Ausgabe 7/2014
Inhalt (17 Artikel)
“Good’s Syndrome Presenting with Recurrent Giardiasis”
Amit Rawat, Varun Dhir, Anju Gupta, Deepti Suri, Deepak K. Burad, Ritambra Nada, Surjit Singh
Inborn errors of metabolism underlying primary immunodeficiencies
Nima Parvaneh, Pierre Quartier, Parastoo Rostami, Jean-Laurent Casanova, Pascale de Lonlay
XLP: Clinical Features and Molecular Etiology due to Mutations in SH2D1A Encoding SAP
Stuart G Tangye
Clinical Course in a Patient With Neutrophil-Specific Granule Deficiency and Rapid Detection of Neutrophil Granules as a Screening Test
Tomonari Shigemura, Takashi Yamazaki, Masaaki Shiohara, Norimoto Kobayashi, Kuniaki Naganuma, Kenich Koike, Kazunaga Agematsu
A Novel Treatment in X-Linked Agammaglobulinaemia - Hyperbaric Oxygen Therapy in Refractory Chronic Wounds
C. L. Steele, C. Cridge, J. D. M. Edgar
Successful Anti-TNF-α Treatment in a Girl with LAD-1 Disease and Autoimmune Manifestations
Manuela Marsili, Vassilios Lougaris, Marta Lucantoni, Daniele Di Marzio, Manuela Baronio, Massimiliano Vitali, Giuliano Lombardi, Francesco Chiarelli, Luciana Breda
Atypical Severe Combined Immunodeficiency Caused by a Novel Homozygous Mutation In Rag1 Gene in a Girl who Presented with Pyoderma Gangrenosum: A Case Report and Literature Review
Turkan Patiroglu, H. Haluk Akar, Kimberly Gilmour, M. Akif Ozdemir, Shahnaz Bibi, Frances Henriquez, Siobhan O. Burns, Ekrem Unal
Identification of Germinal Centres in the Lymph Node of a Patient with Hyperimmunoglobulin M Syndrome Associated with Congenital Rubella
Rohan Ameratunga, Chun-Jen J. Chen, Wikke Koopmans, P. Rod Dunbar, Maia Brewerton, Richard Lloydd, Claudia J. Mansell, Chris van Vliet, See-Tarn Woon
Clinical Experience With an L-Proline–Stabilized 10 % Intravenous Immunoglobulin (Privigen®): Real-Life Effectiveness and Tolerability
Morna J. Dorsey, Viet Ho, Mohsen Mabudian, Pere Soler-Palacín, Nerea Domínguez-Pinilla, Radha Rishi, Rahul Rishi, Duane Wong, Mikhail Rojavin, Alphonse Hubsch, Melvin Berger
Adequate Patient’s Outcome Achieved with Short Immunoglobulin Replacement Intervals in Severe Antibody Deficiencies
Cinzia Milito, Federica Pulvirenti, Anna Maria Pesce, Maria Anna Digiulio, Franco Pandolfi, Marcella Visentini, Isabella Quinti
Infliximab for Treatment of Granulomatous Disease in Patients with Common Variable Immunodeficiency
Timothy J. Franxman, Laura E. Howe, James R. Baker Jr.
Optimal Strategies to Identify Aberrant Intra-Epithelial Lymphocytes in Refractory Coeliac Disease
R. L. J. van Wanrooij, D. M. J. Müller, E. A. Neefjes-Borst, J. Meijer, L. G. Koudstaal, D. A. M. Heideman, H. J. Bontkes, B. M. E. von Blomberg, G. Bouma, C. J. J. Mulder
Primary Immunodeficiency Diseases: A 30-year Patient Registry from the Referral Center for Primary Immunodeficiencies in Greece
Athanasios Michos, Maria Raptaki, Sofia Tantou, Marianna Tzanoudaki, Kleopatra Spanou, Manolis Liatsis, Nikki Constantinidou, Evangelia Paschali, Ioanna Varela, Olga Moraloglou, Chryssa Bakoula, Maria Kanariou
Quality of Life in Children with Primary Antibody Deficiency
P. Titman, Z. Allwood, C. Gilmour, C. Malcolmson, C. Duran-Persson, C. Cale, G. Davies, H. Gaspar, A. Jones
IgA Deficiency, Autoimmunity & Pregnancy: A Population-Based Matched Cohort Study
Jonas F Ludvigsson, Martin Neovius, Olof Stephansson, Lennart Hammarström
Helios Expression in T-regulatory Cells in Patients with di George Syndrome
Adam Klocperk, Jarmila Grecová, Kristýna Šišmová, Jana Kayserová, Eva Froňková, Anna Šedivá
Compound Heterozygous CORO1A Mutations in Siblings with a Mucocutaneous-Immunodeficiency Syndrome of Epidermodysplasia Verruciformis-HPV, Molluscum Contagiosum and Granulomatous Tuberculoid Leprosy
Asbjorg Stray-Pedersen, Emmanuelle Jouanguy, Amandine Crequer, Alison A. Bertuch, Betty S. Brown, Shalini N. Jhangiani, Donna M. Muzny, Tomasz Gambin, Hanne Sorte, Ghadir Sasa, Denise Metry, Judith Campbell, Marianna M. Sockrider, Megan K. Dishop, David M. Scollard, Richard A. Gibbs, Emily M. Mace, Jordan S. Orange, James R. Lupski, Jean-Laurent Casanova, Lenora M. Noroski