Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Magdalena Janzi"'
Autor:
Stephan Borte, Magdalena Janzi, Qiang Pan-Hammarström, Ulrika von Döbeln, Lennart Nordvall, Jacek Winiarski, Anders Fasth, Lennart Hammarström
Publikováno v:
PLoS ONE, Vol 7, Iss 8, p e43419 (2012)
There is a need for neonatal screening tools to improve the long-term clinical outcome of patients with primary immunodeficiency diseases (PID). Recently, a PCR-based screening method for both TRECs and KRECs using Guthrie card samples has been devel
Externí odkaz:
https://doaj.org/article/d70bc6bcd6c94972a023d332c4b174cc
Autor:
Magdalena Janzi, Ronald Sjöberg, Jinghong Wan, Björn Fischler, Ulrika von Döbeln, Lourdes Isaac, Peter Nilsson, Lennart Hammarström
Publikováno v:
PLoS ONE, Vol 4, Iss 4, p e5321 (2009)
BACKGROUND: Dried blood spot samples (DBSS) from newborns are widely used in neonatal screening for selected metabolic diseases and diagnostic possibilities for additional disorders are continuously being evaluated. Primary immunodeficiency disorders
Externí odkaz:
https://doaj.org/article/0e27e9c0d6fe43b1ab48d301c83ba79f
Autor:
Lennart Hammarström, Magdalena Janzi, Bjorn R. Ludviksson, Sveinn Vidar Gudmundsson, Arni E. Ornolfsson, Ari Johannesson, Gudmundur H. Jorgensen, Ning Wang
Publikováno v:
Human Immunology. 72:166-172
Immunoglobulin A deficiency (IgAD) is the most common primary immunodeficiency, with suggested association with various types of autoimmunity, including Graves' disease. This study investigated the association of IgAD with elevated thyrotropin-recept
Autor:
Michael Borte, Lennart Hammarström, Anders Fasth, Ulrika von Döbeln, Qiang Pan-Hammarström, Ning Wang, Magdalena Janzi, Jacek Winiarski, Ulrich Sack, Stephan Borte
Publikováno v:
Blood
Severe combined immunodeficiency (SCID) and X-linked agammaglobulinemia (XLA) are inborn errors of immune function that require prompt diagnosis and treatment to prevent life-threatening infections. The lack of functional T or B lymphocytes in these
Publikováno v:
Genes and immunity. 13(1)
TACI (transmembrane activator and calcium modulator and cyclophilin ligand interactor) mutations seem to be associated with autoimmunity and common variable immunodeficiency in humans. Because of its role in immune responses, we investigated the asso
Autor:
Magdalena Janzi, Lennart Hammarström, Ronald Sjöberg, Narges Bayat, Qiang Pan-Hammarström, Erik Melén, Peter Nilsson, Jinghong Wan, Inger Kull, Eva Östblom
Publikováno v:
Clinical immunology (Orlando, Fla.). 133(1)
Selective IgA deficiency in early life is quite common in Caucasian populations, but it is unclear whether it increases the risk of infections and allergic diseases during childhood. Serum IgA levels were measured in 2423 children at 4 years of age i
Autor:
Jenny Ödling, Mårtenn Sundberg, Joakim Lundeberg, Lennart Hammarström, Magdalena Janzi, Qiang Pan-Hammarström, Mathias Uhlén, Peter Nilsson
Publikováno v:
Molecularcellular proteomics : MCP. 4(12)
There is a great need for comprehensive proteomic analysis of large patient cohorts of plasma and serum samples to identify biomarkers of human diseases. Here we describe a new antibody-based proteomic approach involving a reverse array format where