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The Journal of Allergy and Clinical Immunology
|
September 1, 1995
Immunodeficiency with hyperimmunoglobulinemia M in two female patients is not associated with abnormalities of CD40 or CD40 ligand expression
A Oliva, I Quinti, E Scala, et al.
Journal of Clinical Immunology
|
November 1, 1996
HCV infection in a patient with hyper IgM syndrome
I Quinti, A Giovannetti, R Paganelli, et al.
Folia Biologica
|
August 26, 2014
Complementarity between microarray and immunoblot for the comparative evaluation of IgE repertoire of French and Italian cypress pollen allergic patients
Y Shahali, P Nicaise, A Brázdová, et al.
Allergy
|
May 20, 2003
Distinct delayed T-cell response to beta-methasone and penicillin-G in the same patient
E Scala, M Giani, S Pastore, et al.
The Journal of Allergy and Clinical Immunology
|
May 1, 1995
Immunologic aspects of hyperimmunoglobulinemia E-like syndrome in patients with AIDS
R Paganelli, E Scala, I Mezzaroma, et al.
Brain & Development
|
June 20, 2008
Diagnostic criteria for the Zappella variant of Rett syndrome (the preserved speech variant)
A Renieri, F Mari, M A Mencarelli, et al.
Clinical and Experimental Allergy : Journal of the British Society for Allergy and Clinical Immunology
|
March 11, 2010
Cross-sectional survey on immunoglobulin E reactivity in 23,077 subjects using an allergenic molecule-based microarray detection system
E Scala, C Alessandri, M L Bernardi, et al.
Clinical and Experimental Allergy : Journal of the British Society for Allergy and Clinical Immunology
|
October 31, 2012
Lipid transfer proteins: the most frequent sensitizer in Italian subjects with food-dependent exercise-induced anaphylaxis
A Romano, E Scala, G Rumi, et al.
Journal of Medical Genetics
|
February 4, 2005
CDKL5/STK9 is mutated in Rett syndrome variant with infantile spasms
E Scala, F Ariani, F Mari, et al.
Clinical Genetics
|
July 25, 2012
Exome sequencing overrides formal genetics: ASPM mutations in a case study of apparent X-linked microcephalic intellectual deficit
F Ariani, F Mari, S Amitrano, et al.
Page
of 12
Search research articles
Search
Showing results (81-90 of 114) with videos related to
Sort By:
Page
of 12
The Journal of Allergy and Clinical Immunology
|
September 1, 1995
Immunodeficiency with hyperimmunoglobulinemia M in two female patients is not associated with abnormalities of CD40 or CD40 ligand expression
A Oliva, I Quinti, E Scala, et al.
Journal of Clinical Immunology
|
November 1, 1996
HCV infection in a patient with hyper IgM syndrome
I Quinti, A Giovannetti, R Paganelli, et al.
Folia Biologica
|
August 26, 2014
Complementarity between microarray and immunoblot for the comparative evaluation of IgE repertoire of French and Italian cypress pollen allergic patients
Y Shahali, P Nicaise, A Brázdová, et al.
Allergy
|
May 20, 2003
Distinct delayed T-cell response to beta-methasone and penicillin-G in the same patient
E Scala, M Giani, S Pastore, et al.
The Journal of Allergy and Clinical Immunology
|
May 1, 1995
Immunologic aspects of hyperimmunoglobulinemia E-like syndrome in patients with AIDS
R Paganelli, E Scala, I Mezzaroma, et al.
Brain & Development
|
June 20, 2008
Diagnostic criteria for the Zappella variant of Rett syndrome (the preserved speech variant)
A Renieri, F Mari, M A Mencarelli, et al.
Clinical and Experimental Allergy : Journal of the British Society for Allergy and Clinical Immunology
|
March 11, 2010
Cross-sectional survey on immunoglobulin E reactivity in 23,077 subjects using an allergenic molecule-based microarray detection system
E Scala, C Alessandri, M L Bernardi, et al.
Clinical and Experimental Allergy : Journal of the British Society for Allergy and Clinical Immunology
|
October 31, 2012
Lipid transfer proteins: the most frequent sensitizer in Italian subjects with food-dependent exercise-induced anaphylaxis
A Romano, E Scala, G Rumi, et al.
Journal of Medical Genetics
|
February 4, 2005
CDKL5/STK9 is mutated in Rett syndrome variant with infantile spasms
E Scala, F Ariani, F Mari, et al.
Clinical Genetics
|
July 25, 2012
Exome sequencing overrides formal genetics: ASPM mutations in a case study of apparent X-linked microcephalic intellectual deficit
F Ariani, F Mari, S Amitrano, et al.
Page
of 12