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Current Opinion in Allergy and Clinical Immunology
|
January 11, 2005
Congenital neutropenia: advances in diagnosis and treatment
Raffaele Badolato, Stefania Fontana, Lucia D Notarangelo, et al.
Current Opinion in Allergy and Clinical Immunology
|
November 3, 2005
WASP and the phenotypic range associated with deficiency
Luigi D Notarangelo, Lucia D Notarangelo, Hans D Ochs
Expert Review of Clinical Immunology
|
May 19, 2010
The Wiskott-Aldrich syndrome: from genotype-phenotype correlation to treatment
Daniele Moratto, Silvia Giliani, Lucia D Notarangelo, 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.
Journal of Clinical Immunology
|
September 18, 2015
Diagnosis, Treatment and Long-Term Follow Up of Patients with ADA Deficiency: a Single-Center Experience
Renata Baffelli, Lucia D Notarangelo, Luisa Imberti, et al.
Blood
|
February 5, 2010
Impaired NK-cell migration in WAS/XLT patients: role of Cdc42/WASp pathway in the control of chemokine-induced beta2 integrin high-affinity state
Helena Stabile, Claudia Carlino, Cinzia Mazza, et al.
The Journal of Pediatrics
|
July 4, 2012
Tetralogy of fallot is an uncommon manifestation of warts, hypogammaglobulinemia, infections, and myelokathexis syndrome
Raffaele Badolato, Laura Dotta, Laura Tassone, et al.
The Journal of Allergy and Clinical Immunology
|
March 8, 2011
A peptide derived from the Wiskott-Aldrich syndrome (WAS) protein-interacting protein (WIP) restores WAS protein level and actin cytoskeleton reorganization in lymphocytes from patients with WAS mutations that disrupt WIP binding
Michel J Massaad, Narayanaswamy Ramesh, Severine Le Bras, et al.
Blood
|
August 26, 2010
Defect of plasmacytoid dendritic cells in warts, hypogammaglobulinemia, infections, myelokathexis (WHIM) syndrome patients
Laura Tassone, Daniele Moratto, William Vermi, et al.
Blood
|
March 6, 2002
Missense mutations of the WASP gene cause intermittent X-linked thrombocytopenia
Lucia D Notarangelo, Cinzia Mazza, Silvia Giliani, et al.
Page
of 4
Search research articles
Search
Showing results (1-10 of 33) with videos related to
Sort By:
Page
of 4
Current Opinion in Allergy and Clinical Immunology
|
January 11, 2005
Congenital neutropenia: advances in diagnosis and treatment
Raffaele Badolato, Stefania Fontana, Lucia D Notarangelo, et al.
Current Opinion in Allergy and Clinical Immunology
|
November 3, 2005
WASP and the phenotypic range associated with deficiency
Luigi D Notarangelo, Lucia D Notarangelo, Hans D Ochs
Expert Review of Clinical Immunology
|
May 19, 2010
The Wiskott-Aldrich syndrome: from genotype-phenotype correlation to treatment
Daniele Moratto, Silvia Giliani, Lucia D Notarangelo, 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.
Journal of Clinical Immunology
|
September 18, 2015
Diagnosis, Treatment and Long-Term Follow Up of Patients with ADA Deficiency: a Single-Center Experience
Renata Baffelli, Lucia D Notarangelo, Luisa Imberti, et al.
Blood
|
February 5, 2010
Impaired NK-cell migration in WAS/XLT patients: role of Cdc42/WASp pathway in the control of chemokine-induced beta2 integrin high-affinity state
Helena Stabile, Claudia Carlino, Cinzia Mazza, et al.
The Journal of Pediatrics
|
July 4, 2012
Tetralogy of fallot is an uncommon manifestation of warts, hypogammaglobulinemia, infections, and myelokathexis syndrome
Raffaele Badolato, Laura Dotta, Laura Tassone, et al.
The Journal of Allergy and Clinical Immunology
|
March 8, 2011
A peptide derived from the Wiskott-Aldrich syndrome (WAS) protein-interacting protein (WIP) restores WAS protein level and actin cytoskeleton reorganization in lymphocytes from patients with WAS mutations that disrupt WIP binding
Michel J Massaad, Narayanaswamy Ramesh, Severine Le Bras, et al.
Blood
|
August 26, 2010
Defect of plasmacytoid dendritic cells in warts, hypogammaglobulinemia, infections, myelokathexis (WHIM) syndrome patients
Laura Tassone, Daniele Moratto, William Vermi, et al.
Blood
|
March 6, 2002
Missense mutations of the WASP gene cause intermittent X-linked thrombocytopenia
Lucia D Notarangelo, Cinzia Mazza, Silvia Giliani, et al.
Page
of 4