V. Schuster

发表

Rotavirus Vaccination in Germany: Analysis of Nationwide Surveillance Data 2006 to 2010

H. Uhlig, K. Kostev, U. Uhlig, 2011, The Pediatric infectious disease journal.

Lasting immune memory against hepatitis B in children after primary immunization with 4 doses of DTPa-HBV-IPV/Hib in the first and 2nd year of life

V. Schuster, Gunasekaran Ramakrishnan, O. Van Der Meeren, 2010, BMC Infectious Diseases.

Host response to EBV infection in X-linked lymphoproliferative disease results from mutations in an SH2-domain encoding gene

Jack R. Davis, D. Bentley, M. Ross, 1998, Nature Genetics.

Epstein-Barr virus infection and associated diseases in children

V. Schuster, H. Kreth, Volker Schuster, 1992, European Journal of Pediatrics.

Epstein-Barr virus infection and associated diseases in children

V. Schuster, H. Kreth, 1992, European Journal of Pediatrics.

Addison's Disease and Severe Encephalopathy in an Infant with HIV Infection

J. Allmendinger, V. Schuster, R. Pfäffle, 2010, Journal of pediatric endocrinology & metabolism : JPEM.

Clinical and immunological overlap between autoimmune lymphoproliferative syndrome and common variable immunodeficiency.

K. Schwarz, S. Ehl, S. Fuchs, 2010, Clinical immunology.

Intracardiac calcifications in a case of pseudohypoparathyroidism type Ia (PHP-Ia)

V. Schuster, K. Sandhage, 1992, Pediatric Cardiology.

Serum concentrations of interferon gamma, interleukin-6 and neopterin in patients with infectious mononucleosis and other Epstein-Barr virus-related lymphoproliferative diseases

G. Reibnegger, M. Herold, V. Schuster, 1993, Infection.

Risk Factors for Complicated Lymphadenitis Caused by Nontuberculous Mycobacteria in Children

O. Sommerburg, R. Krüger, H. von Bernuth, 2020, Emerging infectious diseases.

Immunogenicity and Safety Assessments After One and Two Doses of a Refrigerator-Stable Tetravalent Measles-Mumps-Rubella-Varicella Vaccine in Healthy Children During the Second Year of Life

V. Schuster, M. Douha, P. Willems, 2008, The Pediatric infectious disease journal.

[Interdisciplinary AWMF guideline for the diagnostics of primary immunodeficiency].

S. Ehl, H. von Bernuth, K. Warnatz, 2011, Klinische Padiatrie.

Evolution of disease activity and biomarkers on and off rapamycin in 28 patients with autoimmune lymphoproliferative syndrome

K. Schwarz, F. Rieux-Laucat, A. Fischer, 2017, Haematologica.

Detection of a nuclear antigen 2 (EBNA2)‐variant Epstein‐Barr virus strain in two siblings with fatal lymphoproliferative disease

V. Schuster, S. Seidenspinner, H. Kreth, 1996, Journal of medical virology.

Common Epstein-Barr virus (EBV) type-1 variant strains in both malignant and benign EBV-associated disorders.

G. Ott, V. Schuster, S. Seidenspinner, 1996, Blood.

Bruton's tyrosine kinase is activated upon CD40 stimulation in human B lymphocytes.

E. Serfling, A. Avots, V. Schuster, 2002, Immunobiology.

Epstein-Barr virus infection rapidly progressing to monoclonal lymphoproliferative disease in a child with selective immunodeficiency

H. Müller-Hermelink, A. Feller, V. Schuster, 1990, European Journal of Pediatrics.

Crohn’s Disease in a Patient with Juvenile Idiopathic Arthritis after Starting Etanercept Therapy – Causal Link or Only Temporal Coincidence?

V. Schuster, G. Tóth, C. Gébauer, 2013, Klinische Pädiatrie.

An unusual case of refractory Campylobacter jejuni infection in a patient with X-linked agammaglobulinemia: successful combined therapy with maternal plasma and ciprofloxacin.

I. Autenrieth, V. Schuster, D. Harmsen, 1996, Clinical infectious diseases : an official publication of the Infectious Diseases Society of America.

Acquisition of Selective IgA Deficiency in Juvenile Idiopathic Arthritis after Immunosuppressive Treatment

K. Warnatz, V. Schuster, M. Schlesier, 2013 .

Unimpaired Activation of c-Jun NH2-Terminal Kinase (JNK) 1 upon CD40 Stimulation in B Cells of Patients with X-Linked Agammaglobulinemia

H. Ochs, V. Schuster, C. Brunner, 2002, Journal of Clinical Immunology.

Detection of human cytomegalovirus in urine by DNA-DNA and RNA-DNA hybridization.

