-
1
-
-
76549130473
-
Diagnosis andmanagement of duchenne muscular dystrophy, part 2: Implementation of multidisciplinary care
-
PMID: 19945914
-
Bushby K, Finkel R, Birnkrant DJ, Case LE, Clemens PR, et al. (2010) Diagnosis andmanagement of Duchenne muscular dystrophy, part 2: implementation of multidisciplinary care. Lancet Neurol 9: 177-189. doi: 10.1016/S1474-4422(09)70272-8 PMID: 19945914
-
(2010)
Lancet Neurol
, vol.9
, pp. 177-189
-
-
Bushby, K.1
Finkel, R.2
Birnkrant, D.J.3
Case, L.E.4
Clemens, P.R.5
-
2
-
-
72149108443
-
Diagnosis and management of duchenne muscular dystrophy, part 1: Diagnosis, and pharmacological and psychosocial management
-
PMID: 19945913
-
Bushby K, Finkel R, Birnkrant DJ, Case LE, Clemens PR, et al. (2010) Diagnosis and management of Duchenne muscular dystrophy, part 1: diagnosis, and pharmacological and psychosocial management. Lancet Neurol 9: 77-93. doi: 10.1016/S1474-4422(09)70272-8 PMID: 19945913
-
(2010)
Lancet Neurol
, vol.9
, pp. 77-93
-
-
Bushby, K.1
Finkel, R.2
Birnkrant, D.J.3
Case, L.E.4
Clemens, P.R.5
-
3
-
-
80051690306
-
Exon skipping and dystrophin restoration in patients with duchenne muscular dystrophy after systemic phosphorodiamidate morpholino oligomer treatment: An open-label, phase 2, dose-escalation study
-
PMID: 21784508
-
Cirak S, Arechavala-Gomeza V, Guglieri M, Feng L, Torelli S, et al. (2011) Exon skipping and dystrophin restoration in patients with Duchenne muscular dystrophy after systemic phosphorodiamidate morpholino oligomer treatment: an open-label, phase 2, dose-escalation study. Lancet 378: 595-605. doi: 10.1016/S0140-6736(11)60756-3 PMID: 21784508
-
(2011)
Lancet
, vol.378
, pp. 595-605
-
-
Cirak, S.1
Arechavala-Gomeza, V.2
Guglieri, M.3
Feng, L.4
Torelli, S.5
-
4
-
-
79955158683
-
Systemic administration of pro051 in duchenne's muscular dystrophy
-
PMID: 21428760
-
Goemans NM, Tulinius M, van den Akker JT, Burm BE, Ekhart PF, et al. (2011) Systemic administration of PRO051 in Duchenne's muscular dystrophy. N Engl J Med 364: 1513-1522. doi: 10.1056/ NEJMoa1011367 PMID: 21428760
-
(2011)
N Engl J Med
, vol.364
, pp. 1513-1522
-
-
Goemans, N.M.1
Tulinius, M.2
Van Den Akker, J.T.3
Burm, B.E.4
Ekhart, P.F.5
-
5
-
-
84890805770
-
Eteplirsen for the treatment of duchenne muscular dystrophy
-
Mendell J, Rodino-Klapac LR, Sahenk Z, Roush K, Bird L, et al. (2013) Eteplirsen for the treatment of duchenne muscular dystrophy. Ann Neurol.
-
(2013)
Ann Neurol
-
-
Mendell, J.1
Rodino-Klapac, L.R.2
Sahenk, Z.3
Roush, K.4
Bird, L.5
-
6
-
-
84874692333
-
Muscular dystrophies
-
PMID: 23465426
-
Mercuri E, Muntoni F (2013) Muscular dystrophies. Lancet 381: 845-860. doi: 10.1016/S0140-6736 (12)61897-2 PMID: 23465426
-
(2013)
Lancet
, vol.381
, pp. 845-860
-
-
Mercuri, E.1
Muntoni, F.2
-
7
-
-
84883055833
-
The 6-minute walk test and other endpoints in duchenne muscular dystrophy: Longitudinal natural history observations over 48 weeks from a multicenter study
-
McDonald CM, Henricson EK, Abresch RT, Florence JM, Eagle M, et al. (2013) The 6-minute walk test and other endpoints in Duchenne muscular dystrophy: Longitudinal natural history observations over 48 weeks from a multicenter study. Muscle Nerve.
