VENTURA, ALESSANDRO

VENTURA, ALESSANDRO  

Dipartimento Universitario Clinico di Scienze mediche, chirurgiche e della salute  

Settore MED/38 - Pediatria Generale e Specialistica  

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Risultati 1 - 20 di 528 (tempo di esecuzione: 0.055 secondi).
Titolo Data di pubblicazione Autori File
"Automatic" diagnosis of viral enteritis. 1-gen-1997 VENTURA, ALESSANDRO +
"Blaschkoid Dyspigmentation" in a Child: Don't Forget Fibroblast Chromosomal Analysis 1-gen-2015 VENTURA, ALESSANDRO +
"Multicystic dysplastic kidney (Potter type II syndrome) and agenesis of corpus callosum (ACC) in two consecutive pregnancies: a possible teratogenic effect of electromagnetic exposure in utero". 1-gen-2008 VENTURA, ALESSANDRO +
5-Aminoimidazole-4-carboxamide ribonucleotide-transformylase and inosine-triphosphate-pyrophosphatase genes variants predict remission rate during methotrexate therapy in patients with juvenile idiopathic arthritis 1-gen-2015 PASTORE, SERENASTOCCO, GABRIELEMORESSA, VALENTINADECORTI, GIULIANAVENTURA, ALESSANDRO +
A boy with unexplained recurrent abdominal pain. 1-gen-2013 VENTURA, ALESSANDRO +
A Brain and Heart Connection: X-Linked Periventricular Heterotopia 1-gen-2015 NAVIGLIO, SAMUELEVENTURA, ALESSANDRO +
A case of central precocious puberty in a patient with Prader-Willi syndrome 1-gen-2016 Pellegrin MCTornese GVentura A. +
A case of Rubinstein-Taybi syndrome associated with growth hormone deficiency in childhood 1-gen-2015 TORNESE, GIANLUCAPELLEGRIN, MARIA CHIARAVENTURA, ALESSANDRO +
A child with bullous skin lesions. Linear IgA dermatosis. 1-gen-2013 TADDIO, ANDREAVENTURA, ALESSANDRO +
A child with edema, lower limb deformity, and recurrent diarrhea 1-gen-2012 VENTURA, ALESSANDRO +
A Child with Severe Developmental Delay and Growth Retardation 1-gen-2016 MATARAZZO, LORENZATADDIO, ANDREAVENTURA, ALESSANDRO +
A child with severe pneumomediastinum and ABCA3 gene mutation: a puzzling connection. 1-gen-2012 Barbi EVENTURA, ALESSANDRO +
A child with severe pneumomediastinum and ABCA3 gene mutation: a puzzling connection. 1-gen-2012 Copertino, MarcoBarbi, EgidioVentura, Alessandro +
A congenital purplish tumour 1-gen-2017 MATARAZZO, LORENZABUSSANI, ROSSANAVENTURA, ALESSANDRO +
A Functional Idiotype/Anti-Idiotype Network Is Active in Genetically Gluten-Intolerant Individuals Negative for Both Celiac Disease-Related Intestinal Damage and Serum Autoantibodies 1-gen-2019 Quaglia, SaraFerrara, FortunatoDe Leo, LuiginaZiberna, FabianaVatta, SerenaSblattero, DanieleVentura, AlessandroNot, Tarcisio +
A Klinefelter boy with congenital adrenal hyperplasia: too much or too little androgens? 1-gen-2018 Zanella, GiadaTornese, GianlucaMASCHERONI, ELISABETTAVentura, AlessandroBarbi, Egidio +
A new mutation in two siblings with cystinosis presenting with Bartter syndrome. 1-gen-2005 CROVELLA, SERGIOVENTURA, ALESSANDRO +
A new opportunity for thalidomide? Further randomised controlled trial are necessary. 1-gen-2004 VENTURA, ALESSANDRO +
A new, rapid, noninvasive screening test for celiac disease. 1-gen-1993 NOT, TARCISIOVENTURA, ALESSANDRO +
A novel approach based on low field nuclear magnetic resonance for the detection of the pathological components of the sputum of cystic fibrosis patients 1-gen-2017 ABRAMI, MICHELAVENTURA, ALESSANDROCONFALONIERI, MarcoGRASSI, GABRIELEGRASSI, Mario +