X-linked lymphoproliferative disease is caused by deficiency of a novel SH2 domain-containing signal transduction adaptor proteinSCHUSTER, Volker; KRETH, Hans Wolfgang.Immunological reviews. 2000, Vol 178, pp 21-28, issn 0105-2896Article

Efficacy and Immunogenicity of Live-attenuated Human Rotavirus Vaccine in Breast-fed and Formula-fed European InfantsVESIKARI, Timo; PRYMULA, Roman; SCHUSTER, Volker et al.The Pediatric infectious disease journal. 2012, Vol 31, Num 5, pp 509-513, issn 0891-3668, 5 p.Article

Hypoplasminogenemia with ligneous periodontitis : A failed local therapeutic approachKURTULUS, Idil; GOKBUGET, Asian; EFEOGLU, Ahmet et al.Journal of periodontology. 2007, Vol 78, Num 6, pp 1164-1175, issn 0022-3492, 12 p.Article

Inherited plasminogen deficiency presenting as ligneous vaginitis : a case report with molecular correlation and review of the literatureLOTAN, Tamara L; TEFS, Katrin; SCHUSTER, Volker et al.Human pathology. 2007, Vol 38, Num 10, pp 1569-1575, issn 0046-8177, 7 p.Article

Immunogenicity and reactogenicity of a trivalent influenza split vaccine in previously unvaccinated children aged 6-9 and 10-13 yearsSCHMIDT-OTT, Ruprecht; SCHWARZ, Tino; HAASE, Rainer et al.Vaccine. 2007, Vol 26, Num 1, pp 32-40, issn 0264-410X, 9 p.Article

Ligneous (pseudomembranous) inflammation involving the female genital tract associated with type-1 plasminogen deficiencyPANTANOWITZ, Liron; BAUER, Kenneth; TEFS, Katrin et al.International journal of gynecological pathology. 2004, Vol 23, Num 3, pp 292-295, issn 0277-1691, 4 p.Article

Hoffman Syndrome: New Patients, New InsightsHUGLE, Boris; HOFFMAN, Hal; BIRD, Lynne M et al.American journal of medical genetics. Part A. 2011, Vol 155, Num 1, pp 149-153, issn 1552-4825, 5 p.Article

Identification of three novel plasminogen (PLG) gene mutations in a series of 23 patients with low PLG activityKLAMMT, Jürgen; KOBELT, Louise; MENDOZA-LONDONO, Roberto et al.Thrombosis and haemostasis. 2011, Vol 105, Num 3, pp 454-460, issn 0340-6245, 7 p.Article

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Characterization of plasminogen variants in healthy subjects and plasminogen mutants in patients with inherited plasminogen deficiency by isoelectric focusing gel electrophoresisTEFS, Katrin; GEORGIEVA, Maria; SEREGARD, Stefan et al.Thrombosis and haemostasis. 2004, Vol 92, Num 2, pp 352-357, issn 0340-6245, 6 p.Article

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Isoelectric focusing pattern of plasminogen mutants of patients with hypoplasminogenemia: correlation of in-vitro data with computer-predicted isoelectric points (pI)TEFS, Katrin; OTT-GUEORGUIEVA, Maria; KOBELT, Louise et al.Blood coagulation & fibrinolysis. 2011, Vol 22, Num 6, pp 499-505, issn 0957-5235, 7 p.Article

Two new families with X-linked inhibitor of apoptosis deficiency and a review of all 26 published casesHORN, Peter C; BELOHRADSKY, Bernd H; URBAN, Christian et al.Journal of allergy and clinical immunology. 2011, Vol 127, Num 2, pp 544-546, issn 0091-6749, 3 p.Article

A missense mutation in the ZFHX1B gene associated with an atypical Mowat-Wilson syndrome phenotypeHEINRITZ, Wolfram; ZWEIER, Christiane; FROSTER, Ursula G et al.American journal of medical genetics. Part A. 2006, Vol 140, Num 11, pp 1223-1227, issn 1552-4825, 5 p.Article

Ligneous conjunctivitis, hydrocephalus, hydrocele, and pulmonary involvement in a child with homozygous type I plasminogen deficiencyCIFTCI, Ergin; INCE, Erdal; AKAR, Nejat et al.European journal of pediatrics. 2003, Vol 162, Num 7-8, pp 462-465, issn 0340-6199, 4 p.Article

Pulmonary involvement in a child with ligneous conjunctivitis and homozygous type I plasminogen deficiencyÖZCELIK, Ugur; AKCÖREN, Zuhal; ANADOL, Deniz et al.Pediatric pulmonology. 2001, Vol 32, Num 2, pp 179-183, issn 8755-6863Article

Monitoring of 4-hydroxybutyric acid levels in body fluids during vigabatrin treatment in succinic semialdehyde dehydrogenase deficiencyERGEZINGER, Katrin; JESCHKE, Reinhard; FRAUENDIENST-EGGER, Georg et al.Annals of neurology. 2003, Vol 54, Num 5, pp 686-689, issn 0364-5134, 4 p.Article