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Ophthalmic Genetics
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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 challenge
E 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 results
C Pagnini, F Menasci, S Festa, et al.
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of 1
Search research articles
Search
Showing results (1-10 of 3) with videos related to
Sort By:
Page
of 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 challenge
E 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 results
C Pagnini, F Menasci, S Festa, et al.
Page
of 1