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D'Adamo, Adamo Pio
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Preferred name
D'Adamo, Adamo Pio
Main Affiliation
Email
adamopio.dadamo@burlo.trieste.it
ORCID
Scopus Author ID
57211726496
Researcher ID
G-4064-2011
Research Output
Now showing 1 - 10 of 12
- PublicationGNE-related thrombocytopenia: evidence for a mutational hotspot in the ADP/substrate domain of the GNE bifunctional enzyme
; ;Marzollo Antonio ;Marinoni Maddalena ;Athanasakis Emmanouil ;Persico Ilaria; ; ; ;Simoncini Daniela ;Rossini Linda ;Corsolini Fabio; ;Robustelli Giuseppe ;Gabelli Maria ;Agosti Massimo ;Biffi Alessandra ;Grotto Paolo ;Bozzi Valeria ;Noris Patrizia ;Burlina Alberto B; ; ; ;Pastore Annalisa; - PublicationIdentification of a new mutation in RSK2, the gene for coffin¿lowry syndrome (CLS), in two related patients with mild and atypical phenotypes
; ;Bigoni Stefania ;Iuso Nicola ;Vuch Josef ;Selvatici Rita; ; - PublicationSystematic analysis of factors that improve homologous direct repair (HDR) efficiency in CRISPR/Cas9 technique
; ;Foschi Nicola ;Athanasakis Emmanouil; ; - PublicationNew Tools for Congenital Hyperinsulinism
;Da Lozzo Prisca ;Risso Francesco Maria; ;Sirchia Fabio; ;Bussani Rossana; ; - PublicationPlant Antimicrobial Peptides as Potential Tool for Topic Treatment of Hidradenitis Suppurativa
;Dos Santos Silva Carlos Andrè; ;Vilela Lívia Maria Batista ;Roldan-Filho Ricardo Salas ;Amador Vinícius Costa; ;Rêgo Mireli de Santana ;Benko-Iseppon Ana MariaCrovella Sergio - PublicationThe Genetic Diagnosis of Ultrarare DEEs: An Ongoing Challenge
; ; ; ; ; ; ; ;Giulia Ragusa ;Emmanouil Athanasakis; ; ; - PublicationWhat Is the Exact Contribution of PITX1 and TBX4 Genes in Clubfoot Development? An Italian Study
; ;Giulia Ragusa ;Di Carlo Valentina; ;DI STAZIO MARIATERESA ;Costantina Racano ;Giovanni Trisolino ;Cappellani Stefania ;Maurizio De Pellegrin ;Ignazio d¿Addetta ;Giuseppe Carluccio ;Sergio Monforte ;Antonio Andreacchio ;Daniela Dibello; - PublicationIncidence of Congenital Clubfoot: Preliminary Data from Italian CeDAP Registry
;Daniela Dibello ;Lucio Torelli; ; ; ; Giulia Colin - PublicationThings come in threes: A new complex allele and a novel deletion within the CFTR gene complicate an accurate diagnosis of cystic fibrosis
;Ilaria Persico ;Agnese Feresin; ;FONTANA GIORGIA ;Fabio Sirchia; ; ;Suergiu Sarah ;Morgutti Marcello; ; ;Karen S. Raraigh;