Zobrazeno 1 - 4
of 4
pro vyhledávání: '"María V. Paolini"'
Autor:
María V. Paolini, Silvia Danielian, Emma Prieto, María Fernanda Tami, Matías M. Oleastro, Diego S. Fernández Romero
Publikováno v:
Medicina (Buenos Aires), Vol 78, Iss 2, Pp 123-126 (2018)
WHIM syndrome is a primary autosomal dominant immuno deficiency due to CXCR4 mutations characterized by mucocutaneous warts, hypogammaglobulinemia, recurrent bacterial infections and myelokathesis. Treatment consists in prophylactic antibiotics, immu
Autor:
María V, Paolini, Silvia, Danielian, Emma, Prieto, María Fernanda, Tami, Matías M, Oleastro, Diego S, Fernández Romero
Publikováno v:
Medicina. 78(2)
WHIM syndrome is a primary autosomal dominant immuno deficiency due to CXCR4 mutations characterized by mucocutaneous warts, hypogammaglobulinemia, recurrent bacterial infections and myelokathesis. Treatment consists in prophylactic antibiotics, immu
Publikováno v:
Medicina. 76(2)
X-linked agammaglobulinemia (XLA) is characterized by absent or severely reduced B cells, low or undetectable immunoglobulin levels and clinically by extracellular bacterial infections which mainly compromise the respiratory tract as well as recurren
Publikováno v:
CONICET Digital (CONICET)
Consejo Nacional de Investigaciones Científicas y Técnicas
instacron:CONICET
Medicina (Buenos Aires), Vol 73, Iss 4, Pp 315-323 (2013)
Consejo Nacional de Investigaciones Científicas y Técnicas
instacron:CONICET
Medicina (Buenos Aires), Vol 73, Iss 4, Pp 315-323 (2013)
La inmunodeficiencia común variable (IDCV) se caracteriza por una alteración en la producción de anticuerpos y una mayor susceptibilidad a infecciones por bacterias extracelulares capsuladas, principalmente del tracto respiratorio. Analizamos las
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::f805741f7f2dbd323e25c5012c6ca13c
http://ref.scielo.org/rfy9fj
http://ref.scielo.org/rfy9fj