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Lista de obras de Alan D. Irvine

'Peeling paint' dermatitis as a presenting sign of cystic fibrosis

artículo científico publicado en 2006

A case of congenital solitary Langerhans cell histiocytoma

scientific article published on 26 February 2010

A colorimetric bead-binding assay for detection of intermolecular interactions

artículo científico publicado en 2002

A genome-wide association study identifies new psoriasis susceptibility loci and an interaction between HLA-C and ERAP1.

artículo científico publicado en 2010

A genome-wide association study of atopic dermatitis identifies loci with overlapping effects on asthma and psoriasis

artículo científico publicado en 2013

A homozygous frameshift mutation in the mouse Flg gene facilitates enhanced percutaneous allergen priming.

artículo científico publicado en 2009

A longitudinal study of skin barrier function in pregnancy and the postnatal period

artículo científico publicado en 2014

A mutation detection strategy for the human keratin 6A gene and novel missense mutations in two cases of pachyonychia congenita type 1

artículo científico publicado en 1999

A mutation in the V1 domain of keratin 5 causes epidermolysis bullosa simplex with mottled pigmentation

artículo científico publicado en 1997

A novel mutation in KRT12 associated with Meesmann's epithelial corneal dystrophy

artículo científico publicado en 2002

A novel mutation in the 2B domain of keratin 2e causing ichthyosis bullosa of Siemens.

artículo científico publicado en 2000

A randomized controlled trial protocol assessing the effectiveness, safety and cost-effectiveness of methotrexate vs. ciclosporin in the treatment of severe atopic eczema in children: the TREatment of severe Atopic eczema Trial (TREAT)

artículo científico publicado en 2018

A recurrent splice-site mutation in the human hairless gene underlies congenital atrichia in Irish families

artículo científico publicado en 2007

A spectrum of mutations in keratins K6a, K16 and K17 causing pachyonychia congenita

artículo científico publicado en 2007

AP1S3 Mutations Cause Skin Autoinflammation by Disrupting Keratinocyte Autophagy and Up-Regulating IL-36 Production

artículo científico publicado en 2016

Absence of RECQL4 mutations in poikiloderma with neutropenia in Navajo and non-Navajo patients.

artículo científico publicado en 2003

Access to Genetic Diagnostics for Genodermatoses: Who Should Get Tested? Why? Who Pays?

artículo científico publicado en 2016

Activating CARD14 Mutations Are Associated with Generalized Pustular Psoriasis but Rarely Account for Familial Recurrence in Psoriasis Vulgaris.

artículo científico publicado en 2015

Adherence with early infant feeding and complementary feeding guidelines in the Cork BASELINE Birth Cohort Study

artículo científico publicado en 2015

Adhesion of Staphylococcus aureus to Corneocytes from Atopic Dermatitis Patients Is Controlled by Natural Moisturizing Factor Levels

artículo científico publicado en 2018

An unusual N-terminal deletion of the laminin alpha3a isoform leads to the chronic granulation tissue disorder laryngo-onycho-cutaneous syndrome

artículo científico publicado en 2003

An unusual case of genital swelling

artículo científico publicado en 2013

An unusual rash in a neonate. X-linked dominant ichthyosis (XLDI)

artículo científico publicado en 2010

Analysis of the individual and aggregate genetic contributions of previously identified serine peptidase inhibitor Kazal type 5 (SPINK5), kallikrein-related peptidase 7 (KLK7), and filaggrin (FLG) polymorphisms to eczema risk

artículo científico publicado en 2008

Antenatal Vitamin D Status Is Not Associated with Standard Neurodevelopmental Assessments at Age 5 Years in a Well-Characterized Prospective Maternal-Infant Cohort

scientific article published on 01 October 2018

Antenatal vitamin D exposure and childhood eczema, food allergy, asthma and allergic rhinitis at 2 and 5 years of age in the atopic disease-specific Cork BASELINE Birth Cohort Study

scientific article published on 29 August 2018

Antimicrobial resistance in atopic dermatitis: Need for an urgent rethink

scientific article published on 29 November 2018

Assessing the New and Emerging Treatments for Atopic Dermatitis

artículo científico publicado en 2016

Atopic Dermatitis According to GARP: New Mechanistic Insights in Disease Pathogenesis

artículo científico

Atopic dermatitis

artículo científico publicado en 2018

Atopic dermatitis is associated with an increased risk for rheumatoid arthritis and inflammatory bowel disease, and a decreased risk for type 1 diabetes

artículo científico publicado en 2015

Atypical epidermolytic palmoplantar keratoderma presentation associated with a mutation in the keratin 1 gene

artículo científico publicado en 2004

Autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy (APECED) in the Irish population.