V. Schuster, B. Matz, D. Neumann-Haefelin, 1986, The Journal of infectious diseases.

Detection of herpes simplex virus and adenovirus DNA by dot blot hybridization using in vitro synthesized RNA transcripts.

V. Schuster, B. Matz, D. Neumann-Haefelin, 1986, Journal of virological methods.

Nucleic acid hybridization for detection of herpes viruses in clinical specimens

A. Polack, V. Schuster, B. Matz, 1986, Journal of medical virology.

Detection of Human Cytomegalovirus in Urine by DNA-DNA and

V. Schuster, B. Matz, H. Wiegand, 1986 .

Regulary organized lymphoid tissue and CD40 ligand expression in a male fetus carrying the defective gene for X‐linked lymphoproliferative disease (XLP)

A. Greiner, H. Kreipe, V. Schuster, 1997, Histopathology.

Persistent Hypogammaglobulinemia Following Mononucleosis in Boys Is Highly Suggestive of X-Linked Lymphoproliferative Disease—Report of Three Cases

U. Sack, A. Meindl, H. Hellebrand, 2004, Journal of Clinical Immunology.

Hyperactive mTOR pathway promotes lymphoproliferation and abnormal differentiation in autoimmune lymphoproliferative syndrome.

K. Schwarz, S. Ehl, A. Mackensen, 2015, Blood.

Epstein-Barr-Virusinfektionen

V. Schuster, 1995 .

Limited Sequence Heterogeneity of Epstein-Barr Virus Nuclear Antigen 1 in Benign and Malignant EBV-Associated Disorders

G. Ott, V. Schuster, S. Seidenspinner, 2000, Infection.

Epstein-Barr virus and the B cell: a secret romance.

V. Schuster, M. Müschen, 2003, Trends in microbiology.

Activated T lymphocytes in the cerebrospinal fluid of a patient with Epstein-Barr virus-associated meningoencephalitis.

V. Schuster, R. Nanan, S. Seidenspinner, 1996, The Pediatric infectious disease journal.

Autoimmunes lymphoproliferatives Syndrom (ALPS)

V. Schuster, J. Haas, T. Böhler, 2004 .

Lethal influenza B myocarditis in a child and review of the literature for pediatric age groups

U. Liebert, W. Kiess, C. Wittekind, 2010, Infection.

Homozygous mutations in the plasminogen gene of two unrelated girls with ligneous conjunctivitis.

V. Schuster, S. Seidenspinner, H. Kreth, 1997, Blood.

X‐linked lymphoproliferative disease is caused by deficiency of a novel SH2 domain‐containing signal transduction adaptor protein

V. Schuster, H. Kreth, 2000, Immunological reviews.

Epstein-Barr Virus Associated Histio-Lymphoproliferative Syndromes in Two European Families

V. Schuster, H. Kreth, 1991 .

Epstein-Barr virus-negative boys with non-Hodgkin lymphoma are mutated in the SH2D1A gene, as are patients with X-linked lymphoproliferative disease (XLP).

W. Friedrich, A. Meindl, H. Hellebrand, 1999, Human molecular genetics.

A season of aseptic meningitis in Germany: epidemiologic, clinical and diagnostic aspects

U. Liebert, W. Kiess, W. Handrick, 2002, The Pediatric infectious disease journal.

Homozygous and Compound-heterozygous Type I Plasminogen Deficiency Is a Common Cause of Ligneous Conjunctivitis

U. Ozcelik, F. Meire, V. Schuster, 2001, Thrombosis and Haemostasis.

Efficacy of human rotavirus vaccine against rotavirus gastroenteritis during the first 2 years of life in European infants: randomised, double-blind controlled study

T. Vesikari, F. Meurice, V. Schuster, 2007, The Lancet.

S 6.7 – Herpes-simplex-Virus

V. Schuster, 2007 .

Fatal Lymphoproliferative Disease in Two Siblings Lacking Functional FAAP24

A. Borkhardt, B. Kempkes, B. Fleckenstein, 2016, Journal of Clinical Immunology.

Invasive pneumococcal diseases in children and adolescents– a single centre experience

W. Kiess, A. Rodloff, V. Schuster, 2014, BMC Research Notes.

The syndrome of hemophagocytic lymphohistiocytosis in primary immunodeficiencies: implications for differential diagnosis and pathogenesis

W. Al-Herz, A. Gennery, S. Pai, 2015, Haematologica.

Molecular genetic haplotype segregation studies in three families with X-linked lymphoproliferative disease

W. Kress, V. Schuster, T. Grimm, 1994, European Journal of Pediatrics.

Use of peroxidase labelled antibodies for detection of plum pox virus.

