Tải bản đầy đủ (.pdf) (3 trang)

Andersons pediatric cardiology 1586

Bạn đang xem bản rút gọn của tài liệu. Xem và tải ngay bản đầy đủ của tài liệu tại đây (60.85 KB, 3 trang )

146.CarcellerAM,FouronJC,LetarteJ,etal.
Absenceofmitralvalveprolapseinjuvenile
hyperthyroidism.AmJCardiol.1984;54:455–
456.
147.PilapilVR,WatsonDG.Electrocardiogramin
hyperthyroidchildren.AmJDisChild.
1979;119:245–248.
148.ForfarJC,MuirAL,SawersSA,ToftAD.
Abnormalleftventricularfunctionin
hyperthyroidism.Evidenceforapossible
reversiblecardiomyopathy.NEnglJMed.
1982;307:1165–1170.
149.CavalloA,JosephCJ,CastaA.Cardiac
complicationsinjuvenilehyperthyroidism.AmJ
DisChild.1984;138:479–482.
150.ReddyER.Changesinheartsizeandvolumein
certainendocrinalandnutritionaldeficiency
diseases.Acorrelativestudyintwentyadult
patients.JCanAssocRadiol.1984;35(1):17–19.
151.WillisFR,ByrneGC,JonesTW.Fludrocortisone
inducedheartfailureinAddison'sdisease.J
PaediatrChildHealth.1994;30(3):280–281.
152.Barragan-CamposHM,Barrera-RamirezCF,
IturraldeTorresP,etal.Kearns-sayresyndromes
anabsoluteindicationforprohylactic
implantationofdefinitivepacemaker?ArchInst
CardiolMex.1999;69(6):559–565.


153.SubbiahRN,KucharD,BaronD.Torsadesde
pointesinapatientwithkearns-sayresyndrome:


afortunatefinding.PacingClinElectrophysiol.
2007;30(1):137–139.
154.Marin-GarciaJ,GoldenthalMJ,FilianoJJ.
Cardiomyopathyassociatedwithneurologic
disordersandmitochondrialphenotype.JChild
Neurol.2002;17(10):759–765.
155.RashidA,KimMH.Kearns-sayresyndrome:
associationwithlongQTsyndrome?J
CardiovascElectrophysiol.2002;13(2):184–185.
156.Hernandez-LuisC,Garcia-MoranE,Rubio-Sanz
J,Fernandez-AvilesF.Kearns-sayresyndrome:
recurrentsyncopeandatrialflutter.RevEsp
Cardiol.2007;60(1):89–90.
157.KatsanosKH,PappasCJ,PatsourasD,etal.
Alarmingatrioventricularblockandmitralvalve
prolapseintheKearns-sayresyndrome.IntJ
Cardiol.2002;83(2):179–181.
158.ChallaS,KanikannanMA,MurthyJM,
BhoompallyVR,SurathM.Diagnosisof
mitochondrialdiseases:clinicalandhistological
studyofsixtypatientswithraggedredfibers.
NeurolIndia.2004;52(3):353–358.
159.AgapitosE,PavlopoulosPM,PatsourisE,
DavarisP.Subacutenectrozing
encephalomyelopathy(leigh'sdisease):a


clinicopathologicstudyoftencases.GenDiagn
Pathol.1997;142(5–6):335–341.
160.ClarkeSL,IkonN,RyanRO.Barthsyndrome:

connectingcardiolipintocardiomyopathy.
Lipids.2017;52:99–108.
161.RobertsAE,NixonC,StewardCG,etal.The
barthsyndromeregistry:distinguishingdisease
characteristicsandgrowthdatafroma
longitudinalstudy.AmJMedGenetA.
2012;158A:2726–2732.
162.BradyAN,ShehataBM,FernhoffPM.X-linked
fetalcardiomyopathycausedbyanovel
mutationintheTAZgene.PrenatDiagn.
2006;26:462–465.
163.ClarkeSL,BowronA,GonzalezIL,etal.Barth
syndrome.OrphanetJRareDis.2013;8:23.
164.SpencerCT,ByrneBJ,GeqitzMH,etal.
VentriculararrhythmiaintheX-linked
cardiomyopathybarthsyndrome.Pediatr
Cardiol.2005;26(5):632–637.
165.DesviatLR,ClaveroS,Perez-CerdaC,etal.
Newsplicingmutationsinpropionicacidemia.J
HumGenet.2006;51(11):992–997.
166.MassoudAF,LEanordJV.Cardiomyopathyin
proprionicacidemia.EurJPediatr.
1993;152(5):441–445.
167.BaumgartnerD,Scholl-BurgiS,SassJO,etal.



×