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Compound-Heterozygous Mutations in the Plasminogen Gene Predispose to the Development of Ligneous Conjunctivitis

Blood, 1999-05, Vol.93 (10), p.3457-3466

1999

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Homozygous and compound-heterozygous type I plasminogen deficiency is a common cause of ligneous conjunctivitis

Thrombosis and haemostasis, 2001-06, Vol.85 (6), p.1004

2001

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Estimation of the time-dependent vaccine efficacy from a measles epidemic

Statistics in medicine, 2002-08, Vol.21 (16), p.2355-2368

2002

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Demonstration of virus‐specific CD8+ memory T cells in measles‐seropositive individuals by in vitro peptide stimulation

Clinical and experimental immunology, 1995-10, Vol.102 (1), p.40-45

1995

Volltextzugriff (PDF)

Lethal pneumococcal infection in an 18-month-old girl with splenic hypoplasia and dysgammaglobulinemia

Annals of hematology, 2001-11, Vol.80 (11), p.674-676

2001

Volltextzugriff (PDF)

Autoimmune lymphoproliferative syndrome associated with severe humoral immunodeficiency and monoclonal gammopathy

Annals of hematology, 2002-06, Vol.81 (6), p.332-335

2002

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Acute and long-term effects of booster immunisation on frequencies of antigen-specific memory B-lymphocytes

Vaccine, 2001-11, Vol.20 (3), p.498-504

2001

Volltextzugriff (PDF)

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

Blood, 1997-08, Vol.90 (3), p.958-966

1997

Volltextzugriff (PDF)

Measles virus infection causes transient depletion of activated T cells from peripheral circulation

Journal of clinical virology, 1999-05, Vol.12 (3), p.201-210

1999

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Common Epstein-Barr Virus (EBV) Type-1 Variant Strains in Both Malignant and Benign EBV-Associated Disorders

Blood, 1996-02, Vol.87 (4), p.1579-1585

1996

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Reversible monoclonal lymphadenopathy in autoimmune lymphoproliferative syndrome with functional FAS (CD95/APO-1) deficiency

The American journal of surgical pathology, 1999-07, Vol.23 (7), p.829-837

1999

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Combination of von Willebrand disease type 1 and partial factor XII deficiency in children: clinical evidence for a diminished bleeding tendency

Acta Paediatrica, 1999-11, Vol.88 (11), p.1233-1237

1999

Volltextzugriff (PDF)

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

Immunological reviews, 2000-12, Vol.178 (1), p.21-28

2000

Volltextzugriff (PDF)

An Unusual Case of Refractory Campylobacter jejuni Infection in a Patient with X-Linked Agammaglobulinemia: Successful Combined Therapy with Maternal Plasma and Ciprofloxacin

Clinical infectious diseases, 1996-09, Vol.23 (3), p.526-531

1996

Volltextzugriff (PDF)

Expression of measles virus RNA in peripheral blood mononuclear cells of patients with measles, SSPE, and autoimmune diseases

Virology (New York, N.Y.), 1991-06, Vol.182 (2), p.703-711

1991

Volltextzugriff (PDF)

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

European journal of pediatrics, 1993-03, Vol.152 (3), p.185-189

1993

Volltextzugriff (PDF)

Human immunodeficiency virus infection in microglia: Correlation between cells infected in the brain and cells cultured from infectious brain tissue

Annals of neurology, 1992-04, Vol.31 (4), p.361-365

1992

Volltextzugriff (PDF)

A novel sensitive approach for frequency analysis of measles virus-specific memory T-lymphocytes in healthy adults with a childhood history of natural measles

Journal of general virology, 2000-05, Vol.81 (5), p.1313-1319

2000

Volltextzugriff (PDF)

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

Histopathology, 1997-05, Vol.30 (5), p.481-482

1997

Volltextzugriff (PDF)

Epstein-Barr virus infection and associated diseases in children. II: Diagnostic and therapeutic strategies

European journal of pediatrics, 1992-11, Vol.151 (11), p.794-798

1992

Volltextzugriff (PDF)

ACTIVATED T LYMPHOCYTES IN THE CEREBROSPINAL FLUID OF A PATIENT WITH EPSTEIN-BARR VIRUS-ASSOCIATED MENINGOENCEPHALITIS

The Pediatric infectious disease journal, 1996-07, Vol.15 (7), p.631-633

1996

Volltextzugriff (PDF)

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

Journal of medical virology, 1996-01, Vol.48 (1), p.114-120

1996

Volltextzugriff (PDF)

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

Acta Paediatrica, 1994-07, Vol.83 (7), p.783-785

1994

Volltextzugriff (PDF)

Homozygous Type I Plasminogen Deficiency

Seminars in thrombosis and hemostasis, 1997-01, Vol.23 (3), p.259-269

1997

Volltextzugriff (PDF)

Bruton's Tyrosine Kinase is Activated upon CD40 Stimulation in Human B Lymphocytes

Immunobiology (1979), 2002-10, Vol.206 (4), p.432-440

2002

Volltextzugriff (PDF)

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Compound-Heterozygous Mutations in the Plasminogen Gene Predispose to the Development of Ligneous Conjunctivitis

Homozygous and compound-heterozygous type I plasminogen deficiency is a common cause of ligneous conjunctivitis

Estimation of the time-dependent vaccine efficacy from a measles epidemic

Demonstration of virus‐specific CD8+ memory T cells in measles‐seropositive individuals by in vitro peptide stimulation

Lethal pneumococcal infection in an 18-month-old girl with splenic hypoplasia and dysgammaglobulinemia

Autoimmune lymphoproliferative syndrome associated with severe humoral immunodeficiency and monoclonal gammopathy

Acute and long-term effects of booster immunisation on frequencies of antigen-specific memory B-lymphocytes

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

Measles virus infection causes transient depletion of activated T cells from peripheral circulation

Common Epstein-Barr Virus (EBV) Type-1 Variant Strains in Both Malignant and Benign EBV-Associated Disorders

Reversible monoclonal lymphadenopathy in autoimmune lymphoproliferative syndrome with functional FAS (CD95/APO-1) deficiency

Combination of von Willebrand disease type 1 and partial factor XII deficiency in children: clinical evidence for a diminished bleeding tendency

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

An Unusual Case of Refractory Campylobacter jejuni Infection in a Patient with X-Linked Agammaglobulinemia: Successful Combined Therapy with Maternal Plasma and Ciprofloxacin

Expression of measles virus RNA in peripheral blood mononuclear cells of patients with measles, SSPE, and autoimmune diseases

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

Human immunodeficiency virus infection in microglia: Correlation between cells infected in the brain and cells cultured from infectious brain tissue

A novel sensitive approach for frequency analysis of measles virus-specific memory T-lymphocytes in healthy adults with a childhood history of natural measles

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

Epstein-Barr virus infection and associated diseases in children. II: Diagnostic and therapeutic strategies

ACTIVATED T LYMPHOCYTES IN THE CEREBROSPINAL FLUID OF A PATIENT WITH EPSTEIN-BARR VIRUS-ASSOCIATED MENINGOENCEPHALITIS

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

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

Homozygous Type I Plasminogen Deficiency

Bruton's Tyrosine Kinase is Activated upon CD40 Stimulation in Human B Lymphocytes

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