Badolato R - Search Results

1

Primary immunodeficiencies appearing as combined lymphopenia, neutropenia, and monocytopenia.

Dotta L, Badolato R. Dotta L, et al. Among authors: badolato r. Immunol Lett. 2014 Oct;161(2):222-5. doi: 10.1016/j.imlet.2013.11.018. Epub 2013 Dec 4. Immunol Lett. 2014. PMID: 24316408 Review.

2

Congenital neutropenia: advances in diagnosis and treatment.

Badolato R, Fontana S, Notarangelo LD, Savoldi G. Badolato R, et al. Curr Opin Allergy Clin Immunol. 2004 Dec;4(6):513-21. doi: 10.1097/00130832-200412000-00007. Curr Opin Allergy Clin Immunol. 2004. PMID: 15640692 Review.

3

Immunodeficiencies with autoimmune consequences.

Notarangelo LD, Gambineri E, Badolato R. Notarangelo LD, et al. Among authors: badolato r. Adv Immunol. 2006;89:321-70. doi: 10.1016/S0065-2776(05)89008-X. Adv Immunol. 2006. PMID: 16682278 Review.

4

Clinical and genetic features of Warts, Hypogammaglobulinemia, Infections and Myelokathexis (WHIM) syndrome.

Dotta L, Tassone L, Badolato R. Dotta L, et al. Among authors: badolato r. Curr Mol Med. 2011 Jun;11(4):317-25. doi: 10.2174/156652411795677963. Curr Mol Med. 2011. PMID: 21506920 Review.

5

SH2-domain mutations in STAT3 in hyper-IgE syndrome patients result in impairment of IL-10 function.

Giacomelli M, Tamassia N, Moratto D, Bertolini P, Ricci G, Bertulli C, Plebani A, Cassatella M, Bazzoni F, Badolato R. Giacomelli M, et al. Among authors: badolato r. Eur J Immunol. 2011 Oct;41(10):3075-84. doi: 10.1002/eji.201141721. Epub 2011 Sep 6. Eur J Immunol. 2011. PMID: 21792878 Free article.

6

Tetralogy of fallot is an uncommon manifestation of warts, hypogammaglobulinemia, infections, and myelokathexis syndrome.

Badolato R, Dotta L, Tassone L, Amendola G, Porta F, Locatelli F, Notarangelo LD, Bertrand Y, Bachelerie F, Donadieu J. Badolato R, et al. J Pediatr. 2012 Oct;161(4):763-5. doi: 10.1016/j.jpeds.2012.05.058. Epub 2012 Jun 27. J Pediatr. 2012. PMID: 22748845 Free PMC article.

7

Defects of leukocyte migration in primary immunodeficiencies.

Badolato R. Badolato R. Eur J Immunol. 2013 Jun;43(6):1436-40. doi: 10.1002/eji.201243155. Eur J Immunol. 2013. PMID: 23630104 Free article. Review.

8

Clinical, laboratory and molecular signs of immunodeficiency in patients with partial oculo-cutaneous albinism.

Dotta L, Parolini S, Prandini A, Tabellini G, Antolini M, Kingsmore SF, Badolato R. Dotta L, et al. Among authors: badolato r. Orphanet J Rare Dis. 2013 Oct 17;8:168. doi: 10.1186/1750-1172-8-168. Orphanet J Rare Dis. 2013. PMID: 24134793 Free PMC article. Review.

9

Primary immunodeficiences--options for the future.

Badolato R. Badolato R. Pediatr Allergy Immunol. 2014 Feb;25(1):27-9. doi: 10.1111/pai.12192. Pediatr Allergy Immunol. 2014. PMID: 24588485 No abstract available.

10

Autosomal recessive agammaglobulinemia: the third case of Igβ deficiency due to a novel non-sense mutation.

Lougaris V, Vitali M, Baronio M, Moratto D, Tampella G, Biasini A, Badolato R, Plebani A. Lougaris V, et al. Among authors: badolato r. J Clin Immunol. 2014 May;34(4):425-7. doi: 10.1007/s10875-014-0033-4. Epub 2014 Apr 11. J Clin Immunol. 2014. PMID: 24722855

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