Works matching IS 02719142 AND DT 2019 AND VI 39 AND IP 8

Results: 20

Provider Perceptions of Quality of Life, Neurocognition, Physical Well-being, and Psychosocial Health in Patients with Primary Immunodeficiency/Immune Dysregulation Conditions.

Published in:

Journal of Clinical Immunology, 2019, v. 39, n. 8, p. 805, doi. 10.1007/s10875-019-00703-7

By:

Michniacki, Thomas F.;
Walkovich, Kelly J.;
Merz, Lauren E.;
Sturza, Julie;
Abraham, Roshini S.

Publication type:

Article

Interstitial Lung Disease Frequently Precedes CVID Diagnosis.

Published in:

2019

By:

Hanitsch, Leif G.;
Wittke, Kirsten;
Stittrich, Anna Barbara;
Volk, Hans Dieter;
Scheibenbogen, Carmen

Publication type:

Letter

Serum Tryptase Cannot Differentiate Vancomycin-Induced Anaphylaxis From Red Man Syndrome.

Published in:

2019

By:

Noguchi, Satoko;
Takekawa, Daiki;
Saito, Junichi;
Hashiba, Eiji;
Hirota, Kazuyoshi

Publication type:

Letter

Quality of Life Differences for Primary Immunodeficiency Patients on Home SCIG versus IVIG.

Published in:

Journal of Clinical Immunology, 2019, v. 39, n. 8, p. 814, doi. 10.1007/s10875-019-00705-5

By:

Anterasian, Christine;
Duong, Richard;
Gruenemeier, Peg;
Ernst, Carol;
Kitsen, Jessica;
Geng, Bob

Publication type:

Article

The Value of Chromosome Analysis to Interrogate Variants in DNMT3B Causing Immunodeficiency, Centromeric Instability, and Facial Anomaly Syndrome Type I (ICF1).

Published in:

2019

By:

Kellner, Erinn S.;
Rathbun, Pamela A.;
Marshall, Gary S.;
Tolusso, Leandra K.;
Smolarek, Teresa A.;
Sun, Miao;
Chandra, Sharat;
Bleesing, Jack;
Marsh, Rebecca A.

Publication type:

Letter

Correction to: Unusual Severe Seborrheic Dermatitis in Two Siblings with Autosomal Recessive Chronic Granulomatous Disease.

Published in:

2019

By:

Zurro, Nuria Bengala;
de Oliveira Junior, Edgar Borges;
França, Tábata Takahashi;
Dantas, Vera Maria;
Tavares de Albuquerque, Jose Antonio;
Condino-Neto, Antonio

Publication type:

Correction Notice

Editorial, Journal of Clinical Immunology.

Published in:

2019

By:

Casanova, Jean-Laurent;
Bonagura, Vincent

Publication type:

Editorial

Homozygous Splice ADA2 Gene Mutation Causing ADA-2 Deficiency.

Published in:

2019

By:

Chong-Neto, Herberto Jose;
Segundo, Gesmar Rodrigues Silva;
Bandeira, Márcia;
Chong-Silva, Débora Carla;
Rosário, Cristine Secco;
Riedi, Carlos A.;
Hershfield, Michael S.;
Ochs, Hans;
Torgerson, Troy;
Rosário, Nelson Augusto

Publication type:

Letter

A De Novo Frameshift Mutation in TNFAIP3 Impairs A20 Deubiquitination Function to Cause Neuropsychiatric Systemic Lupus Erythematosus.

Published in:

Journal of Clinical Immunology, 2019, v. 39, n. 8, p. 795, doi. 10.1007/s10875-019-00695-4

By:

Duan, Ruonan;
Liu, Qi;
Li, Jiangxia;
Bian, Xianli;
Yuan, Qianqian;
Li, Yan;
Long, Feng;
Gao, Shang;
Wei, Shijun;
Li, Pengyu;
Gao, Fei;
Sun, Wenjie;
Li, Xi;
Liu, Qiji

Publication type:

Article

Altered Monocyte Subsets in Patients with Chronic Idiopathic Neutropenia.

Published in:

2019

By:

Bizymi, Nikoleta;
Velegraki, Maria;
Damianaki, Athina;
Koutala, Helen;
Papadaki, Helen A.

