Found: 36
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H syndrome--four new patients from India.
- Published in:
- 2014
- By:
- Publication type:
- Case Study
H syndrome—Four new patients from India.
- Published in:
- 2014
- By:
- Publication type:
- Letter to the Editor
Secukinumab for the Treatment of Deficiency of Interleukin 36 Receptor Antagonist in an Adolescent.
- Published in:
- 2017
- By:
- Publication type:
- journal article
Topical phage therapy in a mouse model of Cutibacterium acnes-induced acne-like lesions.
- Published in:
- Nature Communications, 2023, v. 14, n. 1, p. 1, doi. 10.1038/s41467-023-36694-8
- By:
- Publication type:
- Article
H Syndrome: A Rare Monogenic Cause of Insulin-Dependent Diabetes Mellitus.
- Published in:
- 2015
- By:
- Publication type:
- Abstract
H Syndrome: A Rare Monogenic Cause of Insulin-Dependent Diabetes Mellitus.
- Published in:
- Journal of Clinical Research in Pediatric Endocrinology, 2015, v. 7, p. 70
- By:
- Publication type:
- Article
Phototherapy for the treatment of cutaneous graft‐versus‐host disease: A systematic review.
- Published in:
- Photodermatology, Photoimmunology & Photomedicine, 2024, v. 40, n. 5, p. 1, doi. 10.1111/phpp.12997
- By:
- Publication type:
- Article
Marie Unna hereditary hypotrichosis caused by a novel mutation in the human hairless transcript.
- Published in:
- Experimental Dermatology, 2010, v. 19, n. 8, p. e320, doi. 10.1111/j.1600-0625.2009.01042.x
- By:
- Publication type:
- Article
A novel splice-site mutation in ECM-1 gene in a consanguineous family with lipoid proteinosis.
- Published in:
- Experimental Dermatology, 2005, v. 14, n. 12, p. 891, doi. 10.1111/j.1600-0625.2005.00374.x
- By:
- Publication type:
- Article
Giant congenital melanocytic naevus with a novel CUX1–BRAF fusion mutation treated with trametinib.
- Published in:
- British Journal of Dermatology, 2022, v. 187, n. 6, p. 1052, doi. 10.1111/bjd.21851
- By:
- Publication type:
- Article
IL36 RN mutation causing generalized pustular psoriasis in a Palestinian patient.
- Published in:
- International Journal of Dermatology, 2014, v. 53, n. 7, p. 866, doi. 10.1111/ijd.12525
- By:
- Publication type:
- Article
Molecular epidemiology of non‐syndromic autosomal recessive congenital ichthyosis in a Middle‐Eastern population.
- Published in:
- Experimental Dermatology, 2021, v. 30, n. 9, p. 1290, doi. 10.1111/exd.14345
- By:
- Publication type:
- Article
Chronic demodicosis in patients with immune dysregulation: An unexpected infectious manifestation of Signal transducer and activator of transcription (STAT)1 gain‐of‐function.
- Published in:
- Clinical & Experimental Immunology, 2021, v. 206, n. 1, p. 56, doi. 10.1111/cei.13636
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- Publication type:
- Article
Tumor necrosis factor‐α inhibitor‐induced follicular psoriasiform eruption.
- Published in:
- Pediatric Dermatology, 2022, v. 39, n. 4, p. 598, doi. 10.1111/pde.14993
- By:
- Publication type:
- Article
Acral peeling skin syndrome resulting from a novel homozygous mutation in the CSTA gene—A report of two cases.
- Published in:
- Pediatric Dermatology, 2021, v. 38, n. 6, p. 1546, doi. 10.1111/pde.14843
- By:
- Publication type:
- Article
Dupilumab for pediatric prurigo nodularis: A case report.
- Published in:
- Pediatric Dermatology, 2021, v. 38, n. 1, p. 334, doi. 10.1111/pde.14464
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- Publication type:
- Article
Subcutaneous granuloma annulare mimicking dermatomyositis.
- Published in:
- Pediatric Dermatology, 2020, v. 37, n. 4, p. 687, doi. 10.1111/pde.14167
- By:
- Publication type:
- Article
The molluscum contagiosum BOTE sign—Infected or inflamed?
- Published in:
- Pediatric Dermatology, 2020, v. 37, n. 3, p. 476, doi. 10.1111/pde.14124
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- Publication type:
- Article
STAT1 gain‐of‐function and chronic demodicosis.
- Published in:
- Pediatric Dermatology, 2020, v. 37, n. 1, p. 153, doi. 10.1111/pde.14011
- By:
- Publication type:
- Article
Atopic Dermatitis in Israeli Adolescents from 1998 to 2013: Trends in Time and Association with Migraine.
