José-Manuel Mascaró (0000-0001-9327-2555)

Personal information

Biography

Professor José M. Mascaró Jr. completed his medical studies at the University of Barcelona, Barcelona, Spain where he obtained his medical degree in 1988. In 1990, after medical school, he began a residency in Dermatology at the Department of Dermatology of the Hospital Clinic of Barcelona in Barcelona, Spain. From 1995 to 1997 he did a two-year research fellowship in Immunodermatology at the Department of Dermatology, Medical College of Wisconsin, Milwaukee, under the direction of Prof. Luis A. Diaz. He is also trained in Dermatopathology, and has the Diploma in Dermatopathology from the International Board of Dermatopathology (2004).
Professor Mascaró Jr. is currently Professor of Dermatology at the University of Barcelona, and Consultant at the Department of Dermatology, Hospital Clínic de Barcelona, Spain. He is in charge of the Dermatology inpatient unit and is also responsible for the autoimmune skin consultation and cutaneous pathology of transplant patients (both solid organ and stem cell transplant) from the Department of Dermatology, Hospital Clínic de Barcelona. He is also responsible for the cutaneous immunofluorescence lab at the Pathology Service of the Hospital Clinic of Barcelona.
His main areas of interest and research are autoimmune blistering diseases, connective tissue diseases, cutaneous manifestations of transplant patients and dermatopathology.

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Hospital Clinic of Barcelona: Barcelona, ES

2012-01-01 to present | Consulltant (Dermatology)

Employment

José-Manuel Mascaró

https://orcid.org/0000-0001-9327-2555

Personal information

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Biography

Activities

Employment (2)

Hospital Clinic of Barcelona: Barcelona, ES

Universitat de Barcelona: Barcelona, Catalunya, ES

Works (50 of 242)

Benznidazole-induced drug reaction with eosinophilia and systemic symptoms syndrome in a patient with human leucocyte antigen (HLA)-A*68

Reply to ‘Comments on the first European guideline for paraneoplastic autoimmune multiorgan syndrome’

A Case Report of Concurrent Pyostomatitis Vegetans-Like/Intercellular Immunoglobulin A Dermatosis and Uveitic Macular Edema Reacting Exclusively with Desmocollins: A Possible Common Pathogenesis

A preterm infant with acral congenital erosions

Case Report: Localized bullous pemphigoid induced by local triggers: a case series and a proposal for diagnostic criteria based on a literature review

Coexistence of junctional epidermolysis bullosa, autosomal recessive deafness type 57, and Angelman syndrome: A case report

Corrigendum: S2k guidelines on the management of paraneoplastic pemphigus/paraneoplastic autoimmune multiorgan syndrome initiated by the European Academy of Dermatology and Venereology (EADV)

Esophageal lichen planus: an unusual case of dysphagia

IgA anti-p200 pemphigoid with areolar tropism

Impact of COVID-19 in patients with autoimmune bullous diseases: Report from an international registry

S2k guidelines on the management of paraneoplastic pemphigus/paraneoplastic autoimmune multiorgan syndrome initiated by the European Academy of Dermatology and Venereology (EADV)

Spanish cohort of VEXAS syndrome: clinical manifestations, outcome of treatments and novel evidences about &lt;i&gt;UBA1&lt;/i&gt; mosaicism

Sweet Syndrome: Clinical Presentation, Malignancy Association, Autoinflammatory Disorders and Treatment Response in a Cohort of 93 Patients with Long-term Follow-up

Treatment of Porokeratosis Ptychotropica With a Topical Combination of Cholesterol and Simvastatin

[Translated article] Indirect Immunofluorescence Findings in a Patient With Toxic Epidermal Necrolysis-Like Cutaneous Lupus Erythematosus

Clinical and molecular response to dasatinib in an adult patient with Penttinen syndrome

Dupilumab in Hailey-Hailey disease: a case series

Knowledge and role of dermatologists in life-threatening infections: a national survey among hospital skin specialists

Reactive perforating collagenosis successfully treated with dupilumab

Skin Manifestations in Patients with Selective Immunoglobulin E Deficiency

Treatment of granuloma annulare with tofacitinib

Updated S2 K guidelines for the management of bullous pemphigoid initiated by the European Academy of Dermatology and Venereology (EADV)

Zosterförmige entzündliche Papeln bei einem Mann mittleren Alters

Zosteriform inflammatory papules in a middle-aged man

Selective IgE deficiency predicts poor or no response of chronic spontaneous urticaria to omalizumab.

Treatment of pemphigoid gestationis with dupilumab

Consensus-Based Recommendations on the Prevention of Squamous Cell Carcinoma in Solid Organ Transplant Recipients: A Delphi Consensus Statement.

Anti-Desmocollin Autoantibodies in Autoimmune Blistering Diseases.

Rapid recurrence of erythema annulare centrifugum following successful treatment with narrowband ultraviolet B phototherapy.

Spectrum of Disease Manifestations in Patients with Selective Immunoglobulin E Deficiency

Stevens-Johnson syndrome/toxic epidermal necrolysis-like cutaneous lupus erythematosus. A case series with long-term follow-up.

High-Frequency Ultrasound to Assess Activity in Connective Tissue Panniculitis

Usefulness of high-frequency ultrasonography in the evaluation and monitoring of sclerosing dermatoses: a cohort study.

Familial drug reaction with eosinophilia and systemic symptoms syndrome.

Successful treatment of two cases of refractory cutaneous lupus erythematosus with belimumab.

Ektodermale Dysplasie-Hautfragilität-Syndrom: zwei neue Fälle mit einer neuartigen Missense-Mutation.

Assessment of Sclerodermoid Chronic Graft-versus-host Disease with Colour Doppler Ultrasound.

Digital ischemia triggered by coronavirus disease 2019 in a patient under cemiplimab treatment

Ultrasound Features of Facial and Extrafacial Granuloma Facial. A Caso Series.

Usefulness of high-frequency Doppler ultrasound skin thickness measurement for disease staging and assessing treatment response in patients with scleredema: a case-control study.

A multidisciplinary registry of patients with autoimmune and immune-mediated diseases with symptomatic COVID-19 from a single center.

Ectodermal dysplasia-skin fragility syndrome: two new cases with a novel missense mutation.

Reactive granulomatous dermatitis as a histological pattern including manifestations of interstitial granulomatous dermatitis and palisaded neutrophilic and granulomatous dermatitis: a study of 52 patients.

Retiform purpura as a dermatological sign of coronavirus disease 2019 (COVID‐19) coagulopathy

Skin Manifestations in COVID-19: Prevalence and Relationship with Disease Severity.

Rupioid psoriasis induced by pembrolizumab.

Autoimmune bullous diseases following hematopoietic cell transplantation.

Giant conjunctival bulla: A rare manifestation of autoimmune fibrosing conjunctivitis.

Updated S2K guidelines on the management of pemphigus vulgaris and foliaceus initiated by the european academy of dermatology and venereology (EADV).

Peer review (11 reviews for 3 publications/grants)

Spanish cohort of VEXAS syndrome: clinical manifestations, outcome of treatments and novel evidences about <i>UBA1</i> mosaicism