artículo científico publicado en 2006

Autosomal recessive hypotrichosis with loose anagen hairs associated with TKFC mutations

scientific article published on 13 August 2020

Blue Rubber Bleb Nevus (BRBN) Syndrome Is Caused by Somatic TEK (TIE2) Mutations

artículo científico publicado en 2016

Body Composition within the First 3 Months: Optimized Correction for Length and Correlation with BMI at 2 Years.

artículo científico publicado en 2016

Breaking the (Un)Sound Barrier: Filaggrin Is a Major Gene for Atopic Dermatitis

article

C3-C4 shingles post haematopoietic stem-cell transplantation

artículo científico publicado en 2014

Cantú syndrome: Report of nine new cases and expansion of the clinical phenotype

article

Carney complex: report of a kindred with predominantly cutaneous manifestations

artículo científico publicado en 1997

Carrier status for the common R501X and 2282del4 filaggrin mutations is not associated with hearing phenotypes in 5,377 children from the ALSPAC cohort.

artículo científico publicado en 2009

Catalogue of inherited disorders found among the Irish Traveller population

artículo científico publicado en 2018

Changes in nano-mechanical properties of human epidermal cornified cells in children with atopic dermatitis

scientific article published on 19 May 2020

Childhood eczema and the importance of the physical environment

artículo científico publicado en 2013

Chromosome 11q13.5 variant associated with childhood eczema: an effect supplementary to filaggrin mutations

artículo científico publicado en 2010

Clarithromycin suspension-associated toxic epidermal necrolysis in a 2-year-old girl

scientific article published on 22 August 2007

Clinical and genetic differences between pustular psoriasis subtypes

artículo científico publicado en 2018

Clumping Factor B Promotes Adherence of Staphylococcus aureus to Corneocytes in Atopic Dermatitis.

artículo científico publicado en 2017

Cohort profile: The Cork BASELINE Birth Cohort Study: Babies after SCOPE: Evaluating the Longitudinal Impact on Neurological and Nutritional Endpoints

artículo científico publicado en 2014

Commentary: Methotrexate and ciclosporin in the treatment of severe eczema in children

artículo científico publicado en 2014

Common loss-of-function variants of the epidermal barrier protein filaggrin are a major predisposing factor for atopic dermatitis

artículo científico publicado en 2006

Comparative PRKAR1A genotype-phenotype analyses in humans with Carney complex and prkar1a haploinsufficient mice

scholarly article

Comprehensive analysis of the gene encoding filaggrin uncovers prevalent and rare mutations in ichthyosis vulgaris and atopic eczema

article

Congenital reticular ichthyosiform erythroderma.

artículo científico publicado en 2016

Congenital-infantile fibrosarcoma of the foot--avoidance of amputation

article by G J Nason et al published May 2014 in Irish Medical Journal

Copy-number mutations on chromosome 17q24.2-q24.3 in congenital generalized hypertrichosis terminalis with or without gingival hyperplasia

artículo científico publicado en 2009

Cord blood leptin and gains in body weight and fat mass during infancy

artículo científico publicado en 2016

Correlation of Insulin-Like Growth Factor-I and -II Concentrations at Birth Measured by Mass Spectrometry and Growth from Birth to Two Months.

artículo científico publicado en 2018

Crossing barriers; restoring barriers? Filaggrin protein replacement takes a bow.

artículo científico publicado en 2014

Cutaneous larva migrans: the case for routine oral treatment

artículo científico publicado en 1997

DOCK8 primary immunodeficiency syndrome

artículo científico publicado en 2015

Deletion of Late Cornified Envelope 3B and 3C genes is not associated with atopic dermatitis.

artículo científico publicado en 2010

Dermatological manifestations of autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy syndrome.

