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1. Full Text Behçet’s disease physiopathology: a contemporary review
by Zeidan, Mohamad J and Saadoun, David and Garrido, Marlene and Klatzmann, David and Six, Adrien and Cacoub, Patrice
Autoimmunity Highlights, ISSN 2038-0305, 12/2016, Volume 7, Issue 1, pp. 1 - 12
Behçet’s disease, also known as the Silk Road Disease, is a rare systemic vasculitis disorder of unknown etiology. Recurrent attacks of acute inflammation... 
Autoimmunity | Inflammation | Biomedicine | Immunology | Behçet disease | Physiopathology | Clinical aspects | Vasculitis | Etiology | Ulcers | Central nervous system | Skin diseases | Gastrointestinal tract | Systemic vasculitis | Morbidity | Life Sciences | Human health and pathology
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2. Full Text The Phenotype and Genotype of Mevalonate Kinase Deficiency: A Series of 114 Cases From the Eurofever Registry
by Haar, N. Ter and Jeyaratnam, J and Lachmann, H.J and Simon, A and Brogan, P.A and Doglio, M and Cattalini, M and Anton, J and Modesto, C and Quartier, P and Hoppenreijs, E.P and Martino, S and Insalaco, A and Cantarini, L and Lepore, L and Alessio, M and Calvo Penades, I and Boros, C and Consolini, R and Rigante, D and Russo, R and Pachlopnik Schmid, J and Lane, T and Martini, A and Ruperto, N and Frenkel, J and Gattorno, M and Paediat Rheumatology Int Trials and Paediatric Rheumatology International Trials Organisation and Eurofever Project
Arthritis & Rheumatology, ISSN 2326-5191, 2016, Volume 68, Issue 11, pp. 2795 - 2805
ObjectiveMevalonate kinase deficiency (MKD) is a rare metabolic disease characterized by recurrent inflammatory episodes. This study was undertaken to describe... 
MVK | HYPER-IGD | PERIODIC FEVER SYNDROME | ACIDURIA | HYPERIMMUNOGLOBULINEMIA-D | AUTOINFLAMMATORY DISEASES | MUTATIONS | SPECTRUM | RHEUMATOLOGY | Arthralgia - etiology | Uveitis - etiology | Humans | Child, Preschool | Lymphadenopathy - etiology | Male | Arthralgia - physiopathology | Arthritis - genetics | Stomatitis, Aphthous - genetics | Cerebellar Diseases - physiopathology | Amyloidosis - genetics | Skin Diseases - physiopathology | Amyloidosis - etiology | Child | Stomatitis, Aphthous - etiology | Infant, Newborn | Myalgia - physiopathology | Amyloidosis - physiopathology | Genotype | Headache - physiopathology | Vomiting - genetics | Phenotype | Diarrhea - genetics | Abdominal Pain - genetics | Adolescent | Age of Onset | Intellectual Disability - etiology | Uveitis - genetics | Vomiting - physiopathology | Conjunctivitis - etiology | Conjunctivitis - genetics | Arthritis - physiopathology | Headache - etiology | Skin Diseases - genetics | Mevalonate Kinase Deficiency - physiopathology | Myalgia - genetics | Cerebellar Diseases - etiology | Diarrhea - physiopathology | Infant | Mevalonate Kinase Deficiency - genetics | Intellectual Disability - genetics | Pharyngitis - genetics | Arthritis - etiology | Female | Registries | Retrospective Studies | Arthralgia - genetics | Pharyngitis - physiopathology | Abdominal Pain - etiology | Pharyngitis - etiology | Lymphadenopathy - genetics | Abdominal Pain - physiopathology | Myalgia - etiology | Phosphotransferases (Alcohol Group Acceptor) - genetics | Headache - genetics | Intellectual Disability - physiopathology | Skin Diseases - etiology | Cerebellar Diseases - genetics | Conjunctivitis - physiopathology | Mevalonate Kinase Deficiency - complications | Stomatitis, Aphthous - physiopathology | Vomiting - etiology | Diarrhea - etiology | Lymphadenopathy - physiopathology | Uveitis - physiopathology | Kinases | Genotype & phenotype | Index Medicus | Abridged Index Medicus
