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S Giliani

Showing results (1-10 of 44) with videos related to

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Mutation Research|September 1, 1991
Xeroderma pigmentosum complementation group H falls into complementation group DW Vermeulen, M Stefanini, S Giliani, et al.
Clinical and Experimental Immunology|February 1, 1997
A boy with X-linked hyper-IgM syndrome and natural killer cell deficiencyB Ostenstad, S Giliani, O J Mellbye, et al.
Mutation Research|March 1, 1992
DNA repair investigations in nine Italian patients affected by trichothiodystrophyM Stefanini, S Giliani, T Nardo, et al.
Immunology Letters|August 27, 2017
Early diagnosis of PI3Kδ syndrome in a 2 years old girl with recurrent otitis and enlarged spleenF Saettini, M A Pelagatti, D Sala, et al.
DNA and Cell Biology|September 1, 1993
Application of molecular analysis to genetic counseling in the Wiskott-Aldrich syndrome (WAS)L D Notarangelo, F Candotti, O Parolini, et al.
Biochemical and Biophysical Research Communications|March 1, 2000
Structural basis for SH2D1A mutations in X-linked lymphoproliferative diseaseI Lappalainen, S Giliani, R Franceschini, et al.
Lancet (London, England)|September 2, 1995
Mutation analysis in Wiskott Aldrich syndrome on chorionic villus DNAG S Wengler, L D Notarangelo, S Giliani, et al.
Journal of Investigational Allergology & Clinical Immunology|September 13, 2011
Evaluation of CARMA1/CARD11 and Bob1 as candidate genes in common variable immunodeficiencyG Tampella, M Baronio, M Vitali, et al.
Genomics|August 10, 1995
The genomic organization of the human transcription factor 3 (TFE3) geneP Macchi, L Notarangelo, S Giliani, et al.
The Journal of Clinical Endocrinology and Metabolism|July 5, 2003
Autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy syndrome: time to review diagnostic criteria?F Buzi, R Badolato, C Mazza, et al.
Pageof 5

Showing results (1-10 of 44) with videos related to

Sort By:
Pageof 5
Mutation Research|September 1, 1991
Xeroderma pigmentosum complementation group H falls into complementation group DW Vermeulen, M Stefanini, S Giliani, et al.
Clinical and Experimental Immunology|February 1, 1997
A boy with X-linked hyper-IgM syndrome and natural killer cell deficiencyB Ostenstad, S Giliani, O J Mellbye, et al.
Mutation Research|March 1, 1992
DNA repair investigations in nine Italian patients affected by trichothiodystrophyM Stefanini, S Giliani, T Nardo, et al.
Immunology Letters|August 27, 2017
Early diagnosis of PI3Kδ syndrome in a 2 years old girl with recurrent otitis and enlarged spleenF Saettini, M A Pelagatti, D Sala, et al.
DNA and Cell Biology|September 1, 1993
Application of molecular analysis to genetic counseling in the Wiskott-Aldrich syndrome (WAS)L D Notarangelo, F Candotti, O Parolini, et al.
Biochemical and Biophysical Research Communications|March 1, 2000
Structural basis for SH2D1A mutations in X-linked lymphoproliferative diseaseI Lappalainen, S Giliani, R Franceschini, et al.
Lancet (London, England)|September 2, 1995
Mutation analysis in Wiskott Aldrich syndrome on chorionic villus DNAG S Wengler, L D Notarangelo, S Giliani, et al.
Journal of Investigational Allergology & Clinical Immunology|September 13, 2011
Evaluation of CARMA1/CARD11 and Bob1 as candidate genes in common variable immunodeficiencyG Tampella, M Baronio, M Vitali, et al.
Genomics|August 10, 1995
The genomic organization of the human transcription factor 3 (TFE3) geneP Macchi, L Notarangelo, S Giliani, et al.
The Journal of Clinical Endocrinology and Metabolism|July 5, 2003
Autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy syndrome: time to review diagnostic criteria?F Buzi, R Badolato, C Mazza, et al.
Pageof 5