SCOPUS 정보 검색 플랫폼

Clinical Pediatrics

Volumn 49, Issue 11, 2010, Pages 1011-1017

Review of duchenne muscular dystrophy (Dmd) for the pediatricians in the community

(3) Verma, Sumit a Anziska, Yaacov a Cracco, Joan a

a STATE UNIVERSITY OF NEW YORK (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ADENYLATE CYCLASE; ALPHA7 INTEGRIN; ANTIFIBROTIC AGENT; ANTISENSE OLIGONUCLEOTIDE; BISPHOSPHONIC ACID DERIVATIVE; CREATINE KINASE; DEFLAZACORT; DYSTROBREVIN; GLUTAMINE; PREDNISONE; SOMATOMEDIN; STAMULUMAB; TUMOR NECROSIS FACTOR ALPHA INHIBITOR; UTROPHIN; GLUCOCORTICOID;

ANAMNESIS; BEHAVIOR DISORDER; CLINICAL FEATURE; COMMUNITY; COMORBIDITY; DIFFERENTIAL DIAGNOSIS; DISEASE COURSE; DUCHENNE MUSCULAR DYSTROPHY; GENE MUTATION; GENETIC COUNSELING; HUMAN; NONHUMAN; REVIEW; SIDE EFFECT; STEROID THERAPY; UNSPECIFIED SIDE EFFECT; VERTEBRA FRACTURE; VIRAL GENE DELIVERY SYSTEM; WEIGHT GAIN; CHILD; COMMUNITY CARE; EARLY DIAGNOSIS; GENETICS; PATHOPHYSIOLOGY; PRACTICE GUIDELINE;

CHILD; COMMUNITY HEALTH SERVICES; COMORBIDITY; CREATINE KINASE; DIAGNOSIS, DIFFERENTIAL; EARLY DIAGNOSIS; GENETIC COUNSELING; GLUCOCORTICOIDS; HUMANS; MUSCULAR DYSTROPHY, DUCHENNE; PRACTICE GUIDELINES AS TOPIC;

EID: 79952276250 PISSN: 00099228 EISSN: None Source Type: Journal
DOI: 10.1177/0009922810378738 Document Type: Review

Times cited : (35)

References (30)

1
- 3042815561
- Dystrophinopathies
- 1st ed. Newton, MA: Butterworth-Heinemann, katriji B
- Darras BT, Menache CC. Dystrophinopathies. In: Katriji B, ed. Neuromuscular Disorders in Clinical Practice. 1st ed. Newton, MA: Butterworth-Heinemann; 2002:1028-1048.
- (2002) Neuromuscular Disorders in Clinical Practice , pp. 1028-1048
- Darras, B.T.¹ Menache, C.C.²

2
- 77949356580
- Duchenne muscular dystrophy: A 30-year population-based incidence study
- Dooley J, Gordon KE, Dodds L, MacSween J. Duchenne muscular dystrophy: a 30-year population-based incidence study. Clin Pediatr (Phila). 2010;49:177-179.
- (2010) Clin Pediatr (Phila) , vol.49 , pp. 177-179
- Dooley, J.¹ Gordon, K.E.² Dodds, L.³ MacSween, J.⁴

3
- 69249230932
- Delayed diagnosis in duchenne muscular dystrophy: Data from the muscular dystrophy surveillance
- Tracking, and Research Network (MD STARnet)
- Ciafaloni E, Fox DJ, Pandya S, et al. Delayed diagnosis in Duchenne muscular dystrophy: data from the Muscular Dystrophy Surveillance, Tracking, and Research Network (MD STARnet). J Pediatr. 2009;155:380-385.
- J Pediatr , vol.155 , pp. 380-385
- Ciafaloni, E.¹ Fox, D.J.² Pandya, S.³

4
- 72149108443
- Diagnosis and management of Duchenne muscular dystrophy part 1: Diagnosis, and pharmacological and psychosocial management
- Bushby K, Finkel R, Birnkrant DJ, et al. Diagnosis and management of Duchenne muscular dystrophy, part 1: diagnosis, and pharmacological and psychosocial management. Lancet Neurol. 2010;9:77-93.
- (2010) Lancet Neurol , vol.9 , pp. 77-93
- Bushby, K.¹ Finkel, R.² Birnkrant, D.J.³

5
- 0020522923
- Clinical investigation in Duchenne dystrophy: II. Determination of the 'power' of therapeutic trials based on the natural history
- Brooke MH, Fenichel GM, Griggs RC, et al: Clinical investigation in Duchenne dystrophy: 2. Determination of the "power" of therapeutic trials based on the natural history. Muscle Nerve. 1983;6:91-103. (Pubitemid 13092078)
- (1983) Muscle and Nerve , vol.6 , Issue.2 , pp. 91-103
- Brooke, M.H.¹ Fenichel, G.M.² Griggs, R.C.³

