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Complement activation in thrombotic thrombocytopenic purpura

Journal of thrombosis and haemostasis, 2012-05, Vol.10 (5), p.791-798

2012

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Short-term prophylaxis in hereditary angioedema due to deficiency of the C1-inhibitor - a long-term survey

Allergy (Copenhagen), 2012-12, Vol.67 (12), p.1586-1593

2012

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F12‐46C/T polymorphism as modifier of the clinical phenotype of hereditary angioedema

Allergy (Copenhagen), 2015-12, Vol.70 (12), p.1661-1664

2015

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High anti-EBNA-1 IgG levels are associated with early-onset myasthenia gravis

European journal of neurology, 2012-06, Vol.19 (6), p.842-846

2012

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Dense deposit disease in an adolescent male mimicking acute post-streptococcal glomerulonephritis

Hippokratia, 2020-01, Vol.24 (4), p.191-193

2020

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Association of Low Ficolin–Lectin Pathway Parameters with Cardiac Syndrome X

Scandinavian journal of immunology, 2016-09, Vol.84 (3), p.174-181

2016

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Complement Activation and its Prognostic role in Post‐cardiac Arrest Patients

Scandinavian journal of immunology, 2014-06, Vol.79 (6), p.404-409

2014

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Management of pregnancies in a hereditary angioedema patient after treatment with attenuated androgens since childhood

Journal of obstetrics and gynaecology, 2015-01, Vol.35 (1), p.89-90

2015

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Complement activation in thrombotic thrombocytopenic purpura

Molecular immunology, 2011-08, Vol.48 (14), p.1719-1719

2011

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Serum concentration of immunoglobulin G‐type antibodies against the whole Epstein–Barr nuclear antigen 1 and its aa35–58 or aa398–404 fragments in the sera of patients with systemic lupus erythematosus and multiple sclerosis

Clinical and experimental immunology, 2013-03, Vol.171 (3), p.255-262

2013

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At-Home Treatment of Patients with Acute Attacks of Hereditary Angioedema with the Bradykinin B2 Receptor-Antagonist Icatibant

Journal of allergy and clinical immunology, 2011-02, Vol.127 (2), p.AB233-AB233

2011

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Abdominal symptoms of hereditary angioedema and early weaning

European journal of clinical nutrition, 2010-09, Vol.64 (9), p.1025-1027

2010

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Cleaved kininogen as a biomarker for bradykinin release in hereditary angioedema

Journal of allergy and clinical immunology, 2017-12, Vol.140 (6), p.1700-1703.e8

2017

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Psychometric study of the SF-36v2 in hereditary angioedema due to C1 inhibitor deficiency (C1-INH-HAE)

Orphanet journal of rare diseases, 2022-03, Vol.17 (1), p.88-88, Article 88

2022

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Genetic Determinants of C1 Inhibitor Deficiency Angioedema Age of Onset

International archives of allergy and immunology, 2017-01, Vol.174 (3-4), p.200-204

2017

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OS004. A link between the complement system and angiogenic imbalance inpreeclampsia: ficolin-2 deficiency

Pregnancy hypertension, 2012-07, Vol.2 (3), p.177-177

2012

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Hereditary Angioedema Due to C1-Inhibitor Deficiency – From a Genetic Point of View

Hereditary genetics, 2015, Vol.4 (1)

Farkas H, Csuka D

2015

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Activation of the ficolin-lectin pathway during attacks of hereditary angioedema

Molecular immunology, 2013-12, Vol.56 (3), p.276-276

2013

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The role of mannose binding lectin in infectious complications of hemato-oncologic diseases

Molecular immunology, 2013-12, Vol.56 (3), p.299-299

2013

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Short‐term prophylaxis in hereditary angioedema due to deficiency of the C 1‐inhibitor – a long‐term survey

Allergy (Copenhagen), 2012-12, Vol.67 (12), p.1586-1593

2012

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Kallikrein-cleaved kininogen as a stable and specific biomarker for bradykinin release in hereditary angioedema

ALLERGY, 2017, Vol.72, p.98

2017

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Use of New Rechargeable Battery and MRI-Friendly Technologies in Sacral Neuromodulation Systems to Treat Fecal Incontinence

Japanese Journal of Gastroenterology and Hepatology, 2020, Vol.5 (5)

2020

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A 65 Year Old Woman with A Nonhealing Lesion of the Right Lower Jaw Four Months After Zoledronic Acid Infusion

Journal of clinical densitometry, 2010, Vol.13 (1), p.124-125

2010

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Management of pregnancies in a hereditary angioedema patient after treatment with attenuated androgens since childhood

Journal of Obstetrics and Gynaecology, 2015, Vol.35 (1), p.89-90

2015

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Can 4GL revolutionize your lab?

Healthcare informatics, 1991-09, Vol.8 (9), p.44, 46, 50

Csuka, J D

1991

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Complement activation in thrombotic thrombocytopenic purpura

Short-term prophylaxis in hereditary angioedema due to deficiency of the C1-inhibitor - a long-term survey

F12‐46C/T polymorphism as modifier of the clinical phenotype of hereditary angioedema

High anti-EBNA-1 IgG levels are associated with early-onset myasthenia gravis

Dense deposit disease in an adolescent male mimicking acute post-streptococcal glomerulonephritis

Association of Low Ficolin–Lectin Pathway Parameters with Cardiac Syndrome X

Complement Activation and its Prognostic role in Post‐cardiac Arrest Patients

Management of pregnancies in a hereditary angioedema patient after treatment with attenuated androgens since childhood

Complement activation in thrombotic thrombocytopenic purpura

Serum concentration of immunoglobulin G‐type antibodies against the whole Epstein–Barr nuclear antigen 1 and its aa35–58 or aa398–404 fragments in the sera of patients with systemic lupus erythematosus and multiple sclerosis

At-Home Treatment of Patients with Acute Attacks of Hereditary Angioedema with the Bradykinin B2 Receptor-Antagonist Icatibant

Abdominal symptoms of hereditary angioedema and early weaning

Cleaved kininogen as a biomarker for bradykinin release in hereditary angioedema

Psychometric study of the SF-36v2 in hereditary angioedema due to C1 inhibitor deficiency (C1-INH-HAE)

Genetic Determinants of C1 Inhibitor Deficiency Angioedema Age of Onset

OS004. A link between the complement system and angiogenic imbalance inpreeclampsia: ficolin-2 deficiency

Hereditary Angioedema Due to C1-Inhibitor Deficiency – From a Genetic Point of View

Activation of the ficolin-lectin pathway during attacks of hereditary angioedema

The role of mannose binding lectin in infectious complications of hemato-oncologic diseases

Short‐term prophylaxis in hereditary angioedema due to deficiency of the C 1‐inhibitor – a long‐term survey

Kallikrein-cleaved kininogen as a stable and specific biomarker for bradykinin release in hereditary angioedema

Use of New Rechargeable Battery and MRI-Friendly Technologies in Sacral Neuromodulation Systems to Treat Fecal Incontinence

A 65 Year Old Woman with A Nonhealing Lesion of the Right Lower Jaw Four Months After Zoledronic Acid Infusion

Management of pregnancies in a hereditary angioedema patient after treatment with attenuated androgens since childhood

Can 4GL revolutionize your lab?

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