Ausgabe 3/2016
Inhalt (10 Artikel)
Primary Immunodeficiency Diseases in Aguascalientes, Mexico: Results from an Educational Program
Aristoteles Alvarez-Cardona, Sara Elva Espinosa-Padilla, Saul Oswaldo Lugo Reyes, Javier Ventura-Juarez, Jaime Asael Lopez-Valdez, Lucila Martínez-Medina, Alberto Santillan-Artolozaga, Adriana Cajero-Avelar, Alma R. De Luna-Sosa, Luis F. Torres-Bernal, Francisco J. Espinosa-Rosales
Deficiency of Adenosine Deaminase 2 Causes Antibody Deficiency
Johanna Schepp, Alla Bulashevska, Wilma Mannhardt-Laakmann, Hongzhi Cao, Fang Yang, Maximilian Seidl, Susan Kelly, Michael Hershfield, Bodo Grimbacher
X-Linked Agammagobulinemia in a Large Series of North African Patients: Frequency, Clinical Features and Novel BTK Mutations
Zahra Aadam, Nadia Kechout, Abdelhamid Barakat, Koon-Wing Chan, Meriem Ben-Ali, Imen Ben-Mustapha, Fethi Zidi, Fatima Ailal, Nabila Attal, Fatouma Doudou, Mohamed-Cherif Abbadi, Chawki Kaddache, Leila Smati, Nabila Touri, Jalel Chemli, Tahar Gargah, Ines Brini, Amina Bakhchane, Hicham Charoute, Leila Jeddane, Sara El Atiqi, Naïma El Hafidi, Mustapha Hida, Rachid Saile, Hanane Salih Alj, Rachida Boukari, Mohamed Bejaoui, Jilali Najib, Mohamed-Ridha Barbouche, Yu-Lung Lau, Fethi Mellouli, Ahmed Aziz Bousfiha
Deletion of the entire interferon-γ receptor 1 gene causing complete deficiency in three related patients
Inge C. de Vor, Pomme M. van der Meulen, Vincent Bekker, Els M. Verhard, Martijn H. Breuning, Esther Harnisch, Maarten J. D. van Tol, Jantien W. Wieringa, Esther van de Vosse, Robbert G. M. Bredius
Chronic and Invasive Fungal Infections in a Family with CARD9 Deficiency
Ana Karina Alves de Medeiros, Evelyn Lodewick, Delfien J. A. Bogaert, Filomeen Haerynck, Sabine Van daele, Bart Lambrecht, Sara Bosma, Laure Vanderdonckt, Olivier Lortholary, Mélanie Migaud, Jean-Laurent Casanova, Anne Puel, Fanny Lanternier, Jo Lambert, Lieve Brochez, Melissa Dullaers
Quantitative Evidence of Wear-Off Effect at the End of the Intravenous IgG (IVIG) Dosing Cycle in Primary Immunodeficiency
Mikhail A. Rojavin, Alphonse Hubsch, John-Philip Lawo
Spondyloenchondrodysplasia Due to Mutations in ACP5: A Comprehensive Survey
Tracy A. Briggs, Gillian I. Rice, Navid Adib, Lesley Ades, Stephane Barete, Kannan Baskar, Veronique Baudouin, Ayse N. Cebeci, Philippe Clapuyt, David Coman, Lien De Somer, Yael Finezilber, Moshe Frydman, Ayla Guven, Sébastien Heritier, Daniela Karall, Muralidhar L. Kulkarni, Pierre Lebon, David Levitt, Martine Le Merrer, Agnes Linglart, John H. Livingston, Vincent Navarro, Ericka Okenfuss, Anne Puel, Nicole Revencu, Sabine Scholl-Bürgi, Marina Vivarelli, Carine Wouters, Brigitte Bader-Meunier, Yanick J. Crow
Erratum to: Severe Mycobacterial Diseases in a Patient with GOF IκBα Mutation Without EDA
Alison Joanne Lee, Marcela Moncada-Vélez, Capucine Picard, Genevieve Llanora, Chiung-Hui Huang, Laurent Abel, Si Min Chan, Bee-Wah Lee, Jean-Laurent Casanova, Jacinta Bustamante, Lynette Pei-Chi Shek, Stéphanie Boisson-Dupuis
Erratum to: Defective Leukocyte Adhesion and Chemotaxis Contributes to Combined Immunodeficiency in Humans with Autosomal Recessive MST1 Deficiency
Tarana Singh Dang, Joseph D. P. Willet, Helen R. Griffin, Neil V. Morgan, Graeme O’Boyle, Peter D. Arkwright, Stephen M. Hughes, Mario Abinun, Louise J. Tee, Dawn Barge, Karin R. Engelhardt, Michael Jackson, Andrew J. Cant, Eamonn R. Maher, Mauro Santibanez Koref, Louise N. Reynard, Simi Ali, Sophie Hambleton