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3. Skin pharmacology and physiology
Skin pharmacology and physiology, ISSN 1660-5535, 2004
Dermatopharmacology | Skin | Physiology | Diseases
Journal
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4. Full Text Clinical manifestations of Behçet's disease depending on sex and age: Results from Japanese nationwide registration
by Ishido, Takehito and Horita, Nobuyuki and Takeuchi, Masaki and Kawagoe, Tatsukata and Shibuya, Etsuko and Yamane, Takahiro and Hayashi, Takahiko and Meguro, Akira and Ishido, Mizuho and Minegishi, Kaoru and Yoshimi, Ryusuke and Kirino, Yohei and Kato, Shingo and Arimoto, Jun and Ishigatsubo, Yoshiaki and Takeno, Mitsuhiro and Kurosawa, Michiko and Kaneko, Takeshi and Mizuki, Nobuhisa
Rheumatology (United Kingdom), ISSN 1462-0324, 2017, Volume 56, Issue 11, pp. 1918 - 1927
Objective. This report aimed to scrutinize the prevalence of Behcet's disease (BD)-related clinical manifestations based on age- and sex-specific subgroups... 
Behçet's syndrome | Surveys and questionnaires | Diagnosis | Epidemiology | Behcet's syndrome | SYSTEMIC-LUPUS-ERYTHEMATOSUS | METAANALYSIS | INVOLVEMENT | SUSCEPTIBILITY LOCI | diagnosis | RISK | RHEUMATOLOGY | FEATURES | epidemiology | SERUM PROLACTIN LEVELS | surveys and questionnaires | ONSET | GENOME-WIDE ASSOCIATION | Epididymitis - etiology | Genital Diseases, Male - physiopathology | Arthritis - physiopathology | Genital Diseases, Female - etiology | Epididymitis - physiopathology | Age Factors | Gastrointestinal Diseases - physiopathology | Vascular Diseases - etiology | Behcet Syndrome - physiopathology | Genital Diseases, Male - etiology | Humans | Middle Aged | Gastrointestinal Diseases - etiology | Genital Diseases, Female - physiopathology | Male | Oral Ulcer - etiology | Skin Ulcer - etiology | Young Adult | Arthritis - etiology | Adult | Female | Registries | Nervous System Diseases - physiopathology | Odds Ratio | Child | Databases, Factual | Skin Ulcer - physiopathology | Japan | Behcet Syndrome - complications | Eye Diseases - etiology | HLA-B51 Antigen - genetics | Oral Ulcer - physiopathology | Vascular Diseases - physiopathology | Phenotype | Adolescent | Sex Factors | Nervous System Diseases - etiology | Aged | Behcet Syndrome - genetics | Eye Diseases - physiopathology | Index Medicus | Abridged Index Medicus
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5. Full Text Global ethnic and geographic differences in the clinical presentations of anti-neutrophil cytoplasm antibody-associated vasculitis
by Pearce, Fiona A and Craven, Anthea and Merkel, Peter A and Luqmani, Raashid A and Watts, Richard A
Rheumatology (United Kingdom), ISSN 1462-0324, 2017, Volume 56, Issue 11, pp. 1962 - 1969
Objectives. There are few data on clinical profiles of ANCA-associated vasculitis (AAV) in different ethnic populations. The aim of this study was to examine... 
