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Results: 1 to 20 of 195

Similar articles for PubMed (Select 22236436)

1.

Newborn screening for primary immunodeficiencies: beyond SCID and XLA.

Borte S, Wang N, Oskarsdóttir S, von Döbeln U, Hammarström L.

Ann N Y Acad Sci. 2011 Dec;1246:118-30. doi: 10.1111/j.1749-6632.2011.06350.x.

PMID:
22236436
2.

[Neonatal screening of severe combined immunodeficiencies].

Thomas C, Mirallié S, Pierres C, Dert C, Clément MC, Mahlaoui N, Durand-Zaleski I, Fischer A, Audrain M; Pour le groupe DEPISTREC.

Arch Pediatr. 2015 Jun;22(6):646-52. doi: 10.1016/j.arcped.2015.03.001. Epub 2015 Apr 18. French.

PMID:
25896629
3.

Gene therapy for primary immunodeficiencies.

Fischer A, Hacein-Bey Abina S, Touzot F, Cavazzana M.

Clin Genet. 2015 Feb 24. doi: 10.1111/cge.12576. [Epub ahead of print]

PMID:
25708106
4.

Primary immunodeficiencies screening: neonatal screening for T/B cell disorders - a triplex PCR method for quantitation of TRECs and KRECs in newborns.

Hammarström L.

Clin Exp Immunol. 2014 Dec;178 Suppl 1:14-5. doi: 10.1111/cei.12494. No abstract available.

PMID:
25546745
5.

Newborn screening for SCID: where are we now?

Buelow BJ, Routes JM, Verbsky JW.

Expert Rev Clin Immunol. 2014 Dec;10(12):1649-57. doi: 10.1586/1744666X.2014.980816. Epub 2014 Nov 12.

PMID:
25387596
6.

[A first pilot study on the neonatal screening of primary immunodeficiencies in Spain: TRECS and KRECS identify severe T- and B-cell lymphopenia].

Olbrich P, de Felipe B, Delgado-Pecellin C, Rodero R, Rojas P, Aguayo J, Marquez J, Casanovas J, Sánchez B, Lucena JM, Ybot-Gonzalez P, Borte S, Neth O.

An Pediatr (Barc). 2014 Nov;81(5):310-7. doi: 10.1016/j.anpedi.2014.08.002. Epub 2014 Sep 30. Spanish.

7.

[Extending neonatal screening to the detection of severe combined immunodeficiencies. A moral imperative].

Alsina L, Llobet-Agulló P, Soler-Palacín P.

An Pediatr (Barc). 2014 Nov;81(5):273-4. doi: 10.1016/j.anpedi.2014.08.003. Epub 2014 Sep 18. Spanish. No abstract available.

8.

Newborn screening for severe T and B cell lymphopenia identifies a fraction of patients with Wiskott-Aldrich syndrome.

Borte S, Fasth A, von Döbeln U, Winiarski J, Hammarström L.

Clin Immunol. 2014 Nov;155(1):74-8. doi: 10.1016/j.clim.2014.09.003. Epub 2014 Sep 15.

PMID:
25217881
9.

Autoimmune and other cytopenias in primary immunodeficiencies: pathomechanisms, novel differential diagnoses, and treatment.

Seidel MG.

Blood. 2014 Oct 9;124(15):2337-44. doi: 10.1182/blood-2014-06-583260. Epub 2014 Aug 27. Review.

10.

Too much of a good thing: immunodeficiency due to hyperactive PI3K signaling.

Walsh CM, Fruman DA.

J Clin Invest. 2014 Sep;124(9):3688-90. doi: 10.1172/JCI77198. Epub 2014 Aug 18.

11.

Good’s syndrome presenting with recurrent giardiasis”.

Rawat A, Dhir V, Gupta A, Suri D, Burad DK, Nada R, Singh S.

J Clin Immunol. 2014 Oct;34(7):751-2. doi: 10.1007/s10875-014-0080-x. Epub 2014 Jul 22. No abstract available.

PMID:
25047153
12.

Antibody immunodeficiency diseases.

Ellenburg JT, deShazo RD.

South Med J. 2014 Feb;107(2):93-100. doi: 10.1097/SMJ.0000000000000055.

PMID:
24926675
13.

Combined newborn screening for familial hemophagocytic lymphohistiocytosis and severe T- and B-cell immunodeficiencies.

Borte S, Meeths M, Liebscher I, Krist K, Nordenskjöld M, Hammarström L, von Döbeln U, Henter JI, Bryceson YT.

J Allergy Clin Immunol. 2014 Jul;134(1):226-8. doi: 10.1016/j.jaci.2014.04.026. Epub 2014 May 29. No abstract available.

PMID:
24882743
14.

Primary immunodeficiency disorders: general classification, new molecular insights, and practical approach to diagnosis and treatment.

Ochs HD, Hagin D.

Ann Allergy Asthma Immunol. 2014 Jun;112(6):489-95. doi: 10.1016/j.anai.2014.04.007. Review. No abstract available.

PMID:
24860921
15.

Clinical characteristics and outcomes of primary antibody deficiency: a 20-year follow-up study.

Chan HY, Yang YH, Yu HH, Chien YH, Chiang LL, Chiang BL.

J Formos Med Assoc. 2014 Jun;113(6):340-8. doi: 10.1016/j.jfma.2012.07.005. Epub 2012 Aug 11.

PMID:
24820629
16.

World Primary Immunodeficiency Week: a call for newborn screening.

Etzioni A.

Eur J Immunol. 2014 Apr;44(4):925-6. doi: 10.1002/eji.201470035. No abstract available.

PMID:
24723167
17.

A case of Bruton's disease with normal immunoglobulin G level.

Alyasin S, Abolnezhadian F, Rezaei A.

Iran J Immunol. 2014 Mar;11(1):59-63. doi: IJIv11i1A7. No abstract available.

PMID:
24632589
18.

First report on the Moroccan registry of primary immunodeficiencies: 15 years of experience (1998-2012).

Bousfiha AA, Jeddane L, El Hafidi N, Benajiba N, Rada N, El Bakkouri J, Kili A, Benmiloud S, Benhsaien I, Faiz I, Maataoui O, Aadam Z, Aglaguel A, Baba LA, Jouhadi Z, Abilkassem R, Bouskraoui M, Hida M, Najib J, Alj HS, Ailal F; Moroccan Society for Primary Immunodeficiencies (MSPID).

J Clin Immunol. 2014 May;34(4):459-68. doi: 10.1007/s10875-014-0005-8. Epub 2014 Mar 12.

PMID:
24619622
19.

ICON: the early diagnosis of congenital immunodeficiencies.

Routes J, Abinun M, Al-Herz W, Bustamante J, Condino-Neto A, De La Morena MT, Etzioni A, Gambineri E, Haddad E, Kobrynski L, Le Deist F, Nonoyama S, Oliveira JB, Perez E, Picard C, Rezaei N, Sleasman J, Sullivan KE, Torgerson T.

J Clin Immunol. 2014 May;34(4):398-424. doi: 10.1007/s10875-014-0003-x. Epub 2014 Mar 12. Review.

PMID:
24619621
20.

Retrospective analysis of TREC based newborn screening results and clinical phenotypes in infants with the 22q11 deletion syndrome.

Lingman Framme J, Borte S, von Döbeln U, Hammarström L, Oskarsdóttir S.

J Clin Immunol. 2014 May;34(4):514-9. doi: 10.1007/s10875-014-0002-y. Epub 2014 Mar 9.

PMID:
24610337
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