Search Results - "Litzman, J"

When to initiate immunoglobulin replacement therapy (IGRT) in antibody deficiency: a practical approach by Jolles, S., Chapel, H., Litzman, J.

“…Summary Primary antibody deficiencies (PAD) constitute the majority of all primary immunodeficiency diseases (PID) and immunoglobulin replacement forms the…”
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Influence of FCRN expression on lung decline and intravenous immunoglobulin catabolism in common variable immunodeficiency patients by Litzman, J.

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Common variants at PVT1, ATG13–AMBRA1, AHI1 and CLEC16A are associated with selective IgA deficiency by Bronson, Paola G, Chang, Diana, Bhangale, Tushar, Seldin, Michael F, Ortmann, Ward, Ferreira, Ricardo C, Urcelay, Elena, Pereira, Luis Fernández, Martin, Javier, Plebani, Alessandro, Lougaris, Vassilios, Friman, Vanda, Freiberger, Tomáš, Litzman, Jiri, Thon, Vojtech, Pan-Hammarström, Qiang, Hammarström, Lennart, Graham, Robert R, Behrens, Timothy W

“…Paola Bronson, Lennart Hammarström and colleagues report a genome-wide association study meta-analysis of selective IgA immunodeficiency in Europeans. They…”
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Possibilities for the analysis of peripheral blood B cell subpopulations in a routine immunological laboratory by Štíchová, J, Nechvátalová, J, Litzman, J, Vlková, M

“…B cells play a vital role in the defence of the body against infectious agents. Apart from their ability to present antigen to T cells, B cells are mainly…”
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Chronic immune activation in common variable immunodeficiency (CVID) is associated with elevated serum levels of soluble CD14 and CD25 but not endotoxaemia by Litzman, J., Nechvatalova, J., Xu, J., Ticha, O., Vlkova, M., Hel, Z.

“…Summary Common variable immunodeficiency (CVID), the most frequent symptomatic immunoglobulin primary immunodeficiency, is associated with chronic T cell…”
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Low ficolin‐2 levels in common variable immunodeficiency patients with bronchiectasis by Metzger, M.‐L., Michelfelder, I., Goldacker, S., Melkaoui, K., Litzman, J., Guzman, D., Grimbacher, B., Salzer, U.

“…Summary Common variable immunodeficiency (CVID) encompasses a heterogeneous group of antibody deficiencies characterized by susceptibility to recurrent…”
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Outcomes of splenectomy in patients with common variable immunodeficiency (CVID): a survey of 45 patients by Wong, G. K., Goldacker, S., Winterhalter, C., Grimbacher, B., Chapel, H., Lucas, M., Alecsandru, D., McEwen, D., Quinti, I., Martini, H., Schmidt, R. E., Ernst, D., Espanol, T., Vidaller, A., Carbone, J., Fernandez‐Cruz, E., Lougaris, V., Plebani, A., Kutukculer, N., Gonzalez‐Granado, L. I., Contreras, R., Kiani‐Alikhan, S., Ibrahim, M. A. A., Litzman, J., Jones, A., Gaspar, H. B., Hammarstrom, L., Baumann, U., Warnatz, K., Huissoon, A. P.

“…Summary Splenectomy has been used in patients with common variable immunodeficiency disorders (CVID), mainly in the context of refractory autoimmune cytopenia…”
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Spectrum and Management of Complement Immunodeficiencies (Excluding Hereditary Angioedema) Across Europe by Turley, A. J., Gathmann, B., Bangs, C., Bradbury, M., Seneviratne, S., Gonzalez-Granado, L. I., Hackett, S., Kutukculer, N., Alachkar, H., Hambleton, S., Ritterbusch, H., Kralickova, P., Marodi, L., Seidel, M. G., Dueckers, G., Roesler, J., Huissoon, A., Baxendale, H., Litzman, J., Arkwright, P. D.

“…Introduction Complement immunodeficiencies (excluding hereditary angioedema and mannose binding lectin deficiency) are rare. Published literature consists…”
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Sequence variants of the TNFRSF13B gene in Czech CVID and IgAD patients in the context of other populations by Freiberger, T, Ravčuková, B, Grodecká, L, Pikulová, Z, Štikarovská, D, Pešák, S, Kuklínek, P, Jarkovský, J, Salzer, U, Litzman, J

“…Abstract Mutations in the TNFRSF13B gene, encoding TACI, have been found in common variable immunodeficiency (CVID) and selective IgA deficient (IgAD)…”
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Matrix metalloproteinase-9 and matrix metalloproteinase-2 as biomarkers of various courses in multiple sclerosis by Benešová, Y, Vašků, A, Novotná, H, Litzman, J, Štourač, P, Beránek, M, Kadaňka, Z, Bednařík, J

