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Lucia D Notarangelo

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Current Opinion in Allergy and Clinical Immunology|January 11, 2005
Congenital neutropenia: advances in diagnosis and treatmentRaffaele 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 deficiencyLuigi 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 treatmentDaniele 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 ExperienceRenata 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 stateHelena 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 syndromeRaffaele 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 bindingMichel 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 patientsLaura Tassone, Daniele Moratto, William Vermi, et al.
Blood|March 6, 2002
Missense mutations of the WASP gene cause intermittent X-linked thrombocytopeniaLucia D Notarangelo, Cinzia Mazza, Silvia Giliani, et al.
Pageof 4

Showing results (1-10 of 33) with videos related to

Sort By:
Pageof 4
Current Opinion in Allergy and Clinical Immunology|January 11, 2005
Congenital neutropenia: advances in diagnosis and treatmentRaffaele 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 deficiencyLuigi 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 treatmentDaniele 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 ExperienceRenata 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 stateHelena 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 syndromeRaffaele 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 bindingMichel 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 patientsLaura Tassone, Daniele Moratto, William Vermi, et al.
Blood|March 6, 2002
Missense mutations of the WASP gene cause intermittent X-linked thrombocytopeniaLucia D Notarangelo, Cinzia Mazza, Silvia Giliani, et al.
Pageof 4