Pigment Cell & Melanoma Research, ISSN 1755-1471, 11/2019, Volume 32, Issue 6, pp. 842 - 847
Multiple reports confirm elevated circulating IL‐17 levels and increased numbers of Th17 lymphocytes in patients with non‐segmental vitiligo. Additionally,...
vitiligo | IL‐17 | Th17 pathway | Vitiligo | Cytokines | Lymphocytes | Medical treatment | Helper cells | Skin | Lymphocytes T | Cell differentiation | Chemokines
vitiligo | IL‐17 | Th17 pathway | Vitiligo | Cytokines | Lymphocytes | Medical treatment | Helper cells | Skin | Lymphocytes T | Cell differentiation | Chemokines
Journal Article
Nature communications, ISSN 2041-1723, 2019, Volume 10, Issue 1, pp. 391 - 10
Vitiligo is an autoimmune disease in which melanocyte destruction causes skin depigmentation, with 49 loci known from previous GWAS. Aiming to define vitiligo...
DISEASES | MULTIDISCIPLINARY SCIENCES | SUSCEPTIBILITY LOCI | DNA ELEMENTS | RISK | PREVALENCE | GENOME-WIDE ASSOCIATION | Haplotypes | Dendritic cells | Health risks | mRNA | Gene expression | Loci | Subgroups | Proteins | Monocytes | Vitiligo | Enhancers | Major histocompatibility complex | Histocompatibility antigen HLA | Variation | Autoimmune diseases | Age
DISEASES | MULTIDISCIPLINARY SCIENCES | SUSCEPTIBILITY LOCI | DNA ELEMENTS | RISK | PREVALENCE | GENOME-WIDE ASSOCIATION | Haplotypes | Dendritic cells | Health risks | mRNA | Gene expression | Loci | Subgroups | Proteins | Monocytes | Vitiligo | Enhancers | Major histocompatibility complex | Histocompatibility antigen HLA | Variation | Autoimmune diseases | Age
Journal Article
FRONTIERS IN IMMUNOLOGY, ISSN 1664-3224, 08/2019, Volume 10, p. 1918
The impressive potential of biologics has been demonstrated in psoriasis, hidradenitis suppurativa, and urticaria. Numerous biologicals are entering the field...
CD20 | biologics | TNF-alpha | IL-1 | IgE | SWEET SYNDROME | LUPUS-ERYTHEMATOSUS | IMMUNOLOGY | IL-12 | IL-23 | RECEPTOR ANTAGONIST | IGE AUTOANTIBODIES | ALOPECIA-AREATA | PYODERMA-GANGRENOSUM | DOUBLE-BLIND | CASE SERIES | HIDRADENITIS SUPPURATIVA | off-label | Omalizumab | Skin diseases | Usage | Care and treatment | Biological products | Risk factors | Psoriasis | Drug therapy | TNF-α
CD20 | biologics | TNF-alpha | IL-1 | IgE | SWEET SYNDROME | LUPUS-ERYTHEMATOSUS | IMMUNOLOGY | IL-12 | IL-23 | RECEPTOR ANTAGONIST | IGE AUTOANTIBODIES | ALOPECIA-AREATA | PYODERMA-GANGRENOSUM | DOUBLE-BLIND | CASE SERIES | HIDRADENITIS SUPPURATIVA | off-label | Omalizumab | Skin diseases | Usage | Care and treatment | Biological products | Risk factors | Psoriasis | Drug therapy | TNF-α
Journal Article
Nature Communications, ISSN 2041-1723, 2019, Volume 10, Issue 1
Vitiligo is an autoimmune disease in which melanocyte destruction causes skin depigmentation, with 49 loci known from previous GWAS. Aiming to define vitiligo...