MPO-ANCA | PR3-ANCA | ANCA-vasculitis | Epidemiology | POLYANGIITIS | epidemiology | SYSTEMIC VASCULITIS | ALLELES | ANCA-ASSOCIATED VASCULITIS | CLASSIFICATION | GRANULOMATOSIS | RHEUMATOLOGY | Kidney Diseases - physiopathology | Japan - epidemiology | United States - epidemiology | Male Urogenital Diseases - physiopathology | Humans | Middle Aged | Anti-Neutrophil Cytoplasmic Antibody-Associated Vasculitis - physiopathology | Female Urogenital Diseases - etiology | Arabs | Male | Anti-Neutrophil Cytoplasmic Antibody-Associated Vasculitis - ethnology | Antibodies, Antineutrophil Cytoplasmic - immunology | Anti-Neutrophil Cytoplasmic Antibody-Associated Vasculitis - complications | Skin Diseases - physiopathology | Female | Otorhinolaryngologic Diseases - physiopathology | Nervous System Diseases - physiopathology | Odds Ratio | Otorhinolaryngologic Diseases - etiology | Female Urogenital Diseases - physiopathology | Peroxidase - immunology | Heart Diseases - physiopathology | Myeloblastin - immunology | Eye Diseases - etiology | Europe - epidemiology | India - epidemiology | European Continental Ancestry Group | China - epidemiology | Skin Diseases - etiology | Male Urogenital Diseases - etiology | Middle East - epidemiology | Asian Continental Ancestry Group | Heart Diseases - etiology | Respiratory Tract Diseases - etiology | Anti-Neutrophil Cytoplasmic Antibody-Associated Vasculitis - immunology | Turkey - epidemiology | Nervous System Diseases - etiology | Respiratory Tract Diseases - physiopathology | Aged | Kidney Diseases - etiology | Eye Diseases - physiopathology | Index Medicus | Abridged Index Medicus
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6. Handbook of hair in health and disease
by Preedy, Victor R
2012, Human health handbooks, ISBN 9789086861743, Volume no. 1, 493
This handbook examines hair in health and disease. It provides an insight into hair growth and loss, molecular and cellular biology of hair, dietary toxicity... 
Hair | Hair Diseases | Diseases | Handbooks, manuals, etc | Care and hygiene
Book
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7. Full Text Phenotypes of organ involvement in sarcoidosis
by Schupp, Jonas Christian and Freitag-Wolf, Sandra and Bargagli, Elena and Mihailović-Vučinić, Violeta and Rottoli, Paola and Grubanovic, Aleksandar and Müller, Annegret and Jochens, Arne and Tittmann, Lukas and Schnerch, Jasmin and Olivieri, Carmela and Fischer, Annegret and Jovanovic, Dragana and Filipovic, Snežana and Videnovic-Ivanovic, Jelica and Bresser, Paul and Jonkers, René and O’Reilly, Kate and Ho, Ling-Pei and Gaede, Karoline I and Zabel, Peter and Dubaniewicz, Anna and Marshall, Ben and Kieszko, Robert and Milanowski, Janusz and Günther, Andreas and Weihrich, Anette and Petrek, Martin and Kolek, Vitezslav and Keane, Michael P and O’Beirne, Sarah and Donnelly, Seamas and Haraldsdottir, Sigridur Olina and Jorundsdottir, Kristin B and Costabel, Ulrich and Bonella, Francesco and Wallaert, Benoît and Grah, Christian and Peroš-Golubičić, Tatjana and Luisetti, Mauritio and Kadija, Zamir and Pabst, Stefan and Grohé, Christian and Strausz, János and Vašáková, Martina and Sterclova, Martina and Millar, Ann and Homolka, Jiří and Slováková, Alena and Kendrick, Yvonne and Crawshaw, Anjali and Wuyts, Wim and Spencer, Lisa and Pfeifer, Michael and Valeyre, Dominique and Poletti, Venerino and Wirtz, Hubertus and Prasse, Antje and Schreiber, Stefan and Krawczak, Michael and Müller-Quernheim, Joachim
European Respiratory Journal, ISSN 0903-1936, 01/2018, Volume 51, Issue 1, pp. 1700991 - 1700991
Sarcoidosis is a highly variable, systemic granulomatous disease of hitherto unknown aetiology. The GenPhenReSa (Genotype-Phenotype Relationship in... 
