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Zeitschrift

Journal of Clinical Immunology

Journal of Clinical Immunology 1/2019

Ausgabe 1/2019

Inhaltsverzeichnis ( 20 Artikel )

23.11.2018 | Letter to Editor | Ausgabe 1/2019

Successful Bone Marrow Transplantation for XMEN: Hemorrhagic Risk Uncovered

Dimana Dimitrova, Jeremy J. Rose, Gulbu Uzel, Jeffrey I. Cohen, Koneti V. Rao, Jacob H. Bleesing, Christopher G. Kanakry, Jennifer A. Kanakry

26.11.2018 | Letter to Editor | Ausgabe 1/2019

MonoMAC Syndrome Caused by a Novel GATA2 Mutation Successfully Treated by Allogeneic Hematopoietic Stem Cell Transplantation

Maria Francisca Moraes-Fontes, Íris Caramalho, Amy P. Hsu, Steven M. Holland, Manuel Abecasis

03.01.2019 | Letter to Editor | Ausgabe 1/2019

Monoclonal Gammopathy of Unclear Significance in a Child with Wiskott-Aldrich Syndrome: a Rare Occurrence

Rashmi Rikhi, Sagar Bhattad, Ankur Jindal, Biman Saikia, Ravinder Garg, Amit Rawat, Deepti Suri, Surjit Singh

05.01.2019 | Letter to Editor | Ausgabe 1/2019

A Novel STK4 Mutation Presenting with Juvenile Idiopathic Arthritis and Epidermodysplasia Verruciformis

Samin Sharafian, Vahid Ziaee, Mohammad Shahrooei, Mahsa Ahadi, Nima Parvaneh

07.01.2019 | Letter to Editor | Ausgabe 1/2019

Two Prenatal Cases of Hyper-IgE Syndrome

Makiko Egawa, Kohsuke Imai, Yoko Taketani, Tomohiro Morio, Naoyuki Miyasaka

10.01.2019 | Letter to Editor | Ausgabe 1/2019

Successful Treatment with SCIG of a Child with Refractory Chronic ITP

Anna Karastaneva, Daniela S. Klobassa, Milen Minkov, Martin Benesch, Markus G. Seidel

10.01.2019 | Letter to Editor | Ausgabe 1/2019

Damaging BTK Variant Demonstrated by Carrier, Allele-Specific BTK Expression in B Cells and Monocytes

Mary T. Bausch-Jurken, Mary Hintermeyer, Jeffrey Woodliff, Shaoying Chen, Amy Rymaszewski, James Verbsky, John Routes

14.01.2019 | Letter to Editor | Ausgabe 1/2019

Childhood Hodgkin Lymphoma: Think DADA2

Fahad Alabbas, Ghaleb Elyamany, Omar Alsharif, Michael Hershfield, Isabelle Meyts

21.11.2018 | Original Article | Ausgabe 1/2019

Autoimmunity and Inflammation in CVID: a Possible Crosstalk between Immune Activation, Gut Microbiota, and Epigenetic Modifications

Silje F. Jørgensen, Børre Fevang, Pål Aukrust

13.12.2018 | Original Article | Ausgabe 1/2019

Hematopoietic Stem Cell Transplantation in Patients with Heterozygous STAT1 Gain-of-Function Mutation

Ayca Kiykim, Louis Marie Charbonnier, Arzu Akcay, Elif Karakoc-Aydiner, Ahmet Ozen, Gulyuz Ozturk, Talal A. Chatila, Safa Baris

13.12.2018 | Original Article | Ausgabe 1/2019

Imaging of Bronchial Pathology in Antibody Deficiency: Data from the European Chest CT Group

Katharina Schütz, Diana Alecsandru, Bodo Grimbacher, Jamanda Haddock, Annemarie Bruining, Gertjan Driessen, Esther de Vries, Peter M. van Hagen, Ieneke Hartmann, Francesco Fraioli, Cinzia Milito, Milica Mitrevski, Isabella Quinti, Goffredo Serra, Peter Kelleher, Michael Loebinger, Jiri Litzman, Vera Postranecka, Vojtech Thon, Judith Babar, Alison M. Condliffe, Andrew Exley, Dinakantha Kumararatne, Nick Screaton, Alison Jones, Maria P. Bondioni, Vassilios Lougaris, Alessandro Plebani, Annarosa Soresina, Cesare Sirignano, Giuseppe Spadaro, Nermeen Galal, Luis I. Gonzalez-Granado, Sabine Dettmer, Robert Stirling, Helen Chapel, Mary Lucas, Smita Patel, Claire-Michele Farber, Isabelle Meyts, Arpan K. Banerjee, Scott Hackett, John R. Hurst, Klaus Warnatz, Benjamin Gathmann, Ulrich Baumann, for the Chest CT in Antibody Deficiency Group