Journal Article
04/2018, ISBN 9781118937419, 536
eBook
Journal of the American Academy of Dermatology, ISSN 0190-9622, 05/2018, Volume 78, Issue 5, pp. 1013 - 1015
Journal Article
Journal of the American Academy of Dermatology, ISSN 0190-9622, 10/2019
Journal Article
Journal of Investigative Dermatology, ISSN 0022-202X, 01/2016, Volume 136, Issue 1, pp. 6 - 7
The impact of vitiligo is generally believed to be underestimated. Salzes et al. propose a questionnaire to measure the actual burden of vitiligo. Using a...
Sickness Impact Profile | Vitiligo - psychology | Humans | Female | Male | Surveys and Questionnaires | Quality of Life - psychology | INSTRUMENT | PSORIASIS | DERMATOLOGY
Sickness Impact Profile | Vitiligo - psychology | Humans | Female | Male | Surveys and Questionnaires | Quality of Life - psychology | INSTRUMENT | PSORIASIS | DERMATOLOGY
Journal Article
American Journal of Clinical Dermatology, ISSN 1175-0561, 10/2018, Volume 19, Issue 5, pp. 625 - 637
New promising treatments have been developed for psoriasis that target different parts of the interleukin (IL)-23/IL-17 pathway. This approach is believed to...
CONTROLLED-TRIAL | EXPERIMENTAL AUTOIMMUNE ENCEPHALOMYELITIS | TUMOR-NECROSIS-FACTOR | DUAL INHIBITION | IFN-GAMMA | SEVERE PLAQUE PSORIASIS | ARTHRITIS PATIENTS | HOST-DEFENSE | EPIDERMAL HYPERPLASIA | T-CELLS | DERMATOLOGY
CONTROLLED-TRIAL | EXPERIMENTAL AUTOIMMUNE ENCEPHALOMYELITIS | TUMOR-NECROSIS-FACTOR | DUAL INHIBITION | IFN-GAMMA | SEVERE PLAQUE PSORIASIS | ARTHRITIS PATIENTS | HOST-DEFENSE | EPIDERMAL HYPERPLASIA | T-CELLS | DERMATOLOGY
Journal Article
Journal of the American Academy of Dermatology, ISSN 0190-9622, 2018, Volume 79, Issue 2, pp. 369 - 371
Journal Article
Lancet, The, ISSN 0140-6736, 2015, Volume 386, Issue 9988, pp. 74 - 84
Summary Vitiligo, an acquired pigmentary disorder of unknown origin, is the most frequent cause of depigmentation worldwide, with an estimated prevalence of...
Internal Medicine | CHILDHOOD VITILIGO | IMMUNE-RESPONSE | MEDICINE, GENERAL & INTERNAL | DEPIGMENTATION THERAPY | GENERALIZED VITILIGO | INCREASED SENSITIVITY | SUSCEPTIBILITY LOCI | QUALITY-OF-LIFE | KOEBNERS PHENOMENON | HUMAN MELANOCYTES | T-CELLS | Phototherapy - methods | Vitiligo - diagnosis | Vitiligo - therapy | Vitiligo - psychology | Humans | Vitiligo - immunology | Dermatologic Agents - therapeutic use | Vitiligo - epidemiology | Mental Disorders - etiology | Skin | Vitiligo | Pathogenesis | Classification | Epidemiology | Patients | Age
Internal Medicine | CHILDHOOD VITILIGO | IMMUNE-RESPONSE | MEDICINE, GENERAL & INTERNAL | DEPIGMENTATION THERAPY | GENERALIZED VITILIGO | INCREASED SENSITIVITY | SUSCEPTIBILITY LOCI | QUALITY-OF-LIFE | KOEBNERS PHENOMENON | HUMAN MELANOCYTES | T-CELLS | Phototherapy - methods | Vitiligo - diagnosis | Vitiligo - therapy | Vitiligo - psychology | Humans | Vitiligo - immunology | Dermatologic Agents - therapeutic use | Vitiligo - epidemiology | Mental Disorders - etiology | Skin | Vitiligo | Pathogenesis | Classification | Epidemiology | Patients | Age
Journal Article
Journal of the American Academy of Dermatology, ISSN 0190-9622, 03/2017, Volume 76, Issue 3, pp. 464 - 471
Background The Vitiligo Extent Score (VES) has recently been introduced as a physicians' score for the clinical assessment of the extent of vitiligo, but a...
severity | patient-reported outcomes | Dermatology | outcome measurement | vitiligo | body surface area
severity | patient-reported outcomes | Dermatology | outcome measurement | vitiligo | body surface area
Journal Article
American journal of clinical dermatology, 12/2017, Volume 18, Issue 6, p. 733
The pathophysiology of vitiligo is becoming increasingly clarified. In non-segmental vitiligo, early factors include activation of innate immunity,...
