Manometric study in Kearns-Sayre syndrome

Diseases of the Esophagus

Volumn 14, Issue 1, 2001, Pages 63-66

  Katsanos, K H ^a   Nastos, D ^a   Noussias, V ^a   Christodoulou, D ^a   Kappas, A ^a   Tsianos, E V ^a  

^a UNIVERSITY OF IOANNINA   (Greece)

Author keywords

[No Author keywords available]

Indexed keywords

CALCIUM; MAGNESIUM; POTASSIUM; UBIDECARENONE; VITAMIN D;

ADULT; ARTICLE; ATAXIA; CASE REPORT; CLINICAL EXAMINATION; CLINICAL FEATURE; CONTROLLED STUDY; DIET THERAPY; DYSPHAGIA; ELECTROCARDIOGRAM; ESOPHAGUS MANOMETRY; ESOPHAGUS MOTILITY; ESOPHAGUS PRESSURE; FEMALE; GROWTH RETARDATION; HEARING IMPAIRMENT; HEMISPHERE; HUMAN; KEARNS SAYRE SYNDROME; LONG QT SYNDROME; MAJOR CLINICAL STUDY; MUSCLE BIOPSY; MUSCLE RELAXATION; NUCLEAR MAGNETIC RESONANCE IMAGING; PHARYNX; PRIORITY JOURNAL; PROGNOSIS; QUALITY OF LIFE; SWALLOWING; TREATMENT OUTCOME; UPPER ESOPHAGUS SPHINCTER; UPPER RESPIRATORY TRACT INFECTION;

ADOLESCENT; DEGLUTITION DISORDERS; ESOPHAGUS; FEMALE; HUMANS; KEARNS-SAYER SYNDROME; MANOMETRY; PHARYNX;

EID: 0034921006     PISSN: 11208694     EISSN: None     Source Type: Journal    
DOI: 10.1046/j.1442-2050.2001.00152.x     Document Type: Article

References (12)

1. Kearns-Sayre syndrome
2. Mitochondrial encephalomyopathy and hypoparathyroidism associated with a duplication and a deletion of mitochondrial deoxyribonucleic acid
3. Kearns-Sayre syndrome, hypoparathyroidism and basal ganglia calcification
4. Endocrine dysfunction in Kearns-Sayre syndrome
5. Manometric characteristics of cervical dysphagia in a patient with the Kearns-Sayre syndrome
6. Oculoskeletal myopathy with abnormal mitochondria
7. Widespread tissue distribution of mitochondrial DNA deletions in Kearns-Sayer syndrome
8. Hypoparathyroidism and deafness associated with pleioplasmic large scale rearrangements of the mitochondrial DNA: A clinical and molecular genetic study of four children with Kearns-Sayre syndrome
9. Kearns-Sayre syndrome with hypoparathyroidism
10. Maternally inherited duplication of the mitochondrial genome in a syndrome of proximal tubulopathy, diabetes mellitus and cerebral ataxia
11. Hypoparathyroidism and insulin-dependent diabetes mellitus in a patient with Kearns-Sayre syndrome harbouring in mitochondrial DNA deletion
12. Renal tubular involvement mimicking Bartter syndrome in a patient with Kearns-Sayre syndrome