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Use of dupilumab for atopic dermatitis in pediatric and young adult patients with inborn errors of immunity.
- Published in:
- Pediatric Allergy & Immunology, 2024, v. 35, n. 8, p. 1, doi. 10.1111/pai.14215
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- Publication type:
- Article
Cross-Sectional Study on Autosomal Recessive Congenital Ichthyoses: Association of Genotype with Disease Severity, Phenotypic, and Ultrastructural Features in 74 Italian Patients.
- Published in:
- Dermatology (10188665), 2024, v. 240, n. 3, p. 397, doi. 10.1159/000536366
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- Publication type:
- Article
Identification of a novel SH3PXD2B::FER fusion in a case of plexiform myofibroblastic tumor and review of the literature.
- Published in:
- Genes, Chromosomes & Cancer, 2024, v. 63, n. 2, p. 1, doi. 10.1002/gcc.23224
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- Publication type:
- Article
Sulfur 17% ointment for topical treatment of scabies in children: old but gold.
- Published in:
- International Journal of Dermatology, 2024, v. 63, n. 1, p. e19, doi. 10.1111/ijd.16898
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- Publication type:
- Article
Staphylococcal Infections and Neonatal Skin: Data from Literature and Suggestions for the Clinical Management from Four Challenging Patients.
- Published in:
- Antibiotics (2079-6382), 2023, v. 12, n. 4, p. 632, doi. 10.3390/antibiotics12040632
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- Publication type:
- Article
Paraneoplastic pemphigus and Castleman's disease: a case report and a revision of the literature.
- Published in:
- Italian Journal of Pediatrics, 2023, v. 49, n. 1, p. 1, doi. 10.1186/s13052-023-01442-7
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- Publication type:
- Article
Auricular leishmaniasis in a child successfully treated with intralesional amphotericin B.
- Published in:
- Pediatric Dermatology, 2022, v. 39, n. 5, p. 832, doi. 10.1111/pde.15046
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- Publication type:
- Article
Radiosensitivity in patients affected by ARPC1B deficiency: a new disease trait?
- Published in:
- Frontiers in Immunology, 2022, v. 13, p. 1, doi. 10.3389/fimmu.2022.919237
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- Publication type:
- Article
Multidisciplinary care for patients with epidermolysis bullosa from birth to adolescence: experience of one Italian reference center.
- Published in:
- Italian Journal of Pediatrics, 2022, v. 48, n. 1, p. 1, doi. 10.1186/s13052-022-01252-3
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- Publication type:
- Article
Narrative review on the management of moderate-severe atopic dermatitis in pediatric age of the Italian Society of Pediatric Allergology and Immunology (SIAIP), of the Italian Society of Pediatric Dermatology (SIDerP) and of the Italian Society of Pediatrics (SIP)
- Published in:
- Italian Journal of Pediatrics, 2022, v. 48, n. 1, p. 1, doi. 10.1186/s13052-022-01278-7
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- Publication type:
- Article
Clinical and Molecular Spectrum of Sporadic Vascular Malformations: A Single-Center Study.
- Published in:
- Biomedicines, 2022, v. 10, n. 6, p. 1460, doi. 10.3390/biomedicines10061460
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- Publication type:
- Article
PIK3CA-related overgrowth with an uncommon phenotype: case report.
- Published in:
- Italian Journal of Pediatrics, 2022, v. 48, n. 1, p. 1, doi. 10.1186/s13052-022-01268-9
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- Publication type:
- Article
Prominent Follicular Keratosis in Multiple Intestinal Atresia with Combined Immune Deficiency Caused by a TTC7A Homozygous Mutation.
- Published in:
- 2022
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- Publication type:
- Case Study
Proteasome-mediated degradation of keratins 7, 8, 17 and 18 by mutant KLHL24 in a foetal keratinocyte model: Novel insight in congenital skin defects and fragility of epidermolysis bullosa simplex with cardiomyopathy.
- Published in:
- Human Molecular Genetics, 2022, v. 31, n. 8, p. 1308, doi. 10.1093/hmg/ddab318
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- Publication type:
- Article
Multidisciplinary care for patients with epidermolysis bullosa from birth to adolescence: experience of one Italian reference center.
- Published in:
- Italian Journal of Pediatrics, 2022, v. 48, n. 1, p. 1, doi. 10.1186/s13052-022-01252-3
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- Publication type:
- Article
Epidermolysis Bullosa in children: the central role of the pediatrician.