Lasers, Excimer | Vitiligo - therapy | Photosensitizing Agents - therapeutic use | Humans | Immunosuppressive Agents - therapeutic use | Skin Pigmentation | Combined Modality Therapy | Plant Extracts - therapeutic use | Vitiligo - physiopathology | Phototherapy
Lasers, Excimer | Vitiligo - therapy | Photosensitizing Agents - therapeutic use | Humans | Immunosuppressive Agents - therapeutic use | Skin Pigmentation | Combined Modality Therapy | Plant Extracts - therapeutic use | Vitiligo - physiopathology | Phototherapy
Journal Article
Pigment Cell and Melanoma Research, ISSN 1755-1471, 06/2011, Volume 24, Issue 3, pp. 564 - 573
P>Koebner's phenomenon (KP) has been observed in a number of skin diseases, including vitiligo. Its clinical significance in vitiligo with respect to disease...
Vitiligo | Pathogenesis | Koebner's phenomenon | Melanocytorrhagy | Isomorphic response | Review | Trauma | trauma | DENDRITIC CELLS | vitiligo | HUMAN MELANOCYTES | isomorphic response | DISEASE-ACTIVITY | REPIGMENTATION | CELL BIOLOGY | DERMATOLOGY | pathogenesis | IN-VITRO | GENERALIZED VITILIGO | melanocytorrhagy | review | SKIN | T-CELLS | PSORIASIS | Vitiligo - therapy | Animals | Vitiligo - pathology | Humans | Chronic Disease | Vitiligo - metabolism | Vitiligo - physiopathology | Skin diseases
Vitiligo | Pathogenesis | Koebner's phenomenon | Melanocytorrhagy | Isomorphic response | Review | Trauma | trauma | DENDRITIC CELLS | vitiligo | HUMAN MELANOCYTES | isomorphic response | DISEASE-ACTIVITY | REPIGMENTATION | CELL BIOLOGY | DERMATOLOGY | pathogenesis | IN-VITRO | GENERALIZED VITILIGO | melanocytorrhagy | review | SKIN | T-CELLS | PSORIASIS | Vitiligo - therapy | Animals | Vitiligo - pathology | Humans | Chronic Disease | Vitiligo - metabolism | Vitiligo - physiopathology | Skin diseases
Journal Article
Pigment Cell and Melanoma Research, ISSN 1755-1471, 2019, Volume 32, Issue 5, pp. 728 - 733
Currently, vitiligo lacks a validated Physician Global Assessment (PGA) for disease extent. This PGA can be used to stratify and interpret the numeric scores...
Journal Article
American Journal of Clinical Dermatology, ISSN 1175-0561, 12/2017, Volume 18, Issue 6, pp. 733 - 744
The pathophysiology of vitiligo is becoming increasingly clarified. In non-segmental vitiligo, early factors include activation of innate immunity,...
