Ausgabe 4/2014
Inhalt (14 Artikel)
The Case for Mandatory Newborn Screening for Severe Combined Immunodeficiency (SCID)
H. B. Gaspar, L. Hammarström, N. Mahlaoui, M. Borte, S. Borte
ICON: The Early Diagnosis of Congenital Immunodeficiencies
John Routes, Mario Abinun, Waleed Al-Herz, Jacinta Bustamante, Antonio Condino-Neto, Maria Teresa De La Morena, Amos Etzioni, Eleonora Gambineri, Elie Haddad, Lisa Kobrynski, Francoise Le Deist, Shigeaki Nonoyama, Joao Bosco Oliveira, Elena Perez, Capucine Picard, Nima Rezaei, John Sleasman, Kathleen E. Sullivan, Troy Torgerson
Autosomal Recessive Agammaglobulinemia: The Third Case of Igβ Deficiency Due to a Novel Non-sense Mutation
Vassilios Lougaris, Massimiliano Vitali, Manuela Baronio, Daniele Moratto, Giacomo Tampella, Augusto Biasini, Raffaele Badolato, Alessandro Plebani
USIDNET: A Strategy to Build a Community of Clinical Immunologists
Kathleen E. Sullivan, Jennifer M. Puck, Luigi D. Notarangelo, Ramsay Fuleihan, Tara Caulder, Connie Wang, Marcia Boyle, Charlotte Cunningham-Rundles
Correlating Interleukin-12 Stimulated Interferon-γ Production and the Absence of Ectodermal Dysplasia and Anhidrosis (EDA) in Patients with Mutations in NF-κB Essential Modulator (NEMO)
Margje H. Haverkamp, Beatriz E. Marciano, David M. Frucht, Ashish Jain, Esther van de Vosse, Steven M. Holland
Association Between IgA Deficiency & Other Autoimmune Conditions: A Population-Based Matched Cohort Study
Jonas F. Ludvigsson, Martin Neovius, Lennart Hammarström
Chronic Granulomatous Disease in Morocco: Genetic, Immunological, and Clinical Features of 12 Patients from 10 Kindreds
Laila Ait Baba, Fatima Ailal, Naima El Hafidi, Marjorie Hubeau, Fabienne Jabot-Hanin, Noufissa Benajiba, Zahra Aadam, Francesca Conti, Caroline Deswarte, Leila Jeddane, Ayoub Aglaguel, Ouafaa El Maataoui, Ahmed Tissent, Chafiq Mahraoui, Jilali Najib, Ruben Martinez-Barricarte, Laurent Abel, Norddine Habti, Rachid Saile, Jean-Laurent Casanova, Jacinta Bustamante, Hanane Salih Alj, Ahmed Aziz Bousfiha
First Report on the Moroccan Registry of Primary Immunodeficiencies: 15 Years of Experience (1998–2012)
A. A. Bousfiha, L. Jeddane, N. El Hafidi, N. Benajiba, N. Rada, J. El Bakkouri, A. Kili, S. Benmiloud, I. Benhsaien, I. Faiz, O. Maataoui, Z. Aadam, A. Aglaguel, L. Ait Baba, Z. Jouhadi, R. Abilkassem, M. Bouskraoui, M. Hida, J. Najib, H. Salih Alj, F. Ailal
Novel STAT3 Mutation Causing Hyper-IgE Syndrome: Studies of the Clinical Course and Immunopathology
Mikael Sundin, Bianca Tesi, Maria Sund Böhme, Yenan T. Bryceson, Katrin Pütsep, Samuel C. Chiang, Sarah Thunberg, Jacek Winiarski, Ann-Charlotte Wikström
Primary Immunodeficiency Disorders in Iran: Update and New Insights from the Third Report of the National Registry
Asghar Aghamohammadi, Payam Mohammadinejad, Hassan Abolhassani, Babak Mirminachi, Masoud Movahedi, Mohammad Gharagozlou, Nima Parvaneh, Vaheid Zeiaee, Bahram Mirsaeed-Ghazi, Zahra Chavoushzadeh, Alireza Mahdaviani, Mahboubeh Mansouri, Sedigheh Yousefzadegan, Bahareh Sharifi, Fariborz Zandieh, Ehsan Hedayat, Ali Nadjafi, Roya Sherkat, Behzad Shakerian, Mahnaz Sadeghi-Shabestari, Reza Farid Hosseini, Farahzad Jabbari-Azad, Hamid Ahanchian, Fatemeh Behmanesh, Mohammadreza Zandkarimi, Afshin Shirkani, Taher Cheraghi, Abbas Fayezi, Iraj Mohammadzadeh, Reza Amin, Soheila Aleyasin, Mojgan Moghtaderi, Javad Ghaffari, Saba Arshi, Naser Javahertrash, Mohammad Nabavi, Mohammad Hassan Bemanian, Alireza Shafiei, Najmedin Kalantari, Akefeh Ahmadiafshar, Hossein Ali Khazaei, Lida Atarod, Nima Rezaei
Differential microRNA Profile and Post-Transcriptional Regulation Exist in Systemic Lupus Erythematosus Patients with Distinct Autoantibody Specificities
Sudhir Kumar Chauhan, Vikas Vikram Singh, Richa Rai, Madhukar Rai, Geeta Rai
Highly Efficient Neutralization by Plasma Antibodies from Human Immunodeficiency Virus Type-1 Infected Individuals on Antiretroviral Drug Therapy
Raiees Andrabi, M. A. Makhdoomi, Rajesh Kumar, Manju Bala, Hilal Parray, Arjun Gupta, Ankita Kotnala, Velpandian Thirumurthy, Kalpana Luthra
Retrospective Analysis of TREC Based Newborn Screening Results and Clinical Phenotypes in Infants with the 22q11 Deletion Syndrome
Jenny Lingman Framme, Stephan Borte, Ulrika von Döbeln, Lennart Hammarström, Sólveig Óskarsdóttir
Erratum to: Efficacy and Safety of IgPro20, a Subcutaneous Immunoglobulin, in Japanese Patients with Primary Immunodeficiency Diseases
Hirokazu Kanegane, Kohsuke Imai, Masafumi Yamada, Hidetoshi Takada, Tadashi Ariga, Martin Bexon, Mikhail Rojavin, Wilson Hu, Midori Kobayashi, John-Philip Lawo, Shigeaki Nonoyama, Toshiro Hara, Toshio Miyawaki