6
- 36349015997
- Duchenne muscular dystrophy: Issues in expanding newborn screening
- DOI 10.1097/MOP.0b013e3282f19f65, PII 0000848020071200000017
- Kemper AR, Wake MA. Duchenne muscular dystrophy: ssues in expanding newborn screening. Curr Opin Pediatr. 2007;19:700-704. (Pubitemid 350145241)
- (2007) Current Opinion in Pediatrics , vol.19 , Issue.6 , pp. 700-704
- Kemper, A.R.¹ Wake, M.A.²

7
- 33846658426
- Strategy for comprehensive molecular testing for Duchenne and Becker muscular dystrophies
- DOI 10.1089/gte.2006.10.229
- Stockley TL, Akber S, Bulgin N, Ray PN. Strategy for comprehensive molecular testing for Duchenne and Becker muscular dystrophies. Genet Test. 2006;10:229-243. (Pubitemid 46193273)
- (2006) Genetic Testing , vol.10 , Issue.4 , pp. 229-243
- Stockley, T.L.¹ Akber, S.² Bulgin, N.³ Ray, P.N.⁴

8
- 79952823522
- Online mendelian inheritance in man. muscular dystrophy, Accessed July
- Online Mendelian Inheritance in Man. Muscular dystrophy, Duchenne type; DMD. http://www.ncbi.nlm.nih.gov/omim/310200. Accessed July 13, 2010.
- Duchenne type; Dmd , vol.13 , pp. 2010

9
- 0024430346
- Molecular and phenotypic analysis of patients with deletions within the deletion-rich region of the Duchenne muscular dystrophy (DMD) gene
- Gillard EF, Chamberlain JS, Murphy EG, et al. Molecular and phenotypic analysis of patients with deletions within the deletion-rich region of the Duchenne muscular dystrophy (DMD) gene. Am J Hum Genet. 1989;45:507-520. (Pubitemid 19261438)
- (1989) American Journal of Human Genetics , vol.45 , Issue.4 , pp. 507-520
- Gillard, E.F.¹ Chamberlain, J.S.² Murphy, E.G.³ Duff, C.L.⁴ Smith, B.⁵ Burghes, A.H.M.⁶ Thompson, M.W.⁷ Sutherland, J.⁸ Oss, I.⁹ Bodrug, S.E.¹⁰ Klamut, H.J.¹¹ Ray, P.N.¹² Worton, R.G.¹³

10
- 0026766161
- Genetic and clinical correlations of Xp21 muscular dystrophy
- Bushby KM. Genetic and clinical correlations of Xp21 muscular dystrophy. J Inherit Metab Dis. 1992;15:551-564.
- (1992) J Inherit Metab Dis , vol.15 , pp. 551-564
- Bushby, K.M.¹

11
- 0023718118
- An explanation for the phenotypic differences between patients bearing partial deletions of the DMD locus
- Monaco AP, Bertelson CJ, Liechti-Gallati S, et al. An explanation for the phenotypic differences between patients bearing partial deletions of the DMD locus. Genomics. 1988;2:90-95.
- (1988) Genomics , vol.2 , pp. 90-95
- Monaco, A.P.¹ Bertelson, C.J.² Liechti-Gallati, S.³

12
- 0033794163
- Diagnosis of pediatric neuromuscular disorders in the era of DNA analysis
- Darras BT, Jones HR. Diagnosis of pediatric neuromuscular disorders in the era of DNA analysis. Pediatr Neurol. 2000;23:289-300.
- (2000) Pediatr Neurol , vol.23 , pp. 289-300
- Darras, B.T.¹ Jones, H.R.²

13
- 0033583984
- Signs and symptoms of Duchenne muscular dystrophy and Becker muscular dystrophy among carriers in the Netherlands: A cohort study
- DOI 10.1016/S0140-6736(98)10028-4
- Hoogerwaard EM, Bakker E, Ippel PF, et al. Signs and symptoms of Duchenne muscular dystrophy and Becker muscular dystrophy among carriers in The Netherlands: a cohort study. Lancet. 1999;353:2116-2119. (Pubitemid 29278481)
- (1999) Lancet , vol.353 , Issue.9170 , pp. 2116-2119
- Hoogerwaard, E.M.¹ Bakker, E.² Ippel, P.F.³ Oosterwijk, J.C.⁴ Majoor-Krakauer, D.F.⁵ Leschot, N.J.⁶ Van Essen, A.J.⁷ Brunner, H.G.⁸ Van Der Wouw, P.A.⁹ Wilde, A.A.M.¹⁰ De Visser, M.¹¹

