Electrocardiographic changes following exercise in the congenitally deaf school children: relationship with Jervell Lange Neilsen syndrome (the Long QT syndrome).

No abstract is available for this paper.

• Publication year

  1998

• Venue

  Indian journal of physiology and pharmacology

• Publication date

  1998-10-01

• Fields of study

  Medicine

• Identifiers
  PMID 10874353
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar, PubMed

• No claims are published for this paper.

• No concepts are published for this paper.

• The long-QT syndrome.

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• CONGENITAL DEAF‐MUTISM, FUNCTIONAL HEART DISEASE WITH PROLONGATION OF THE Q‐T INTERVAL, AND SUDDEN DEATH

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• Quantitative analysis of T wave abnormalities and their prognostic implications in the idiopathic long QT syndrome.

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• The idiopathic long QT syndrome: the need for a prospective registry.

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• Romano-Ward prolonged QT syndrome with intermittent T wave alternans and atrioventricular block.

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• Effect of unilateral stellate ganglion blockade and stimulation on experimental arrhythmias.

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• Congenital deafness and cardiac arrhythmias.

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• THE CARDIO AUDITORY SYNDROME OF JERVELL AND LANGENIELSON: REPORT OF AN ADDITIONAL CASE WITH RADIOELECTROCARDIOGRAPHIC MONITORING DURING EXERCISE

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

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• A NEW FAMILIAL CARDIAC SYNDROME IN CHILDREN.

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

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