- Published in:
- 2022
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- Publication type:
- journal article
ITGB4-mutated Junctional Epidermolysis Bullosa without Pyloric Atresia Presenting with Severe Urinary Involvement and Late-onset Minimal Skin Fragility: Diagnostic and Therapeutic Challenges.
- Published in:
- 2022
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- Publication type:
- Case Study
A multicenter study on quality of life of the "greater patient" in congenital ichthyoses.
- Published in:
- 2021
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- Publication type:
- journal article
Severe adverse events during sirolimus "off‐label" therapy for vascular anomalies.
- Published in:
- Pediatric Blood & Cancer, 2021, v. 68, n. 8, p. 1, doi. 10.1002/pbc.28936
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- Publication type:
- Article
Congenital self-healing reticulohistiocytosis in a newborn: unusual oral and cutaneous manifestations.
- Published in:
- Italian Journal of Pediatrics, 2021, v. 47, n. 1, p. 1, doi. 10.1186/s13052-021-01082-9
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- Publication type:
- Article
The Burden of Autosomal Recessive Congenital Ichthyoses on Patients and their Families: An Italian Multicentre Study.
- Published in:
- Acta Dermato-Venereologica, 2021, v. 101, n. 6, p. 1, doi. 10.2340/00015555-3822
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- Publication type:
- Article
The Role of KRAS Mutations in Cortical Malformation and Epilepsy Surgery: A Novel Report of Nevus Sebaceous Syndrome and Review of the Literature.
- Published in:
- Brain Sciences (2076-3425), 2021, v. 11, n. 6, p. 793, doi. 10.3390/brainsci11060793
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- Publication type:
- Article
Cutaneous venous malformations as a clue for possible gastrointestinal tract involvement: Diagnosis and treatment of six cases.
- Published in:
- Dermatologic Therapy, 2021, v. 34, n. 3, p. 1, doi. 10.1111/dth.14932
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- Publication type:
- Article
Ectodermal Dysplasia-Syndactyly Syndrome with Toe-Only Minimal Syndactyly Due to a Novel Mutation in NECTIN4: A Case Report and Literature Review.
- Published in:
- Genes, 2021, v. 12, n. 5, p. 748, doi. 10.3390/genes12050748
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- Publication type:
- Article
Two Italian Patients with ELOVL4 -Related Neuro-Ichthyosis: Expanding the Genotypic and Phenotypic Spectrum and Ultrastructural Characterization.
- Published in:
- Genes, 2021, v. 12, n. 3, p. 343, doi. 10.3390/genes12030343
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- Publication type:
- Article
First Case of KRT2 Epidermolytic Nevus and Novel Clinical and Genetic Findings in 26 Italian Patients with Keratinopathic Ichthyoses.
- Published in:
- International Journal of Molecular Sciences, 2020, v. 21, n. 20, p. 7707, doi. 10.3390/ijms21207707
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- Publication type:
- Article
Cutaneous Infantile Haemangiomas with Intracranial and Intraspinal Involvement: A European Multicentre Experience and Review.
- Published in:
- Acta Dermato-Venereologica, 2020, v. 100, n. 9, p. 1, doi. 10.2340/00015555-3608
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- Publication type:
- Article
Membranous aplasia cutis congenita in trisomy 18.
- Published in:
- Italian Journal of Pediatrics, 2020, v. 46, n. 1, p. N.PAG, doi. 10.1186/s13052-020-00885-6
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- Publication type:
- Article
Diffuse infantile hepatic hemangiomas in a patient with Beckwith–Wiedemann syndrome: A new association?
- Published in:
- American Journal of Medical Genetics. Part A, 2020, v. 182, n. 8, p. 1972, doi. 10.1002/ajmg.a.61718
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- Publication type:
- Article
Successful topical treatment of anal giant condylomata acuminata in an infant.
- Published in:
- Dermatologic Therapy, 2020, v. 33, n. 4, p. 1, doi. 10.1111/dth.13624
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- Publication type:
- Article
Juvenile idiopathic arthritis in infants with Harlequin Ichthyosis: two cases report and literature review.
- Published in:
- Italian Journal of Pediatrics, 2020, v. 46, n. 1, p. 1, doi. 10.1186/s13052-020-0817-5
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- Publication type:
- Article
Correction to: Italian translation, cultural adaptation, and pilot testing of a questionnaire to assess family burden in inherited ichthyoses.
