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A Plebani

Showing results (141-150 of 163) with videos related to

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The Journal of Clinical Investigation|March 13, 1999
HLA class I deficiencies due to mutations in subunit 1 of the peptide transporter TAP1H de la Salle, J Zimmer, D Fricker, et al.
European Journal of Medical Genetics|March 31, 2007
A case report of a patient with microcephaly, facial dysmorphism, chromosomal radiosensitivity and telomere length alterations closely resembling "Nijmegen breakage syndrome" phenotypeF Berardinelli, A di Masi, M Salvatore, et al.
European Journal of Neurology|March 1, 2018
Minimum effective betamethasone dosage on the neurological phenotype in patients with ataxia-telangiectasia: a multicenter observer-blind studyE Cirillo, E Del Giudice, R Micheli, et al.
Clinical Immunology (Orlando, Fla.)|May 4, 2000
Development of autologous T lymphocytes in two males with X-linked severe combined immune deficiency: molecular and cellular characterizationP Mella, L Imberti, D Brugnoni, et al.
Nature Medicine|November 14, 1997
In vivo evolution of HIV-1 co-receptor usage and sensitivity to chemokine-mediated suppressionG Scarlatti, E Tresoldi, A Björndal, et al.
Human Immunology|January 8, 2000
HLA-DRB1* and allergy to Parietaria: linkage and association analysesM D'Amato, A Picardi, T Menna, et al.
Autoimmunity Reviews|September 4, 2012
Aicardi-Goutieres syndrome, a rare neurological disease in children: a new autoimmune disorder?Elisa Fazzi, Marco Cattalini, Simona Orcesi, et al.
Haematologica|December 13, 2000
Cytokine gene expression and T-cell proliferative responses in lymph node mononuclear cells from children with early stage human immunodeficiency virus infectionI Airoldi, D Saverino, A Favre, et al.
Arthritis and Rheumatism|January 13, 2011
Long-term clinical profile of children with the low-penetrance R92Q mutation of the TNFRSF1A geneM A Pelagatti, A Meini, R Caorsi, et al.
Immunological Reviews|February 24, 2001
Of genes and phenotypes: the immunological and molecular spectrum of combined immune deficiency. Defects of the gamma(c)-JAK3 signaling pathway as a modelL D Notarangelo, S Giliani, C Mazza, et al.
Pageof 17

Showing results (141-150 of 163) with videos related to

Sort By:
Pageof 17
The Journal of Clinical Investigation|March 13, 1999
HLA class I deficiencies due to mutations in subunit 1 of the peptide transporter TAP1H de la Salle, J Zimmer, D Fricker, et al.
European Journal of Medical Genetics|March 31, 2007
A case report of a patient with microcephaly, facial dysmorphism, chromosomal radiosensitivity and telomere length alterations closely resembling "Nijmegen breakage syndrome" phenotypeF Berardinelli, A di Masi, M Salvatore, et al.
European Journal of Neurology|March 1, 2018
Minimum effective betamethasone dosage on the neurological phenotype in patients with ataxia-telangiectasia: a multicenter observer-blind studyE Cirillo, E Del Giudice, R Micheli, et al.
Clinical Immunology (Orlando, Fla.)|May 4, 2000
Development of autologous T lymphocytes in two males with X-linked severe combined immune deficiency: molecular and cellular characterizationP Mella, L Imberti, D Brugnoni, et al.
Nature Medicine|November 14, 1997
In vivo evolution of HIV-1 co-receptor usage and sensitivity to chemokine-mediated suppressionG Scarlatti, E Tresoldi, A Björndal, et al.
Human Immunology|January 8, 2000
HLA-DRB1* and allergy to Parietaria: linkage and association analysesM D'Amato, A Picardi, T Menna, et al.
Autoimmunity Reviews|September 4, 2012
Aicardi-Goutieres syndrome, a rare neurological disease in children: a new autoimmune disorder?Elisa Fazzi, Marco Cattalini, Simona Orcesi, et al.
Haematologica|December 13, 2000
Cytokine gene expression and T-cell proliferative responses in lymph node mononuclear cells from children with early stage human immunodeficiency virus infectionI Airoldi, D Saverino, A Favre, et al.
Arthritis and Rheumatism|January 13, 2011
Long-term clinical profile of children with the low-penetrance R92Q mutation of the TNFRSF1A geneM A Pelagatti, A Meini, R Caorsi, et al.
Immunological Reviews|February 24, 2001
Of genes and phenotypes: the immunological and molecular spectrum of combined immune deficiency. Defects of the gamma(c)-JAK3 signaling pathway as a modelL D Notarangelo, S Giliani, C Mazza, et al.
Pageof 17