Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.

Combined evaluation of genotype and phenotype of thiopurine S-methyltransferase (TPMT) in the clinical management of patients in chronic therapy with azathioprine.

Autor: Rucci, Francesco, Cigoli, Maria Sole, Marini, Valeria, Fucile, Carmen, Mattioli, Francesca, Robbiano, Luigi, Cavallari, Ugo, Scaglione, Francesco, Perno, Carlo F., Penco, Silvana, Marocchi, Alessandro

Publikováno v: Drug Metabolism & Personalized Therapy; Mar2019, Vol. 34 Issue 1, pN.PAG-N.PAG, 10p

Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.

CCM3/PDCD10 gene mutation in cerebral cavernous malformations associated with hyperkeratotic cutaneous capillary venous malformations

Autor: Giuseppe De Michele, Enrico Maria Procaccini, Mario Quarantelli, Silvio Peluso, Gelsomina Mansueto, Maria Sole Cigoli, Silvana Penco, Antonella Antenora, Leonilda Bilo

Publikováno v: Journal of dermatology
43 (2016): 962–963. doi:10.1111/1346-8138.13317
info:cnr-pdr/source/autori:Bilo, Leonilda; Antenora, Antonella; Peluso, Silvio; Procaccini, Enrico Maria; Quarantelli, Mario; Mansueto, Gelsomina; Cigoli, Maria Sole; Penco, Silvana; De Michele, Giuseppe/titolo:CCM3%2FPDCD10 gene mutation in cerebral cavernous malformations associated with hyperkeratotic cutaneous capillary venous malformations/doi:10.1111%2F1346-8138.13317/rivista:Journal of dermatology (Print)/anno:2016/pagina_da:962/pagina_a:963/intervallo_pagine:962–963/volume:43

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c39ed4b6aac83ede83c6f4ae34efd929
https://publications.cnr.it/doc/444051