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M Martinetti

Showing results (61-70 of 116) with videos related to

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Clinica Chimica Acta; International Journal of Clinical Chemistry|July 20, 2011
A new approach to safely type for HLA the HIV infected people eligible to abacavir therapy: saliva or buccal swab as reliable DNA sourcesC Badulli, I Sbarsi, D Di Giorgio, et al.
Genes and Immunity|November 13, 2001
Family study of non-responsiveness to hepatitis B vaccine confirms the importance of HLA class III C4A locusA De Silvestri, A Pasi, M Martinetti, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|February 19, 2014
Immunogenetic factors in mycosis fungoides: can the HLA system influence the susceptibility and prognosis of the disease? Long-term follow-up study of 46 patientsV Brazzelli, N Rivetti, C Badulli, et al.
International Journal of Immunopathology and Pharmacology|October 14, 2009
Molecular study of receptor for advanced glycation endproduct gene promoter and identification of specific HLA haplotypes possibly involved in chronic fatigue syndromeN Carlo-Stella, S Bozzini, A De Silvestri, et al.
Vaccine|April 1, 1995
Anti-HBV neonatal immunization with recombinant vaccine. Part II. Molecular basis of the impaired alloreactivityM Martinetti, M Cuccia, C Daielli, et al.
Disease Markers|June 22, 2006
Non classical HLA genes and non-HLA genes in a population of infants at familial risk of atopyA De Silvestri, C Belloni, M De Amici, et al.
Leukemia|February 1, 1996
Hemophagocytic lymphohistiocytosis. Report of 122 children from the International Registry. FHL Study Group of the Histiocyte SocietyM Aricò, G Janka, A Fischer, et al.
The European Respiratory Journal|April 1, 1990
Familial elevation of serum angiotensin converting enzyme activityM Luisetti, M Martinetti, M Cuccia, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|May 5, 2001
Hypersomnia in the Prader Willi syndrome: clinical-electrophysiological features and underlying factorsR Manni, L Politini, L Nobili, et al.
Progress in Clinical and Biological Research|January 1, 1985
21-Hydroxylase deficiency: HLA genotypes and hormonal phenotypes in the families of 32 Italian patientsC Livieri, M Belvedere, M Martinetti, et al.
Pageof 12

Showing results (61-70 of 116) with videos related to

Sort By:
Pageof 12
Clinica Chimica Acta; International Journal of Clinical Chemistry|July 20, 2011
A new approach to safely type for HLA the HIV infected people eligible to abacavir therapy: saliva or buccal swab as reliable DNA sourcesC Badulli, I Sbarsi, D Di Giorgio, et al.
Genes and Immunity|November 13, 2001
Family study of non-responsiveness to hepatitis B vaccine confirms the importance of HLA class III C4A locusA De Silvestri, A Pasi, M Martinetti, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|February 19, 2014
Immunogenetic factors in mycosis fungoides: can the HLA system influence the susceptibility and prognosis of the disease? Long-term follow-up study of 46 patientsV Brazzelli, N Rivetti, C Badulli, et al.
International Journal of Immunopathology and Pharmacology|October 14, 2009
Molecular study of receptor for advanced glycation endproduct gene promoter and identification of specific HLA haplotypes possibly involved in chronic fatigue syndromeN Carlo-Stella, S Bozzini, A De Silvestri, et al.
Vaccine|April 1, 1995
Anti-HBV neonatal immunization with recombinant vaccine. Part II. Molecular basis of the impaired alloreactivityM Martinetti, M Cuccia, C Daielli, et al.
Disease Markers|June 22, 2006
Non classical HLA genes and non-HLA genes in a population of infants at familial risk of atopyA De Silvestri, C Belloni, M De Amici, et al.
Leukemia|February 1, 1996
Hemophagocytic lymphohistiocytosis. Report of 122 children from the International Registry. FHL Study Group of the Histiocyte SocietyM Aricò, G Janka, A Fischer, et al.
The European Respiratory Journal|April 1, 1990
Familial elevation of serum angiotensin converting enzyme activityM Luisetti, M Martinetti, M Cuccia, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|May 5, 2001
Hypersomnia in the Prader Willi syndrome: clinical-electrophysiological features and underlying factorsR Manni, L Politini, L Nobili, et al.
Progress in Clinical and Biological Research|January 1, 1985
21-Hydroxylase deficiency: HLA genotypes and hormonal phenotypes in the families of 32 Italian patientsC Livieri, M Belvedere, M Martinetti, et al.
Pageof 12