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Leukoderma induced by rhododendrol is different from leukoderma of vitiligo in pathogenesis: A novel comparative morphological study.
- Published in:
- Journal of Cutaneous Pathology, 2019, v. 46, n. 2, p. 123, doi. 10.1111/cup.13396
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- Publication type:
- Article
Agminated pigmented matricoma: a case of a unique tumor with a multifocal appearance composed of neoplastic matrical cells with a significant component of melanocyte.
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- Journal of Cutaneous Pathology, 2013, v. 40, n. 9, p. 823, doi. 10.1111/cup.12185
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- Publication type:
- Article
Nonsegmental Vitiligo and Autoimmune Mechanism.
- Published in:
- Dermatology Research & Practice, 2011, v. 2011, p. 1, doi. 10.1155/2011/518090
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- Publication type:
- Article
Nonsegmental Vitiligo and Autoimmune Mechanism.
- Published in:
- 2011
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- Publication type:
- Journal Article
The Surprising Effect of Phenformin on Cutaneous Darkening and Characterization of Its Underlying Mechanism by a Forward Chemical Genetics Approach.
- Published in:
- International Journal of Molecular Sciences, 2020, v. 21, n. 4, p. 1451, doi. 10.3390/ijms21041451
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- Publication type:
- Article
Dermoscopy is useful for the diagnosis of milia‐like idiopathic calcinosis cutis.
- Published in:
- 2018
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- Publication type:
- Letter to the Editor
Pulmonary and Intestinal Involvement in a Patient with Myeloperoxidase-specific Antineutrophil Cytoplasmic Antibody-positive Hermansky-Pudlak Syndrome.
- Published in:
- Internal Medicine, 2023, v. 62, n. 1, p. 103, doi. 10.2169/internalmedicine.9350-22
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- Publication type:
- Article
Hermansky-Pudlak syndrome is caused by mutations in HPS4, the human homolog of the mouse light-ear gene.
- Published in:
- Nature Genetics, 2002, v. 30, n. 3, p. 321, doi. 10.1038/ng835
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- Publication type:
- Article
Depigmentation of the skin induced by 4-(4-hydroxyphenyl)-2-butanol is spontaneously re-pigmented in brown and black guinea pigs.
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- Journal of Toxicological Sciences, 2014, v. 39, n. 4, p. 615, doi. 10.2131/jts.39.615
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- Publication type:
- Article
Role of endothelin-1/endothelin receptor signaling in fibrosis and calcification in nephrogenic systemic fibrosis.
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- Experimental Dermatology, 2014, v. 23, n. 9, p. 664, doi. 10.1111/exd.12500
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- Publication type:
- Article
A missense mutation c.G2747A (p.R916Q) of ADAR1 gene in dyschromatosis symmetrica hereditaria is not a novel mutation.
- Published in:
- 2010
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- Publication type:
- Letter
IL36 RN gene analysis of two Japanese patients with generalized pustular psoriasis.
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- International Journal of Dermatology, 2015, v. 54, n. 2, p. e60, doi. 10.1111/ijd.12657
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- Publication type:
- Article
Gene expression and in situ localization of ADAM17 during skin wound healing.
- Published in:
- International Journal of Dermatology, 2014, v. 53, n. 3, p. e229, doi. 10.1111/ijd.12119
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- Publication type:
- Article
ADAM17 is involved in the regulation of chemokine expression in keratinocytes.
- Published in:
- International Journal of Dermatology, 2014, v. 53, n. 3, p. e233, doi. 10.1111/ijd.12090
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- Publication type:
- Article
Mucinous eccrine naevus.
- Published in:
- 2009
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- Publication type:
- Letter
A Patient with Subclinical Oculocutaneous Albinism Type 2 Diagnosed on Getting Severely Sunburned.
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- Dermatology (10188665), 2005, v. 210, n. 4, p. 322, doi. 10.1159/000084758
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- Publication type:
- Article
Melanin accumulation in acanthotic seborrheic keratosis: Reduced proliferation and early differentiation of keratinocytes and increased number of melanocytes.
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- Experimental Dermatology, 2024, v. 33, n. 7, p. 1, doi. 10.1111/exd.15138
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- Publication type:
- Article
Metastatic Orbital Tumor From Breast Ductal Carcinoma With Neuroendocrine Differentiation Initially Presenting as Ocular Symptoms: A Case Report and Literature Review.
