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Skin Colonization by Staphylococcus aureus Precedes the Clinical Diagnosis of Atopic Dermatitis in Infancy

Journal of investigative dermatology, 2017-12, Vol.137 (12), p.2497-2504

2017

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PASS Syndrome: An IL-1-Driven Autoinflammatory Disease

Dermatology (Basel), 2016-01, Vol.232 (2), p.254-258

2016

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Diaper dermatitis prevalence and severity: Global perspective on the impact of caregiver behavior

Pediatric dermatology, 2020-01, Vol.37 (1), p.130-136

2020

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Bilateral Alopecia in a Six-year-old Boy: A Quiz

Acta dermato-venereologica, 2020-04, Vol.100 (8), p.adv00104-2

2020

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UVB-Induced Skin Inflammation and Cutaneous Tissue Injury Is Dependent on the MHC Class I–Like Protein, CD1d

Journal of investigative dermatology, 2014-01, Vol.134 (1), p.192-202

2014

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5-Hydroxymethylcytosine Expression in Proliferative Nodules Arising within Congenital Nevi Allows Differentiation from Malignant Melanoma

Journal of investigative dermatology, 2016-12, Vol.136 (12), p.2453-2461

2016

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Mutations in the human connexin gene GJB3 cause erythrokeratodermia variabilis

Nature genetics, 1998-12, Vol.20 (4), p.366-369

1998

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Interleukin 23-Helper T Cell 17 Axis as a Treatment Target for Pityriasis Rubra Pilaris

JAMA dermatology (Chicago, Ill.), 2017-04, Vol.153 (4), p.304

2017

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Mutations of Keratinocyte Transglutaminase in Lamellar Ichthyosis

Science (American Association for the Advancement of Science), 1995-01, Vol.267 (5197), p.525-528

1995

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Mutations of the gene encoding the transmembrane transporter protein ABC-C6 cause pseudoxanthoma elasticum

Journal of molecular medicine (Berlin, Germany), 2000-01, Vol.78 (5), p.282-286

2000

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Mutations in ACTRT1 and its enhancer RNA elements lead to aberrant activation of Hedgehog signaling in inherited and sporadic basal cell carcinomas

Nature Medicine, 2017-10, Vol.23 (10), p.1226-1233

2017

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Revised nomenclature and classification of inherited ichthyoses: Results of the First Ichthyosis Consensus Conference in Sorèze 2009

Journal of the American Academy of Dermatology, 2010-10, Vol.63 (4), p.607-641

2010

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Unclassified sclerosing malignant melanomas with AKAP9-BRAF gene fusion: a report of two cases and review of BRAF fusions in melanocytic tumors

Virchows Archiv : an international journal of pathology, 2018-03, Vol.472 (3), p.469-476

2018

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Cutaneous presentation of hepatosplenic T-cell lymphoma—a potential mimicker of primary cutaneous gamma-delta T-cell lymphoma

Virchows Archiv : an international journal of pathology, 2016-11, Vol.469 (5), p.591-596

2016

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Consequences of Seven Novel Mutations on the Expression and Structure of Keratinocyte Transglutaminase

The Journal of biological chemistry, 1997-08, Vol.272 (34), p.21018-21026

1997

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The TRAF-Interacting Protein (TRIP) Is a Regulator of Keratinocyte Proliferation

Journal of investigative dermatology, 2011-02, Vol.131 (2), p.349-357

2011

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A novel Q378X mutation exists in the transmembrane transporter protein ABCC6 and its pseudogene : implications for mutation analysis in pseudoxanthoma elasticum

Journal of molecular medicine (Berlin, Germany), 2001-09, Vol.79 (9), p.536-546

2001

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Syndrome of Birt-Hogg-Dubé, a histopathological pitfall with similarities to tuberous sclerosis: a report of three cases

The American journal of dermatopathology, 2013-04, Vol.35 (2), p.241-245

2013

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Five New CYLD Mutations in Skin Appendage Tumors and Evidence that Aspartic Acid 681 in CYLD Is Essential for Deubiquitinase Activity