artículo científico publicado en 2006

Dermatological manifestations of hereditary fibrosing poikiloderma with tendon contractures, myopathy and pulmonary fibrosis (POIKTMP): a case series of 28 patients

scientific article published on 10 April 2019

Dermatological presentation of disease associated with antineutrophil cytoplasmic antibodies: a report of two contrasting cases and a review of the literature

artículo científico publicado en 1996

Desmoglein 1 deficiency results in severe dermatitis, multiple allergies and metabolic wasting

scientific article published on 25 August 2013

Development of allele-specific therapeutic siRNA in Meesmann epithelial corneal dystrophy

artículo científico publicado en 2011

Development of mycosis fungoides after bone marrow transplantation for chronic myeloid leukaemia: transmission from an allogeneic donor

article

Disease trajectories in childhood atopic dermatitis: an update and practitioner's guide

scientific article published on 15 May 2019

Disorders of keratinisation: from rare to common genetic diseases of skin and other epithelial tissues.

artículo científico publicado en 2007

Double Trouble: Homozygous Dominant Mutations and Hair Loss in Pachyonychia Congenita

Drug rash with eosinophilia and systemic symptoms (DRESS) syndrome induced by cidofovir.

artículo científico publicado en 2010

Early life regional and temporal variation in filaggrin-derived natural moisturising factor, filaggrin processing enzyme activity, corneocyte phenotypes and plasmin activity: Implications for atopic dermatitis.

artículo científico publicado en 2018

Erratum: Corrigendum: Loss-of-function mutations of an inhibitory upstream ORF in the human hairless transcript cause Marie Unna hereditary hypotrichosis

scholarly article published in Nature Genetics

Erratum: Corrigendum: Transcriptional regulator PRDM12 is essential for human pain perception

artículo científico publicado en 2015

Erythema elevatum diutinum in a healthy child

artículo científico publicado en 2017

Evidence for a second genetic locus in Carney complex

artículo científico publicado en 1998

Exome Sequencing and Rare Variant Analysis Reveals Multiple Filaggrin Mutations in Bangladeshi Families with Atopic Eczema and Additional Risk Genes

scientific article published on 30 May 2018

Expanding the clinical spectrum of hereditary fibrosing poikiloderma with tendon contractures, myopathy and pulmonary fibrosis due to FAM111B mutations

artículo científico publicado en 2015

FOXN1 Duplication and Congenital Hypertrichosis

artículo científico publicado en 2017

Filaggrin Expression and Processing Deficiencies Impair Corneocyte Surface Texture and Stiffness in Mice

artículo científico publicado en 2019

Filaggrin breakdown products determine corneocyte conformation in patients with atopic dermatitis

artículo científico publicado en 2015

Filaggrin gene mutation associations with peanut allergy persist despite variations in peanut allergy diagnostic criteria or asthma status

artículo científico publicado en 2013

Filaggrin in atopic dermatitis

artículo científico publicado en 2009

Filaggrin in atopic dermatitis.

scientific article published on 05 September 2008

Filaggrin in the frontline: role in skin barrier function and disease

artículo científico publicado en 2009

Filaggrin loss-of-function mutations are associated with enhanced expression of IL-1 cytokines in the stratum corneum of patients with atopic dermatitis and in a murine model of filaggrin deficiency.

artículo científico publicado en 2012

Filaggrin mutations associated with skin and allergic diseases.

artículo científico publicado en 2011

Filaggrin mutations, atopic eczema, hay fever, and asthma in children

artículo científico publicado en 2008

Filaggrin null alleles are not associated with psoriasis

artículo científico publicado en 2007

Filaggrin variants confer susceptibility to asthma

article

Filaggrin's fuller figure: a glimpse into the genetic architecture of atopic dermatitis.

artículo científico publicado en 2007

Filaggrin-stratified transcriptomic analysis of pediatric skin identifies mechanistic pathways in patients with atopic dermatitis

artículo científico publicado en 2014

Fleshing out filaggrin phenotypes

scientific article published on 01 March 2007

Focal dermal hypoplasia (Goltz syndrome) associated with intestinal malrotation and mediastinal dextroposition.

artículo científico publicado en 1996

Gender- and gestational age-specific body fat percentage at birth

artículo científico publicado en 2011

Generalized lymphatic anomaly successfully treated with long-term, low-dose sirolimus.

artículo científico publicado en 2018

Genetical, clinical, and functional analysis of a large international cohort of patients with autosomal recessive congenital ichthyosis due to mutations in NIPAL4

artículo científico publicado en 2019

Genetics of Hidradenitis Suppurativa

article

Genome-wide Comparative Analysis of Atopic Dermatitis and Psoriasis Gives Insight into Opposing Genetic Mechanisms.

