello, L

AU - Bonfiglio, S

AU - Zucchini, E

AU - De Sanctis, R

AU - Scutifero, M

AU - Bianco, Flaviana

AU - Rossi, F

AU - Motta, Mc

AU - Sacco, Angela

AU - Donati, Maria Benedetta

AU - Mongini, T

AU - Pini, A

AU - Battini, R

AU - Pegoraro, E

AU - Pane, Marika

AU - Gasperini, S

AU - Previtali, S

AU - Napolitano, S

AU - Martinelli, Danilo

AU - Bruno, Cristina

AU - Vita, G

AU - Comi, G

AU - Bertini, E

AU - Mercuri, Eugenio Maria

PY - 2011

Y1 - 2011

N2 - The aim of the study was to assess different outcome measures in a cohort of ambulant boys with Duchenne muscular dystrophy (DMD) over 12 months in order to establish the spectrum of possible changes in relation to age and steroid treatment.

AB - The aim of the study was to assess different outcome measures in a cohort of ambulant boys with Duchenne muscular dystrophy (DMD) over 12 months in order to establish the spectrum of possible changes in relation to age and steroid treatment.

KW - Adolescent

KW - Anti-Inflammatory Agents

KW - Child

KW - Child, Preschool

KW - Cohort Studies

KW - Cross-Sectional Studies

KW - Disease Progression

KW - Female

KW - Humans

KW - Male

KW - Muscular Dystrophy, Duchenne

KW - Prednisolone

KW - Pregnenediones

KW - Reproducibility of Results

KW - Severity of Illness Index

KW - Statistics as Topic

KW - Walking

KW - Adolescent

KW - Anti-Inflammatory Agents

KW - Child

KW - Child, Preschool

KW - Cohort Studies

KW - Cross-Sectional Studies

KW - Disease Progression

KW - Female

KW - Humans

KW - Male

KW - Muscular Dystrophy, Duchenne

KW - Prednisolone

KW - Pregnenediones

KW - Reproducibility of Results

KW - Severity of Illness Index

KW - Statistics as Topic

KW - Walking

UR - http://hdl.handle.net/10807/6684

U2 - 10.1212/WNL.0b013e318225ab2e

DO - 10.1212/WNL.0b013e318225ab2e

M3 - Article

SN - 0028-3878

VL - 77

SP - 250

EP - 256

JO - Neurology

JF - Neurology

ER -

Functional changes in Duchenne muscular dystrophy: a 12-month longitudinal cohort study

Abstract

Keywords

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