FERESIN, AGNESE

FERESIN, AGNESE  

Dipartimento Universitario Clinico di Scienze mediche, chirurgiche e della salute  

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Case Report: Two cases of apparent discordance between non-invasive prenatal testing (NIPT) and amniocentesis resulting in feto-placental mosaicism of trisomy 21. Issues in diagnosis, investigation and counselling 1-gen-2022 Feresin, AgneseStampalija, TamaraCappellani, StefaniaBussani, RossanaFaletra, FlavioBosio, BarbaraArdisia, Carmela +
Differential and shared genetic effects on kidney function between diabetic and non-diabetic individuals 1-gen-2022 Cocca, MassimilianoFeresin, AgneseMorgan, AnnaSpedicati, BeatriceCatamo, EulaliaRizzi, FedericaGirotto, GiorgiaPistis, GiorgioFrancescatto, MargheritaConcas, Maria PinaBianca, Martina LaPirastu, NicolaGasparini, Paolo +
Modeling postnatal hearing case finding within the Italian National Health System 1-gen-2021 giulia pizzamigliolucio torelliagnese feresin +
Obliterated cavum septi pellucidi: is it always a benign finding? A case report and narrative review of the literature 1-gen-2023 Fantasia, IlariaFaletra, FlavioBussani, RossanaOttaviani Giammarco, ChiaraTravan, LauraFeresin, AgneseStampalija, Tamara +
Prenatal findings of cataract and arthrogryposis: recurrence of cerebro-oculo-facio-skeletal syndrome and review of differential diagnosis 1-gen-2021 Fantasia I.Feresin A.Faletra F.Mordeglia D.Barbieri M.Stampalija T. +
TBC1D24 and non-syndromic autosomal dominant hearing loss: the identification of an additional Italo-American family carrying the p.(S178L) mutation 1-gen-2021 Beatrice SpedicatiAnna MorganFlavio FaletraAgnese FeresinPaolo GaspariniGiorgia Girotto +
The clinical impact of the first-trimester nuchal translucency between the 95th-99th percentiles 1-gen-2023 Fantasia, IlariaBianchini, IreneBussolaro, SofiaQuadrifoglio, MariachiaraLo Bello, LeilaRicci, GiuseppeFaletra, FlavioFeresin, AgneseStampalija, Tamara +
The role of knockout olfactory receptor genes in odor discrimination 1-gen-2021 Concas M. P.Cocca M.Francescatto M.Spedicati B.Feresin A.Morgan A.Gasparini P.Girotto G. +
Things come in threes: A new complex allele and a novel deletion within the CFTR gene complicate an accurate diagnosis of cystic fibrosis 1-gen-2022 Persico I.Feresin A.Faleschini M.Fontana G.Faletra F.La Bianca M.Morgutti M.D'Adamo A. P.Savoia A.Bottega R. +
TTC5 syndrome: Clinical and molecular spectrum of a severe and recognizable condition 1-gen-2022 Faletra, FlavioZanus, CaterinaMagnolato, AndreaLa Bianca, MartinaFeresin, AgneseGirotto, GiorgiaGasparini, PaoloCosta, PaolaCarrozzi, Marco +