Publication type:

Letter

Management of ADA-Deficient SCID Patient on Adagen During Pregnancy.

Published in:

2019

By:

Shams, Marissa;
Kobrynski, Lisa

Publication type:

Letter

Quality of Life of Patients with Wiskott Aldrich Syndrome and X-Linked Thrombocytopenia: a Study of the Primary Immune Deficiency Consortium (PIDTC), Immune Deficiency Foundation, and the Wiskott-Aldrich Foundation.

Published in:

Journal of Clinical Immunology, 2019, v. 39, n. 8, p. 786, doi. 10.1007/s10875-019-00689-2

By:

Shah, Ami J.;
Sokolic, Robert;
Logan, Brent;
Yin, Ziyan;
Iyengar, Sumathi;
Scalchunes, Chris;
Mangurian, Christina;
Albert, Michael;
Cowan, Morton J.

Publication type:

Article

Novel Gain-of-Function Mutation in Stat1 Sumoylation Site Leads to CMC/CID Phenotype Responsive to Ruxolitinib.

Published in:

Journal of Clinical Immunology, 2019, v. 39, n. 8, p. 776, doi. 10.1007/s10875-019-00687-4

By:

Al Shehri, Tariq;
Gilmour, Kimberly;
Gothe, Florian;
Loughlin, Sam;
Bibi, Shahnaz;
Rowan, Andrew D.;
Grainger, Angela;
Mohanadas, Thivytra;
Cant, Andrew J.;
Slatter, Mary A.;
Hambleton, Sophie;
Lilic, Desa;
Leahy, Timothy R.

Publication type:

Article

Abnormal Newborn Screen in a WHIM Syndrome Infant.

Published in:

2019

By:

Evans II, Martin O.;
McDermott, David H.;
Murphy, Philip M.;
Petersen, Maureen M.

Publication type:

Letter

Successful Treatment of PAPA Syndrome with Dual Adalimumab and Tacrolimus Therapy.

Published in:

2019

By:

Sood, Amika K.;
McShane, Diana B.;
Googe, Paul B.;
Wu, Eveline Y.

Publication type:

Letter

Autosomal Dominant Hyper-IgE Syndrome Without Significantly Elevated IgE.

Published in:

2019

By:

Larsen, Carsten S.;
Christiansen, Mette;
Mogensen, Trine H.

Publication type:

Letter

STK4 Deficiency in a Patient with Immune Complex Glomerulonephritis, Salt-Losing Tubulopathy, and Castleman's-Like Disease.

Published in:

2019

By:

Al-Saud, Bandar;
Alajlan, Huda;
Sabar, Haneen;
Anwar, Siddiq;
Alruwaili, Hibah;
Al-Hussain, Turki;
Alamri, Nada;
Alazami, Anas M.

Publication type:

Letter

Unusual Severe Seborrheic Dermatitis in Two Siblings with Autosomal Recessive Chronic Granulomatous Disease.

Published in:

2019

By:

Zurro, Nuria B.;
de Oliveira Junior, Edgar B.;
França, Tábata T.;
Dantas, Vera M.;
Tavares de Albuquerque, Jose A.;
Condino-Neto, Antonio

Publication type:

Letter

Clinical and Molecular Features of Chronic Granulomatous Disease in Mainland China and a XL-CGD Female Infant Patient After Prenatal Diagnosis.

Published in:

Journal of Clinical Immunology, 2019, v. 39, n. 8, p. 762, doi. 10.1007/s10875-019-00680-x

By:

Wang, Shiyu;
Wang, Tao;
Xiang, Qingqing;
Xiao, Min;
Cao, Yao;
Xu, Huan;
Li, Shujuan;
Tian, Wen;
Zhao, Xiaodong;
Tang, Xuemei;
Jiang, Liping

Publication type:

Article

Survey of Infection Control Precautions for Patients with Severe Combined Immune Deficiency.

Published in:

Journal of Clinical Immunology, 2019, v. 39, n. 8, p. 753, doi. 10.1007/s10875-019-00671-y

By:

Dergousoff, Brieanne A.;
Vayalumkal, Joseph V.;
Wright, Nicola A. M.

Publication type:

Article