Protein-energy malnutrition as the first manifestation of cystic fibrosis in infancy

Pediatrics International

Volumn 51, Issue 5, 2009, Pages 678-683

  Fustik, Stojka ^a   Jacovska, Tanja ^a   Spirevska, Lidija ^a   Koceva, Svetlana ^b  

^a UNIVERSITY CHILDREN S HOSPITAL   (Macedonia)

^b MACEDONIAN ACADEMY OF SCIENCES AND ARTS   (Macedonia)

Author keywords

Anemia; Cystic fibrosis; Cystic fibrosis transmembrane conductance regulator mutations; Edema; Hypoproteinemia

Indexed keywords

ALBUMIN; HEMOGLOBIN;

ARTICLE; BREAST MILK; CLINICAL ARTICLE; CLINICAL EXAMINATION; CLINICAL FEATURE; CONTROLLED STUDY; CYSTIC FIBROSIS; DISEASE COURSE; EARLY DIAGNOSIS; ERYTHROCYTE; ERYTHROCYTE COUNT; F508 GENE; FEMALE; G542X GENE; GENE; GENE MUTATION; GENOTYPE; HEALTH PROGRAM; HUMAN; INFANT; LABORATORY TEST; MALE; N130K GENE; PREVALENCE; PRIORITY JOURNAL; PROTEIN BLOOD LEVEL; PROTEIN CALORIE MALNUTRITION; RISK FACTOR;

COMORBIDITY; CYSTIC FIBROSIS; FEMALE; GREECE; HOSPITALS, UNIVERSITY; HUMANS; INFANT; INFANT, NEWBORN; MALE; PROTEIN-ENERGY MALNUTRITION; RISK FACTORS;

EID: 70349586105     PISSN: 13288067     EISSN: 1442200X     Source Type: Journal    
DOI: 10.1111/j.1442-200X.2009.02855.x     Document Type: Article

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