C. Gómez-Traseira

发表

Management of angioedema without urticaria in the emergency department

I. Jáuregui, M. Pedrosa, C. Marcos, 2014, Annals of medicine.

Development of a disease-specific quality of life questionnaire for adult patients with hereditary angioedema due to C1 inhibitor deficiency (HAE-QoL): Spanish multi-centre research project

E. Remor, V. Cardona, C. Marcos, 2012, Health and Quality of Life Outcomes.

Consensus statement on the diagnosis, management, and treatment of angioedema mediated by bradykinin. Part II. Treatment, follow-up, and special situations.

M. López-Trascasa, M. Pedrosa, C. Marcos, 2011, Journal of investigational allergology & clinical immunology.

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

W. Aberer, R. A. Campos, H. Farkas, 2021, Orphanet Journal of Rare Diseases.

Psychometric Field Study of Hereditary Angioedema Quality of Life Questionnaire for Adults: HAE-QoL.

W. Aberer, H. Farkas, E. Remor, 2016, The journal of allergy and clinical immunology. In practice.

Adverse reaction with hexavalent vaccine: An unusual case.

S. Quirce, M. González‐Muñoz, C. Gómez-Traseira, 2020, Allergologia et immunopathologia.

Paracetamol-induced fixed drug eruption at an unusual site.

L. Sánchez-Morillas, P. Rojas-Pérez-Ezquerra, C. Gómez-Traseira, 2013, Recent patents on inflammation & allergy drug discovery.

HAE-AS: A Specific Disease Activity Scale for Hereditary Angioedema With C1-Inhibitor Deficiency

H. Farkas, P. Staubach, G. Porebski, 2021 .

Fixed Food Eruption Caused by Peanut Confirmed by Open Oral Food Challenge and in Vitro Cellular Testing.

M. González‐Muñoz, C. Gómez-Traseira, F. Vílchez-Sánchez, 2020, Contact dermatitis.

Drug Provocation Tests for Assessing Antibiotic Hypersensitivity

S. Quirce, A. Umpiérrez, C. Gómez-Traseira, 2020, The Pediatric infectious disease journal.

Clinical Pattern and Acute and Long-term Management of Hereditary Angioedema Due to C1-Esterase Inhibitor Deficiency.

M. López-Trascasa, M. Pedrosa, M. García-Ara, 2015, Journal of investigational allergology & clinical immunology.

Usefulness of abdominal ultrasonography in the follow-up of patients with hereditary C1-inhibitor deficiency.

M. Pedrosa, A. Olveira, T. Caballero, 2009, Annals of allergy, asthma & immunology : official publication of the American College of Allergy, Asthma, & Immunology.

Consensus statement on the diagnosis, management, and treatment of angioedema mediated by bradykinin. Part I. Classification, epidemiology, pathophysiology, genetics, clinical symptoms, and diagnosis.

M. López-Trascasa, M. Pedrosa, C. Marcos, 2011, Journal of investigational allergology & clinical immunology.

Hereditary angioedema caused by the p.Thr309Lys mutation in the F12 gene: a multifactorial disease.

M. López-Trascasa, C. Drouet, N. Prior, 2013, The Journal of allergy and clinical immunology.

Hypersensitivity to nabumetone: cross reactivity with naproxen.

C. Gómez-Traseira, J. L. Laguna Martínez, P. R. Pérez-Ezquerra, 2013, Annals of allergy, asthma & immunology : official publication of the American College of Allergy, Asthma, & Immunology.

Selective hypersensitivity reactions to acetaminophen: a 13-case series.

P. Rojas-Pérez-Ezquerra, C. Gómez-Traseira, R. González-Mendiola, 2014, The journal of allergy and clinical immunology. In practice.

The Lymphocyte Transformation Test in delayed hypersensitivity reactions induced by ibuprofen and/or metamizole.

A. Fiandor, R. Cabañas, J. Domínguez-Ortega, 2022, Journal of investigational allergology & clinical immunology.

Trimethoprim–sulfamethoxazole (cotrimoxazole) desensitization in an HIV‐infected 5‐yr‐old girl

F. Martín-Muñoz, S. Quirce, M. Pedrosa, 2015, Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology.