| scholarly article | Q13442814 |
| P356 | DOI | 10.1002/HEP.510290318 |
| P698 | PubMed publication ID | 10051464 |
| P2093 | author name string | Bardella MT | |
| Vecchi M | |||
| Conte D | |||
| Minola E | |||
| Del Ninno E | |||
| Fraquelli M | |||
| Cesana BM | |||
| De Franchis R | |||
| Landoni M | |||
| Pacchetti S | |||
| P2860 | cites work | Screening for hemochromatosis | Q34335860 |
| Molecular biology and genetics of alpha 1-antitrypsin deficiency | Q35532429 | ||
| Hepatic injury in adult coeliac disease | Q39446125 | ||
| The humoral immune system in coeliac disease | Q40406366 | ||
| Where have all the American celiacs gone? | Q41092382 | ||
| Hemochromatosis after the gene discovery: revisiting the diagnostic strategy | Q41758975 | ||
| Wilson disease in 1998: genetic, diagnostic and therapeutic aspects | Q41758992 | ||
| Coeliac disease hidden by cryptogenic hypertransaminasaemia | Q57014316 | ||
| Hypertransaminasemia as the first symptom in infant celiac disease | Q68613302 | ||
| Elevated serum aminotransferase activity as an early manifestation of gluten-sensitive enteropathy | Q70579868 | ||
| High prevalence of undiagnosed coeliae disease in 5280 Italian students screened by antigliadin antibodies | Q72047646 | ||
| Childhood coeliac disease in Sweden | Q72687215 | ||
| P433 | issue | 3 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 654-657 | |
| P577 | publication date | 1999-03-01 | |
| P1433 | published in | Hepatology | Q15724398 |
| P1476 | title | Chronic unexplained hypertransaminasemia may be caused by occult celiac disease | |
| P478 | volume | 29 |
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