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Human Genetics|January 1, 1985
Mapping of human thyroglobulin gene on the long arm of chromosome 8 by in situ hybridizationV E Avvedimento, R Di Lauro, A Monticelli, et al.Human Mutation|January 1, 1996
Mutation pattern in clinically asymptomatic coagulation factor VII deficiencyF Bernardi, G Castaman, M Pinotti, et al.The European Respiratory Journal|May 8, 1999
Pulmonary function abnormalities in children with Henoch-Schönlein purpuraS Cazzato, F Bernardi, C Cinti, et al.Acta Paediatrica Scandinavica|March 1, 1978
Hypophyso-gonadal function in the diabetic childA Cicognani, F Zappulla, F Bernardi, et al.Cell Death & Disease|October 21, 2016
Functional KCa1.1 channels are crucial for regulating the proliferation, migration and differentiation of human primary skeletal myoblastsRajeev B Tajhya, Xueyou Hu, Mark R Tanner, et al.European Journal of Endocrinology|January 23, 1998
Hormonal replacement therapy affects calcitonin gene-related peptide and atrial natriuretic peptide secretion in postmenopausal womenA Spinetti, A Margutti, S Bertolini, et al.Journal of Clinical Medicine|January 11, 2022
Evolution in Real-World Therapeutic Strategies for HIV Treatment: A Retrospective Study in Southern Italy, 2014-2020Nunzia Papa, Simona Cammarota, Anna Citarella, et al.Human Genetics|September 1, 1987
De novo complex autosomal translocation involving chromosomes 8, 13 and 15 in a girl with a sporadic retinoblastomaE Calzolari, P Palazzi, V Aiello, et al.Acta Paediatrica Scandinavica|May 1, 1976
GH, ACTH, LH and FSH behaviour in the first seven days of lifeE Cacciari, A Cicognani, P Pirazoli, et al.Pageof 34