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Results: 1 to 20 of 114

Similar articles for PubMed (Select 21274562)

1.

Study of patients with Hyper-IgM type IV phenotype who recovered spontaneously during late childhood and review of the literature.

Karaca NE, Durandy A, Gulez N, Aksu G, Kutukculer N.

Eur J Pediatr. 2011 Aug;170(8):1039-47. doi: 10.1007/s00431-011-1400-2. Epub 2011 Jan 28. Review.

PMID:
21274562
2.

Onychomadesis in a patient with immunoglobulin class switch recombination deficiency.

Safari M, Rezaei N, Hajilooi M, Aghamohammadi A, Pan-Hammarstrom Q, Hammarstrom L.

Iran J Allergy Asthma Immunol. 2008 Mar;7(1):41-4. doi: 07.01/ijaai.4144.

3.

Hyper-IgM, neutropenia, mild infections and low response to polyclonal stimulation: hyper-IgM syndrome or common variable immunodeficiency?

Rosado MM, Picchianti Diamanti A, Cascioli S, Ceccarelli S, Caporuscio S, D'Amelio R, Carsetti R, Lagana B.

Int J Immunopathol Pharmacol. 2011 Oct-Dec;24(4):983-91.

PMID:
22230404
4.

Pathophysiology of B-cell intrinsic immunoglobulin class switch recombination deficiencies.

Durandy A, Taubenheim N, Peron S, Fischer A.

Adv Immunol. 2007;94:275-306. Review.

PMID:
17560278
5.

Clinical and laboratory findings in hyper-IgM syndrome with novel CD40L and AICDA mutations.

Aghamohammadi A, Parvaneh N, Rezaei N, Moazzami K, Kashef S, Abolhassani H, Imanzadeh A, Mohammadi J, Hammarström L.

J Clin Immunol. 2009 Nov;29(6):769-76. doi: 10.1007/s10875-009-9315-7. Epub 2009 Jul 3.

PMID:
19575287
6.

Clinical features and genetic analysis of Taiwanese patients with the hyper IgM syndrome phenotype.

Lee WI, Huang JL, Yeh KW, Yang MJ, Lai MC, Chen LC, Ou LS, Yao TC, Lin SJ, Jaing TH, Chen SH, Hsieh MY, Yu HH, Chien YH, Shyur SD.

Pediatr Infect Dis J. 2013 Sep;32(9):1010-6. doi: 10.1097/INF.0b013e3182936280.

PMID:
23538518
7.

A novel mouse model for the hyper-IgM syndrome: a spontaneous activation-induced cytidine deaminase mutation leading to complete loss of Ig class switching and reduced somatic hypermutation.

Dahlberg CI, He M, Visnes T, Torres ML, Cortizas EM, Verdun RE, Westerberg LS, Severinson E, Ström L.

J Immunol. 2014 Nov 1;193(9):4732-8. doi: 10.4049/jimmunol.1401242. Epub 2014 Sep 24.

8.

Isolated growth hormone deficiency in a patient with immunoglobulin class switch recombination deficiency.

Kashef S, Ghaedian MM, Rezaei N, Karamizadeh Z, Aghamohammadi A, Durandy A, Pan-Hammarstrom Q, Hammarstrom L.

J Investig Allergol Clin Immunol. 2009;19(3):233-6. Erratum in: J Investig Allergol Clin Immunol. 2009;19(5):422.

9.

The outcome of patients with unclassified hypogammaglobulinemia in early childhood.

Kutukculer N, Gulez N.

Pediatr Allergy Immunol. 2009 Nov;20(7):693-8. doi: 10.1111/j.1399-3038.2008.00845.x. Epub 2009 Jan 31.

PMID:
19196447
10.

Pitfalls of "hyper"-IgM syndrome: a new CD40 ligand mutation in the presence of low IgM levels. A case report and a critical review of the literature.

Heinold A, Hanebeck B, Daniel V, Heyder J, Tran TH, Döhler B, Greil J, Müller FM.

Infection. 2010 Dec;38(6):491-6. doi: 10.1007/s15010-010-0061-9. Epub 2010 Oct 28. Review.

PMID:
20981468
11.

Update on the hyper immunoglobulin M syndromes.

Davies EG, Thrasher AJ.

Br J Haematol. 2010 Apr;149(2):167-80. doi: 10.1111/j.1365-2141.2010.08077.x. Epub 2010 Feb 23. Review.

12.

Symptomatic hypogammaglobulinemia in infancy and childhood - clinical outcome and in vitro immune responses.

Kidon MI, Handzel ZT, Schwartz R, Altboum I, Stein M, Zan-Bar I.

BMC Fam Pract. 2004 Oct 21;5:23.

13.

Hyper-IgM syndrome type 4 with a B lymphocyte-intrinsic selective deficiency in Ig class-switch recombination.

Imai K, Catalan N, Plebani A, Maródi L, Sanal O, Kumaki S, Nagendran V, Wood P, Glastre C, Sarrot-Reynauld F, Hermine O, Forveille M, Revy P, Fischer A, Durandy A.

J Clin Invest. 2003 Jul;112(1):136-42.

14.

Hyper-immunoglobulin M syndromes caused by intrinsic B-lymphocyte defects.

Durandy A, Revy P, Imai K, Fischer A.

Immunol Rev. 2005 Feb;203:67-79. Review.

PMID:
15661022
15.

The different process of class switching and somatic hypermutation; a novel analysis by CD27(-) naive B cells.

Nagumo H, Agematsu K, Kobayashi N, Shinozaki K, Hokibara S, Nagase H, Takamoto M, Yasui K, Sugane K, Komiyama A.

Blood. 2002 Jan 15;99(2):567-75.

16.

Clinical, immunological, and molecular characterization of hyper-IgM syndrome due to CD40 deficiency in eleven patients.

Al-Saud BK, Al-Sum Z, Alassiri H, Al-Ghonaium A, Al-Muhsen S, Al-Dhekri H, Arnaout R, Alsmadi O, Borrero E, Abu-Staiteh A, Rawas F, Al-Mousa H, Hawwari A.

J Clin Immunol. 2013 Nov;33(8):1325-35. Review.

PMID:
24122029
17.

Class switch recombination process in ataxia telangiectasia patients with elevated serum levels of IgM.

Mohammadinejad P, Abolhassani H, Aghamohammadi A, Pourhamdi S, Ghosh S, Sadeghi B, Nasiri Kalmarzi R, Durandy A, Borkhardt A.

J Immunoassay Immunochem. 2015;36(1):16-26. doi: 10.1080/15321819.2014.891525.

PMID:
24568663
18.
19.

[Hyper-IgM syndrome in a boy with recurrent pneumonia and hepatosplenomegaly].

Janić D, Radlović N, Dokmanović L, Krstovski N, Leković Z, Janković S, Ristić D.

Srp Arh Celok Lek. 2009 Jan-Feb;137(1-2):81-5. Serbian.

PMID:
19370972
20.

Autoimmunity in hyper-IgM syndrome.

Jesus AA, Duarte AJ, Oliveira JB.

J Clin Immunol. 2008 May;28 Suppl 1:S62-6. doi: 10.1007/s10875-008-9171-x. Epub 2008 Feb 2. Review.

PMID:
18246414
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