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Journal of Hepatology|June 12, 1999
Serum ferritin and hepatic glutathione concentrations in chronic hepatitis C patients related to the hepatitis C virus genotypeG Barbaro, G Di Lorenzo, M Ribersani, et al.
Journal of Endocrinological Investigation|January 1, 1982
Familial thyroxine-binding globulin deficiency detected in a pilot screening program for congenital hypothyroidismM Carta Sorcini, L Moschini, L Fiore, et al.
Hepatology (Baltimore, Md.)|February 1, 1995
Differential distribution of hepatitis C virus genotypes in patients with and without liver function abnormalitiesE Silini, F Bono, A Cividini, et al.
Helvetica Paediatrica Acta|December 1, 1986
Longitudinal assessment of children with congenital hypothyroidism detected by neonatal screeningL Moschini, P Costa, E Marinelli, et al.
Thyroid : Official Journal of the American Thyroid Association|June 1, 1997
Mutations in the gene encoding thyroid transcription factor-1 (TTF-1) are not a frequent cause of congenital hypothyroidism (CH) with thyroid dysgenesisP Lapi, P E Macchia, L Chiovato, et al.
European Journal of Emergency Medicine : Official Journal of the European Society for Emergency Medicine|December 10, 1998
Flumazenil for hepatic coma in patients with liver cirrhosis: an Italian multicentre double-blind, placebo-controlled, crossover studyG Barbaro, G Di Lorenzo, M Soldini, et al.
Medical Hypotheses|March 1, 1995
Adjuvant therapy with essential fatty acids (EFAs) for primary liver tumors: some hypothesesG F Baronzio, L Solbiati, T Ierace, et al.
Clinical Therapeutics|January 1, 1988
Treatment of anxiety with ketazolam in elderly patientsN Bresolin, G Monza, E Scarpini, et al.
Genes & Development|April 1, 1997
UbcD1, a Drosophila ubiquitin-conjugating enzyme required for proper telomere behaviorG Cenci, R B Rawson, G Belloni, et al.
Acta Anthropogenetica|January 1, 1983
Screening for cytogenetic polymorphisms in a random sample of liveborn infants from Italian populationG Belloni, A Benincasa, A Bosi, et al.
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