-
(2013)
Muscle Nerve
-
-
McDonald, C.M.1
Henricson, E.K.2
Abresch, R.T.3
Florence, J.M.4
Eagle, M.5
-
8
-
-
77950210043
-
The 6-minute walk test as a new outcome measure in duchenne muscular dystrophy
-
PMID: 19941337
-
McDonald CM, Henricson EK, Han JJ, Abresch RT, Nicorici A, et al. (2010) The 6-minute walk test as a new outcome measure in Duchenne muscular dystrophy. Muscle Nerve 41: 500-510. doi: 10.1002/ mus.21544 PMID: 19941337
-
(2010)
Muscle Nerve
, vol.41
, pp. 500-510
-
-
McDonald, C.M.1
Henricson, E.K.2
Han, J.J.3
Abresch, R.T.4
Nicorici, A.5
-
9
-
-
53249098299
-
Towards harmonisation of outcomemeasures for dmd and sma within treat-nmd
-
PMID: 18818076,Report of three expert workshops: Treat-nmd/enmc workshop on outcomemeasures, 12th-13thmay 2007, naarden, the netherlands; Treat-nmd workshop on outcomemeasures in experimental trials for dmd, 30th june-1st july 2007, naarden, the netherlands; Conjoint institute ofmyology treat-nmdmeeting on physical activitymonitoring in neuromuscular disorders, 11th july 2007, paris, france
-
Mercuri E,Mayhew A, Muntoni F, Messina S, Straub V, et al. (2008) Towards harmonisation of outcomemeasures for DMD and SMA within TREAT-NMD; report of three expert workshops: TREAT-NMD/ENMC workshop on outcomemeasures, 12th-13thMay 2007, Naarden, The Netherlands; TREAT-NMD workshop on outcomemeasures in experimental trials for DMD, 30th June-1st July 2007, Naarden, The Netherlands; conjoint Institute ofMyology TREAT-NMDmeeting on physical activitymonitoring in neuromuscular disorders, 11th July 2007, Paris, France. Neuromuscul Disord 18: 894-903. PMID: 18818076
-
(2008)
Neuromuscul Disord
, vol.18
, pp. 894-903
-
-
Mercuri Emayhew, A.1
Muntoni, F.2
Messina, S.3
Straub, V.4
-
10
-
-
84868104653
-
International workshop on assessment of upper limb function in duchenne muscular dystrophy: Rome, 15-16 february 2012
-
PMID: 22795657
-
Mercuri E, McDonald C, Mayhew A, Florence J, Mazzone E, et al. (2012) International workshop on assessment of upper limb function in Duchenne Muscular Dystrophy: Rome, 15-16 February 2012. Neuromuscul Disord 22: 1025-1028. doi: 10.1016/j.nmd.2012.06.006 PMID: 22795657
-
(2012)
Neuromuscul Disord
, vol.22
, pp. 1025-1028
-
-
Mercuri, E.1
McDonald, C.2
Mayhew, A.3
Florence, J.4
Mazzone, E.5
-
11
-
-
84866424753
-
A critical review of functional assessment tools for upper limbs in duchenne muscular dystrophy
-
PMID: 22713125
-
Mazzone ES, Vasco G, Palermo C, Bianco F, Galluccio C, et al. (2012) A critical review of functional assessment tools for upper limbs in Duchenne muscular dystrophy. Dev Med Child Neurol 54: 879-885. doi: 10.1111/j.1469-8749.2012.04345.x PMID: 22713125
-
(2012)
Dev Med Child Neurol
, vol.54
, pp. 879-885
-
-
Mazzone, E.S.1
Vasco, G.2
Palermo, C.3
Bianco, F.4
Galluccio, C.5
-
12
-
-
84885175848
-
Development of the performance of the upper limb module for duchenne muscular dystrophy
-
Mayhew A, Mazzone ES, Eagle M, Duong T, Ash M, et al. (2013) Development of the Performance of the Upper Limb module for Duchenne muscular dystrophy. Dev Med Child Neurol.