14
- 0030453801
- Prenatal diagnosis of Duchenne and Becker muscular dystrophy
- DOI 10.1002/(SICI)1097-0223(199612)16:13<1187::AID-PD94>3.0.CO;2-2
- Abbs S. Prenatal diagnosis of Duchenne and Becker muscular dystrophy. Prenat Diagn. 1996;16:1187-1198. (Pubitemid 27107723)
- (1996) Prenatal Diagnosis , vol.16 , Issue.13 , pp. 1187-1198
- Abbs, S.¹

15
- 13144288103
- Dystrophinassociated proteins in muscular dystrophy
- Ozawa E, Yoshida M, Hagiwara Y, et al. Dystrophinassociated proteins in muscular dystrophy. Hum Mol Genet. 1990;4:11711-11716.
- (1990) Hum Mol Genet , vol.4 , pp. 11711-11716
- Ozawa, E.¹ Yoshida, M.² Hagiwara, Y.³

16
- 0027458614
- Diagnosis of occult muscular dystrophy: Importance of the 'chance' finding of elevated serum aminotransferase activities
- Morse RP, Rosman NP: Diagnosis of occult muscular dystrophy: importance of the "chance" finding of elevated serum aminotransferase activities. J Pediatr. 1993;122: 254-256. (Pubitemid 23041557)
- (1993) Journal of Pediatrics , vol.122 , Issue.2 , pp. 254-256
- Morse, R.P.¹ Rosman, N.P.²

17
- 41749096186
- Glucocorticoid corticosteroids for Duchenne muscular dystrophy
- CD003725
- Manzur AY, Kuntzer T, Pike M, Swan A. Glucocorticoid corticosteroids for Duchenne muscular dystrophy. Cochrane Database Syst Rev. 2008;(1):CD003725.
- (2008) Cochrane Database Syst Rev. , vol.1
- Manzur, A.Y.¹ Kuntzer, T.² Pike, M.³ Swan, A.⁴

18
- 19944427852
- Practice Parameter: Corticosteroid treatment of Duchenne dystrophy - Report of the Quality Standards Subcommittee of the American Academy of Neurology and the Practice Committee of the Child Neurology Society
- Moxley RT III, Ashwal S, Pandya S, et al. Practice parameter: corticosteroid treatment of Duchenne dystrophy: report of the Quality Standards Subcommittee of the American Academy of Neurology and the Practice Committee of the Child Neurology Society. Neurology. 2005;64:13-20. (Pubitemid 40082930)
- (2005) Neurology , vol.64 , Issue.1 , pp. 13-20
- Moxley III, R.T.¹ Ashwal, S.² Pandya, S.³ Connolly, A.⁴ Florence, J.⁵ Mathews, K.⁶ Baumbach, L.⁷ McDonald, C.⁸ Sussman, M.⁹ Wade, C.¹⁰

19
- 0035140165
- Deflazacort treatment of Duchenne muscular dystrophy
- DOI 10.1067/mpd.2001.109601
- Biggar WD, Gingras M, Fehlings DL, Harris VA, Steele CA. Deflazacort treatment of Duchenne muscular dystrophy. J Pediatr. 2001;138:45-50. (Pubitemid 32097140)
- (2001) Journal of Pediatrics , vol.138 , Issue.1 , pp. 45-50
- Biggar, W.D.¹ Gingras, M.² Fehlings, D.L.³ Harris, V.A.⁴ Steele, C.A.⁵

20
- 0041846566
- Vertebral fractures in boys with Duchenne muscular dystrophy
- Bothwell JE, Gordon KE, Dooley JM, MacSween J, Cummings EA, Salisbury S. Vertebral fractures in boys with Duchenne muscular dystrophy. Clin Pediatr (Phila). 2003;42:353-356. (Pubitemid 36909149)
- (2003) Clinical Pediatrics , vol.42 , Issue.4 , pp. 353-356
- Bothwell, J.E.¹ Gordon, K.E.² Dooley, J.M.³ MacSween, J.⁴ Cummings, E.A.⁵ Salisbury, S.⁶

21
- 30344435305
- Gene therapy strategies for Duchenne muscular dystrophy utilizing recombinant adeno-associated virus vectors
- DOI 10.1016/j.ymthe.2005.11.001, PII S1525001605016734
- Blankinship MJ, Gregorevic P, Chamberlain JS. Gene therapy strategies for Duchenne muscular dystrophy utilizing recombinant adeno-associated virus vectors. Mol Ther. 2006;13:241-249. (Pubitemid 43056889)
- (2006) Molecular Therapy , vol.13 , Issue.2 , pp. 241-249
- Blankinship, M.J.¹ Gregorevic, P.² Chamberlain, J.S.³