V. Schuster, I. Barna-Vetró, R. Varró, 1981 .

Sequential decisions on FAS sequencing guided by biomarkers in patients with lymphoproliferation and autoimmune cytopenia

K. Schwarz, W. Vach, E. Mejstrikova, 2013, Haematologica.

Hypersensitivity to Warfarin, Fix Can Be Adjusted to a Rather Stable Level with a Suggested Therapeutic Goal of 8% to 16%. Autoimmunity in Severe Combined Immunodeficiency (scid)

S. Kristensen, F. Horn, V. Schuster, 2002 .

Prenatal diagnosis of X linked lymphoproliferative disease using multiplex polymerase chain reaction.

V. Schuster, S. Seidenspinner, H. Kreth, 1995, Journal of medical genetics.

[Rare case of an epidemiologically important tuberculosis in childhood].

W. Kiess, V. Schuster, R. Schille, 2006, Klinische Padiatrie.

Alexander's disease: Cranial MRI and ultrasound findings

V. Schuster, H. Kreth, A. Horwitz, 1991, Pediatric Radiology.

Decreased Factor XIII Activity during Severe Henoch-Schoenlein Purpura - Does It Play a Role?

V. Schuster, R. Pfäffle, F. Prenzel, 2006, Klinische Padiatrie.

[Gianotti-Crosti syndrome in an infant following immunization].

V. Schuster, L. Vogler, N. Schwerk, 2005, Klinische Pädiatrie.

Immunogenicity and safety of the human rotavirus vaccine Rotarix co-administered with routine infant vaccines following the vaccination schedules in Europe.

T. Vesikari, V. Schuster, A. Bouckenooghe, 2010, Vaccine.

Efficacy and Immunogenicity of Live-attenuated Human Rotavirus Vaccine in Breast-fed and Formula-fed European Infants

T. Vesikari, V. Schuster, R. Cohen, 2012, The Pediatric infectious disease journal.

Report of the Third European Expert Meeting on Rotavirus Vaccination: Progress in rotavirus universal mass vaccination in Europe.

C. Giaquinto, T. Vesikari, V. Schuster, 2014, Vaccine.

Gastritis and colitis can be associated with XLP‐1 (SAP deficiency)

H. Kanegane, V. Schuster, Xi Yang, 2012, Pediatrics international : official journal of the Japan Pediatric Society.

Two new families with X-linked inhibitor of apoptosis deficiency and a review of all 26 published cases.

A. Meindl, V. Schuster, C. Urban, 2011, The Journal of allergy and clinical immunology.

Detection of a novel mutation in the SRC homology domain 2 (SH2) of Bruton's tyrosine kinase and direct female carrier evaluation in a family with X-linked agammaglobulinemia.

V. Schuster, S. Seidenspinner, H. Kreth, 1996, American journal of medical genetics.

[Evaluation and Utilization - Quality Management in a Paediatric University Outpatient Department].

W. Kiess, V. Schuster, T. Kapellen, 2016, Klinische Padiatrie.

Congenital varicella syndrome: studies of the virus‐specific humoral and cell‐mediated immune responses

V. Schuster, H. Kreth, J. Pannenbecker, 1994, Acta paediatrica.

Twenty Year Follow up of a Patient with a New De-Novo NLRP3 Mutation (S595G) and CINCA Syndrome

A. Rösen‐Wolff, V. Schuster, J. Roesler, 2009, Klinische Padiatrie.

Impact of Rotavirus Vaccination in Germany: Rotavirus Surveillance, Hospitalization, Side Effects and Comparison of Vaccines

H. Uhlig, K. Kostev, S. Koletzko, 2014, The Pediatric infectious disease journal.

A hospital based study on inter- and intragenotypic diversity of human rotavirus A VP4 and VP7 gene segments, Germany.

U. Liebert, V. Schuster, C. Pietsch, 2011, Journal of clinical virology : the official publication of the Pan American Society for Clinical Virology.

Konnatale Epstein-Barr-Virus-Infektion

V. Schuster, S. Seidenspinner, H. Kreth, 1993 .

Dexamethasone in childhood meningitis [2]

G. Mccracken, V. Schuster, T. Newman, 1991 .

Clinical Course and Laboratory Findings in a Patient with a New Mutation Causing Wiskott-Aldrich Syndrome

U. Sack, A. Meindl, V. Schuster, 2002 .

Antinuclear Antibody-Positive Juvenile Idiopathic Arthritis Despite IRAK-4 Deficiency

K. Schwarz, V. Schuster, M. Borte, 2018, Journal of Clinical Immunology.

Endocrine and molecular biological studies in a German family with Albright hereditary osteodystrophy

P. Gierschik, V. Schuster, V. Schuster, 1993, European Journal of Pediatrics.

X-linked lymphoproliferative disease. Detection of a paternally inherited mutation in a German family using haplotype analysis.

W. Friedrich, W. Kress, V. Schuster, 1993, American journal of diseases of children.

Hoffman syndrome: New patients, new insights

U. Sack, L. Bird, V. Schuster, 2011, American Journal of Medical Genetics. Part A.