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- Frontiers in Endocrinology, 2021, v. 11, p. N.PAG, doi. 10.3389/fendo.2021.625663
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- Publication type:
- Article
A case of Hailey‐Hailey disease with novel ATP2C1 gene variant (c.G925C) showing unusual phenotype.
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- Journal of Dermatology, 2024, v. 51, n. 10, p. e346, doi. 10.1111/1346-8138.17258
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- Publication type:
- Article
Post‐COVID‐19 vaccination diffuse cutaneous sarcoidosis.
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- Journal of Dermatology, 2024, v. 51, n. 8, p. e282, doi. 10.1111/1346-8138.17194
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- Publication type:
- Article
Amelanotic melanoma in oculocutaneous albinism type 4 detected using violet‐light dermoscopy.
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- Journal of Dermatology, 2024, v. 51, n. 8, p. e261, doi. 10.1111/1346-8138.17164
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- Publication type:
- Article
Successful treatment of recurrent subcutaneous abscesses using granulocyte and monocyte adsorptive apheresis.
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- Journal of Dermatology, 2024, v. 51, n. 8, p. e287, doi. 10.1111/1346-8138.17198
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- Publication type:
- Article
Rosemary extract and rosmarinic acid accelerate elastic fiber formation by increasing the expression of elastic fiber components in dermal fibroblasts.
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- Journal of Dermatology, 2024, v. 51, n. 6, p. 816, doi. 10.1111/1346-8138.17185
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- Publication type:
- Article
A case of acute localized exanthematous pustulosis following COVID‐19 infection.
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- Journal of Dermatology, 2024, v. 51, n. 2, p. e37, doi. 10.1111/1346-8138.16983
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- Publication type:
- Article
Rhododendrol‐induced leukoderma update II: Pathophysiology, mechanisms, risk evaluation, and possible mechanism‐based treatments in comparison with vitiligo.
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- Journal of Dermatology, 2021, v. 48, n. 7, p. 969, doi. 10.1111/1346-8138.15878
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- Publication type:
- Article
Rhododendrol‐induced leukoderma update I: Clinical findings and treatment.
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- Journal of Dermatology, 2021, v. 48, n. 7, p. 961, doi. 10.1111/1346-8138.15835
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- Publication type:
- Article
Immunohistopathological observation of a case recovering from leukotrichia after suction blister transplantation.
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- Journal of Dermatology, 2021, v. 48, n. 6, p. e263, doi. 10.1111/1346-8138.15855
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- Publication type:
- Article
Efficient isolation of human metapneumovirus using MNT-1, a human malignant melanoma cell line with early and distinct cytopathic effects.
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- Microbiology & Immunology, 2017, v. 61, n. 11, p. 497, doi. 10.1111/1348-0421.12542
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- Publication type:
- Article
Efficient isolation of human parainfluenza viruses 1 and 3 using MNT-1, a human malignant melanoma cell line system that exhibits an apparent cytopathic effect.
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- Microbiology & Immunology, 2016, v. 60, n. 11, p. 801, doi. 10.1111/1348-0421.12446
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- Publication type:
- Article
Novel AP3B1 mutations in a Hermansky–Pudlak syndrome type2 with neonatal interstitial lung disease.
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- Pediatric Allergy & Immunology, 2022, v. 33, n. 2, p. 1, doi. 10.1111/pai.13748
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- Publication type:
- Article
Linear IgA Bullous Dermatosis in a Pregnant Woman with Autoantibodies to the Non-collagenous 16A Domain of Type XVII Collagen.
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- Acta Dermato-Venereologica, 2017, v. 97, n. 3, p. 404, doi. 10.2340/00015555-2557
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- Publication type:
- Article
Melanotic Malignant Melanoma in Oculocutaneous Albinism Type 4.
- Published in:
- 2017
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- Publication type:
- Case Study
Diacylglycerol Kinase Regulates Tyrosinase Expression and Function in Human Melanocytes.
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- Journal of Investigative Dermatology, 2012, v. 132, n. 12, p. 2791, doi. 10.1038/jid.2012.261
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- Publication type:
- Article
ABCA12 Is a Major Causative Gene for Non-Bullous Congenital Ichthyosiform Erythroderma.
- Published in:
- 2009
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- Publication type:
- Letter
Ten Novel Mutations of the ADAR1 Gene in Japanese Patients with Dyschromatosis Symmetrica Hereditaria.
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- Journal of Investigative Dermatology, 2007, v. 127, n. 2, p. 309, doi. 10.1038/sj.jid.5700528
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- Publication type:
- Article
High Frequency of Hermansky–Pudlak Syndrome Type 1 (HPS1) Among Japanese Albinism Patients and Functional Analysis of HPS1 Mutant Protein.
