Tải bản đầy đủ (.pdf) (3 trang)

Andersons pediatric cardiology 1591

Bạn đang xem bản rút gọn của tài liệu. Xem và tải ngay bản đầy đủ của tài liệu tại đây (60.83 KB, 3 trang )

conductionsystemstudy.Chest.1984;86:444–
450.
243.PerloffJK,StevensonWG,RobertsNK,Cabeen
W,WeissJ.Cardiacinvolvementinmyotonic
musculardystrophy(steinert'sdisease):a
prospectivestudyof25patients.AmJCardiol.
1984;54:1074–1081.
244.IBID190.
245.ChakrabartiA,PearceJMS.Scapuloperoneal
syndromewithcardiomyopathy:reportofa
familywithautosomaldominantinheritanceand
unusualfeatures.JNeurolNeurosurg
Psychiatry.1981;44(12):1146–1152.
246.ThomasPK,SchottGD,Morgan-HughesJA.
Adultonsetofscapuloperonealmyopathy.J
NeurolNeurosurgPsychiatry.
1975;38(10):1008–1015.
247.NigroG,ComiLI,PolitanoL,etal.Evaluation
ofthecardiomyopathyinbeckermuscular
dystrophy.MuscleNerve.1995;18(3):283–291.
248.SaitoM,KawaiH,AkaikeM,etal.Cardiac
dysfunctionwithbeckermusculardystrophy.Am
HeartJ.1996;132(3):642–647.
249.AmmendolaE,RussoV,PolitanoL,Santangelo
L,CalabroR.Isheartratevariabilityavalid
parametertopredictsuddendeathinpatients
withBecker'smusculardystrophy?Heart.


2006;92(11):1686–1687.
250.FinstererJ,StollbergerC.Theheartinhuman


dystrophinopathies.Cardiology.2003;99(1):1–
19.
251.KomanapalliCB,SeraV,SlaterMS,etal.
Becker'smusculardystrophyandorthotopic
hearttransplantation:perioperative
considerations.HeartSurgForum.
2006;9(2):E604–E606.
252.OsborneRJ,WelleS,VenanceSL,ThorntonCA,
TawilR.ExpressionprofileofFSHDsupportsa
linkbetweenretinalvasculopathyandmuscular
dystrophy.Neurology.2007;68(9):569–577.
253.TrevisanCP,PastorelloE,ArmaniM,etal.
Facioscapulohumeralmusculardystrophyand
occurrenceofheartarrhythmia.EurNeurol.
2006;56(1):1–5.
254.StevensonWG,PerloffJK,WeissJN,Anderson
TL.Facioscapulohumeralmusculardystrophy:
evidenceforselective,genetic
electrophysiologiccardiacinvolvement.JAm
CollCardiol.1990;15(2):292–299.
255.RaffaeleDiBarlettaM,RicciE,GalluzziG,et
al.DifferentmutationsintheLMNAgenecause
autosomaldominantandautosomalrecessive
Emery-driefussmusculardystrophy.AmJHum
Genet.2000;66(4):1407–1412.


256.MerliniL,GranataC,DominiciP,BonfiglioloS.
Emery-dreifussmusculardystrophy:reportof
fivecasesinafamilyandreviewofthe

literature.MuscleNerve.1986;9(6):481–485.
257.YoshiokaM,SaidaK,ItagakiY,KamiyaT.
Followupstudyofcardiacinvolvementin
Emery-dreifussmusculardystrophy.ArchDis
Child.1989;64(5):713–715.
258.KichukChrisantMR,Drummond-WebbJ,
HallowellS,FriedmanNR.Cardiac
transplantationintwinswithautosomal
dominantEmery-dreifussmusculardystrophy.J
HeartLungTransplant.2004;23(4):496–498.
259.Al-RuwaishidA,VajsarJ,TeinI,BensonL,Jay
V.Centronuclearmyopathyandcardiomyopathy
requiringhearttransplant.BrainDev.
2003;25(1):62–66.
260.IlkovskiB,CooperST,NowakK,etal.
Nemalinemyopathycausedbymutationsinthe
musclealpha-skeletal-actingene.AmJHum
Genet.2001;68(6):1333–1343.
261.D'AmicoA,GrazianoC,PacileoG,etal.Fatal
hypertrophiccardiomyopathyandnemaline
myopathyassociatedwithACTA1k336e
mutation.NeuromusculDisord.2006;16(9–
10):548–552.
262.NowakKJ,WattanasirichaigoonD,GoebelHH,



×