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Items: 1 to 20 of 199

1.

Clinical, Immunological, Molecular Analyses and Outcomes of Iranian Patients with LRBA Deficiency: A Longitudinal Study.

Azizi G, Abolhassani H, Mahdaviani SA, Chavoshzadeh Z, Eshghi P, Yazdani R, Kiaee F, Shaghaghi M, Mohammadi J, Rezaei N, Hammarström L, Aghamohammadi A.

Pediatr Allergy Immunol. 2017 May 17. doi: 10.1111/pai.12735. [Epub ahead of print]

PMID:
28512785
2.

Treatment of Severe Forms of LPS-Responsive Beige-like Anchor Protein (LRBA) Deficiency by Allogeneic Hematopoietic Stem Cell Transplantation.

Seidel MG, Böhm K, Dogu F, Worth A, Thrasher A, Florkin B, İkincioğulları A, Peters A, Bakhtiar S, Meeths M, Stepensky P, Meyts I, Sharapova SO, Gámez-Díaz L, Hammarström L, Ehl S, Grimbacher B, Gennery AR; Inborn Errors Working Party (IEWP) of the European Group for Blood and Marrow Transplantation (EBMT)..

J Allergy Clin Immunol. 2017 May 10. pii: S0091-6749(17)30747-9. doi: 10.1016/j.jaci.2017.04.023. [Epub ahead of print]

PMID:
28502825
3.

Human sera collected during 1979-2010 possess blocking antibody titers to pandemic GII.4 noroviruses isolated during 3 decades.

Sharma S, Carlsson B, Czakó R, Vene S, Haglund M, Ludvigsson J, Larson G, Hammarström L, Sosnovtsev SV, Atmar RL, Green KY, Estes MK, Svensson L.

J Virol. 2017 May 3. pii: JVI.00567-17. doi: 10.1128/JVI.00567-17. [Epub ahead of print]

PMID:
28468886
4.

NEIL1 is a candidate gene associated with common variable immunodeficiency in a patient with a chromosome 15q24 deletion.

Romano R, Zaravinos A, Liadaki K, Caridha R, Lundin J, Carlsson G, Winiarski J, Pan-Hammarström Q, Hammarström L.

Clin Immunol. 2017 Mar;176:71-76. doi: 10.1016/j.clim.2017.01.006. Epub 2017 Jan 14.

PMID:
28093361
5.

Costs associated with treatment of severe combined immunodeficiency-rationale for newborn screening in Sweden.

Gardulf A, Winiarski J, Thorin M, Heibert Arnlind M, von Döbeln U, Hammarström L.

J Allergy Clin Immunol. 2017 May;139(5):1713-1716.e6. doi: 10.1016/j.jaci.2016.10.043. Epub 2016 Dec 21. No abstract available.

PMID:
28012934
6.

Combined immunodeficiency and Epstein-Barr virus-induced B cell malignancy in humans with inherited CD70 deficiency.

Abolhassani H, Edwards ES, Ikinciogullari A, Jing H, Borte S, Buggert M, Du L, Matsuda-Lennikov M, Romano R, Caridha R, Bade S, Zhang Y, Frederiksen J, Fang M, Bal SK, Haskologlu S, Dogu F, Tacyildiz N, Matthews HF, McElwee JJ, Gostick E, Price DA, Palendira U, Aghamohammadi A, Boisson B, Rezaei N, Karlsson AC, Lenardo MJ, Casanova JL, Hammarström L, Tangye SG, Su HC, Pan-Hammarström Q.

J Exp Med. 2017 Jan;214(1):91-106. doi: 10.1084/jem.20160849. Epub 2016 Dec 23.

PMID:
28011864
7.

Newborn Screening for Severe Primary Immunodeficiency Diseases in Sweden-a 2-Year Pilot TREC and KREC Screening Study.

Barbaro M, Ohlsson A, Borte S, Jonsson S, Zetterström RH, King J, Winiarski J, von Döbeln U, Hammarström L.

J Clin Immunol. 2017 Jan;37(1):51-60. doi: 10.1007/s10875-016-0347-5. Epub 2016 Nov 21.

8.

Common variants at PVT1, ATG13-AMBRA1, AHI1 and CLEC16A are associated with selective IgA deficiency.

Bronson PG, Chang D, Bhangale T, Seldin MF, Ortmann W, Ferreira RC, Urcelay E, Pereira LF, Martin J, Plebani A, Lougaris V, Friman V, Freiberger T, Litzman J, Thon V, Pan-Hammarström Q, Hammarström L, Graham RR, Behrens TW.

Nat Genet. 2016 Nov;48(11):1425-1429. doi: 10.1038/ng.3675. Epub 2016 Oct 10.

9.

Oral Delivery of Pentameric Glucagon-Like Peptide-1 by Recombinant Lactobacillus in Diabetic Rats.

Lin Y, Krogh-Andersen K, Pelletier J, Marcotte H, Östenson CG, Hammarström L.

PLoS One. 2016 Sep 9;11(9):e0162733. doi: 10.1371/journal.pone.0162733. eCollection 2016.

10.

Heterozygosity for transmembrane activator and calcium modulator ligand interactor A144E causes haploinsufficiency and pneumococcal susceptibility in mice.

Jabara HH, Lee JJ, Janssen E, Ullas S, Liadaki K, Garibyan L, Benson H, Sannikova T, Bram R, Hammarstrom L, Cruz AC, Siegel R, Manis J, Malley R, Geha RS.