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- Journal of Investigative Dermatology, 2005, v. 125, n. 4, p. 715, doi. 10.1111/j.0022-202X.2005.23884.x
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- Publication type:
- Article
Five Novel Mutations in Tyrosinase Gene of Japanese and Indian Patients with Oculocutaneous Albinism Type I (OCA1).
- Published in:
- 2005
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- Publication type:
- Letter
Ultrastructural Features of Trafficking Defects Are Pronounced in Melanocytic Nevus in Hermansky–Pudlak Syndrome Type 1.
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- Journal of Investigative Dermatology, 2005, v. 125, n. 1, p. 154, doi. 10.1111/j.0022-202X.2005.23743.x
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- Publication type:
- Article
Mutation Analysis of the ADAR1 Gene in Dyschromatosis Symmetrica Hereditaria and Genetic Differentiation from both Dyschromatosis Universalis Hereditaria and Acropigmentatio Reticularis.
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- Journal of Investigative Dermatology, 2005, v. 124, n. 6, p. 1186, doi. 10.1111/j.0022-202X.2005.23732.x
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- Publication type:
- Article
Analysis ofKIT,SCF, and Initial Screening ofSLUGin Patients with Piebaldism.
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- Journal of Investigative Dermatology, 2005, v. 124, n. 3, p. 670, doi. 10.1111/j.0022-202X.2005.23637.x
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- Publication type:
- Article
Six Novel P Gene Mutations and Oculocutaneous Albinism Type 2 Frequency in Japanese Albino Patients.
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- Journal of Investigative Dermatology, 2003, v. 120, n. 5, p. 781, doi. 10.1046/j.1523-1747.2003.12127.x
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- Publication type:
- Article
Whole-exome sequencing identifies ADAM10 mutations as a cause of reticulate acropigmentation of Kitamura, a clinical entity distinct from Dowling-Degos disease.
- Published in:
- Human Molecular Genetics, 2013, v. 22, n. 17, p. 3524, doi. 10.1093/hmg/ddt207
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- Publication type:
- Article
Pathological Findings of Pemphigus Vulgaris Showing Giant Cobblestone-Like Conjunctival Papillae.
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- Case Reports in Ophthalmology, 2013, v. 4, n. 3, p. 114, doi. 10.1159/000355374
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- Publication type:
- Article
Detection of Minimal Bone Marrow involvement of Blastic Plasmacytoid Dendritic Cell Neoplastic Cells - CD303 immunostaining as a diagnostic tool-.
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- Journal of Clinical & Experimental Hematopathology, 2018, v. 58, n. 1, p. 1, doi. 10.3960/jslrt.17030
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- Publication type:
- Article
Worldwide expert recommendations for the diagnosis and management of vitiligo: Position statement from the international Vitiligo Task Force—Part 2: Specific treatment recommendations.
- Published in:
- Journal of the European Academy of Dermatology & Venereology, 2023, v. 37, n. 11, p. 2185, doi. 10.1111/jdv.19450
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- Publication type:
- Article
Report of two Japanese patients with piebaldism including a novel mutation in KIT.
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- Journal of Dermatology, 2021, v. 48, n. 2, p. e94, doi. 10.1111/1346-8138.15684
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- Publication type:
- Article
Identification of two novel mutations in a Japanese patient with Hermansky–Pudlak syndrome type 5.
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- Journal of Dermatology, 2020, v. 47, n. 11, p. e392, doi. 10.1111/1346-8138.15560
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- Publication type:
- Article
Expression of discoidin domain receptor 1 and E‐cadherin in epidermis affects melanocyte behavior in rhododendrol‐induced leukoderma mouse model.
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- Journal of Dermatology, 2020, v. 47, n. 11, p. 1330, doi. 10.1111/1346-8138.15534
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- Publication type:
- Article
Japanese case of Papillon–Lefèvre syndrome with novel compound heterozygous mutations.
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- Journal of Dermatology, 2020, v. 47, n. 8, p. e293, doi. 10.1111/1346-8138.15412
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- Publication type:
- Article
Case of phaeohyphomycosis caused by Cladophialophora boppii successfully treated with local hyperthermia and systemic terbinafine.
- Published in:
- Journal of Dermatology, 2020, v. 47, n. 7, p. e250, doi. 10.1111/1346-8138.15357
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- Publication type:
- Article