Pediatric ferroportin disease

Journal of Pediatric Gastroenterology and Nutrition

Volumn 63, Issue 6, 2016, Pages e205-e207

  Galicia Poblet, Gonzalo ^a,b   Cid París, Ester ^a   López Andrés, Nerea ^a   Losada Pajares, Alba ^a   Jurado López, Juan Carlos ^a   Moreno Carralero, María Isabel ^c   Morán Jiménez, María Josefa ^c  

^a HOSPITAL UNIVERSITARIO DE GUADALAJARA   (Spain)

^b UNIVERSITY OF ALCALÁ   (Spain)

^c Universidad Complutense   (Spain)

Author keywords

[No Author keywords available]

Indexed keywords

ALANINE AMINOTRANSFERASE; ASPARTATE AMINOTRANSFERASE; FERRITIN; IMMUNOGLOBULIN E; IRON; TRANSFERRIN; CATION TRANSPORT PROTEIN; METAL TRANSPORTING PROTEIN 1;

ALANINE AMINOTRANSFERASE BLOOD LEVEL; ASPARTATE AMINOTRANSFERASE BLOOD LEVEL; AUTOSOMAL DOMINANT DISORDER; CASE REPORT; CHILD; FEMALE; FERRITIN BLOOD LEVEL; FERROPORTIN DISEASE; GENE; GENE MUTATION; HEMOCHROMATOSIS; HETEROZYGOSITY; HUMAN; IMMUNOGLOBULIN BLOOD LEVEL; IRON BLOOD LEVEL; IRON OVERLOAD; NUCLEAR MAGNETIC RESONANCE IMAGING; PRIORITY JOURNAL; SCHOOL CHILD; SHORT SURVEY; SLC40A1 GENE; TRANSFERRIN BLOOD LEVEL; APHERESIS; BLOOD; CHEMISTRY; DEFICIENCY; DIAGNOSTIC IMAGING; GENETICS; HETEROZYGOTE; LIVER; MUTATION;

ALANINE TRANSAMINASE; ASPARTATE AMINOTRANSFERASES; BLOOD COMPONENT REMOVAL; CATION TRANSPORT PROTEINS; CHILD; FEMALE; FERRITINS; HEMOCHROMATOSIS; HETEROZYGOTE; HUMANS; IRON; LIVER; MAGNETIC RESONANCE IMAGING; MUTATION;

EID: 85003794634     PISSN: 02772116     EISSN: 15364801     Source Type: Journal    
DOI: 10.1097/MPG.0000000000000648     Document Type: Short Survey

References (7)

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