Novel insight into Chronic Inflammatory Demyelinating Polineuropathy in APECED syndrome: molecular mechanisms and clinical implications in children-Reference-Cited by-同舟云学术

Novel insight into Chronic Inflammatory Demyelinating Polineuropathy in APECED syndrome: molecular mechanisms and clinical implications in children

Published:2017-01-19 Issue:1 Volume:43 Page:
ISSN:1824-7288
Container-title:Italian Journal of Pediatrics
language:en
Short-container-title:Ital J Pediatr

Author:

Valenzise Mariella,Aversa Tommaso,Salzano Giuseppina,Zirilli Giuseppina,De Luca Filippo,Su Maureen

Publisher

Springer Science and Business Media LLC

Subject

General Medicine

Link

http://link.springer.com/content/pdf/10.1186/s13052-017-0331-6.pdf

Reference16 articles.

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2. Valenzise M, Wasniewska M, Mirabelli S, De Luca F, Cervato S, Betterle C. Identification of two novel mutations in the first Sicilian APECED patient with no R203X mutation in AIRE gene and review of Italian APECED genotypes. Gene. 2012;499(2):343–6.

3. Perri V, Gianchecchi E, Scarpa R, Valenzise M, Rosado MM, Giorda E et a.Altered B cell homeostasis and Toll-like receptor 9-driven response in patients affected by autoimmune polyglandular syndrome Type 1: Altered B cell phenotype and dysregulation of the B cell function in APECED patients. Immunobiology. 2017; 222(2):372–383.

4. Valenzise M, Alessi L, Bruno E, Cama V, Costanzo D, Genovese C, et al. APECED syndrome in childhood: clinical spectrum is enlarging. Minerva Pediatr. 2016;68(3):226–9. 25502918.

5. De Luca F, Valenzise M, Alaggio R, Arrigo T, Crisafulli G, Salzano G, et al. Sicilian family with autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy (APECED) and lethal lung disease in one of the affected brothers. Eur J Pediatr. 2008;167(11):1283–8.

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