Search Results - "Skattum, L"

Molecular basis of hereditary C1q deficiency-revisited: identification of several novel disease-causing mutations by Schejbel, L, Skattum, L, Hagelberg, S, Åhlin, A, Schiller, B, Berg, S, Genel, F, Truedsson, L, Garred, P

“…C1q is the central pattern-recognition molecule in the classical pathway of the complement system and is known to have a key role in the crossroads between…”
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Treatment with belimumab in systemic lupus erythematosus does not impair antibody response to 13-valent pneumococcal conjugate vaccine by Nagel, J, Saxne, T, Geborek, P, Bengtsson, A A, Jacobsen, S, Svaerke Joergensen, C, Nilsson, J-Å, Skattum, L, Jönsen, A, Kapetanovic, M C

“…Background/purpose The objective of this study was to explore the impact of systemic lupus erythematosus and belimumab given in addition to standard of care…”
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Eculizumab treatment in pregnancy complicated with APS – Effects on mother and infant by Gustavsen, A, Bergseth, G, Volokhina, E, van den Heuvel, L.P, Skattum, L, Mollnes, T.E, Barratt-Due, A

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Heat differentiated complement factor profiling by Hamsten, Carl, Skattum, Lillemor, Truedsson, Lennart, von Döbeln, Ulrika, Uhlén, Mathias, Schwenk, Jochen M., Hammarström, Lennart, Nilsson, Peter, Neiman, Maja

“…Complement components and their cascade of reactions are important defense mechanisms within both innate and adaptive immunity. Many complement deficient…”
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Molecular basis of hereditary C1q deficiency-revisited: Identification of several novel disease causing mutations by Schejbel, L., Skattum, L., Hagelberg, S., Åhlin, A., Berg, S., Genel, F., Truedsson, L., Garred, P.

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Acute renal failure in dense deposit disease: complete recovery after combination therapy with immunosuppressant and plasma exchange by Krmar, R T, Holtbäck, U, Linné, T, Berg, U B, Celsi, G, Söderberg, M P, Wernerson, A, Szakos, A, Larsson, S, Skattum, L, Bárány, P

“…We describe the clinical course of a female adolescent who was followed because of isolated microhematuria and hypocomplementemia before admission to hospital…”
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Influence of IgG allotypes on defense against Haemophilus influenzae type b in children—A complement-dependent mechanism? by Skattum, L., Gullstrand, B., Jönsson, G., Truedsson, L.

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Homozygosity for a novel mutation in the C1q C chain gene in a Turkish family with hereditary C1q deficiency by Gulez, N, Genel, F, Atlihan, F, Gullstrand, B, Skattum, L, Schejbel, L, Garred, P, Truedsson, L

“…Hereditary complete deficiency of complement component C1q is associated with a high prevalence of systemic lupus erythematosus and increased susceptibility to…”
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Serum bactericidal activity against Neisseria meningitidis in patients with C3 nephritic factors is dependent on IgG allotypes by Skattum, L, Gullstrand, B, Holmström, E, Oxelius, V.-A, Truedsson, L

“…Abstract The main mechanisms of immune defense against Neisseria meningitidis are serum bactericidal activity (SBA) and opsonophagocytosis. Many complement…”
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Antibodies against four proteins from a Streptococcus pyogenes serotype M1 strain and levels of circulating mannan-binding lectin in acute poststreptococcal glomerulonephritis by Skattum, L, Akesson, P, Truedsson, L, Sjöholm, A G

“…Responses against antigens from the potentially nephritogenic Streptococcus pyogenes serotype M1 in patients with acute poststreptococcal glomerulonephritis…”
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Hypocomplementaemia caused by C3 nephritic factors (C3 NeF): clinical findings and the coincidence of C3 NeF type II with anti‐C1q autoantibodies by SKATTUM, L., MARTENSSON, U., SJÖHOLM, A. G.

“… Skattum L, MBrtensson U, Sjoholm AG (Lund University, Lund, Sweden). Hypocomple‐mentaemia caused by C3 nephritic factors (C3 NeF): clinical findings and the…”
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Evaluation of a Novel Immunoassay for Quantification of C1q for Clinical Diagnostic Use by Sandholm, Kerstin, Persson, Barbro, Skattum, Lillemor, Eggertsen, Gösta, Nyman, Dag, Gunnarsson, Iva, Svenungson, Elisabet, Nilsson, Bo, Ekdahl, Kristina N

“…C1q is a valuable biomarker of disease activity in systemic lupus erythematosus (SLE). The "gold standard" assay, rocket immunoelectrophoresis (RIE), is…”
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Newborn Screening for Presymptomatic Diagnosis of Complement and Phagocyte Deficiencies by Dezfouli, Mahya, Bergström, Sofia, Skattum, Lillemor, Abolhassani, Hassan, Neiman, Maja, Torabi-Rahvar, Monireh, Franco Jarava, Clara, Martin-Nalda, Andrea, Ferrer Balaguer, Juana M, Slade, Charlotte A, Roos, Anja, Fernandez Pereira, Luis M, López-Trascasa, Margarita, Gonzalez-Granado, Luis I, Allende-Martinez, Luis M, Mizuno, Yumi, Yoshida, Yusuke, Friman, Vanda, Lundgren, Åsa, Aghamohammadi, Asghar, Rezaei, Nima, Hernández-Gonzalez, Manuel, von Döbeln, Ulrika, Truedsson, Lennart, Hara, Toshiro, Nonoyama, Shigeaki, Schwenk, Jochen M, Nilsson, Peter, Hammarström, Lennart

“…The clinical outcomes of primary immunodeficiencies (PIDs) are greatly improved by accurate diagnosis early in life. However, it is not common to consider PIDs…”
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Heat differentiated multiplex complement factor profiling by Neiman, M, Hamsten, C, Skattum, L, Truedsson, L, Uhlen, M, Schwenk, J, Hammarstrom, L, Nilsson, P

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Anti-C1q antibodies and C1q in SLE: Comparison between methods and relation to nephritis and disease activity by Skattum, L.S., Tydén, H., Orsander, K., Sturfelt, G., Bengtsson, A.A., Jönsen, A.

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Screening for anti-factor B autoantibody in a patient with acute renal injury due to dense deposit disease by Krmar, Rafael T, Skattum, Lillemor, Bárány, Peter, Józsi, Mihály

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Complement factor I deficiency associated with recurrent infections, vasculitis and immune complex glomerulonephritis by Genel, Ferah, Sjöholm, Anders G., Skattum, Lillemor, Truedsson, Lennart

“…Here we report complement factor I deficiency in an 11-y-old girl from a consanguineous Turkish family, who presented with recurrent pyogenic infections,…”
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