22
- 68649123826
- Therapy for neuromuscular disorders
- Arnett AL, Chamberlain JR, Chamberlain JS. Therapy for neuromuscular disorders. Curr Opin Genet Dev. 2009;19: 290-297.
- (2009) Curr Opin Genet Dev , vol.19 , pp. 290-297
- Arnett, A.L.¹ Chamberlain, J.R.² Chamberlain, J.S.³

23
- 68249119765
- Evaluation of vascular delivery methodologies to enhance rAAV6- mediated gene transfer to canine striated musculature
- Gregorevic P, Schultz BR, Allen JM, et al. Evaluation of vascular delivery methodologies to enhance rAAV6- mediated gene transfer to canine striated musculature. Mol Ther. 2009;17:1427-1433.
- (2009) Mol Ther , vol.17 , pp. 1427-1433
- Gregorevic, P.¹ Schultz, B.R.² Allen, J.M.³

24
- 43449113543
- Optimizing exon skipping therapies for DMD
- Yokota T, Duddy W, Partridge T. Optimizing exon skipping therapies for DMD. Acta Myol. 2007;26:179-184. (Pubitemid 351668927)
- (2007) Acta Myologica , vol.26 , Issue.3 , pp. 179-184
- Yokota, T.¹ Duddy, W.² Partridge, T.³

25
- 70349667577
- Emerging genetic therapies to treat Duchenne muscular dystrophy
- Nelson SF, Crosbie RH, Miceli MC, Spencer MJ. Emerging genetic therapies to treat Duchenne muscular dystrophy. Curr Opin Neurol. 2009;22:532-538.
- (2009) Curr Opin Neurol , vol.22 , pp. 532-538
- Nelson, S.F.¹ Crosbie, R.H.² Miceli, M.C.³ Spencer, M.J.⁴

26
- 0027382464
- Blood pressure nomograms for children and adolescents
- by height,sex, and age, in the United States
- Rosner B, Prineas RJ, Loggie JM, Daniels SR. Blood pressure nomograms for children and adolescents, by height,sex, and age, in the United States. J Pediatr. 1993;123:871-886.
- (1993) J Pediatr , vol.123 , pp. 871-886
- Rosner, B.¹ Prineas, R.J.² Loggie, J.M.³ Daniels, S.R.⁴

27
- 34247142867
- Delayed Developmental Language Milestones in Children with Duchenne's Muscular Dystrophy
- DOI 10.1016/j.jpeds.2006.12.045, PII S0022347607000133
- Cyrulnik SE, Fee RJ, De Vivo DC, Goldstein E, Hinton VJ. Delayed developmental language milestones in children with Duchenne's muscular dystrophy. J Pediatr. 2007;150:474-478. (Pubitemid 46602323)
- (2007) Journal of Pediatrics , vol.150 , Issue.5 , pp. 474-478
- Cyrulnik, S.E.¹ Fee, R.J.² De Vivo, D.C.³ Goldstein, E.⁴ Hinton, V.J.⁵

28
- 33644670773
- American Academy of pediatrics section on cardiology and cardiac surgery. cardiovascular health supervision for individuals affected by duchenne or becker muscular dystrophy
- American Academy of Pediatrics Section on Cardiology and Cardiac Surgery. Cardiovascular health supervision for individuals affected by Duchenne or Becker muscular dystrophy. Pediatrics. 2005;116:1569-1573.
- (2005) Pediatrics , vol.116 , pp. 1569-1573

29
- 4544272373
- Respiratory care of the patient with duchenne muscular dystrophy: ATS consensus statement
- DOI 10.1164/rccm.200307-885ST
- Finder JD, Birnkrant D, Carl J, et al. Respiratory care of the patient with Duchenne muscular dystrophy: an official ATS consensus statement. Am J Respir Crit Care Med. 2004;170:456-465. (Pubitemid 39214623)
- (2004) American Journal of Respiratory and Critical Care Medicine , vol.170 , Issue.4 , pp. 456-465
- Finder, J.D.¹ Birnkrant, D.² Carl, J.³ Farber, H.J.⁴ Gozal, D.⁵ Iannaccone, S.T.⁶ Kovesi, T.⁷ Kravitz, R.M.⁸ Panitch, H.⁹ Schramm, C.¹⁰ Schroth, M.¹¹ Sharma, G.¹² Sievers, L.¹³ Silvestri, J.M.¹⁴ Sterni, L.¹⁵

30
- 76549130473
- Diagnosis and management of Duchenne muscular dystrophy
- part 2: implementation of multidisciplinary care
- Bushby K, Finkel R, Birnkrant DJ, et al. Diagnosis and management of Duchenne muscular dystrophy, part 2: implementation of multidisciplinary care. Lancet Neurol. 2010;9:177-189.
- (2010) Lancet Neurol , vol.9 , pp. 177-189
- Bushby, K.¹ Finkel, R.² Birnkrant, D.J.³

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.