Hereditary prolongation of QT interval . Study of two families. - Wikidata - wikimedia - TriplyDB

Hereditary prolongation of QT interval . Study of two families.

Hereditary prolongation of QT interval . Study of two families.

http://www.wikidata.org/entity/Q33170558

about

Hypoxia at the heart of sudden infant death syndrome?Familial qt prolongation and risk of sudden death.Hereditary prolongation of QT interval Atrioventricular dissociation with prolonged QT interval and syncopal attacks in a 10-year-old boy.Observation on a case of Jervell and Lange-Neilsen syndrome in an adult A study of the inheritance pattern of Romano-Ward syndrome. Prolonged Q-T interval, syncope, and sudden death.Prolonged QT interval and cardiac arrhythmias in two neonates: sudden infant death syndrome in one case QT interval in right and left bundle-branch block.Sudden unexpected death in infants. Evidence on a lethal cardiac arrhythmia.An unusual cause of apparent epilepsy: ECG and EEG findings in a case of Jervell Lange-Neilson syndrome

P2860

Q26825254-EDB9DC67-2077-4285-92CB-D0593AA696EF Q33146961-414BFDC2-C925-4A2D-ACCC-B511B6CDF53E Q33170564-318B484F-51F7-4CD0-AD4E-C2A2339EC2ED Q33171053-0CE09E98-C5D5-417C-A9EB-8F2F37FC0F95 Q33171223-8C3DFB3B-9815-4176-9B21-7901E540C968 Q33173085-AD94E832-7099-4DA4-8ADE-5D437908401B Q34988059-F6A147EA-310A-40D6-8BAC-8B1F102BEE2B Q36100371-16D0D919-03F0-458E-8FFA-AD2EAE3B4CE1 Q36659743-AD89DEF1-D40A-4BE3-A2B9-273E024301E9 Q37056507-FE8CAB77-892C-43E7-BFDD-A8227294411F

P2860

Hereditary prolongation of QT interval . Study of two families.

http://www.wikidata.org/entity/Q33170558

description

1970 nî lūn-bûn

@nan

1970 թուականի Յուլիսին հրատարակուած գիտական յօդուած

@hyw

1970 թվականի հուլիսին հրատարակված գիտական հոդված

@hy

1970年の論文

@ja

1970年論文

@yue

1970年論文

@zh-hant

1970年論文

@zh-hk

1970年論文

@zh-mo

1970年論文

@zh-tw

1970年论文

@wuu

name

Hereditary prolongation of QT interval . Study of two families.

@ast

Hereditary prolongation of QT interval . Study of two families.

@en

type

label

Hereditary prolongation of QT interval . Study of two families.

@ast

Hereditary prolongation of QT interval . Study of two families.

@en

prefLabel

Hereditary prolongation of QT interval . Study of two families.

@ast

Hereditary prolongation of QT interval . Study of two families.

@en

P1433

Q33170558-E8005F3D-1008-48D4-9FE2-DDDE6F37A2F1

P1476

Q33170558-E52ECB7B-3380-498B-9A91-0DC1E83F94CA

P2093

Q33170558-3ED0E4DE-07D9-4529-B34A-C7546A338CA6

Q33170558-7BA39BC1-8FAF-4A84-818C-981BACC041C6

Q33170558-7D11A8AB-AEA4-4929-9EF2-7052B98FFDD0

Q33170558-8A936D5A-7F51-4873-867B-743F3E75E44B

P2860

Q33170558-23B99FCF-DF48-4F1E-A3C6-E5F93D55487B

Q33170558-7511B2C8-A525-4A7C-9DA3-5668FBB2A79B

Q33170558-7DF499C2-A89C-4A99-90D8-E08EF35E81DA

Q33170558-8AC34048-53D8-4980-B5DB-07F47AD650E6

Q33170558-B3306B4D-C2E5-4CAA-9640-EBA62DEFE5D4

Q33170558-B66FEAE5-A42B-48ED-B7BA-858F1DD26E57

Q33170558-B764C6BD-21E4-4A93-A207-04E9185E79F3

Q33170558-DD78E997-D705-4574-895F-50244911B9AC

Q33170558-F0306701-0EC8-457C-84C2-C71E26832100

P304

Q33170558-313ED07B-0D76-413E-BF5B-BF4A1E8A5462

P31

Q33170558-E1070D3F-55D0-45AE-B072-84DF9D144A77

P356

Q33170558-A98A8838-4684-4A36-B5F5-F1FE1485F959

P433

Q33170558-70D579BB-DAE3-4022-AB91-8FB400CAA436

P478

Q33170558-93A302AD-A416-4CF9-B8EE-58C1907E3206

P577

Q33170558-0B45D7CD-2570-4A40-9E23-B78DE02F3AAA

P5875

Q33170558-2ED57350-DBB2-4FDB-9EDE-DE32E30F570A

P698

Q33170558-6E416E90-CECE-4BD8-9CE6-183C99C29963

P932

Q33170558-59DBDCCF-1DD9-43E8-A340-ED338021C51B

P356

P1433

British heart journal

P1476

Hereditary prolongation of QT interval . Study of two families.

@en

P2093

Barlow JB

http://www.w3.org/2001/XMLSchema#string

Bosman CK

http://www.w3.org/2001/XMLSchema#string

Gale GE

http://www.w3.org/2001/XMLSchema#string

Tucker RB

http://www.w3.org/2001/XMLSchema#string

P2860

Congenital deaf-mutism, prolonged QT interval, syncopal attacks and sudden death.

A NEW FAMILIAL CARDIAC SYNDROME IN CHILDREN.

[RARE CARDIAC ARRYTHMIAS OF THE PEDIATRIC AGE. II. SYNCOPAL ATTACKS DUE TO PAROXYSMAL VENTRICULAR FIBRILLATION. (PRESENTATION OF 1ST CASE IN ITALIAN PEDIATRIC LITERATURE)].

CONGENITAL DEAFNESS ASSOCIATED WITH ELECTROCARDIOGRAPHIC ABNORMALITIES, FAINTING ATTACKS AND SUDDEN DEATH. A RECESSIVE SYNDROME.

CONGENITAL CARDIAC ARRHYTHMIA.

GENETICAL ASPECTS OF THE CARDIO-AUDITORY SYNDROME OF JERVELL AND LANGE-NIELSEN (CONGENITAL DEAFNESS AND ELECTROCARDIOGRAPHIC ABNORMALITIES).

The surdo-cardiac syndrome: three new cases of congenital deafness with syncopal attacks and Q-T prolongation in the electrocardiogram.

Congenital deaf-mutism, functional heart disease with prolongation of the Q-T interval and sudden death.

Fundamental mechanisms in the genesis and evolution of myocardial fibrillation.

P304

505-509

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

P356

10.1136/HRT.32.4.505

http://www.w3.org/2001/XMLSchema#string

P433

4

http://www.w3.org/2001/XMLSchema#string

P478

32

http://www.w3.org/2001/XMLSchema#string

P577

1970-07-01T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P5875

18771520

http://www.w3.org/2001/XMLSchema#string

P698

4393533

http://www.w3.org/2001/XMLSchema#string

P932

487362

http://www.w3.org/2001/XMLSchema#string