- Published in:
- 2020
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- Publication type:
- Correction Notice
Hoarse cry in a newborn with epidermolysis bullosa simplex, generalized severe.
- Published in:
- Pediatric Dermatology, 2020, v. 37, n. 2, p. 393, doi. 10.1111/pde.14105
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- Publication type:
- Article
EGFR inhibition for metastasized cutaneous squamous cell carcinoma in dystrophic epidermolysis bullosa.
- Published in:
- 2019
- By:
- Publication type:
- letter
X‐linked ichthyosis: Clinical and molecular findings in 35 Italian patients.
- Published in:
- Experimental Dermatology, 2019, v. 28, n. 10, p. 1156, doi. 10.1111/exd.13667
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- Publication type:
- Article
Fibrolipomatous hamartomas not only on the soles.
- Published in:
- Pediatric Dermatology, 2019, v. 36, n. 5, p. 728, doi. 10.1111/pde.13874
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- Publication type:
- Article
Management of chronic urticaria in children: a clinical guideline.
- Published in:
- Italian Journal of Pediatrics, 2019, v. 45, n. 1, p. N.PAG, doi. 10.1186/s13052-019-0695-x
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- Publication type:
- Article
Novel clinical features associated with Clouston syndrome.
- Published in:
- International Journal of Dermatology, 2019, v. 58, n. 8, p. e143, doi. 10.1111/ijd.14507
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- Publication type:
- Article
Agminated Spitzoid Naevi after Remission of Langerhans Cell Histiocytosis: First Italian Case and Literature Review.
- Published in:
- Acta Dermato-Venereologica, 2019, v. 99, n. 9, p. 824, doi. 10.2340/00015555-3156
- By:
- Publication type:
- Article
Next Generation Sequencing Uncovers a Rare Case of X-linked Ichthyosis in an Adopted Girl Homozygous for a Novel Nonsense Mutation in the STS Gene.
- Published in:
- Acta Dermato-Venereologica, 2019, v. 99, n. 9, p. 828, doi. 10.2340/00015555-3162
- By:
- Publication type:
- Article
Efficacy and Adverse Events During Janus Kinase Inhibitor Treatment of SAVI Syndrome.
- Published in:
- Journal of Clinical Immunology, 2019, v. 39, n. 5, p. 476, doi. 10.1007/s10875-019-00645-0
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- Publication type:
- Article
Angioma serpiginosum: a case report and review of the literature.
- Published in:
- Italian Journal of Pediatrics, 2019, v. 45, n. 1, p. N.PAG, doi. 10.1186/s13052-019-0644-8
- By:
- Publication type:
- Article
Italian translation, cultural adaptation, and pilot testing of a questionnaire to assess family burden in inherited ichthyoses.
- Published in:
- Italian Journal of Pediatrics, 2019, v. 45, n. 1, p. N.PAG, doi. 10.1186/s13052-019-0618-x
- By:
- Publication type:
- Article
Phenotypic Features of Epidermolysis Bullosa Simplex due to KLHL24 Mutations in 3 Italian Cases.
- Published in:
- 2019
- By:
- Publication type:
- Case Study
A novel dermoscopic pattern observed in furuncular myiasis.
- Published in:
- 2019
- By:
- Publication type:
- Case Study
An additional patient with a homozygous mutation in DCPS contributes to the delination of Al‐Raqad syndrome.
- Published in:
- American Journal of Medical Genetics. Part A, 2018, v. 176, n. 12, p. 2781, doi. 10.1002/ajmg.a.40488
- By:
- Publication type:
- Article
Ichthyosis Prematurity Syndrome due to a Novel SLC27A4 Homozygous Mutation in an Italian Patient.
- Published in:
- 2018
- By:
- Publication type:
- Case Study
Cardiopulmonary anomalies in incontinentia pigmenti patients.
- Published in:
- International Journal of Dermatology, 2018, v. 57, n. 1, p. 40, doi. 10.1111/ijd.13835
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- Publication type:
- Article
Local anesthesia in pediatric dermatologic surgery: Evaluation of a patient‐centered approach.
- Published in:
- Pediatric Dermatology, 2018, v. 35, n. 1, p. 112, doi. 10.1111/pde.13347
- By:
- Publication type:
- Article
Lipoid Proteinosis: A Previously Unrecognized Mutation and Therapeutic Response to Acitretin.
- Published in:
- 2017
- By:
- Publication type:
- Case Study