14.a Contributo in Rivista

14.a Contributo in Rivista: [71318] Home page macrotipologia

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14.a.1 Articolo su rivista 64001
14.a.2 Proceedings in extenso su rivista 1597
14.a.3 Recensione in rivista 1703
14.a.4 Scheda bibliografica 83
14.a.5 Nota a sentenza 538
14.a.6 Abstract in rivista 3351
14.a.7 Traduzione in rivista 45

Prodotti recenti

Il diritto ecclesiastico: un eterno incompreso o mal compreso

The text examines the effects that the problematic definition of “diritto ecclesiastico” has had on the general understanding of a democratically advanced model of legal “laicità” that engages all sources (common and special) of Italian law.

Evaluation of Intrinsic Hand Musculature Reinnervation following Supercharge End-to-Side Anterior Interosseous-to-Ulnar Motor Nerve Transfer

Relazioni tra genitori e figli: il ruolo della libertà di religione e di coscienza

Lo scritto analizza la più recente giurisprudenza sul ruolo della libertà di religione e di coscienza nelle relazioni genitori-figli. Le questioni controverse sono essenzialmente due: la prima, fino a che punto la accresciuta capacità di scelta del bambino può entrare in conflitto con il ruolo educativo dei genitori; la seconda, in che modo promuovere la crescita del bambino in un ambiente aperto e pacifico, conciliando i diritti dei suoi genitori.

Vedolizumab-associated pulmonary manifestations in children with ulcerative colitis

What is known and Objective: The off-label use of vedolizumab (VDZ) for inflammatory bowel disease in children is increasing. We report on possibly the first case of VDZ-associated pulmonary manifestations in paediatrics. Case summary: This report details the case of a 13-year-old child with ulcerative colitis who was initiated on VDZ due to persistent active disease. After the first three doses, he developed a persistent and productive cough. Microbiological work-up was normal. VDZ discontin...

First Case of Mature Teratoma and Yolk Sac Testis Tumor Associated to Inherited MEN-1 Syndrome

Introduction: Multiple endocrine neoplasia type 1 (MEN1) is an autosomal dominantly inherited endocrine tumor syndrome characterized by the development of cancer in various endocrine organs, particularly in the pituitary, parathyroid and pancreas. Moreover, in some cases, also non-endocrine tumors can be diagnosed, developing atypical phenotypes.Case report: We report herein the clinical history of a patient affected by MEN-1 syndrome who developed atypical features for this disease. The pati...

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