-
(2013)
Dev Med Child Neurol
-
-
Mayhew, A.1
Mazzone, E.S.2
Eagle, M.3
Duong, T.4
Ash, M.5
-
13
-
-
84894248468
-
Reliability of the performance of upper limb assessment in duchenne muscular dystrophy
-
Pane M, Mazzone ES, Fanelli L, De Sanctis R, Bianco F, et al. (2013) Reliability of the Performance of Upper Limb assessment in Duchenne muscular dystrophy. Neuromuscul Disord.
-
(2013)
Neuromuscul Disord
-
-
Pane, M.1
Mazzone, E.S.2
Fanelli, L.3
De Sanctis, R.4
Bianco, F.5
-
14
-
-
84866454704
-
Development and application of stereo camera-based upper extremity workspace evaluation in patients with neuromuscular diseases
-
PMID: 23028947
-
Kurillo G, Han JJ, Abresch RT, Nicorici A, Yan P, et al. (2012) Development and application of stereo camera-based upper extremity workspace evaluation in patients with neuromuscular diseases. PLoS One 7: e45341. doi: 10.1371/journal.pone.0045341 PMID: 23028947
-
(2012)
PLoS One
, vol.7
-
-
Kurillo, G.1
Han, J.J.2
Abresch, R.T.3
Nicorici, A.4
Yan, P.5
-
15
-
-
84922323625
-
Upper extremity reachable workspace evaluation in dmd using kinect
-
Kurillo G, Han JJ, Nicorici A, Johnson LB, Abresch RT, et al. (2013) Upper extremity reachable workspace evaluation in DMD using Kinect. Neuromuscular Disorders 23: 749-750. doi: 10.1016/j.nmd.2013.06.409
-
(2013)
Neuromuscular Disorders
, vol.23
, pp. 749-750
-
-
Kurillo, G.1
Han, J.J.2
Nicorici, A.3
Johnson, L.B.4
Abresch, R.T.5
-
16
-
-
84875453982
-
Proof of concept of the ability of the kinect to quantify upper extremity function in dystrophinopathy
-
Lowes LP, Alfano LN, Yetter BA, Worthen-Chaudhari L, Hinchman W, et al. (2013) Proof of concept of the ability of the kinect to quantify upper extremity function in dystrophinopathy. PLoS Curr 5.
