Metabolic mimics: The disorders of N-linked glycosylation

Seminars in Pediatric Neurology

Volumn 12, Issue 3, 2005, Pages 144-151

  Patterson, Marc C ^a  

^a NewYork Presbyterian Hospital   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CARBOHYDRATE; FUCOSE; MANNOSE; TRANSFERRIN;

ATAXIA; BLOOD CLOTTING DISORDER; CHEMICAL ANALYSIS; CLINICAL FEATURE; CONGENITAL DISORDER OF GLYCOSYLATION TYPE 1; CONGENITAL DISORDER OF GLYCOSYLATION TYPE 1A; CONGENITAL DISORDER OF GLYCOSYLATION TYPE 1B; CONGENITAL DISORDER OF GLYCOSYLATION TYPE 2C; DEVELOPMENTAL DISORDER; DIAGNOSTIC TEST; DISEASE CLASSIFICATION; GENOTYPE; GLYCOBIOLOGY; GLYCOSYLATION; HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; HISTOPATHOLOGY; HUMAN; IMMUNOASSAY; IMMUNOELECTROPHORESIS; ION EXCHANGE CHROMATOGRAPHY; LABORATORY TEST; NERVOUS SYSTEM; RECURRENT INFECTION; REVIEW; SCREENING; SEIZURE; STROKE;

GLYCOSYLATION; HUMANS; METABOLIC DISEASES; MOLECULAR BIOLOGY; MOLECULAR MIMICRY;

EID: 33644759171     PISSN: 10719091     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.spen.2005.10.002     Document Type: Review

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