artículo científico publicado en 2015

Genome-wide comparative analysis of atopic dermatitis and psoriasis gives insight into opposing genetic mechanisms

artículo científico publicado en 2015

Genotype-phenotype correlations with TGM1: clustering of mutations in the bathing suit ichthyosis and self-healing collodion baby variants of lamellar ichthyosis

artículo científico publicado en 2009

Global Allergy Forum and 3rd Davos Declaration 2015: Atopic dermatitis/Eczema: challenges and opportunities toward precision medicine

artículo científico publicado en 2016

Haploinsufficiency for AAGAB causes clinically heterogeneous forms of punctate palmoplantar keratoderma.

artículo científico publicado en 2012

Heritable filaggrin disorders: the paradigm of atopic dermatitis

artículo científico publicado en 2012

High dose Bilastine for the treatment of Bascule Syndrome

artículo científico publicado en 2020

High-density genotyping study identifies four new susceptibility loci for atopic dermatitis

scientific article published on 02 June 2013

Human and computational models of atopic dermatitis: a review and perspectives by an expert panel of the International Eczema Council

artículo científico publicado en 2019

IL36RN mutations define a severe autoinflammatory phenotype of generalized pustular psoriasis

artículo científico publicado en 2014

Ichthyosis prematurity syndrome: a case report and review of known mutations

artículo científico

Identification of a novel C16orf57 mutation in Athabaskan patients with Poikiloderma with Neutropenia

article

Identification of a novel genetic locus for familial cardiac myxomas and Carney complex

scientific article published on 01 December 1998

Identification of novel mutations in basic hair keratins hHb1 and hHb6 in monilethrix: implications for protein structure and clinical phenotype.

artículo científico publicado en 1999

Impact of maternal, antenatal and birth-associated factors on iron stores at birth: data from a prospective maternal-infant birth cohort

artículo científico publicado en 2016

Insight into IKBKG/NEMO locus: report of new mutations and complex genomic rearrangements leading to incontinentia pigmenti disease

artículo científico

Intragenic copy number variation within filaggrin contributes to the risk of atopic dermatitis with a dose-dependent effect

artículo científico publicado en 2011

Iron intakes and status of 2-year-old children in the Cork BASELINE Birth Cohort Study

artículo científico publicado en 2016

Iron status, body size, and growth in the first 2 years of life

artículo científico publicado en 2017

Juvenile localised scleroderma: a retrospective review of response to systemic treatment.

artículo científico publicado en 2008

Kaposi sarcoma in an patient with atopic dermatitis treated with ciclosporin

artículo científico publicado en 2013

Kasabach-Merritt syndrome, kaposiform haemangioendothelioma and platelet blockade

artículo científico publicado en 2015

Levels of filaggrin degradation products are influenced by both filaggrin genotype and atopic dermatitis severity.

artículo científico publicado en 2011

Lipoatrophic panniculitis of the ankles

artículo científico publicado en 2006

Loss-of-Function Mutations in the Filaggrin Gene Lead to Reduced Level of Natural Moisturizing Factor in the Stratum Corneum

article

Loss-of-function mutations in the gene encoding filaggrin cause ichthyosis vulgaris.

artículo científico publicado en 2006

Loss-of-function mutations of an inhibitory upstream ORF in the human hairless transcript cause Marie Unna hereditary hypotrichosis

artículo científico publicado en 2009

Loss-of-function variants in the filaggrin gene are a significant risk factor for peanut allergy.

artículo científico publicado en 2011

Loss-of-function variations within the filaggrin gene predispose for atopic dermatitis with allergic sensitizations

artículo científico publicado en 2006

Low vitamin D deficiency in Irish toddlers despite northerly latitude and a high prevalence of inadequate intakes

artículo científico publicado en 2016

Lymphangioma circumscriptum associated with paravesical cystic retroperitoneal lymphangioma

artículo científico publicado en 1996

Management of vascular birthmarks: review of a multidisciplinary clinic.

artículo científico publicado en 2007

Mathematical modeling of atopic dermatitis reveals "double-switch" mechanisms underlying 4 common disease phenotypes.

