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Science and technology in Argentina according to the World Bank

Medicina (Buenos Aires), 2017, Vol.77 (5), p.442-442

Malbrán, Alejandro

2017

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On scientific research in health institutions of the city of Buenos Aires

Medicina (Buenos Aires), 2014, Vol.74 (2), p.179-179

Malbrán, Alejandro

2014

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Epidemiology of Angioedema without Wheels in an Allergy and Immunology Clinic

Journal of allergy and clinical immunology, 2015-02, Vol.135 (2), p.AB199-AB199

2015

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Treatment of hereditary angioedema due to C1 inhibitor deficiency in Argentina

Medicina (Buenos Aires), 2017-01, Vol.77 (4), p.279-282

2017

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Progressive reduction of circulating B lymphocytes in patients with X‐linked lymphoproliferative disease (XLP)

British journal of haematology, 2017-05, Vol.177 (4), p.648-650

2017

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Phosphorylation of Mitogen-Activated Protein Kinases Contributes to Interferon γ Production in Response to Mycobacterium tuberculosis

The Journal of infectious diseases, 2013-01, Vol.207 (2), p.340-350

2013

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Allergy to drugs. Experience in 771 procedures

Medicina (Buenos Aires), 2017, Vol.77 (3), p.180-184

2017

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IVIG Trademark Head to Head Analysis of Adverse Events in 1394 Intravenous Immunoglobulin Replacement Treatments

Journal of allergy and clinical immunology, 2013-02, Vol.131 (2), p.AB70-AB70

2013

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Epidemiology of angioedema without wheals in an allergy and immunology center

Medicina (Buenos Aires), 2015-01, Vol.75 (5), p.273-276

2015

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Anaphylaxis and allergic reactions during surgery and medical procedures

Medicina (Buenos Aires), 2017, Vol.77 (5), p.382-387

2017

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Hereditary angioedema. Treatment of acute attacks in Argentina

Medicina (Buenos Aires), 2014, Vol.74 (3), p.198-200

2014

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Rituximab and hypogammaglobulinemia

Medicina (Buenos Aires), 2015, Vol.75 (5), p.319-323

2015

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Relapses in inflammatory myopathies

Medicina (Buenos Aires), 2016, Vol.76 (6), p.379-382

2016

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Common variable immunodeficiency and granulomatosis treated with infliximab

Clinical immunology (Orlando, Fla.), 2010-03, Vol.134 (3), p.359-360

2010

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Hereditary angioedema. A therapeutic guide

Medicina (Buenos Aires), 2012, Vol.72 (2), p.119-123

2012

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Deep immunophenotyping shows altered immune cell subsets in CTLA‐4 haploinsufficiency

Pediatric allergy and immunology, 2023-07, Vol.34 (7), p.e13994-n/a

2023

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Long Term Follow-Up of a Common Variable Immunodeficiency Patient with Infliximab Responsive Granulomatous Disease

Journal of allergy and clinical immunology, 2019-02, Vol.143 (2), p.AB17-AB17

2019

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Common variable immunodeficiency. Epidemiology and clinical manifestations in 69 patients

Medicina (Buenos Aires), 2013, Vol.73 (4), p.315-323

2013

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Adverse events in 1395 infusions with different intravenous gammaglobulin products

Medicina (Buenos Aires), 2013, Vol.73 (5), p.433-437

2013

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Common Variable Immunodeficiency and Circulating TFH

Journal of Immunology Research, 2016-01, Vol.2016 (2016), p.1-10

2016

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Analysis of cold activation of the contact system in hereditary angioedema with normal C1 inhibitor

Molecular immunology, 2021-08, Vol.136, p.150-160

2021

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Evidence-based recommendations for the therapeutic management of angioedema owing to hereditary C1 inhibitor deficiency: consensus report of an International Working Group

Allergy, 2012-02, Vol.67 (2), p.147-157

2012

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sgp120 and the contact system in hereditary angioedema: A diagnostic tool in HAE with normal C1 inhibitor

Molecular immunology, 2020-03, Vol.119, p.27-34

2020

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Science and technology in Argentina according to the World Bank

On scientific research in health institutions of the city of Buenos Aires

Epidemiology of Angioedema without Wheels in an Allergy and Immunology Clinic

Treatment of hereditary angioedema due to C1 inhibitor deficiency in Argentina

Progressive reduction of circulating B lymphocytes in patients with X‐linked lymphoproliferative disease (XLP)

Phosphorylation of Mitogen-Activated Protein Kinases Contributes to Interferon γ Production in Response to Mycobacterium tuberculosis

Allergy to drugs. Experience in 771 procedures

IVIG Trademark Head to Head Analysis of Adverse Events in 1394 Intravenous Immunoglobulin Replacement Treatments

Epidemiology of angioedema without wheals in an allergy and immunology center

Anaphylaxis and allergic reactions during surgery and medical procedures

Hereditary angioedema. Treatment of acute attacks in Argentina

Rituximab and hypogammaglobulinemia

IHAE-Qol: Specific Health-Related Quality Of Life (HRQoL) Questionnaire In Hereditary Angioedema Due To C1 Inhibitor Deficiency (HAE-C1INH)

Health-Related Quality Of Life (HRQoL) In Adult Patients With Hereditary Angioedema Due To C1 Inhibitor Deficiency (HAE-C1-INH) Assessed By SF-36v2

Relapses in inflammatory myopathies

Common variable immunodeficiency and granulomatosis treated with infliximab

Hereditary angioedema. A therapeutic guide

Deep immunophenotyping shows altered immune cell subsets in CTLA‐4 haploinsufficiency

Long Term Follow-Up of a Common Variable Immunodeficiency Patient with Infliximab Responsive Granulomatous Disease

Common variable immunodeficiency. Epidemiology and clinical manifestations in 69 patients

Adverse events in 1395 infusions with different intravenous gammaglobulin products

Common Variable Immunodeficiency and Circulating TFH

Analysis of cold activation of the contact system in hereditary angioedema with normal C1 inhibitor

Evidence-based recommendations for the therapeutic management of angioedema owing to hereditary C1 inhibitor deficiency: consensus report of an International Working Group

sgp120 and the contact system in hereditary angioedema: A diagnostic tool in HAE with normal C1 inhibitor

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