Ausgabe 4/2016
Inhalt (14 Artikel)
Ligase-4 Deficiency Causes Distinctive Immune Abnormalities in Asymptomatic Individuals
Kerstin Felgentreff, Sachin N. Baxi, Yu Nee Lee, Kerry Dobbs, Lauren A. Henderson, Krisztian Csomos, Erdyni N. Tsitsikov, Mary Armanios, Jolan E. Walter, Luigi D. Notarangelo
Presenting features and platelet anomalies in WAS: one centre’s experience
Christo Tsilifis, Andrew R. Gennery, Andrew Cant
Immune Complex-Mediated Glomerulonephritis in a Patient with Wiskott–Aldrich Syndrome
Tomonari Shigemura, Yozo Nakazawa, Hisashi Shimojo, Norimoto Kobayashi, Kazunaga Agematsu
Spondylodiscitis in a Boy with X-linked Agammaglobulinemia: an Unusual Occurrence
Sagar Bhattad, Pandiarajan Vignesh, Amit Rawat, Deepti Suri, Anju Gupta, Sameer Vyas, Surjit Singh
Visceral Leishmaniasis May Unmask X-linked Hyper-IgM Syndrome
Luis Ignacio Gonzalez-Granado, Nerea Dominguez-Pinilla, Fernando Gallego-Bustos, Jesús Ruiz-Contreras, Luis M. Allende
Myelodysplastic Syndrome and Acute Lymphocytic Leukemia in Common Variable Immunodeficiency (CVID)
Jennifer Toh, Rachel Eisenberg, Kamila Bakirhan, Amit Verma, Arye Rubinstein
A Clinical Approach to a Child with Hypoalbuminemia and Lymphopenia
Ayse Sevgi Köstel-Bal, Suna Kaymak, Şule Haskoloğlu, Zarife Kuloğlu, Arzu Ensari, Figen Doğu, Aydan Kansu, Aydan İkincioğulları
A ‘Too Negative’ ANA Test Predicts Antibody Deficiency
Mike Recher, Christoph T. Berger, Thomas Daikeler, Christoph Hess, Ingmar A. F. M. Heijnen
Copa Syndrome: a Novel Autosomal Dominant Immune Dysregulatory Disease
Timothy J. Vece, Levi B. Watkin, Sarah K. Nicholas, Debra Canter, Michael C. Braun, Robert Paul Guillerman, Karen W. Eldin, Grant Bertolet, Scott D. McKinley, Marietta de Guzman, Lisa R. Forbes, Ivan Chinn, Jordan S. Orange
Novel Mutations Causing C5 Deficiency in Three North-African Families
Roger Colobran, Clara Franco-Jarava, Andrea Martín-Nalda, Neus Baena, Elisabeth Gabau, Natàlia Padilla, Xavier de la Cruz, Ricardo Pujol-Borrell, David Comas, Pere Soler-Palacín, Manuel Hernández-González
WHIM Syndrome Caused by Waldenström’s Macroglobulinemia-Associated Mutation CXCR4 L329fs
Qian Liu, Catherina Pan, Lizbeeth Lopez, Jiliang Gao, Daniel Velez, Sandra Anaya-O’Brien, Jean Ulrick, Patricia Littel, John S. Corns, Donald T. Ellenburg, Harry L. Malech, Philip M. Murphy, David H. McDermott
Secondary Antibody Deficiency in Glucocorticoid Therapy Clearly Differs from Primary Antibody Deficiency
Clemens Wirsum, Cornelia Glaser, Sylvia Gutenberger, Baerbel Keller, Susanne Unger, Reinhard E. Voll, Werner Vach, Thomas Ness, Klaus Warnatz
Erratum to: Adenosine Deaminase Deficient Severe Combined Immunodeficiency Presenting as Atypical Haemolytic Uraemic Syndrome
Olga Nikolajeva, Austen Worth, Rosie Hague, Nuria Martinez-Alier, Joanne Smart, Stuart Adams, E. Graham Davies, H. Bobby Gaspar