artículo científico publicado en 2016

Mediastinal and neck kaposiform hemangioendothelioma: report of three cases

artículo científico publicado en 2009

Meta-analysis of filaggrin polymorphisms in eczema and asthma: Robust risk factors in atopic disease

artículo científico publicado en 2009

Methotrexate for Severe Childhood Atopic Dermatitis: Clinical Experience in a Tertiary Center

artículo científico publicado en 2017

Methylenetetrahydrofolate reductase (MTHFR) deficiency presenting as a rash

scientific article published on 27 July 2012

Microcytosis is associated with low cognitive outcomes in healthy 2-year-olds in a high-resource setting

artículo científico publicado en 2017

Microscopic polyangiitis. Delineation of a cutaneous-limited variant associated with antimyeloperoxidase autoantibody

artículo científico publicado en 1997

Miliary neonatal hemangiomatosis with fulminant heart failure and cardiac septal hypertrophy in two infants

artículo científico publicado en 2004

Molecular genetics of the inherited disorders of cornification: an update.

artículo científico publicado en 2002

Multi-ancestry genome-wide association study of 21,000 cases and 95,000 controls identifies new risk loci for atopic dermatitis

artículo científico publicado en 2015

Multiple dermatofibromas in a patient with HIV infection

artículo científico publicado en 1995

Mutations in cornea-specific keratin K3 or K12 genes cause Meesmann's corneal dystrophy

artículo científico publicado en 1997

Mutations in desmoglein 1 cause diverse inherited palmoplantar keratoderma phenotypes: implications for genetic screening

artículo científico publicado en 2016

Mutations in keratin K9 in kindreds with epidermolytic palmoplantar keratoderma and epidemiology in Northern Ireland.

artículo científico publicado en 1998

Mutations in the SASPase gene (ASPRV1) are not associated with atopic eczema or clinically dry skin

artículo científico publicado en 2012

Neonatal adiposity increases the risk of atopic dermatitis during the first year of life

artículo científico publicado en 2015

Netherton syndrome: disease expression and spectrum of SPINK5 mutations in 21 families

artículo científico publicado en 2002

Newborn transepidermal water loss values: a reference dataset

artículo científico publicado en 2013

Next-generation anti-Staphylococcus aureus vaccines: A potential new therapeutic option for atopic dermatitis?

scientific article published on 12 September 2018

No association between food allergens in the complementary feeding diet and eczema during the first 12-months in the Cork BASELINE Birth Cohort

artículo científico publicado en 2015

Nottingham Eczema Severity Scoring tool can identify children at high risk of food allergy to cow’s milk, egg and peanut

artículo científico publicado en 2015

O08 - Increased early life Transepidermal Water Loss (TEWL) values can predate atopic dermatitis in asymptomatic infants: results from the BASELINE study.

artículo científico publicado en 2014

Ocular surface reconstruction in LOGIC syndrome by amniotic membrane transplantation.

artículo científico publicado en 2001

Old King coal - molecular mechanisms underlying an ancient treatment for atopic eczema

artículo científico publicado en 2013

Optimization of placebo use in clinical trials with systemic treatments for atopic dermatitis: an International Eczema Council survey-based position statement

artículo científico publicado en 2019

PHACE syndrome: MRI of intracerebral vascular anomalies and clinical findings in a series of 12 patients.

artículo científico publicado en 2011

PLACK syndrome resulting from a novel homozygous variant in CAST

scientific article published on 03 October 2020

Parental atopy and risk of atopic dermatitis in the first two years of life in the BASELINE birth cohort study

artículo científico publicado en 2022

Prevalent and Rare Mutations in the Gene Encoding Filaggrin Cause Ichthyosis Vulgaris and Predispose Individuals to Atopic Dermatitis

article

Primary cutaneous adenoid cystic carcinoma

scientific article published on 01 May 1996

Propranolol in the treatment of infantile haemangiomas: lessons from the European Propranolol In the Treatment of Complicated Haemangiomas (PITCH) Taskforce survey.