-
(2013)
PLoS Curr
, pp. 5
-
-
Lowes, L.P.1
Alfano, L.N.2
Yetter, B.A.3
Worthen-Chaudhari, L.4
Hinchman, W.5
-
17
-
-
33845989867
-
Reliable surrogate outcome measures in multicenter clinical trials of duchenne muscular dystrophy
-
PMID: 16969838
-
Mayhew JE, Florence JM, Mayhew TP, Henricson EK, Leshner RT, et al. (2007) Reliable surrogate outcome measures in multicenter clinical trials of Duchenne muscular dystrophy. Muscle Nerve 35: 36-42. doi: 10.1002/mus.20654 PMID: 16969838
-
(2007)
Muscle Nerve
, vol.35
, pp. 36-42
-
-
Mayhew, J.E.1
Florence, J.M.2
Mayhew, T.P.3
Henricson, E.K.4
Leshner, R.T.5
-
18
-
-
0023886555
-
Reliability of quantitative muscle testing in healthy children and in children with duchenne muscular dystrophy using a hand-held dynamometer
-
PMID: 3375322
-
Stuberg WA, Metcalf WK (1988) Reliability of quantitative muscle testing in healthy children and in children with Duchenne muscular dystrophy using a hand-held dynamometer. Phys Ther 68: 977-982. PMID: 3375322
-
(1988)
Phys Ther
, vol.68
, pp. 977-982
-
-
Stuberg, W.A.1
Metcalf, W.K.2
-
19
-
-
80054680303
-
Upper limb function in adults with duchenne muscular dystrophy
-
PMID: 21826385
-
Bartels B, Pangalila RF, Bergen MP, Cobben NA, Stam HJ, et al. (2011) Upper limb function in adults with Duchenne muscular dystrophy. J Rehabil Med 43: 770-775. doi: 10.2340/16501977-0841 PMID: 21826385
-
(2011)
J Rehabil Med
, vol.43
, pp. 770-775
-
-
Bartels, B.1
Pangalila, R.F.2
Bergen, M.P.3
Cobben, N.A.4
Stam, H.J.5
-
20
-
-
79956124923
-
Assessing upper limb function in nonambulant sma patients: Development of a new module
-
PMID: 21421316
-
Mazzone E, Bianco F, Martinelli D, Glanzman AM, Messina S, et al. (2011) Assessing upper limb function in nonambulant SMA patients: development of a new module. Neuromuscul Disord 21: 406-412. doi: 10.1016/j.nmd.2011.02.014 PMID: 21421316
-
(2011)
Neuromuscul Disord
, vol.21
, pp. 406-412
-
-
Mazzone, E.1
Bianco, F.2
Martinelli, D.3
Glanzman, A.M.4
Messina, S.5
-
21
-
-
0027194376
-
Assessment of hand function in duchenne muscular dystrophy
-
PMID: 8347064
-
Wagner MB, Vignos PJ Jr, Carlozzi C, Hull AL (1993) Assessment of hand function in Duchenne muscular dystrophy. Arch Phys Med Rehabil 74: 801-804. doi: 10.1016/0003-9993(93)90004-T PMID: 8347064
-
(1993)
Arch Phys Med Rehabil
, vol.74
, pp. 801-804
-
-
Wagner, M.B.1
Vignos, P.J.2
Carlozzi, C.3
Hull, A.L.4
-
22
-
-
84879551615
-
The cooperative international neuromuscular research group duchenne natural history study: Glucocorticoid treatment preserves clinically meaningful functional milestones and reduces rate of disease progression as measured by manual muscle testing and other commonly used clinical trial outcome measures
-
PMID: 23649481
-
Henricson EK, Abresch RT, Cnaan A, Hu F, Duong T, et al. (2013) The cooperative international neuromuscular research group Duchenne natural history study: glucocorticoid treatment preserves clinically meaningful functional milestones and reduces rate of disease progression as measured by manual muscle testing and other commonly used clinical trial outcome measures. Muscle Nerve 48: 55-67. doi: 10.1002/mus.23808 PMID: 23649481
-
(2013)
Muscle Nerve
, vol.48
, pp. 55-67
-
-
Henricson, E.K.1
