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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 sources
C 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 locus
A 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 patients
V 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 syndrome
N 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 alloreactivity
M 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 atopy
A 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 Society
M Aricò, G Janka, A Fischer, et al.
The European Respiratory Journal
|
April 1, 1990
Familial elevation of serum angiotensin converting enzyme activity
M 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 factors
R 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 patients
C Livieri, M Belvedere, M Martinetti, et al.
Page
of 12
Search research articles
Search
Showing results (61-70 of 116) with videos related to
Sort By:
Page
of 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 sources
C 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 locus
A 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 patients
V 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 syndrome
N 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 alloreactivity
M 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 atopy
A 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 Society
M Aricò, G Janka, A Fischer, et al.
The European Respiratory Journal
|
April 1, 1990
Familial elevation of serum angiotensin converting enzyme activity
M 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 factors
R 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 patients
C Livieri, M Belvedere, M Martinetti, et al.
Page
of 12