INSTRUMENT | INFLAMMATORY-BOWEL-DISEASE | RESPIRATORY SYSTEM | JAPAN | RISK | COHORT | PREVALENCE | EPIDEMIOLOGY | Sarcoidosis - diagnosis | Acute Disease | Europe | Humans | Middle Aged | European Continental Ancestry Group | Genotype | Male | Lung - physiopathology | Tertiary Healthcare | Lymph Nodes - physiopathology | Abdomen | Forced Expiratory Volume | Phenotype | Sarcoidosis - physiopathology | Skin Diseases - physiopathology | Adult | Female | Aged | Lung Diseases - physiopathology | Skin - physiopathology | Eye Diseases - physiopathology | Eye - physiopathology | Joint Diseases - physiopathology | Phenotypes | Sarcoidosis | Central nervous system | Fatigue | Skin | Heart diseases | Genotypes | Lymph nodes | Index Medicus
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8. Skin
: a natural history
by Jablonski, Nina G
2006, 1, ISBN 9780520242814, xiii, 266 p., [12] p. of plates
We expose it, cover it, paint it, tattoo it, scar it, and pierce it. Our intimate connection with the world, skin protects us while advertising our health, our... 
Skin | Anthropology | Social sciences | Publicaciones periodicas | Ciencias sociales | Articulos | Publicaciones periódicas | Periodicals | Libros electronicos | Artículos
Book
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9. Full Text Digital ulcers predict a worse disease course in patients with systemic sclerosis
by Mihai, Carina and Landewé, Robert and van der Heijde, Désirée and Walker, Ulrich A and Constantin, Paul I and Gherghe, Ana Maria and Ionescu, Ruxandra and Rednic, Simona and Allanore, Yannick and Avouac, Jérôme and Czirják, László and Hachulla, Eric and Riemekasten, Gabriela and Cozzi, Franco and Airò, Paolo and Cutolo, Maurizio and Mueller-Ladner, Ulf and Matucci-Cerinic, Marco and EUSTAR and EUSTAR co-authors
Annals of the Rheumatic Diseases, ISSN 0003-4967, 04/2016, Volume 75, Issue 4, pp. 681 - 686
ObjectiveSystemic sclerosis (SSc) is a systemic autoimmune disease with high morbidity and significant mortality. There is a great need of predictors that... 
ORGAN INVOLVEMENT | RISK-FACTORS | DATABASE | 5-YEAR SURVIVAL | COHORT | MODEL | RHEUMATOLOGY | EULAR SCLERODERMA TRIALS | LESIONS | Care and treatment | Usage | Systemic scleroderma | Mortality | Analysis | Scleroderma (Disease) | Ultrasonic waves | Outcome and process assessment (Health Care) | Hypertension | Studies | Heart failure | Ultrasonic imaging | Medical prognosis | Clinical medicine | Scleroderma | Patients | Data bases | Index Medicus
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10. Full Text Development of an Autoimmune Syndrome Affecting the Skin and Internal Organs in P‐Selectin Glycoprotein Ligand 1 Leukocyte Receptor–Deficient Mice
by Pérez‐Frías, A and González‐Tajuelo, R and Núñez‐Andrade, N and Tejedor, R and García‐Blanco, M. J and Vicente‐Rabaneda, E and Castañeda, S and Gamallo, C and Silván, J and Esteban‐Villafruela, A and Cubero‐Rueda, L and García‐García, C and Muñoz‐Calleja, C and García‐Diez, A and Urzainqui, A
Arthritis & Rheumatology, ISSN 2326-5191, 11/2014, Volume 66, Issue 11, pp. 3178 - 3189
Objective. To define and characterize the progression of the spontaneous autoimmune disease that develops in mice in the absence of the leukocyte adhesion... 