Abresch, R.T.2
Cnaan, A.3
Hu, F.4
Duong, T.5
-
23
-
-
0019948028
-
Quantitation of muscle function in children: A prospective study in duchenne muscular dystrophy
-
PMID: 7099196
-
Scott OM, Hyde SA, Goddard C, Dubowitz V (1982) Quantitation of muscle function in children: a prospective study in Duchenne muscular dystrophy. Muscle Nerve 5: 291-301. doi: 10.1002/mus. 880050405 PMID: 7099196
-
(1982)
Muscle Nerve
, vol.5
, pp. 291-301
-
-
Scott, O.M.1
Hyde, S.A.2
Goddard, C.3
Dubowitz, V.4
-
24
-
-
79956111449
-
Idebenone as a novel, therapeutic approach for duchenne muscular dystrophy: Results from a 12 month, double-blind, randomized placebo-controlled trial
-
PMID: 21435876
-
Buyse GM, Goemans N, van den Hauwe M, Thijs D, de Groot IJ, et al. (2011) Idebenone as a novel, therapeutic approach for Duchenne muscular dystrophy: results from a 12 month, double-blind, randomized placebo-controlled trial. Neuromuscul Disord 21: 396-405. doi: 10.1016/j.nmd.2011.02.016 PMID: 21435876
-
(2011)
Neuromuscul Disord
, vol.21
, pp. 396-405
-
-
Buyse, G.M.1
Goemans, N.2
Van Den Hauwe, M.3
Thijs, D.4
De Groot, I.J.5
-
25
-
-
84866064194
-
Quantitative muscle strength assessment in duchenne muscular dystrophy: Longitudinal study and correlation with functional measures
-
PMID: 22974002
-
Lerario A, Bonfiglio S, Sormani M, Tettamanti A, Marktel S, et al. (2012) Quantitative muscle strength assessment in duchenne muscular dystrophy: longitudinal study and correlation with functional measures. BMC Neurol 12: 91. doi: 10.1186/1471-2377-12-91 PMID: 22974002
-
(2012)
BMC Neurol
, vol.12
, pp. 91
-
-
Lerario, A.1
Bonfiglio, S.2
Sormani, M.3
Tettamanti, A.4
Marktel, S.5
-
26
-
-
84873117388
-
Innovativemethods to assess upper limb strength and function in non-ambulant duchenne patients
-
PMID: 23219352
-
Servais L, Deconinck N, Moraux A, Benali M, Canal A, et al. (2013) Innovativemethods to assess upper limb strength and function in non-ambulant Duchenne patients. Neuromuscul Disord 23: 139-148. doi: 10. 1016/j.nmd.2012.10.022 PMID: 23219352
-
(2013)
Neuromuscul Disord
, vol.23
, pp. 139-148
-
-
Servais, L.1
Deconinck, N.2
Moraux, A.3
Benali, M.4
Canal, A.5
-
27
-
-
70349573300
-
Analysis of dp71 contribution in the severity of mental retardation through comparison of duchenne and becker patients differing by mutation consequences on dp71 expression
-
PMID: 19602481
-
Daoud F, Angeard N, Demerre B, Martie I, Benyaou R, et al. (2009) Analysis of Dp71 contribution in the severity of mental retardation through comparison of Duchenne and Becker patients differing by mutation consequences on Dp71 expression. Hum Mol Genet 18: 3779-3794. doi: 10.1093/hmg/ddp320 PMID: 19602481
-
(2009)
Hum Mol Genet
, vol.18
, pp. 3779-3794
-
-
Daoud, F.1
Angeard, N.2
Demerre, B.3
Martie, I.4
Benyaou, R.5
-
28
-
-
0036644465
-
ATS statement: Guidelines for the six-minute walk test
-
PMID: 12091180
-
- (2002) ATS statement: guidelines for the six-minute walk test. AmJ Respir Crit CareMed 166: 111-117. doi: 10.1164/ajrccm.166.1.at1102 PMID: 12091180
-
(2002)
AmJ Respir Crit CareMed
, vol.166
, pp. 111-117
-
-
-
30
-
-
84887212371
-
Clinical heterogeneity of duchenne muscular dystrophy (dmd): Definition of sub-phenotypes and predictive criteria by long-term follow-up
