Original languageEnglish
Article numbere0218683
JournalPLoS One
Volume14
Issue number6
DOIs
Publication statusPublished - 2019

Keywords

  • Article
  • child
  • cohort analysis
  • controlled study
  • disease course
  • Duchenne muscular dystrophy
  • exon
  • exon 44
  • exon 45
  • exon 51
  • exon 53
  • exon skipping
  • follow up
  • gene deletion
  • gene mutation
  • genotype
  • human
  • intermethod comparison
  • major clinical study
  • male
  • medical history
  • outpatient care
  • six minute walk test

Cite this

Long-term natural history data in Duchenne muscular dystrophy ambulant patients with mutations amenable to skip exons 44, 45, 51 and 53. / Brogna, C.; Coratti, G.; Pane, M.; Ricotti, V.; Messina, S.; D’Amico, A.; Bruno, C.; Vita, G.; Berardinelli, A.; Mazzone, E.; Magri, F.; Ricci, F.; Mongini, T.; Battini, R.; Bello, L.; Pegoraro, E.; Baranello, G.; Previtali, S.C.; Politano, L.; Comi, G.P.; Sansone, V.A.; Donati, A.; Bertini, E.; Muntoni, F.; Goemans, N.; Mercuri, E.

In: PLoS One, Vol. 14, No. 6, e0218683, 2019.

Research output: Contribution to journalArticle

@article{e3509b93570348969d44d26c8721e92c,
title = "Long-term natural history data in Duchenne muscular dystrophy ambulant patients with mutations amenable to skip exons 44, 45, 51 and 53",
keywords = "Article, child, cohort analysis, controlled study, disease course, Duchenne muscular dystrophy, exon, exon 44, exon 45, exon 51, exon 53, exon skipping, follow up, gene deletion, gene mutation, genotype, human, intermethod comparison, major clinical study, male, medical history, outpatient care, six minute walk test",
author = "C. Brogna and G. Coratti and M. Pane and V. Ricotti and S. Messina and A. D’Amico and C. Bruno and G. Vita and A. Berardinelli and E. Mazzone and F. Magri and F. Ricci and T. Mongini and R. Battini and L. Bello and E. Pegoraro and G. Baranello and S.C. Previtali and L. Politano and G.P. Comi and V.A. Sansone and A. Donati and E. Bertini and F. Muntoni and N. Goemans and E. Mercuri",
note = "Export Date: 4 September 2019 CODEN: POLNC Correspondence Address: Mercuri, E.; Pediatric Neurology, Department of Woman and Child Health and Public Health, Child Health Area, Universit{\`a} Cattolica del Sacro CuoreItaly; email: eugeniomaria.mercuri@unicatt.it",
year = "2019",
doi = "10.1371/journal.pone.0218683",
language = "English",
volume = "14",
journal = "PLoS One",
issn = "1932-6203",
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number = "6",

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TY - JOUR

T1 - Long-term natural history data in Duchenne muscular dystrophy ambulant patients with mutations amenable to skip exons 44, 45, 51 and 53

AU - Brogna, C.

AU - Coratti, G.

AU - Pane, M.

AU - Ricotti, V.

AU - Messina, S.

AU - D’Amico, A.

AU - Bruno, C.

AU - Vita, G.

AU - Berardinelli, A.

AU - Mazzone, E.

AU - Magri, F.

AU - Ricci, F.

AU - Mongini, T.

AU - Battini, R.

AU - Bello, L.

AU - Pegoraro, E.

AU - Baranello, G.

AU - Previtali, S.C.

AU - Politano, L.

AU - Comi, G.P.

AU - Sansone, V.A.

AU - Donati, A.

AU - Bertini, E.

AU - Muntoni, F.

AU - Goemans, N.

AU - Mercuri, E.

N1 - Export Date: 4 September 2019 CODEN: POLNC Correspondence Address: Mercuri, E.; Pediatric Neurology, Department of Woman and Child Health and Public Health, Child Health Area, Università Cattolica del Sacro CuoreItaly; email: eugeniomaria.mercuri@unicatt.it

PY - 2019

Y1 - 2019

KW - Article

KW - child

KW - cohort analysis

KW - controlled study

KW - disease course

KW - Duchenne muscular dystrophy

KW - exon

KW - exon 44

KW - exon 45

KW - exon 51

KW - exon 53

KW - exon skipping

KW - follow up

KW - gene deletion

KW - gene mutation

KW - genotype

KW - human

KW - intermethod comparison

KW - major clinical study

KW - male

KW - medical history

KW - outpatient care

KW - six minute walk test

U2 - 10.1371/journal.pone.0218683

DO - 10.1371/journal.pone.0218683

M3 - Article

VL - 14

JO - PLoS One

JF - PLoS One

SN - 1932-6203

IS - 6

M1 - e0218683

ER -