Mitochondrial neurogastrointestinal encephalomyopathy (MNGIE): Case report with a new mutation

European Journal of Pediatrics

Volumn 169, Issue 11, 2010, Pages 1375-1378

  Barış, Zeren ^a   Eminoğlu, Tuba ^a   Dalgıç, Buket ^a   Tümer, Leyla ^a   Hasanoğlu, Alev ^a  

^a GAZI UNIVERSITY FACULTY OF MEDICINE   (Turkey)

Author keywords

Gastrointestinal dysmotility; Mitochondrial neurogastrointestinal encephalomyopathy; New mutation

Indexed keywords

DEOXYURIDINE; LACTIC ACID; THYMIDINE; THYMIDINE PHOSPHORYLASE;

ADULT; ANOREXIA NERVOSA; ARTICLE; CARDIOPULMONARY ARREST; CASE REPORT; CATALYSIS; CLINICAL FEATURE; COMPUTER ASSISTED TOMOGRAPHY; DIAGNOSTIC ERROR; ENZYME ANALYSIS; FEMALE; GENE MUTATION; GENETIC ANALYSIS; HUMAN; HYPONATREMIA; INTESTINE OBSTRUCTION; LABORATORY TEST; METABOLIC ACIDOSIS; MNGIE SYNDROME; NEUROIMAGING; NUCLEAR MAGNETIC RESONANCE IMAGING; PARENTERAL NUTRITION; PHYSICAL EXAMINATION; PNEUMONIA; PRIORITY JOURNAL; ULTRASOUND;

EID: 77957684211     PISSN: 03406199     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00431-010-1237-0     Document Type: Article

References (8)

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