-
PMID: 19194511
-
Desguerre I, Christov C, Mayer M, Zeller R, Becane HM, et al. (2009) Clinical heterogeneity of duchenne muscular dystrophy (DMD): definition of sub-phenotypes and predictive criteria by long-term follow-up. PLoS One 4: e4347. doi: 10.1371/journal.pone.0004347 PMID: 19194511
-
(2009)
PLoS One
, vol.4
, pp. e4347
-
-
Desguerre, I.1
Christov, C.2
Mayer, M.3
Zeller, R.4
Becane, H.M.5
-
31
-
-
77955533579
-
Impact of steroids on surgical experiences of patients with duchenne muscular dystrophy
-
PMID: 20691938
-
Dooley JM, Gordon KE, MacSween JM (2010) Impact of steroids on surgical experiences of patients with duchenne muscular dystrophy. Pediatr Neurol 43: 173-176. doi: 10.1016/j.pediatrneurol.2010.04. 013 PMID: 20691938
-
(2010)
Pediatr Neurol
, vol.43
, pp. 173-176
-
-
Dooley, J.M.1
Gordon, K.E.2
Macsween, J.M.3
-
32
-
-
79959852658
-
The natural history of cardiac and pulmonary function decline in patients with duchenne muscular dystrophy
-
Roberto R, Fritz A, Hagar Y, Boice B, Skalsky A, et al. (2011) The natural history of cardiac and pulmonary function decline in patients with duchenne muscular dystrophy. Spine (Phila Pa 1976) 36: E1009-1017. doi: 10.1097/BRS.0b013e3181fea1ed
-
(2011)
Spine (Phila Pa 1976)
, vol.36
, pp. E1009-1017
-
-
Roberto, R.1
Fritz, A.2
Hagar, Y.3
Boice, B.4
Skalsky, A.5
-
33
-
-
84869491156
-
Responsiveness of the motor function measure in neuromuscular diseases
-
e2251., PMID: 22705238
-
Vuillerot C, Payan C, Girardot F, Fermanian J, Iwaz J, et al. (2012) Responsiveness of the motor function measure in neuromuscular diseases. Arch Phys Med Rehabil 93: 2251-2256 e2251. doi: 10.1016/ j.apmr.2012.05.025 PMID: 22705238
-
(2012)
Arch Phys Med Rehabil
, vol.93
, pp. 2251-2256
-
-
Vuillerot, C.1
Payan, C.2
Girardot, F.3
Fermanian, J.4
Iwaz, J.5
-
34
-
-
84897449030
-
6 minute walk test in duchenne md patients with different mutations: 12 month changes
-
PMID: 24421885
-
Pane M, Mazzone ES, Sormani MP, Messina S, Vita GL, et al. (2014) 6 minute walk test in duchenne MD patients with different mutations: 12 month changes. PLoS One 9: e83400. doi: 10.1371/journal. pone.0083400 PMID: 24421885
-
(2014)
PLoS One
, vol.9
-
-
Pane, M.1
Mazzone, E.S.2
Sormani, M.P.3
Messina, S.4
Vita, G.L.5
-
35
-
-
41549112444
-
Hand weakness in duchenne muscular dystrophy and its relation to physical disability
-
PMID: 18207403
-
Mattar FL, Sobreira C (2008) Hand weakness in Duchenne muscular dystrophy and its relation to physical disability. Neuromuscul Disord 18: 193-198. doi: 10.1016/j.nmd.2007.11.004 PMID: 18207403
-
(2008)
Neuromuscul Disord
, vol.18
, pp. 193-198
-
-
Mattar, F.L.1
Sobreira, C.2
-
36
-
-
84857358770
-
Motor and respiratory heterogeneity in duchenne patients: Implication for clinical trials
-
PMID: 21920787
-
Humbertclaude V, Hamroun D, Bezzou K, Berard C, Boespflug-Tanguy O, et al. (2012) Motor and respiratory heterogeneity in Duchenne patients: implication for clinical trials. Eur J Paediatr Neurol 16: 149-160. doi: 10.1016/j.ejpn.2011.07.001 PMID: 21920787
-
(2012)
Eur J Paediatr Neurol
, vol.16
, pp. 149-160
-
-
Humbertclaude, V.1
Hamroun, D.2
Bezzou, K.3
Berard, C.4
Boespflug-Tanguy, O.5
|