Works matching IS 02719142 AND DT 2018 AND VI 38 AND IP 4

Results: 20

Editorial.

Published in:

2018

By:

Casanova, Jean-Laurent;
Bonagura, Vincent

Publication type:

Editorial

The International Alliance of Primary Immune Deficiency Societies.

Published in:

2018

By:

Gennery, Andrew R.;
Abraham, Roshini S.;
Torgerson, Troy R.;
Etzioni, Amos;
Cant, Andrew J.;
Meyts, Isabelle;
Chipeta, James;
Bousfiha, Ahmed Aziz;
Dieye, Tandakha D.;
Condino-Neto, Antonio;
Espinosa, Francisco;
Besrodnik, Liliana;
Lau, Yu-Lung;
Singh, Surjit;
Chan, Godfrey C. F.;
Orange, Jordan S.;
on behalf of the European Society for Immunodeficiencies;
Clinical Immunology Society;
African Society for Immunodeficiencies;
Latin American Society for Immunodeficiencies

Publication type:

Editorial

Cerebral Lymphoproliferation in a Patient with Kabuki Syndrome.

Published in:

2018

By:

Marzollo, Antonio;
Colavito, Davide;
Sartori, Stefano;
Fanelli, Giuseppe Nicolò;
Putti, Maria Caterina

Publication type:

Letter to the Editor

Novel LRBA Mutation and Possible Germinal Mosaicism in a Slavic Family.

Published in:

2018

By:

Sharapova, Svetlana O.;
Haapaniemi, Emma;
Sakovich, Inga S.;
Rojas, Jessica;
Gámez-Díaz, Laura;
Mareika, Yuliya E.;
Guryanova, Irina E.;
Migas, Alexandr A.;
Mikhaleuskaya, Taisiya M.;
Grimbacher, Bodo;
Aleinikova, Olga V.

Publication type:

Letter to the Editor

T<sup>+</sup> NK<sup>+</sup> IL-2 Receptor γ Chain Mutation: a Challenging Diagnosis of Atypical Severe Combined Immunodeficiency.

Published in:

Journal of Clinical Immunology, 2018, v. 38, n. 4, p. 527, doi. 10.1007/s10875-018-0514-y

By:

Stepensky, Polina;
Keller, Baerbel;
Shamriz, Oded;
von Spee-Mayer, Caroline;
Friedmann, David;
Shadur, Bella;
Unger, Susanne;
Fuchs, Sebastian;
NaserEddin, Adeeb;
Rumman, Nisreen;
Amro, Sara;
Molho Pessach, Vered;
Abuzaitoun, Omar;
Somech, Raz;
Elpeleg, Orly;
Ehl, Stephan;
Warnatz, Klaus

Publication type:

Article

Lethal Influenza in Two Related Adults with Inherited GATA2 Deficiency.

Published in:

Journal of Clinical Immunology, 2018, v. 38, n. 4, p. 513, doi. 10.1007/s10875-018-0512-0

By:

Sologuren, Ithaisa;
Martínez-Saavedra, María Teresa;
Solé-Violán, Jordi;
de Borges de Oliveira Jr, Edgar;
Betancor, Eva;
Casas, Inmaculada;
Oleaga-Quintas, Carmen;
Martínez-Gallo, Mónica;
Zhang, Shen-Ying;
Pestano, Jose;
Colobran, Roger;
Herrera-Ramos, Estefanía;
Pérez, Carmen;
López-Rodríguez, Marta;
Ruiz-Hernández, José Juan;
Franco, Nieves;
Ferrer, José María;
Bilbao, Cristina;
Andújar-Sánchez, Miguel;
Álvarez Fernández, Mercedes

Publication type:

Article

Aortic Calcification in a Patient with a Gain-of-Function STAT1 Mutation.

Published in:

2018

By:

Smyth, Anna E.;
Kaleviste, Epp;
Snow, Aisling;
Kisand, Kai;
McMahon, Colin J.;
Cant, Andrew J.;
Leahy, T. Ronan

Publication type:

Letter to the Editor

Treatment of Intracerebral Lesions with Abatacept in a CTLA4-Haploinsufficient Patient.

Published in:

2018

By:

van Leeuwen, Ester M.;
Cuadrado, Eloy;
Gerrits, Anke M.;
Witteveen, Esther;
de Bree, Godelieve J.

Publication type:

Letter to the Editor

Correction to: Use of Genetic Testing for Primary Immunodeficiency Patients.

Published in:

2018

By:

Heimall, Jennifer R.;
Hagin, David;
Hajjar, Joud;
Henrickson, Sarah E.;
Hernandez-Trujillo, Hillary S.;
Itan, Yuval;
Kobrynski, Lisa;
Paris, Kenneth;
Torgerson, Troy R.;
Verbsky, James W.;
Wasserman, Richard L.;
Hsieh, Elena W. Y.;
Bleesing, Jack J.;
Chou, Janet S.;
Lawrence, Monica G.;
Marsh, Rebecca A.;
Rosenzweig, Sergio D.;
Orange, Jordan S.;
Abraham, Roshini S.

Publication type:

Correction Notice

Autosomal Dominant IFN-γR1 Deficiency Presenting with both Atypical Mycobacteriosis and Tuberculosis in a BCG-Vaccinated South African Patient.