“…Background Matrix metalloproteinases are notable contributors to neuroinflammation and blood-brain barrier disruption in multiple sclerosis (MS). Objective The…”
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Hereditary angio-oedema with C1 inhibitor deficiency: Characteristics and diagnostic delay of Czech patients from one centre by Hakl, R, Kuklínek, P, Kadlecová, P, Litzman, J

“…Hereditary angio-oedema (HAE) is manifested by repeated episodes of localised subcutaneous or sub-mucosal oedema. Symptoms are extremely variable in frequency,…”
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Reduced memory B cells in patients with hyper IgE syndrome by Speckmann, C, Enders, A, Woellner, C, Thiel, D, Rensing-Ehl, A, Schlesier, M, Rohr, J, Jakob, T, Oswald, E, Kopp, M.V, Sanal, O, Litzman, J, Plebani, A, Pietrogrande, M.C, Franco, J.L, Espanol, T, Grimbacher, B, Ehl, S

“…Abstract Dominant-negative mutations in STAT-3 have recently been found in the majority of patients with sporadic or autosomal-dominant hyper IgE syndrome…”
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Association of FcRn expression with lung abnormalities and IVIG catabolism in patients with common variable immunodeficiency by Freiberger, T, Grodecká, L, Ravčuková, B, Kuřecová, B, Postránecká, V, Vlček, J, Jarkovský, J, Thon, V, Litzman, J

“…Abstract The neonatal Fc receptor (FcRn) acts as a key regulator of IgG homeostasis and is an important sensor of luminal infection. We analyzed the influence…”
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Mannose-binding lectin gene polymorphic variants predispose to the development of bronchopulmonary complications but have no influence on other clinical and laboratory symptoms or signs of common variable immunodeficiency by Litzman, J, Freiberger, T, Grimbacher, B, Gathmann, B, Salzer, U, Pavlík, T, Vlček, J, Postránecká, V, Trávníčková, Z, Thon, V

“…Mannose-binding lectin (MBL), activating protein of the lectin pathway of the complement system, is an important component of the non-specific immune response…”
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Age dependency and mutual relations in T and B lymphocyte abnormalities in common variable immunodeficiency patients by Vlková, M., Thon, V., Šárfyová, M., Bláha, L., Svobodník, A., Lokaj, J., Litzman, J.

“…Summary Common variable immunodeficiency (CVID) is primary hypogammaglobulinaemia with an unknown aetiopathogenesis. Although various abnormalities of T and B…”
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Recurrent meningitis and inherited complement deficiency by Šrotová, A, Litzman, J, Rumlarová, Š, Drahošová, M, Bartoňková, D, Krčmová, I, Roberts, A, Jolles, S, Králíčková, P

“…Complement deficiency represents 5% of primary immunodeficiencies worldwide. A total of seven patients with deficiencies of the classical complement pathway…”
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NOD2 polymorphisms in clinical phenotypes of common variable immunodeficiency disorders by Packwood, K, Drewe, E, Staples, E, Webster, D, Witte, T, Litzman, J, Egner, W, Sargur, R, Sewell, W, Lopez-Granados, E, Seneviratne, S.L, Powell, R.J, Ferry, B.L, Chapel, H.M

“…Common variable immunodeficiency disorders (CVIDs) are a heterogeneous group of diseases characterized by hypogammaglobulinaemia and consequent susceptibility…”
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T and B lymphocyte subpopulations and activation/differentiation markers in patients with selective IgA deficiency by Litzman, J., Vlková, M., Pikulová, Z., Štikarovská, D., Lokaj, J.

“…Summary Selective deficiency of immunoglobulin A (IgAD) and common variable immunodeficiency (CVID) are genetically closely related diseases, both of unknown…”
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No Evidence for Linkage between the Hereditary Angiooedema Clinical Phenotype and the BDKR1, BDKR2, ACE or MBL2 gene by Freiberger, T., Grombiříková, H., Ravčuková, B., Jarkovský, J., Kuklínek, P., Kryštůfková, O., Hanzlíková, J., Daňková, E., Kopecký, O., Zachová, R., Lahodná, M., Vašáková, M., Grodecká, L., Litzman, J.

“…Hereditary angiooedema (HAE) is a life‐threatening disease with poor clinical phenotype correlation with its causal mutation in the C1 inhibitor (SERPING1)…”
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Spectrum and Management of Complement Immunodeficiencies (Excluding Hereditary Angioedema) Across Europe by Turley, A. J., Gathmann, B., Bangs, C., Bradbury, M., Seneviratne, S., Gonzalez-Granado, L. I., Hackett, S., Kutukculer, N., Alachkar, H., Hambleton, S., Ritterbusch, H., Kralickova, P., Marodi, L., Seidel, M. G., Dueckers, G., Roesler, J., Huissoon, A., Baxendale, H., Litzman, J., Arkwright, P. D.

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