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Volumn 197, Issue 10, 2001, Pages 699-709
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Hepatic failure with neonatal tissue siderosis of hemochromatotic type in an infant presenting with meconium ileus. Case report and differential diagnosis of the perinatal iron storage disorders
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Author keywords
Atomic absorption spectroscopy; Gene sequencing; Histochemistry; Neonatal iron storage disease
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Indexed keywords
FERRITIN;
IRON;
PHENYLALANINE;
TOXIC SUBSTANCE;
ADRENAL GLAND;
AMNIONITIS;
ANTIPHOSPHOLIPID SYNDROME;
ARTICLE;
ATOMIC ABSORPTION SPECTROMETRY;
AUTOPSY;
BLOOD GROUP ABO INCOMPATIBILITY;
CASE REPORT;
CHROMOSOME ABERRATION;
COLLAPSE;
CONGENITAL HEART DISEASE;
CYSTIC FIBROSIS;
CYTOMEGALOVIRUS;
DEATH;
DISEASE CLASSIFICATION;
DISEASE COURSE;
EVIDENCE BASED MEDICINE;
FEMALE;
GENE SEQUENCE;
GESTATIONAL AGE;
HEART;
HEMOCHROMATOSIS;
HEMOSIDEROSIS;
HISTOCHEMISTRY;
HUMAN;
HUMAN TISSUE;
HYALINE MEMBRANE DISEASE;
HYPERFERRITINEMIA;
IMMATURITY;
IMMUNOPATHOLOGY;
INFANT;
INFECTION;
INTENSIVE CARE;
INTENSIVE CARE UNIT;
KIDNEY;
LIVER;
LIVER FAILURE;
LIVER REGENERATION;
LUNG DYSPLASIA;
MECONIUM ASPIRATION;
MECONIUM ILEUS;
METABOLIC DISORDER;
MUTATION;
NEWBORN PERIOD;
PANCREAS;
PREMATURITY;
RETICULOENDOTHELIAL SYSTEM;
RHESUS INCOMPATIBILITY;
SALIVARY GLAND;
STATISTICAL ANALYSIS;
TRISOMY 18;
TRISOMY 21;
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EID: 0034748825
PISSN: 03440338
EISSN: None
Source Type: Journal
DOI: 10.1016/s0344-0338(04)70148-x Document Type: Article |
Times cited : (14)
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References (60)
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