NARROW-BAND-UVB | GENERALIZED VITILIGO | DOUBLE-BLIND | SUSCEPTIBILITY LOCI | TERM-FOLLOW-UP | TOPICAL TACROLIMUS | TACROLIMUS OINTMENT | NON-SEGMENTAL VITILIGO | DISEASE-ACTIVITY | B PHOTOTHERAPY | DERMATOLOGY
NARROW-BAND-UVB | GENERALIZED VITILIGO | DOUBLE-BLIND | SUSCEPTIBILITY LOCI | TERM-FOLLOW-UP | TOPICAL TACROLIMUS | TACROLIMUS OINTMENT | NON-SEGMENTAL VITILIGO | DISEASE-ACTIVITY | B PHOTOTHERAPY | DERMATOLOGY
Journal Article
Melanoma Research, ISSN 0960-8931, 07/2015, Volume 25, Issue 4, pp. 357 - 361
Interferon-α (IFN-α) is the only approved adjuvant treatment for high-risk melanoma patients in Europe, but the impact on overall survival is low. Although it...
melanoma | negative feedback mechanism | indoleamine 2,3-dioxygenase | programmed-death ligand-1 | adjuvant interferon-α | Indoleamine-Pyrrole 2,3,-Dioxygenase - biosynthesis | T-Lymphocytes, Cytotoxic - immunology | Indoleamine-Pyrrole 2,3,-Dioxygenase - blood | Skin Neoplasms - drug therapy | Skin Neoplasms - immunology | Dendritic Cells - immunology | Europe | Humans | Middle Aged | Interferon-alpha - therapeutic use | Male | CTLA-4 Antigen - biosynthesis | Indoleamine-Pyrrole 2,3,-Dioxygenase - immunology | T-Lymphocytes, Regulatory - immunology | Flow Cytometry | Melanoma - immunology | Myeloid Cells - immunology | B7-H1 Antigen - biosynthesis | Leukocytes, Mononuclear - immunology | Melanoma - drug therapy | Adult | Female | Aged | Neoplasm Staging
melanoma | negative feedback mechanism | indoleamine 2,3-dioxygenase | programmed-death ligand-1 | adjuvant interferon-α | Indoleamine-Pyrrole 2,3,-Dioxygenase - biosynthesis | T-Lymphocytes, Cytotoxic - immunology | Indoleamine-Pyrrole 2,3,-Dioxygenase - blood | Skin Neoplasms - drug therapy | Skin Neoplasms - immunology | Dendritic Cells - immunology | Europe | Humans | Middle Aged | Interferon-alpha - therapeutic use | Male | CTLA-4 Antigen - biosynthesis | Indoleamine-Pyrrole 2,3,-Dioxygenase - immunology | T-Lymphocytes, Regulatory - immunology | Flow Cytometry | Melanoma - immunology | Myeloid Cells - immunology | B7-H1 Antigen - biosynthesis | Leukocytes, Mononuclear - immunology | Melanoma - drug therapy | Adult | Female | Aged | Neoplasm Staging
Journal Article
American journal of clinical dermatology, 10/2018, Volume 19, Issue 5, p. 625
New promising treatments have been developed for psoriasis that target different parts of the interleukin (IL)-23/IL-17 pathway. This approach is believed to...
Psoriasis - immunology | Severity of Illness Index | Psoriasis - drug therapy | Humans | Immunosuppressive Agents - therapeutic use | Psoriasis - diagnosis | Receptors, Interleukin-17 - immunology | Interleukin-17 - immunology | Treatment Outcome | Receptors, Interleukin-17 - antagonists & inhibitors | Molecular Targeted Therapy | Interleukin-23 - immunology | Patient Selection | Interleukin-17 - metabolism | Signal Transduction - immunology | Interleukin-23 - metabolism | Interleukin-17 - antagonists & inhibitors | Signal Transduction - drug effects | Interleukin-23 - antagonists & inhibitors | Receptors, Interleukin-17 - metabolism | Immunosuppressive Agents - pharmacology
Psoriasis - immunology | Severity of Illness Index | Psoriasis - drug therapy | Humans | Immunosuppressive Agents - therapeutic use | Psoriasis - diagnosis | Receptors, Interleukin-17 - immunology | Interleukin-17 - immunology | Treatment Outcome | Receptors, Interleukin-17 - antagonists & inhibitors | Molecular Targeted Therapy | Interleukin-23 - immunology | Patient Selection | Interleukin-17 - metabolism | Signal Transduction - immunology | Interleukin-23 - metabolism | Interleukin-17 - antagonists & inhibitors | Signal Transduction - drug effects | Interleukin-23 - antagonists & inhibitors | Receptors, Interleukin-17 - metabolism | Immunosuppressive Agents - pharmacology
Journal Article
European Journal of Dermatology, ISSN 1167-1122, 01/2013, Volume 23, Issue 1, pp. 33 - 39
Background: Pemphigus is a potentially life-threatening auto-immune blistering disease and consequently it is important to monitor disease activity....