- Published in:
- Pediatric Dermatology, 2017, v. 34, n. 3, p. 247, doi. 10.1111/pde.13084
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- Publication type:
- Article
Two Novel Homozygous Desmoplakin Mutations in Carvajal Syndrome.
- Published in:
- Pediatric Dermatology, 2015, v. 32, n. 5, p. 641, doi. 10.1111/pde.12541
- By:
- Publication type:
- Article
Agenesis of the Inferior Vena Cava in H Syndrome Due to a Novel SLC29A3 Mutation.
- Published in:
- Pediatric Dermatology, 2013, v. 30, n. 5, p. e70, doi. 10.1111/pde.12085
- By:
- Publication type:
- Article
Cutaneous Adverse Events to Targeted Therapies and Immunotherapies in Children: A Retrospective Study of 103 Patients from Two Tertiary Haemato-Oncology Referral Centres.
- Published in:
- Acta Dermato-Venereologica, 2021, v. 101, n. 7, p. 1, doi. 10.2340/00015555-3867
- By:
- Publication type:
- Article
Oral and Topical Sirolimus for Vascular Anomalies: A Multicentre Study and Review.
- Published in:
- Acta Dermato-Venereologica, 2019, v. 99, n. 11, p. 990, doi. 10.2340/00015555-3262
- By:
- Publication type:
- Article
Ulcers and Scars on the Trunk of a 20-month-old Boy: A Quiz.
- Published in:
- Acta Dermato-Venereologica, 2019, v. 99, n. 6, p. 629, doi. 10.2340/00015555-3153
- By:
- Publication type:
- Article
Cutaneous Chronic Graft Versus Host Disease Following Allogeneic Haematopoietic Stem Cell Transplantation in Children: A Retrospective Study.
- Published in:
- Acta Dermato-Venereologica, 2018, v. 98, n. 2, p. 206, doi. 10.2340/00015555-2824
- By:
- Publication type:
- Article
Paediatric Erythema Multiforme: Epidemiological, Clinical and Laboratory Characteristics.
- Published in:
- Acta Dermato-Venereologica, 2017, v. 97, n. 4, p. 489, doi. 10.2340/00015555-2569
- By:
- Publication type:
- Article
Coxsackievirus A6 Polymorphic Exanthem in Israeli Children.
- Published in:
- Acta Dermato-Venereologica, 2016, v. 96, n. 4, p. 546, doi. 10.2340/00015555-2261
- By:
- Publication type:
- Article
H Syndrome: A Multifaceted Histiocytic Disorder with Hyperpigmentation and Hypertrichosis.
- Published in:
- Acta Dermato-Venereologica, 2015, v. 95, n. 8, p. 1021, doi. 10.2340/00015555-2145
- By:
- Publication type:
- Article
Management of Atopy with Dupilumab and Omalizumab in CADINS Disease.
- Published in:
- Journal of Clinical Immunology, 2024, v. 44, n. 2, p. 1, doi. 10.1007/s10875-023-01636-y
- By:
- Publication type:
- Article
T<sup>+</sup> NK<sup>+</sup> IL-2 Receptor γ Chain Mutation: a Challenging Diagnosis of Atypical Severe Combined Immunodeficiency.
- Published in:
- Journal of Clinical Immunology, 2018, v. 38, n. 4, p. 527, doi. 10.1007/s10875-018-0514-y
- By:
- Publication type:
- Article
Homozygous Splice Site Mutations in PKP1 Result in Loss of Epidermal Plakophilin 1 Expression and Underlie Ectodermal Dysplasia/Skin Fragility Syndrome in Two Consanguineous Families.
- Published in:
- Journal of Investigative Dermatology, 2004, v. 122, n. 3, p. 647, doi. 10.1111/j.0022-202X.2004.22335.x
- By:
- Publication type:
- Article
Lymphatic Dissemination in Cutaneous Leishmaniasis Following Local Treatment.
- Published in:
- American Journal of Tropical Medicine & Hygiene, 2015, v. 93, n. 4, p. 770, doi. 10.4269/ajtmh.14-0787
- By:
- Publication type:
- Article
Coexistence of Two Rare Autosomal Recessive Disorders: Activation-Induced Cytidine Deaminase Deficiency and Sjogren-Larsson Syndrome.
- Published in:
- Israel Medical Association Journal, 2016, v. 18, n. 10, p. 636
- By:
- Publication type:
- Article
Skin toxicity following treosulfan‐thiotepa‐fludarabine‐based conditioning regimen in non‐malignant pediatric patients undergoing hematopoietic stem cell transplantation.
- Published in:
- Pediatric Transplantation, 2020, v. 24, n. 1, p. N.PAG, doi. 10.1111/petr.13626
- By:
- Publication type:
- Article
Alopecia Areata and Down Syndrome: A True Association or a Coincidence.
- Published in:
- 2013
- By:
- Publication type:
- Letter to the Editor