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Hydrocolloid dressing for the treatment of severe diaper dermatitis

Pediatric dermatology, 2023-01, Vol.40 (1), p.224-225

2023

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A 9‐year‐old girl with frontotemporal hair thinning and peripilar hair casts

Pediatric dermatology, 2022-01, Vol.39 (1), p.124-125

2022

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Report of a case of RAVEN, hair heterochromia and autism in the setting of FGFR2 mutation

Pediatric dermatology, 2023-03, Vol.40 (2), p.382-384

2023

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Patient with atopic dermatitis, hyper IgE syndrome and ulcerative colitis, treated successfully with dupilumab during pregnancy

Dermatologic therapy, 2022-02, Vol.35 (2), p.e15237-n/a

2022

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Multiple rhabdomyomatous mesenchymal hamartomas in a patient with mosaic Barber-Say syndrome

Pediatric dermatology, 2024-03, Vol.41 (2), p.307-310

2024

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Grover‐like skin eruption: another cutaneous manifestation in a COVID‐19 patient

International journal of dermatology, 2020-10, Vol.59 (10), p.1290-1292

2020

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Leukoplakia, skin pigmentation and microcephaly in a 4‐year‐old boy

Pediatric dermatology, 2020-11, Vol.37 (6), p.e79-e80

2020

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Facial hemihypertrophy in a girl with sturge‐weber syndrome: Treatment with oral sirolimus

Pediatric dermatology, 2021-03, Vol.38 (2), p.469-471

2021

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Chronic urticaria in children under 15 years of age: Clinical experience beyond the clinical trials

Pediatric dermatology, 2021-03, Vol.38 (2), p.385-389

2021

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Exserohilum rostratum, a rare cause of opportunistic skin infection in children: Case report and review of the literature

Pediatric dermatology, 2020-09, Vol.37 (5), p.918-921

2020

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Timolol for the treatment of pyogenic granuloma (PG) in children

Journal of the American Academy of Dermatology, 2016-09, Vol.75 (3), p.e105-e106

2016

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Erosions and vesicles following the lines of Blaschko in a neonate

Pediatric dermatology, 2018-07, Vol.35 (4), p.519-520

2018

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Safety Profile and Tolerability of Topical Phosphodiesterase 4 Inhibitors for the Treatment of Atopic Dermatitis: A Systematic Review and Meta-Analysis

Current therapeutic research, 2022-01, Vol.96, p.100679-100679, Article 100679

2022

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Prominent venous circulation and thick lips in an 8‐year‐old boy with congenital neutropenia

Pediatric dermatology, 2019-05, Vol.36 (3), p.e69-e70

2019

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Improving the relationship between soil characteristics and metal bioavailability by using reactive fractions of soil parameters in calcareous soils

Environmental toxicology and chemistry, 2015-01, Vol.34 (1), p.37-44

2015

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Annular paraneoplastic bullous pemphigoid mimicking linear IgA bullous dermatosis in a 40‐year‐old patient

Journal der Deutschen Dermatologischen Gesellschaft, 2018-04, Vol.16 (4), p.482-484

2018

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Dermoscopic Visualization of Vellus Hair Involvement in Tinea Corporis: A Criterion for Systemic Antifungal Therapy?

Pediatric dermatology, 2015-09, Vol.32 (5), p.e226-e227

2015

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ABCA12 mutations in patients with autosomal recessive congenital ichthyosis: evidence of a founder effect in the Spanish population and phenotype-genotype implications

Journal of dermatological science, 2018-09, Vol.91 (3), p.328-331

2018

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Patient with H syndrome, cardiogenic shock, multiorgan infiltration, and digital ischemia

Pediatric rheumatology online journal, 2021-06, Vol.19 (1), p.104-104, Article 104

2021

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Flagellate erythema in parvovirus B19 infection

International journal of dermatology, 2014-12, Vol.53 (12), p.e583-e585

2014

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Dermoscopy “clears” out the diagnosis: An erythematous nodule in a psoriatic patient

Journal of the American Academy of Dermatology, 2015-01, Vol.72 (1), p.S68-S70

2015

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Diagnostic Value of the Skin Lesions in Immune Dysregulation, Polyendocrinopathy, Enteropathy, X-Linked Syndrome

Pediatric dermatology, 2013-11, Vol.30 (6), p.e221-e222

2013

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Novel CYP4F22 mutations associated with autosomal recessive congenital ichthyosis (ARCI). Study of the CYP4F22 c.1303C>T founder mutation

PloS one, 2020-02, Vol.15 (2), p.e0229025-e0229025

2020

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Varicella Precipitating Febrile Ulceronecrotic Mucha-Habermann Disease

Pediatric dermatology, 2013-11, Vol.30 (6), p.e216-e217

2013

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Novel CYP4F22 mutations associated with autosomal recessive congenital ichthyosis . Study of the CYP4F22 c.1303CT founder mutation

PloS one, 2020-02, Vol.15 (2), p.e0229025

2020

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Hydrocolloid dressing for the treatment of severe diaper dermatitis

A 9‐year‐old girl with frontotemporal hair thinning and peripilar hair casts

Report of a case of RAVEN, hair heterochromia and autism in the setting of FGFR2 mutation

Patient with atopic dermatitis, hyper IgE syndrome and ulcerative colitis, treated successfully with dupilumab during pregnancy

Multiple rhabdomyomatous mesenchymal hamartomas in a patient with mosaic Barber-Say syndrome

Grover‐like skin eruption: another cutaneous manifestation in a COVID‐19 patient

Leukoplakia, skin pigmentation and microcephaly in a 4‐year‐old boy

Facial hemihypertrophy in a girl with sturge‐weber syndrome: Treatment with oral sirolimus

Chronic urticaria in children under 15 years of age: Clinical experience beyond the clinical trials

Exserohilum rostratum, a rare cause of opportunistic skin infection in children: Case report and review of the literature

Timolol for the treatment of pyogenic granuloma (PG) in children

Erosions and vesicles following the lines of Blaschko in a neonate

Safety Profile and Tolerability of Topical Phosphodiesterase 4 Inhibitors for the Treatment of Atopic Dermatitis: A Systematic Review and Meta-Analysis

Prominent venous circulation and thick lips in an 8‐year‐old boy with congenital neutropenia

Improving the relationship between soil characteristics and metal bioavailability by using reactive fractions of soil parameters in calcareous soils

Annular paraneoplastic bullous pemphigoid mimicking linear IgA bullous dermatosis in a 40‐year‐old patient

Dermoscopic Visualization of Vellus Hair Involvement in Tinea Corporis: A Criterion for Systemic Antifungal Therapy?

ABCA12 mutations in patients with autosomal recessive congenital ichthyosis: evidence of a founder effect in the Spanish population and phenotype-genotype implications

Patient with H syndrome, cardiogenic shock, multiorgan infiltration, and digital ischemia

Flagellate erythema in parvovirus B19 infection

Dermoscopy “clears” out the diagnosis: An erythematous nodule in a psoriatic patient

Diagnostic Value of the Skin Lesions in Immune Dysregulation, Polyendocrinopathy, Enteropathy, X-Linked Syndrome

Novel CYP4F22 mutations associated with autosomal recessive congenital ichthyosis (ARCI). Study of the CYP4F22 c.1303C>T founder mutation

Varicella Precipitating Febrile Ulceronecrotic Mucha-Habermann Disease

Novel CYP4F22 mutations associated with autosomal recessive congenital ichthyosis . Study of the CYP4F22 c.1303CT founder mutation

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