Published in:

2018

By:

Glanzmann, Brigitte;
Möller, Marlo;
Moncada-Velez, Marcela;
Peter, Jonny;
Urban, Michael;
van Helden, Paul D.;
Hoal, Eileen G.;
de Villiers, Nikola;
Glashoff, Richard H.;
Nortje, Rina;
Bustamante, Jacinta;
Abel, Laurent;
Casanova, Jean-Laurent;
Boisson-Dupuis, Stephanie;
Esser, Monika;
Kinnear, Craig J.

Publication type:

Letter to the Editor

Insights into Mutation Effect in Three Poikiloderma with Neutropenia Patients by Transcript Analysis and Disease Evolution of Reported Patients with the Same Pathogenic Variants.

Published in:

Journal of Clinical Immunology, 2018, v. 38, n. 4, p. 494, doi. 10.1007/s10875-018-0508-9

By:

Colombo, Elisa A.;
Elcioglu, Nursel H.;
Graziano, Claudio;
Farinelli, Pamela;
Di Fede, Elisabetta;
Neri, Iria;
Facchini, Elena;
Greco, Mariangela;
Gervasini, Cristina;
Larizza, Lidia

Publication type:

Article

Rapid Push vs Pump-Infused Subcutaneous Immunoglobulin Treatment: a Randomized Crossover Study of Quality of Life in Primary Immunodeficiency Patients.

Published in:

Journal of Clinical Immunology, 2018, v. 38, n. 4, p. 503, doi. 10.1007/s10875-018-0507-x

By:

Bienvenu, Boris;
Cozon, Grégoire;
Mataix, Yves;
Lachaud, Dominique;
Alix, Antoine;
Hoarau, Cyrille;
Antier, Daniel;
Hachulla, Eric;
Brice, Sylvie;
Viallard, Jean-François;
Tamisier, Stéphanie;
Fauchais, Anne-Laure;
Renon-Carron, Françoise;
Clerson, Pierre;
Fardini, Yann;
Crave, Jean-Charles;
Miossec, Pierre

Publication type:

Article

First Identification of an Inherited TPSAB1 Quintuplication in a Patient with Clonal Mast Cell Disease.

Published in:

2018

By:

Sabato, Vito;
Chovanec, Jack;
Faber, Margaretha;
Milner, Joshua D.;
Ebo, Didier;
Lyons, Jonathan J.

Publication type:

Letter to the Editor

Disseminated Cutaneous Warts in X-Linked Hyper IgM Syndrome.

Published in:

2018

By:

Ho, Hsi-en;
Byun, Minji;
Cunningham-Rundles, Charlotte

Publication type:

Letter to the Editor

Correction to: Assessment of Local Adverse Reactions to Subcutaneous Immunoglobulin (SCIG) in Clinical Trials.

Published in:

2018

By:

Ballow, Mark;
Wasserman, Richard L.;
Jolles, Stephen;
Chapel, Helen;
Berger, Mel;
Misbah, Siraj A.

Publication type:

Correction Notice

Correction to: Circulating T Cells of Patients with Nijmegen Breakage Syndrome Show Signs of Senescence.

Published in:

2018

By:

Meijers, Ruud W. J.;
Dzierzanowska-Fangrat, Katarzyna;
Zborowska, Magdalena;
Solarska, Iwona;
Tielemans, Dennis;
van Turnhout, Bob A. C.;
Driessen, Gertjan;
van der Burg, Mirjam;
van Dongen, Jacques J. M.;
Chrzanowska, Krystyna H.;
Langerak, Anton W.

Publication type:

Correction Notice

Correction to: Raised Serum IL-8 Levels Are Associated with Excessive Fatigue in Female Carriers of X-Linked Chronic Granulomatous Disease in the UK.

Published in:

2018

By:

Battersby, Alexandra C.;
Martin, Alexander J.;
Tarn, Jessica;
Ng, W. F.;
Cale, Catherine M.;
Goldblatt, David;
Gennery, Andrew R.

Publication type:

Correction Notice

Antinuclear Antibody-Positive Juvenile Idiopathic Arthritis Despite IRAK-4 Deficiency.

Published in:

2018

By:

Hügle, Boris;
Händel, Norman;
Schwarz, Klaus;
Borte, Michael;
Schuster, Volker

Publication type:

Letter to the Editor

Dual Threat of Epstein-Barr Virus: an Autopsy Case Report of HIV-Positive Plasmablastic Lymphoma Complicating EBV-Associated Hemophagocytic Lymphohistiocytosis.

Published in:

2018

By:

Koizumi, Yusuke;
Imadome, Ken-Ichi;
Ota, Yasunori;
Minamiguchi, Hitoshi;
Kodama, Yoshinori;
Watanabe, Dai;
Mikamo, Hiroshige;
Uehira, Tomoko;
Okada, Seiji;
Shirasaka, Takuma

Publication type:

Case Study

ADA Deficiency: Evaluation of the Clinical and Laboratory Features and the Outcome.

Published in:

Journal of Clinical Immunology, 2018, v. 38, n. 4, p. 484, doi. 10.1007/s10875-018-0496-9

By:

Cagdas, Deniz;
Gur Cetinkaya, Pınar;
Karaatmaca, Betül;
Esenboga, Saliha;
Tan, Cagman;
Yılmaz, Togay;
Gümüş, Ersin;
Barış, Safa;
Kuşkonmaz, Barış;
Ozgur, Tuba Turul;
Bali, Pawan;
Santisteban, Ines;
Orhan, Diclehan;
Yüce, Aysel;
Cetinkaya, Duygu;
Boztug, Kaan;
Hershfield, Michael;
Sanal, Ozden;
Tezcan, İlhan

Publication type:

Article