artículo científico publicado en 2015

Pseudoporphyria induced by mefenamic acid

artículo científico publicado en 1998

Pyodermatitis-pyostomatitis vegetans: evidence for an entirely mucocutaneous variant

artículo científico publicado en 1998

RASA1 mosaic mutations in patients with capillary malformation-arteriovenous malformation

artículo científico publicado en 2019

RASA1 mutations and associated phenotypes in 68 families with capillary malformation-arteriovenous malformation

artículo científico publicado en 2013

Raised limb bands developing in infancy

artículo científico publicado en 2003

Raman profiles of the stratum corneum define 3 filaggrin genotype-determined atopic dermatitis endophenotypes

artículo científico publicado en 2010

Rapidly Involuting Congenital Hemangioma with Pustules: Two Cases

article published in 2014

Recent advances in the pathobiology and management of Kasabach-Merritt phenomenon

artículo científico publicado en 2015

Report from the National Institute of Allergy and Infectious Diseases workshop on "Atopic dermatitis and the atopic march: Mechanisms and interventions"

artículo científico publicado en 2019

Resolution of the plantar hyperkeratosis of pachyonychia congenita during chemotherapy for Ewing sarcoma

artículo científico publicado en 2013

Response to "Comment on: 'When does atopic dermatitis warrant systemic therapy? Recommendations from an expert panel of the International Eczema Council'"

artículo científico publicado en 2018

Response to "Dental caries as a side effect of infantile hemangioma treatment with propranolol solution"

scientific article published on 01 September 2011

Response to IL-1-receptor antagonist in a child with familial cold autoinflammatory syndrome

scientific article published on 01 January 2007

Review of Critical Issues in the Pathogenesis of Atopic Dermatitis

artículo científico publicado en 2016

SVEP1 plays a crucial role in epidermal differentiation

artículo científico publicado en 2017

Second International Conference on a classification of ectodermal dysplasias: Development of a multiaxis model

article

Severe dermatitis, multiple allergies, and metabolic wasting syndrome caused by a novel mutation in the N-terminal plakin domain of desmoplakin

artículo científico publicado en 2015

Skin barrier dysfunction measured by transepidermal water loss at 2 days and 2 months predates and predicts atopic dermatitis at 1 year

artículo científico publicado en 2015

Skin barrier impairment at birth predicts food allergy at 2 years of age

artículo científico publicado en 2016

Skin involvement in Down syndrome transient abnormal myelopoiesis

artículo científico publicado en 2012

Skin microbiome before development of atopic dermatitis: Early colonization with commensal staphylococci at 2 months is associated with a lower risk of atopic dermatitis at 1 year

artículo científico publicado en 2016

South African amaXhosa patients with atopic dermatitis have decreased levels of filaggrin breakdown products but no loss-of-function mutations in filaggrin

artículo científico publicado en 2014

Spontaneous atopic dermatitis in mice with a defective skin barrier is independent of ILC2 and mediated by IL-1β

scientific article published on 29 April 2019

Spontaneous atopic dermatitis is mediated by innate immunity, with the secondary lung inflammation of the atopic march requiring adaptive immunity

artículo científico publicado en 2015

Spontaneous regression of cutaneous metastases of squamous cell carcinoma.

artículo científico publicado en 2013

Staphylococcus aureus and Atopic Dermatitis: A Complex and Evolving Relationship.

artículo científico publicado en 2017

Successful treatment of a refractory verruca in a child with acute lymphoblastic leukaemia with topical cidofovir.

artículo científico publicado en 2005

Successful treatment of florid cutaneous warts with intravenous cidofovir in an 11-year-old girl

artículo científico publicado en 2008

Sweet syndrome revealing systemic lupus erythematosus.

artículo científico publicado en 2015

Systemic and stratum corneum biomarkers of severity in infant atopic dermatitis include markers of innate and T helper cell-related immunity and angiogenesis

artículo científico publicado en 2018

Systemic therapies for severe atopic dermatitis in children and adults

artículo científico publicado en 2013

Systemic treatments in the management of atopic dermatitis: a systematic review and meta-analysis

artículo científico publicado en 2020

TREatment of ATopic eczema (TREAT) Registry Taskforce: an international Delphi exercise to identify a core set of domains and domain items for national atopic eczema photo- and systemic therapy registries

artículo científico publicado en 2018

TREatment of ATopic eczema (TREAT) Registry Taskforce: consensus on how and when to measure the core dataset for atopic eczema treatment research registries

artículo científico publicado en 2019

TREatment of ATopic eczema (TREAT) Registry Taskforce: protocol for a European safety study of dupilumab and other systemic therapies in patients with atopic eczema

artículo científico publicado en 2019

TREatment of ATopic eczema (TREAT) Registry Taskforce: protocol for an international Delphi exercise to identify a core set of domains and domain items for national atopic eczema registries

artículo científico publicado en 2017

The Changing Paradigm of Atopic Dermatitis Therapy

artículo científico publicado en 2016

The European TREatment of ATopic eczema (TREAT) Registry Taskforce survey: prescribing practices in Europe for phototherapy and systemic therapy in adult patients with moderate-to-severe atopic eczema

artículo científico publicado en 2020

The International TREatment of ATopic Eczema (TREAT) Registry Taskforce: An Initiative to Harmonize Data Collection across National Atopic Eczema Photo- and Systemic Therapy Registries.

