Literature DB >> 14176667

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

G R FRASER, P FROGGATT, T N JAMES.   

Abstract

Entities:  

Keywords:  ABNORMALITIES; ADOLESCENCE; ANEMIA, HYPOCHROMIC; CHILD; COCHLEA; CONVULSIONS; DEAFNESS; DEATH, SUDDEN; ELECTROCARDIOGRAPHY; ENGLAND; GENETICS, HUMAN; HEART CONDUCTION SYSTEM; HEART DEFECTS, CONGENITAL; IRELAND; PATHOLOGY; PHONOCARDIOGRAPHY; STRESS; SYNCOPE

Mesh：

Year:  1964        PMID： 14176667

Source DB:  PubMed          Journal:  Q J Med        ISSN： 0033-5622


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  22 in total

1.  Bidirectional tachycardia in a child. A study using His bundle electrography.

Authors:  D S Reid; M Tynan; L Braidwood; G R Fitzgerald
Journal:  Br Heart J       Date:  1975-03

Review 2.  Drug-induced QT interval shortening: potential harbinger of proarrhythmia and regulatory perspectives.

Authors:  Rashmi R Shah
Journal:  Br J Pharmacol       Date:  2009-06-25       Impact factor: 8.739

3.  Assessment of deafmute patients: a study of ten years.

Authors:  Mangal Singh; S C Gupta; Alok Singla
Journal:  Indian J Otolaryngol Head Neck Surg       Date:  2009-03-31

4.  Hereditary prolongation of QT interval . Study of two families.

Authors:  G E Gale; C K Bosman; R B Tucker; J B Barlow
Journal:  Br Heart J       Date:  1970-07

5.  A family with heritable electrocardiographic QT-prolongation.

Authors:  P J van der Straaten; C L Bruins
Journal:  J Med Genet       Date:  1973-06       Impact factor: 6.318

6.  Observation on a case of Jervell and Lange-Neilsen syndrome in an adult.

Authors:  F Furlanello; F Maccà; C Dal Palù
Journal:  Br Heart J       Date:  1972-06

7.  Surdo-cardiac syndrome: incidence among children in schools for the deaf.

Authors:  J E Fay; P M Olley; M W Partington; V B Kavety; G Ahmad
Journal:  Can Med Assoc J       Date:  1971-10-09       Impact factor: 8.262

Review 8.  Inherited diseases of the inner ear in man in the light of studies on the mouse.

Authors:  M S Deol
Journal:  J Med Genet       Date:  1968-06       Impact factor: 6.318

9.  Conductive hearing loss and malformed low-set ears, as a possible recessive syndrome.

Authors:  M C Mengel; B W Konigsmark; C I Berlin; V A McKusick
Journal:  J Med Genet       Date:  1969-03       Impact factor: 6.318

10.  An unusual cause of apparent epilepsy: ECG and EEG findings in a case of Jervell Lange-Neilson syndrome.

Authors:  P J Selby; M V Driver
Journal:  J Neurol Neurosurg Psychiatry       Date:  1977-11       Impact factor: 10.154
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