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Pathologica|May 1, 1989
[Type-III acrocephalosyndactylia (Saethre-Chotzen syndrome). Description of 2 cases]O Gabrielli, E Moroni, M Barbato, et al.Scandinavian Journal of Gastroenterology|September 6, 2000
Antiendomysium versus antigliadin antibodies in screening the general population for coeliac diseaseC Catassi, G Fanciulli, A R D'Appello, et al.Acta Paediatrica (Oslo, Norway : 1992). Supplement|May 1, 1996
Dietary compliance in screening-detected coeliac disease adolescentsE Fabiani, C Catassi, A Villari, et al.Lancet (London, England)|January 22, 1994
Coeliac disease in the year 2000: exploring the icebergC Catassi, I M Rätsch, E Fabiani, et al.Mediators of Inflammation|January 1, 1994
Effect of nedocromil sodium on polymorphonuclear leukocyte plasma membraneA Kantar, N Oggiano, P L Giorgi, et al.Cancer Genetics and Cytogenetics|August 1, 1987
ins(6;11) in a case of peripheral T-cell lymphomaE Donti, B Falini, S Bordoni, et al.Minerva Pediatrica|September 24, 2013
Hunter syndrome (Mucopolysaccharidosis type II), severe phenotype: long term follow-up on patients undergone to hematopoietic stem cell transplantationR Annibali, L Caponi, A Morganti, et al.Minerva Pediatrica|December 1, 1989
[Cohen syndrome. Description of a new case and study of the central nervous system using nuclear magnetic resonance]O Gabrielli, C Pierleoni, M Barbato, et al.Acta Haematologica|January 1, 1986
Redox and energetic state of red blood cells in G6PD deficiency, heterozygous beta-thalassemia and the combination of bothM Magnani, V Stocchi, F Canestrari, et al.Gut|November 1, 1993
Dose dependent effects of protracted ingestion of small amounts of gliadin in coeliac disease children: a clinical and jejunal morphometric studyC Catassi, M Rossini, I M Rätsch, et al.Pageof 9