@ARTICLE{
author={Ruperto Nicolino,Garcia-Munitis P,Villa L,Pesce M,Aggarwal A,Fasth A,Avcin Tadej,Bae SC,Balogh Zoltan,Li C,De Inocencio J,Dibra M,Dolezalova Pavla,El Miedany Y,Flato B,Harjacek Miroslav,Huppertz HI,Kanakoudi-Tsakalidou F,Wulffraat N,Lahdenne P,Melo-Gomes JA,Mihaylova D,Nielsen S,Nikishima I,Ozdogan H,Pagava K,Panaviene V,Prieur AM,Romicka AM,Rumba I,Shafaie N,Susic Gordana Z,Takei S,Uziel Y,Vesely R,Woo P,Martini Alberto},
year={2005},
title={PRINTO/PRES international website for families of children with rheumatic diseases: www.pediatric-rheumatology.printo.it},
journal={ANNALS OF THE RHEUMATIC DISEASES},
volume={64},
number={7},
pages={1101-1106},
document_type={Article},
} 

@ARTICLE{
author={Sobacchi Cristina,Frattini A,Orchard PJ,Porras O,Tezcan I,Andolina M,Babul-Hirji R,Baric I,Canham N,Chitayat D,Dupuis-Girod S,Ellis I,Etzioni A,Fasth A,Fisher A,Gerritsen B,Gulino V,Horwitz EM,Klamroth V,Lanino E,Mirolo M,Musio A,Matthijs G,Nonomaya S,Notarangelo LD,Ochs HD,Furga AS,Valiaho J,van Hove JLK,Vihinen M,Vujic Dragana S,Vezzoni P,Villa A},
year={2001},
title={The mutational spectrum of human malignant autosomal recessive osteopetrosis},
journal={HUMAN MOLECULAR GENETICS},
volume={10},
number={17},
pages={1767-1773},
document_type={Article},
} 

@ARTICLE{
author={Villa A,Sobacchi Cristina,Notarangelo LD,Bozzi F,Abinun Mario,Abrahamsen TG,Arkwright PD,Baniyash M,Brooks EG,Conley ME,Cortes P,Duse M,Fasth A,Filipovic Aleksandra M,Infante AJ,Jones A,Mazzolari E,Muller SM,Pasic Srdjan S,Rechavi G,Sacco MG,Santagata S,Schroeder ML,Seger R,Strina D,Ugazio A,Valiaho J,Vihinen M,Vogler LB,Ochs H,Vezzoni P,Friedrich W,Schwarz K},
year={2001},
title={V(D)J recombination defects in lymphocytes due to RAG mutations: severe immunodeficiency with a spectrum of clinical presentations},
journal={BLOOD},
volume={97},
number={1},
pages={81-88},
document_type={Article},
} 

@ARTICLE{
author={Villa A,Bozzi F,Sobacchi Cristina,Strina D,Fasth A,Pasic Srdjan S,Notarangelo LD,Vezzoni P},
year={2000},
title={Prenatal diagnosis of RAG-deficient Omenn syndrome},
journal={PRENATAL DIAGNOSIS},
volume={20},
number={1},
pages={56-59},
document_type={Article},
}