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M Delle Fave

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Ophthalmic Genetics|March 11, 2021
Congenital stationary night blindness in a patient with mild learning disability due to a compound heterozygous microdeletion of 15q13 and a missense mutation in <i>TRPM1</i>M Delle Fave, M Cordonnier, L Vallee, et al.
Acta Gastro-Enterologica Belgica|February 9, 2016
Portosystemic encephalopathy in an 86-year-old patient : a clinical challengeE Merola, M Cao, S La Starza, et al.
European Review for Medical and Pharmacological Sciences|October 28, 2015
Application of clinical indexes in ulcerative colitis patients in regular follow-up visit: correlation with endoscopic 'mucosal healing' and implication for management. Preliminary resultsC Pagnini, F Menasci, S Festa, et al.
Pageof 1

Showing results (1-10 of 3) with videos related to

Sort By:
Pageof 1
Ophthalmic Genetics|March 11, 2021
Congenital stationary night blindness in a patient with mild learning disability due to a compound heterozygous microdeletion of 15q13 and a missense mutation in <i>TRPM1</i>M Delle Fave, M Cordonnier, L Vallee, et al.
Acta Gastro-Enterologica Belgica|February 9, 2016
Portosystemic encephalopathy in an 86-year-old patient : a clinical challengeE Merola, M Cao, S La Starza, et al.
European Review for Medical and Pharmacological Sciences|October 28, 2015
Application of clinical indexes in ulcerative colitis patients in regular follow-up visit: correlation with endoscopic 'mucosal healing' and implication for management. Preliminary resultsC Pagnini, F Menasci, S Festa, et al.
Pageof 1