Dsg1 | Pemphigus vulgaris | Dsg3 | ELISA | Pemphigus foliaceus | AUTOANTIBODIES | ANTIBODIES | pemphigus foliaceus | PHAGE DISPLAY | RECOMBINANT DESMOGLEINS | DERMATOLOGY | pemphigus vulgaris | DISEASE | VULGARIS | CLINICAL PHENOTYPE | Severity of Illness Index | Desmoglein 3 - immunology | Predictive Value of Tests | Confidence Intervals | Prospective Studies | Enzyme-Linked Immunosorbent Assay | Immunoglobulin G - blood | Autoantibodies - blood | Humans | Middle Aged | Desmoglein 1 - immunology | Male | Time Factors | Adult | Female | Pemphigus - immunology | ROC Curve | Aged | Longitudinal Studies
Dsg1 | Pemphigus vulgaris | Dsg3 | ELISA | Pemphigus foliaceus | AUTOANTIBODIES | ANTIBODIES | pemphigus foliaceus | PHAGE DISPLAY | RECOMBINANT DESMOGLEINS | DERMATOLOGY | pemphigus vulgaris | DISEASE | VULGARIS | CLINICAL PHENOTYPE | Severity of Illness Index | Desmoglein 3 - immunology | Predictive Value of Tests | Confidence Intervals | Prospective Studies | Enzyme-Linked Immunosorbent Assay | Immunoglobulin G - blood | Autoantibodies - blood | Humans | Middle Aged | Desmoglein 1 - immunology | Male | Time Factors | Adult | Female | Pemphigus - immunology | ROC Curve | Aged | Longitudinal Studies
Journal Article
20.
Full Text
Clinical Significance of Serum Soluble CD Molecules to Assess Disease Activity in Vitiligo
JAMA Dermatology, ISSN 2168-6068, 11/2016, Volume 152, Issue 11, pp. 1194 - 1200
IMPORTANCE: It is difficult to determine disease activity in vitiligo owing to the absence of inflammatory signs, such as erythema or scaling. A biomarker that...
GAMMA | CXCL10 | CELLS | ACTIVATION | SKIN | EXPRESSION | DERMATOLOGY | Predictive Value of Tests | Vitiligo - diagnosis | Prospective Studies | Cross-Sectional Studies | Interleukin-2 Receptor alpha Subunit - blood | CD40 Ligand - blood | Humans | Middle Aged | Hospitals, University | Male | Biomarkers - blood | Tumor Necrosis Factor Receptor Superfamily, Member 7 - blood | Disease Progression | Vitiligo - blood | Sensitivity and Specificity | Adult | Female | Vitiligo | Usage | Interleukin-2 | Development and progression | Diagnosis | Research | Biological markers
GAMMA | CXCL10 | CELLS | ACTIVATION | SKIN | EXPRESSION | DERMATOLOGY | Predictive Value of Tests | Vitiligo - diagnosis | Prospective Studies | Cross-Sectional Studies | Interleukin-2 Receptor alpha Subunit - blood | CD40 Ligand - blood | Humans | Middle Aged | Hospitals, University | Male | Biomarkers - blood | Tumor Necrosis Factor Receptor Superfamily, Member 7 - blood | Disease Progression | Vitiligo - blood | Sensitivity and Specificity | Adult | Female | Vitiligo | Usage | Interleukin-2 | Development and progression | Diagnosis | Research | Biological markers
Journal Article
No results were found for your search.
Cannot display more than 1000 results, please narrow the terms of your search.