Progressive nature of aspartylglucosaminuria

Acta Paediatrica, International Journal of Paediatrics

Volumn 91, Issue 3, 2002, Pages 255-257

  Arvio, P ^a   Arvio, M ^a  

^a NONE   (Finland)

Author keywords

Finnish disease heritage; Lysosomal storage disorder; Metabolic disease

Indexed keywords

ADOLESCENT; ADULT; AGE; AGED; ASPARTYLGLYCOSAMINURIA; CHILD; CLINICAL FEATURE; DISEASE COURSE; DISEASE SIMULATION; FINLAND; HEALTH STATUS; HUMAN; INFANT; MAJOR CLINICAL STUDY; MENTAL DEFICIENCY; MOTOR PERFORMANCE; NEWBORN; PERSONALITY; PHYSICAL EXAMINATION; PRIORITY JOURNAL; SELF HELP; SHORT SURVEY; SPEECH; SYMPTOM; TREATMENT OUTCOME;

ADOLESCENT; ADULT; ASPARTYLGLUCOSYLAMINASE; CHILD; CHILD, PRESCHOOL; DISEASE PROGRESSION; FEMALE; FINLAND; GENETIC PREDISPOSITION TO DISEASE; HUMANS; INCIDENCE; INFANT, NEWBORN; MALE; METABOLISM, INBORN ERRORS; MIDDLE AGED; RISK ASSESSMENT;

EID: 0036212391     PISSN: 08035253     EISSN: None     Source Type: Journal    
DOI: 10.1080/08035250252833842     Document Type: Article

References (19)

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