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Autori: Sobacchi Cristina

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Naslov Severe Combined Immunodeficiency in Serbia and Montenegro Between Years 1986 and 2010: A Single-Center Experience (Article)
Autori Pasic Srdjan S Vujic Dragana S Veljkovic Dobrila K Slavkovic Bojana Mostarica-Stojkovic Marija B Minic Predrag B Minic Aleksandra  Ristic Goran G Giliani Silvia Villa Anna Sobacchi Cristina Lilic Desa Abinun Mario 
Info JOURNAL OF CLINICAL IMMUNOLOGY, (2014), vol. 34 br. 3, str. 304-308
Ispravka Web of Science   Članak   Elečas   Rang časopisa   Citati: Web of Science   Scopus  
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Naslov Chloride channel ClCN7 mutations are responsible for severe recessive, dominant, and intermediate osteopetrosis (Article)
Autori Frattini A Pangrazio A Susani L Sobacchi Cristina Mirolo M Abinun Mario Andolina M Flanagan A Horwitz EM Mihci E Notarangelo LD Ramenghi U Teti A van Hove JLK Vujic Dragana S Young T Albertini A Orchard PJ Vezzoni P Villa A 
Info JOURNAL OF BONE AND MINERAL RESEARCH, (2003), vol. 18 br. 10, str. 1740-1747
Ispravka Web of Science   Članak   Elečas   Rang časopisa   Citati: Web of Science   Scopus  
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Naslov The mutational spectrum of human malignant autosomal recessive osteopetrosis (Article)
Autori 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 
Info HUMAN MOLECULAR GENETICS, (2001), vol. 10 br. 17, str. 1767-1773
Ispravka Web of Science   Članak   Elečas   Rang časopisa   Citati: Web of Science   Scopus  
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Naslov V(D)J recombination defects in lymphocytes due to RAG mutations: severe immunodeficiency with a spectrum of clinical presentations (Article)
Autori 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 
Info BLOOD, (2001), vol. 97 br. 1, str. 81-88
Ispravka Web of Science   Članak   Elečas   Rang časopisa   Citati: Web of Science   Scopus  
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Naslov N-terminal RAG1 frameshift mutations in Omenn's syndrome: Internal methionine usage leads to partial V(D)J recombination activity and reveals a fundamental role in vivo for the N-terminal domains (Article)
Autori Santagata S Gomez CA Sobacchi Cristina Bozzi F Abinun Mario Pasic Srdjan S Cortes P Vezzoni P Villa A 
Info PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, (2000), vol. 97 br. 26, str. 14572-14577
Ispravka Web of Science   Članak   Elečas   Rang časopisa   Citati: Web of Science   Scopus  
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Naslov Prenatal diagnosis of RAG-deficient Omenn syndrome (Article)
Autori Villa A Bozzi F Sobacchi Cristina Strina D Fasth A Pasic Srdjan S Notarangelo LD Vezzoni P 
Info PRENATAL DIAGNOSIS, (2000), vol. 20 br. 1, str. 56-59
Ispravka Web of Science   Članak   Elečas   Rang časopisa   Citati: Web of Science   Scopus  
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