6-SULFO LACNAC | DENDRITIC CELLS | SPECIALIZED FORM | INFLAMMATION | REGULATORY T-CELLS | ANIMAL-MODEL | PSGL-1 | RHEUMATOLOGY | STEM-CELL TRANSPLANTATION | SYSTEMIC-SCLEROSIS | EPIDEMIOLOGY | Kidney Diseases - physiopathology | Autoimmune Diseases - physiopathology | Autoantibodies - metabolism | Prevalence | Connective Tissue Diseases - epidemiology | Kidney - pathology | Scleroderma, Systemic - pathology | Male | Membrane Glycoproteins - physiology | Fibrosis - epidemiology | Kidney Diseases - epidemiology | Scleroderma, Systemic - physiopathology | Skin Diseases - physiopathology | Female | Lung Diseases, Interstitial - physiopathology | Skin Diseases - epidemiology | Autoimmune Diseases - pathology | Kidney - physiopathology | Lung Diseases, Interstitial - epidemiology | Skin - pathology | Disease Models, Animal | Connective Tissue Diseases - physiopathology | Lung - pathology | Fibrosis - physiopathology | Mice, Inbred C57BL | Lung - physiopathology | Membrane Glycoproteins - genetics | Mice, Knockout | Animals | Mice | Skin - physiopathology | Membrane Glycoproteins - deficiency | Ligands | Autoimmune diseases | Rodents | Immune system | Index Medicus | Abridged Index Medicus
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11. Full Text Climacteric symptoms in middle-aged women with chronic somatic diseases
by Katainen, Riina E and Engblom, Janne R and Siirtola, Tiina J and Erkkola, Risto U and Polo-Kantola, Päivi
Maturitas, ISSN 0378-5122, 2016, Volume 86, pp. 17 - 24
Highlights • This cross-sectional study included 3421 women, aged 41–54. • We studied associations between chronic diseases and climacteric symptoms. • We used... 
Internal Medicine | Obstetrics and Gynecology | Climacteric | Middle-age | Medical condition | Menopausal symptoms | Menopause | Quality of life | RISK-FACTORS | COGNITIVE IMPAIRMENT | DEPRESSIVE SYMPTOMS | PREVALENCE | NIGHT SWEATS | GERIATRICS & GERONTOLOGY | OBSTETRICS & GYNECOLOGY | DIABETES-MELLITUS | PSYCHIATRIC-DISORDERS | QUALITY-OF-LIFE | HEALTH | HOT FLASHES | Urologic Diseases - psychology | Gastrointestinal Diseases - physiopathology | Humans | Middle Aged | Musculoskeletal Diseases - physiopathology | Nervous System Diseases - psychology | Menopause - psychology | Depression - etiology | Skin Diseases - psychology | Vasomotor System - physiopathology | Cognition Disorders - etiology | Skin Diseases - physiopathology | Adult | Female | Surveys and Questionnaires | Nervous System Diseases - physiopathology | Neoplasms - physiopathology | Urologic Diseases - physiopathology | Sleep Wake Disorders - etiology | Cardiovascular Diseases - physiopathology | Cross-Sectional Studies | Gastrointestinal Diseases - psychology | Aging - psychology | Lung Diseases - psychology | Neoplasms - psychology | Diabetes Mellitus - physiopathology | Sexuality | Cardiovascular Diseases - psychology | Lung Diseases - physiopathology | Musculoskeletal Diseases - psychology | Chronic Disease | Menopause - physiology | Anxiety - etiology | Diabetes Mellitus - psychology | Women | Chronic diseases | Analysis | Index Medicus
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12. Skin pharmacology and applied skin physiology
Skin pharmacology and applied skin physiology, ISSN 1422-2906, 1998
Periodicals | Dermatopharmacology | Skin | Physiology | Diseases
Journal
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13. Full Text Global Skin Disease Morbidity and Mortality: An Update From the Global Burden of Disease Study 2013
by Karimkhani, Chante and Dellavalle, Robert P and Coffeng, Luc E and Flohr, Carsten and Hay, Roderick J and Langan, Sinéad M and Nsoesie, Elaine O and Ferrari, Alize J and Erskine, Holly E and Silverberg, Jonathan I and Vos, Theo and Naghavi, Mohsen
JAMA Dermatology, ISSN 2168-6068, 05/2017, Volume 153, Issue 5, pp. 406 - 412
IMPORTANCE: Disability secondary to skin conditions is substantial worldwide. The Global Burden of Disease Study 2013 includes estimates of global morbidity... 