14.12.2018 | Original Article | Ausgabe 1/2019

Progressive Multifocal Leukoencephalopathy in Primary Immunodeficiencies

Jérôme Hadjadj, Aurélien Guffroy, Christophe Delavaud, Guillaume Taieb, Isabelle Meyts, Anne Fresard, Nathalie Streichenberger, Anne-Sophie L’Honneur, Flore Rozenberg, Maud D’Aveni, Claire Aguilar, Jérémie Rosain, Capucine Picard, Nizar Mahlaoui, Marc Lecuit, Olivier Hermine, Olivier Lortholary, Felipe Suarez

19.12.2018 | Original Article | Ausgabe 1/2019

Lymphocyte Apoptosis and FAS Expression in Patients with 22q11.2 Deletion Syndrome

Dina M. Aresvik, Torstein Øverland, Kari Lima, Rolf D. Pettersen, Tore G. Abrahamsen

20.12.2018 | Original Article | Ausgabe 1/2019 Open Access

DDX58 and Classic Singleton-Merten Syndrome

Carlos R. Ferreira, Yanick J. Crow, William A. Gahl, Pamela J. Gardner, Raphaela Goldbach-Mansky, Sun Hur, Adriana Almeida de Jesús, Michele Nehrebecky, Ji Woo Park, Tracy A. Briggs

03.01.2019 | Original Article | Ausgabe 1/2019

Rubella Virus-Associated Cutaneous Granulomatous Disease: a Unique Complication in Immune-Deficient Patients, Not Limited to DNA Repair Disorders

David Buchbinder, Fabian Hauck, Michael H. Albert, Anita Rack, Shahrzad Bakhtiar, Anna Shcherbina, Elena Deripapa, Kathleen E. Sullivan, Ludmila Perelygina, Marc Eloit, Bénédicte Neven, Philippe Pérot, Despina Moshous, Félipe Suarez, Christine Bodemer, Francisco A. Bonilla, Louise E. Vaz, Alfons L. Krol, Christoph Klein, Mikko Seppanen, Diane J. Nugent, Jasjit Singh, Hans D. Ochs

04.01.2019 | Original Article | Ausgabe 1/2019

Differing Performance of the Warning Signs for Immunodeficiency in the Diagnosis of Pediatric Versus Adult Patients in a Two-Center Tertiary Referral Population

Jaclyn A. Bjelac, Jennifer R. Yonkof, James Fernandez

08.01.2019 | Original Article | Ausgabe 1/2019

A Novel Missense LIG4 Mutation in a Patient With a Phenotype Mimicking Behçet’s Disease

Ekim Z. Taskiran, Hafize E. Sonmez, Can Kosukcu, Ece Tavukcuoglu, Gozde Yazici, Gunes Esendagli, Ezgi D. Batu, Pelin O. S. Kiper, Yelda Bilginer, Mehmet Alikasifoglu, Seza Ozen

12.01.2019 | Original Article | Ausgabe 1/2019

Mosaicism of an ELANE Mutation in an Asymptomatic Mother

Tomonari Shigemura, Norimoto Kobayashi, Kazunaga Agematsu, Osamu Ohara, Yozo Nakazawa

24.01.2019 | Original Article | Ausgabe 1/2019

Outcomes for Nitazoxanide Treatment in a Case Series of Patients with Primary Immunodeficiencies and Rubella Virus-Associated Granuloma

Ludmila Perelygina, David Buchbinder, Morna J. Dorsey, Marc Eloit, Fabian Hauck, Timo Hautala, Despina Moshous, Ignacio Uriarte, Elena Deripapa, Joseph Icenogle, Kathleen E. Sullivan

26.01.2019 | Original Article | Ausgabe 1/2019

TREX-1-Related Disease Associated with the Presence of Cryofibrinogenemia

C. Paradis, M. Cadieux-Dion, C. Meloche, M. Gravel, J. Paradis, A. Des Roches, G. Leclerc, P. Cossette, P. Begin

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