J Allergy Clin Immunol. 2017 Apr;139(4):1293-1301.e4. doi: 10.1016/j.jaci.2016.07.028. Epub 2016 Sep 5.

PMID:
27609654
11.

Reply.

Bonilla FA, Chapel H, Costa-Carvalho BT, Cunningham-Rundles C, de la Morena MT, Espinosa-Rosales FJ, Hammarström L, Nonoyama S, Quinti I, Routes JM, Tang ML, Warnatz K.

J Allergy Clin Immunol Pract. 2016 Sep-Oct;4(5):1019-20. doi: 10.1016/j.jaip.2016.04.029. No abstract available.

PMID:
27587326
12.

[Study on immunoglobulin A Deficiency(IgAD) in Chinese Shanghai Blood Donors].

Lu P, Ling B, Wang N, Hammarstrom L.

Zhongguo Shi Yan Xue Ye Xue Za Zhi. 2016 Aug;24(4):1216-20. doi: 10.7534/j.issn.1009-2137.2016.04.047. Chinese.

PMID:
27531803
13.

Fusion of the mouse IgG1 Fc domain to the VHH fragment (ARP1) enhances protection in a mouse model of rotavirus.

Günaydın G, Yu S, Gräslund T, Hammarström L, Marcotte H.

Sci Rep. 2016 Jul 21;6:30171. doi: 10.1038/srep30171.

14.

Monogenic mutations associated with IgA deficiency.

Abolhassani H, Aghamohammadi A, Hammarström L.

Expert Rev Clin Immunol. 2016 Dec;12(12):1321-1335. Epub 2016 Jun 21. Review.

PMID:
27266541
15.

Deep sequencing of the MHC region in the Chinese population contributes to studies of complex disease.

Zhou F, Cao H, Zuo X, Zhang T, Zhang X, Liu X, Xu R, Chen G, Zhang Y, Zheng X, Jin X, Gao J, Mei J, Sheng Y, Li Q, Liang B, Shen J, Shen C, Jiang H, Zhu C, Fan X, Xu F, Yue M, Yin X, Ye C, Zhang C, Liu X, Yu L, Wu J, Chen M, Zhuang X, Tang L, Shao H, Wu L, Li J, Xu Y, Zhang Y, Zhao S, Wang Y, Li G, Xu H, Zeng L, Wang J, Bai M, Chen Y, Chen W, Kang T, Wu Y, Xu X, Zhu Z, Cui Y, Wang Z, Yang C, Wang P, Xiang L, Chen X, Zhang A, Gao X, Zhang F, Xu J, Zheng M, Zheng J, Zhang J, Yu X, Li Y, Yang S, Yang H, Wang J, Liu J, Hammarström L, Sun L, Wang J, Zhang X.

Nat Genet. 2016 Jul;48(7):740-6. doi: 10.1038/ng.3576. Epub 2016 May 23.

PMID:
27213287
16.

Multiple IgH Isotypes Including IgD, Subclasses of IgM, and IgY Are Expressed in the Common Ancestors of Modern Birds.

Han B, Yuan H, Wang T, Li B, Ma L, Yu S, Huang T, Li Y, Fang D, Chen X, Wang Y, Qiu S, Guo Y, Fei J, Ren L, Pan-Hammarström Q, Hammarström L, Wang J, Wang J, Hou Y, Pan Q, Xu X, Zhao Y.

J Immunol. 2016 Jun 15;196(12):5138-47. doi: 10.4049/jimmunol.1600307. Epub 2016 May 16.

PMID:
27183632
17.

Internal Duplications of DH, JH, and C Region Genes Create an Unusual IgH Gene Locus in Cattle.

Ma L, Qin T, Chu D, Cheng X, Wang J, Wang X, Wang P, Han H, Ren L, Aitken R, Hammarström L, Li N, Zhao Y.

J Immunol. 2016 May 15;196(10):4358-66. doi: 10.4049/jimmunol.1600158. Epub 2016 Apr 6.

18.

Next Generation Sequencing Data Analysis in Primary Immunodeficiency Disorders - Future Directions.

Fang M, Abolhassani H, Lim CK, Zhang J, Hammarström L.

J Clin Immunol. 2016 May;36 Suppl 1:68-75. doi: 10.1007/s10875-016-0260-y. Epub 2016 Mar 18.

PMID:
26993986
19.

Evaluation of Known Defective Signaling-Associated Molecules in Patients Who Primarily Diagnosed as Common Variable Immunodeficiency.

Yazdani R, Abolhassani H, Rezaei N, Azizi G, Hammarström L, Aghamohammadi A.

Int Rev Immunol. 2016;35(1):7-24. doi: 10.3109/08830185.2015.1136306. Review.

PMID:
26959802
20.

Cohort of Iranian Patients with Congenital Agammaglobulinemia: Mutation Analysis and Novel Gene Defects.

Abolhassani H, Vitali M, Lougaris V, Giliani S, Parvaneh N, Parvaneh L, Mirminachi B, Cheraghi T, Khazaei H, Mahdaviani SA, Kiaei F, Tavakolinia N, Mohammadi J, Negahdari B, Rezaei N, Hammarstrom L, Plebani A, Aghamohammadi A.

Expert Rev Clin Immunol. 2016;12(4):479-86. doi: 10.1586/1744666X.2016.1139451. Epub 2016 Feb 24.

PMID:
26910880

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