INJURIES | HEALTH | LIFE YEARS DALYS | METRICS | DERMATOLOGY | Quality-Adjusted Life Years | Prevalence | Global Health | Humans | Middle Aged | Child, Preschool | Infant | Male | Young Adult | Global Burden of Disease | Adolescent | Bayes Theorem | Skin Diseases - physiopathology | Aged, 80 and over | Adult | Disabled Persons - statistics & numerical data | Female | Aged | Skin Diseases - epidemiology | Child | Infant, Newborn | Skin Diseases - mortality | Index Medicus | Abridged Index Medicus | Online First | Original Investigation | Research
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14. Full Text Anti-TNF antibody-induced psoriasiform skin lesions in patients with inflammatory bowel disease are characterised by interferon-γ-expressing Th1 cells and IL-17A/IL-22-expressing Th17 cells and respond to anti-IL-12/IL-23 antibody treatment
by Tillack, Cornelia and Ehmann, Laura Maximiliane and Friedrich, Matthias and Laubender, Rüdiger P and Papay, Pavol and Vogelsang, Harald and Stallhofer, Johannes and Beigel, Florian and Bedynek, Andrea and Wetzke, Martin and Maier, Harald and Koburger, Maria and Wagner, Johanna and Glas, Jürgen and Diegelmann, Julia and Koglin, Sarah and Dombrowski, Yvonne and Schauber, Jürgen and Wollenberg, Andreas and Brand, Stephan
Gut, ISSN 0017-5749, 04/2014, Volume 63, Issue 4, pp. 567 - 577
Background We analysed incidence, predictors, histological features and specific treatment options of anti-tumour necrosis factor α (TNF-α) antibody-induced... 
RHEUMATOID-ARTHRITIS | ULCERATIVE-COLITIS | DOUBLE-BLIND | PROINFLAMMATORY GENE-EXPRESSION | ACTIVE CROHNS-DISEASE | NECROSIS FACTOR THERAPY | GASTROENTEROLOGY & HEPATOLOGY | MAINTENANCE THERAPY | HUMAN KERATINOCYTES | INTERLEUKIN-12/23 MONOCLONAL-ANTIBODY | GENOME-WIDE ASSOCIATION | Th1 Cells - physiology | Prospective Studies | Humans | Inflammatory Bowel Diseases - immunology | Interleukin-12 - physiology | Interleukin-17 - immunology | Interleukin-17 - physiology | Psoriasis - etiology | Ustekinumab | Inflammatory Bowel Diseases - physiopathology | Male | Th1 Cells - immunology | Interleukins - physiology | Inflammatory Bowel Diseases - pathology | Interleukins - immunology | Tumor Necrosis Factor-alpha - immunology | Antibodies - immunology | Adult | Female | Inflammatory Bowel Diseases - complications | Interleukin-23 - physiology | Skin - pathology | Skin - immunology | Psoriasis - immunology | Antibodies - therapeutic use | Antibodies, Monoclonal, Humanized - therapeutic use | Interferon-gamma - physiology | Interleukin-23 - immunology | Psoriasis - physiopathology | Interferon-gamma - immunology | Interleukin-12 - immunology | Tumor Necrosis Factor-alpha - physiology | Skin - physiopathology | Antibodies, Monoclonal, Humanized - immunology | Complications and side effects | Inflammatory bowel diseases | Care and treatment | Psoriasis | Tumor necrosis factor | Influence | Risk factors | Index Medicus | Abridged Index Medicus
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