Journal of investigative dermatology, 2008-03, Vol.128 (3), p.587-593

2008

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EBV+ cutaneous B‐cell lymphoproliferation of the leg in an elderly patient with mycosis fungoides and methotrexate treatment

APMIS : acta pathologica, microbiologica et immunologica Scandinavica, 2013-01, Vol.121 (1), p.79-84

2013

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A human keratin 10 knockout causes recessive epidermolytic hyperkeratosis

Human molecular genetics, 2006-04, Vol.15 (7), p.1133-1141

2006

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A Novel Dinucleotide Mutation in Keratin 10 in the Annular Epidermolytic Ichthyosis Variant of Bullous Congenital Ichthyosiform Erythroderma

Journal of investigative dermatology, 1997-03, Vol.108 (3), p.357-361

1997

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Mutation in the Gene for Connexin 30.3 in a Family with Erythrokeratodermia Variabilis

American journal of human genetics, 2000-11, Vol.67 (5), p.1296-1301

2000

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Skin Colonization by Staphylococcus aureus Precedes the Clinical Diagnosis of Atopic Dermatitis in Infancy

PASS Syndrome: An IL-1-Driven Autoinflammatory Disease

Diaper dermatitis prevalence and severity: Global perspective on the impact of caregiver behavior

Bilateral Alopecia in a Six-year-old Boy: A Quiz

UVB-Induced Skin Inflammation and Cutaneous Tissue Injury Is Dependent on the MHC Class I–Like Protein, CD1d

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

5-Hydroxymethylcytosine Expression in Proliferative Nodules Arising within Congenital Nevi Allows Differentiation from Malignant Melanoma

Mutations in the human connexin gene GJB3 cause erythrokeratodermia variabilis

Interleukin 23-Helper T Cell 17 Axis as a Treatment Target for Pityriasis Rubra Pilaris

Mutations of Keratinocyte Transglutaminase in Lamellar Ichthyosis

Mutations of the gene encoding the transmembrane transporter protein ABC-C6 cause pseudoxanthoma elasticum

Mutations in ACTRT1 and its enhancer RNA elements lead to aberrant activation of Hedgehog signaling in inherited and sporadic basal cell carcinomas

Revised nomenclature and classification of inherited ichthyoses: Results of the First Ichthyosis Consensus Conference in Sorèze 2009

Unclassified sclerosing malignant melanomas with AKAP9-BRAF gene fusion: a report of two cases and review of BRAF fusions in melanocytic tumors

Cutaneous presentation of hepatosplenic T-cell lymphoma—a potential mimicker of primary cutaneous gamma-delta T-cell lymphoma

Consequences of Seven Novel Mutations on the Expression and Structure of Keratinocyte Transglutaminase

The TRAF-Interacting Protein (TRIP) Is a Regulator of Keratinocyte Proliferation

A novel Q378X mutation exists in the transmembrane transporter protein ABCC6 and its pseudogene : implications for mutation analysis in pseudoxanthoma elasticum

Syndrome of Birt-Hogg-Dubé, a histopathological pitfall with similarities to tuberous sclerosis: a report of three cases

Five New CYLD Mutations in Skin Appendage Tumors and Evidence that Aspartic Acid 681 in CYLD Is Essential for Deubiquitinase Activity

EBV+ cutaneous B‐cell lymphoproliferation of the leg in an elderly patient with mycosis fungoides and methotrexate treatment

Identification of the familial cylindromatosis tumour-suppressor gene

A human keratin 10 knockout causes recessive epidermolytic hyperkeratosis

A Novel Dinucleotide Mutation in Keratin 10 in the Annular Epidermolytic Ichthyosis Variant of Bullous Congenital Ichthyosiform Erythroderma

Mutation in the Gene for Connexin 30.3 in a Family with Erythrokeratodermia Variabilis

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