Clinical and genetic spectrum of mitochondrial neurogastrointestinal encephalomyopathy

Brain

Volumn 134, Issue 11, 2011, Pages 3326-3332

  Garone, Caterina ^a,b,c   Tadesse, Saba ^a   Hirano, Michio ^a  

^a New York Presbyterian Morgan Stanley Children's Hospital   (United States)

^b UNIVERSITY OF TURIN   (Italy)

^c UNIVERSITY OF BOLOGNA   (Italy)

Author keywords

BMT; encephalomyopathy; mitochondrial disease; MNGIE; TYMP

Indexed keywords

PHOSPHORYLASE; THYMIDINE;

ALLOGENEIC HEMATOPOIETIC STEM CELL TRANSPLANTATION; ARTICLE; BLOOD BUFFY COAT; CACHEXIA; CHILD; CLINICAL FEATURE; CONTROLLED STUDY; DIAGNOSTIC ERROR; DISEASE COURSE; DOMINICAN REPUBLIC; ENVIRONMENTAL FACTOR; EUROPE; FEMALE; GASTROINTESTINAL MOTILITY DISORDER; GENE MUTATION; GENETIC SCREENING; GENETIC VARIABILITY; GENETICS; GENOTYPE; HUMAN; HUMAN TISSUE; KAPLAN MEIER METHOD; LEUKODYSTROPHY; MAJOR CLINICAL STUDY; MALE; MEDICAL RECORD; METABOLIC DISORDER; MNGIE SYNDROME; MORTALITY; PANCREAS EXOCRINE INSUFFICIENCY; PERIPHERAL NEUROPATHY; PHENOTYPE; PRESCHOOL CHILD; PREVALENCE; PRIORITY JOURNAL; SCHOOL CHILD; TYMPANIC TEMPERATURE;

EID: 81055133547     PISSN: 00068950     EISSN: 14602156     Source Type: Journal    
DOI: 10.1093/brain/awr245     Document Type: Article

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