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Primary immunodeficiencies in Switzerland: first report of the national registry in adults and children

Journal of clinical immunology, 1988-11, Vol.8 (6), p.479-485

1988

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Wiskott-Aldrich syndrome : a truly interdisciplinary problem

Nephrology, dialysis, transplantation, 1996-10, Vol.11 (10), p.2093-2095

1996

Volltextzugriff (PDF)

History of primary immunodeficiency diseases

Current opinion in allergy and clinical immunology, 2012-12, Vol.12 (6), p.577-587

2012

Volltextzugriff (PDF)

Immunoblot analysis of antibody binding to polypeptides of Borrelia burgdorferi in children with different clinical manifestations of Lyme disease

Pediatric research, 1989-10, Vol.26 (4), p.377-382

1989

Volltextzugriff (PDF)

Uptake, intracellular activity, and influence of rifampin on normal function of polymorphonuclear leukocytes

Antimicrobial Agents and Chemotherapy, 1985-11, Vol.28 (5), p.667-674

1985

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Infants born to mothers with antibodies against Borrelia burgdorferi at delivery

European journal of pediatrics, 1989-02, Vol.148 (5), p.426-427

1989

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Craniosynostosis in hyper-IgE-syndrome

European journal of pediatrics, 1985-11, Vol.144 (4), p.414-417

1985

Volltextzugriff (PDF)

Antibody deficiency syndrome: new facts

Schweizerische medizinische Wochenschrift, 1991-02, Vol.121 (5), p.131

Hitzig, W H

1991

Volltextzugriff (PDF)

Chronic granulomatous disease, a heterogeneous syndrome

Human genetics, 1983-01, Vol.64 (3), p.207-215

1983

Volltextzugriff (PDF)

IgG2/IgG4 subclass deficiency in a patient with chronic mucocutaneous candidiasis and bronchiectases

European journal of pediatrics, 1989-12, Vol.149 (3), p.168-169

1989

Volltextzugriff (PDF)

Clinical biochemistry: Principles and methods

Curtius, H. C

2018

Volltextzugriff (PDF)

Infection with Staphylococcus aureus producing toxic shock syndrome (TSS) toxin-1 without TSS

European journal of pediatrics, 1989, Vol.148 (4), p.318-319

1989

Volltextzugriff (PDF)

Congenital acatalasemia: a study of neutrophil functions after provocation with hydrogen peroxide

Pediatric research, 1985-11, Vol.19 (11), p.1187-1190

1985

Volltextzugriff (PDF)

Chronic granulomatous disease: uptake and intracellular activity of fosfomycin in granulocytes

Pediatric research, 1985, Vol.19 (1), p.38-44

1985

Volltextzugriff (PDF)

Clinical biochemistry: Principles and methods

2018

Volltextzugriff (PDF)

Absence of complement receptor type 3 and lymphocyte function antigen 1 causing deficient phagocyte and lymphocyte functions

European journal of pediatrics, 1988-10, Vol.148 (1), p.58-61

1988

Volltextzugriff (PDF)

Bone marrow transplantation for severe combined immunodeficiency disease. Reported from 1968 to 1977

European journal of pediatrics, 1979-09, Vol.131 (3), p.155-177

1979

Volltextzugriff (PDF)

Hereditary transcobalamin II deficiency: Clinical findings in a new family

The Journal of pediatrics, 1974-11, Vol.85 (5), p.622-628

1974

Volltextzugriff (PDF)

Nitroblue-Tetrazolium Test for the Detection of Chronic Granulomatous Disease-Technical Modification

European journal of clinical investigation, 1971-12, Vol.1 (6), p.409-412

1971

Volltextzugriff (PDF)

Chronic granulomatous disease: fatal septicemia caused by an unnamed gram-negative bacterium

Journal of Clinical Microbiology, 1982-11, Vol.16 (5), p.821-825

1982

Volltextzugriff (PDF)

IgG subclasses: Development of the serum concentrations in “normal” infants and children

The Journal of pediatrics, 1972-06, Vol.80 (6), p.960-964

1972

Volltextzugriff (PDF)

Oral chloramphenicol therapy for multiple liver abscesses in hyperimmunoglobulinemia E syndrome

European journal of pediatrics, 1984-09, Vol.142 (4), p.292-295

1984

Volltextzugriff (PDF)

Human IgG antibodies to carbohydrate and protein antigens in mouse protection tests with group B streptococci

Pediatric research, 1984-05, Vol.18 (5), p.478-482

1984

Volltextzugriff (PDF)

Hereditary Severe Combined Immunodeficiency and Adenosine Deaminase Deficiency

Pediatric research, 1976-01, Vol.10 (1), p.67-70

1976

Volltextzugriff (PDF)

The Wiskott-Aldrich syndrome. Results of transfer factor therapy

The Journal of clinical investigation, 1972-12, Vol.51 (12), p.3216-3224

1972

Volltextzugriff (PDF)

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Primary immunodeficiencies in Switzerland: first report of the national registry in adults and children

Wiskott-Aldrich syndrome : a truly interdisciplinary problem

History of primary immunodeficiency diseases

Immunoblot analysis of antibody binding to polypeptides of Borrelia burgdorferi in children with different clinical manifestations of Lyme disease

Uptake, intracellular activity, and influence of rifampin on normal function of polymorphonuclear leukocytes

Infants born to mothers with antibodies against Borrelia burgdorferi at delivery

Craniosynostosis in hyper-IgE-syndrome

Antibody deficiency syndrome: new facts

Chronic granulomatous disease, a heterogeneous syndrome

IgG2/IgG4 subclass deficiency in a patient with chronic mucocutaneous candidiasis and bronchiectases

Clinical biochemistry: Principles and methods

Infection with Staphylococcus aureus producing toxic shock syndrome (TSS) toxin-1 without TSS

Congenital acatalasemia: a study of neutrophil functions after provocation with hydrogen peroxide

Chronic granulomatous disease: uptake and intracellular activity of fosfomycin in granulocytes

Clinical biochemistry: Principles and methods

Absence of complement receptor type 3 and lymphocyte function antigen 1 causing deficient phagocyte and lymphocyte functions

Bone marrow transplantation for severe combined immunodeficiency disease. Reported from 1968 to 1977

Hereditary transcobalamin II deficiency: Clinical findings in a new family

Nitroblue-Tetrazolium Test for the Detection of Chronic Granulomatous Disease-Technical Modification

Chronic granulomatous disease: fatal septicemia caused by an unnamed gram-negative bacterium

IgG subclasses: Development of the serum concentrations in “normal” infants and children

Oral chloramphenicol therapy for multiple liver abscesses in hyperimmunoglobulinemia E syndrome

Human IgG antibodies to carbohydrate and protein antigens in mouse protection tests with group B streptococci

Hereditary Severe Combined Immunodeficiency and Adenosine Deaminase Deficiency

The Wiskott-Aldrich syndrome. Results of transfer factor therapy

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