artículo científico publicado en 2017

The atopic march and atopic multimorbidity: Many trajectories, many pathways

artículo científico publicado en 2018

The burden of disease associated with filaggrin mutations: a population-based, longitudinal birth cohort study

artículo científico publicado en 2008

The exposome in atopic dermatitis

scientific article published on 19 August 2019

The microbiome in patients with atopic dermatitis

scientific article published on 23 November 2018

The molecular genetics of the genodermatoses: progress to date and future directions.

artículo científico publicado en 2003

The multifunctional role of filaggrin in allergic skin disease

artículo científico

The relationship between IGF-I and -II concentrations and body composition at birth and over the first 2 months

artículo científico publicado en 2019

The role of bacterial skin infections in atopic dermatitis: expert statement and review from the International Eczema Council Skin Infection Group

artículo científico publicado en 2019

The role of filaggrin in atopic dermatitis and allergic disease

scientific article published on 14 October 2019

The role of filaggrin in the atopic diathesis.

artículo científico publicado en 2010

The spectrum of manifestations in desmoplakin gene (DSP) spectrin repeat 6 domain mutations: Immunophenotyping and response to ustekinumab.

artículo científico publicado en 2017

The treatment of viral warts with topical cidofovir 1%: our experience of seven paediatric patients

artículo científico publicado en 2008

The value of a baseline liver biopsy prior to methotrexate treatment

artículo científico publicado en 1994

The widespread use of topical antimicrobials enriches for resistance in Staphylococcus aureus isolated from Atopic Dermatitis patients.

artículo científico publicado en 2018

Tmem79/Matt is the matted mouse gene and is a predisposing gene for atopic dermatitis in human subjects

scientific journal article

Too Much, Too Little or Just Enough: A Goldilocks Effect for IL-13 and Skin Barrier Regulation?

article published in 2016

Topical Corticosteroids Normalize both Skin and Systemic Inflammatory Markers in Infant Atopic Dermatitis

scientific article published on 02 December 2020

Topical cidofovir for the treatment of recalcitrant viral warts and molluscum contagiosum in Jacobsen syndrome

artículo científico publicado en 2020

Toward a major risk factor for atopic eczema: meta-analysis of filaggrin polymorphism data

artículo científico publicado en 2007

Transcriptional regulator PRDM12 is essential for human pain perception

artículo científico publicado en 2015

Two Cases of Primarily Palmoplantar Keratoderma Associated with Novel Mutations in Keratin 1

article

Update on Epidemiology, Diagnosis, and Disease Course of Atopic Dermatitis

artículo científico publicado en 2016

Use of Systemic Corticosteroids in Management of a Large Congenital Haemangioma of the Scalp

Use of ruxolitinib to successfully treat chronic mucocutaneous candidiasis caused by gain-of-function signal transducer and activator of transcription 1 (STAT1) mutation.

artículo científico publicado en 2015

Use of systemic corticosteroids for atopic dermatitis: International Eczema Council consensus statement ⬇️

artículo científico publicado en 2017

Variation in iodine food composition data has a major impact on estimates of iodine intake in young children.

artículo científico publicado en 2017

Vitamin D metabolite concentrations in umbilical cord blood serum and associations with clinical characteristics in a large prospective mother-infant cohort in Ireland

artículo científico publicado en 2016

What is the evidence for interactions between filaggrin null mutations and environmental exposures in the aetiology of atopic dermatitis? A systematic review

artículo científico publicado en 2019

When does atopic dermatitis warrant systemic therapy? Recommendations from an expert panel of the International Eczema Council.

artículo científico publicado en 2017

Wide spectrum of filaggrin-null mutations in atopic dermatitis highlights differences between Singaporean Chinese and European populations.

artículo científico publicado en 2011

siRNA silencing of the mutant keratin 12 allele in corneal limbal epithelial cells grown from patients with Meesmann's epithelial corneal dystrophy.

artículo científico publicado en 2014

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