Lista de obras - Chao-Kai Hsu - Dominio Público Uruguay

"Spade sign" and inflammation/fibrosis limited to the upper and mid-dermis as the pathognomonic features of acne keloidalis

scientific article published on 23 October 2019

A new superficial needle-scraping method for assessing Demodex density in papulopustular rosacea

artículo científico publicado en 2019

Adjuvant Radiotherapy After Keloid Excision: Preliminary Experience in Taiwan

artículo científico publicado en 2019

Analysis of Taiwanese ichthyosis vulgaris families further demonstrates differences in FLG mutations between European and Asian populations.

artículo científico publicado en 2009

Beneficial effect of ustekinumab in familial pityriasis rubra pilaris with a new missense mutation in CARD14.

artículo científico publicado en 2017

Broadband absorption and reduced scattering spectra of in-vivo skin can be noninvasively determined using δ-P1 approximation based spectral analysis

artículo científico publicado en 2015

Caveolin-1 Controls Hyperresponsiveness to Mechanical Stimuli and Fibrogenesis-Associated RUNX2 Activation in Keloid Fibroblasts

artículo científico publicado en 2017

Central retinal vein occlusion and subsequent neovascular glaucoma after adalimumab treatment for psoriasis.

artículo científico publicado en 2013

Clinicopathological study of Fox-Fordyce disease

artículo científico publicado en 2009

Coagulation Factor XIII-A Subunit Missense Mutation in the Pathobiology of Autosomal Dominant Multiple Dermatofibromas

scientific article published on 04 September 2019

Congenital Anonychia and Uncombable Hair Syndrome: Coinheritance of Homozygous Mutations in RSPO4 and PADI3

artículo científico publicado en 2017

Conjunctival geographic ulcer: an overlooked sign of herpes simplex virus infection

artículo científico publicado en 2015

Dissecting folliculitis (dissecting cellulitis) of the scalp: a 66-patient case series and proposal of classification

scientific article published on 31 August 2018

Early intervention with high-dose steroid pulse therapy prolongs disease-free interval of severe alopecia areata: a retrospective study.

artículo científico publicado en 2013

Ectodermal dysplasia-skin fragility syndrome resulting from a new atypical homozygous cryptic acceptor splice site mutation in PKP1.

artículo científico publicado en 2016

Erythema multiforme, Stevens-Johnson syndrome, and toxic epidermal necrolysis: acute ocular manifestations, causes, and management

scientific article published on 01 February 2007

Erythema multiforme-like secondary syphilis in a HIV-positive bisexual man

artículo científico publicado en 2010

Erythrokeratoderma Variabilis Caused by p.Gly45Glu in Connexin 31: Importance of the First Extracellular Loop Glycine Residue for Gap Junction Function.

artículo científico publicado en 2015

Evanescent and persistent pruritic eruptions of adult-onset still disease: a clinical and pathologic study of 36 patients

artículo científico publicado en 2012

Filaggrin: an emerging star in atopic march

scientific article published on 01 June 2008

Further evidence for genotype-phenotype disparity in Griscelli syndrome.

artículo científico publicado en 2016

Genetic variants associated with phenytoin-related severe cutaneous adverse reactions

artículo científico publicado en 2014

Good cosmesis of a large rhinophyma after carbon dioxide laser treatment

scientific article published on 01 March 2006

Granulomatous rosacea-like demodicidosis.

artículo científico publicado en 2007

Higher body mass index is associated with greater severity of alopecia in men with male-pattern androgenetic alopecia in Taiwan: a cross-sectional study.

artículo científico publicado en 2013

Homozygous acceptor splice site mutation in DSG1 disrupts plakoglobin localization and results in keratoderma and skin fragility.

artículo científico publicado en 2017

Ichthyosis Prematurity Syndrome: From Fetus to Adulthood

artículo científico publicado en 2016

Improved molecular diagnosis of the common recurrent intragenic deletion mutation in IKBKG in a Filipino family with incontinentia pigmenti.

artículo científico publicado en 2015

Incontinentia pigmenti in a father and daughter

artículo científico publicado en 2016

Insect bite-like reaction in association with chronic lymphocytic leukemia

artículo científico publicado en 2014

Large Intragenic Deletion in DSTYK Underlies Autosomal-Recessive Complicated Spastic Paraparesis, SPG23.

artículo científico publicado en 2017

Large, papillomatous and pedunculated nevus sebaceus

artículo científico publicado en 2010

Late-onset comedonal Darier's disease caused by a recurrent ATP2A2 mutation

artículo científico publicado en 2019

Lichen planus and lichenoid dermatoses: Clinical overview and molecular basis

artículo científico publicado en 2018

Lichen planus and lichenoid dermatoses: Conventional and emerging therapeutic strategies

artículo científico publicado en 2018

Linear lupus panniculitis of the scalp presenting as alopecia along Blaschko's lines: a distinct variant of lupus panniculitis in East Asians?

artículo científico publicado en 2011

Lipodystrophia centrifugalis abdominalis infantilis: report of four cases

scientific article published on 09 December 2011

Mechanical coupling of cytoskeletal elasticity and force generation is crucial for understanding the migrating nature of keloid fibroblasts.

artículo científico publicado en 2015

Mechanical forces in skin disorders.

artículo científico publicado en 2018

Mechanobiological dysregulation of the epidermis and dermis in skin disorders and in degeneration ⬇️

artículo científico publicado el 15 de mayo de 2013

Mutations in KLHL24 Add to the Molecular Heterogeneity of Epidermolysis Bullosa Simplex

scientific article published on 19 January 2017

Non-invasive evaluation of therapeutic response in keloid scar using diffuse reflectance spectroscopy

artículo científico publicado en 2015

Noninvasive evaluation of collagen and hemoglobin contents and scattering property of in vivo keloid scars and normal skin using diffuse reflectance spectroscopy: pilot study.

artículo científico publicado en 2012

Novel homozygous missense mutation in NT5C2 underlying hereditary spastic paraplegia SPG45.

artículo científico publicado en 2017

Novel indel mutation of STS underlies a new phenotype of self-healing recessive X-linked ichthyosis

artículo científico publicado en 2015

Novel p.Ala675Thr missense mutation in TRPV3 in Olmsted syndrome

scientific article published on 14 May 2020

PLACK syndrome resulting from a new homozygous insertion mutation in CAST.

artículo científico publicado en 2017

Paper-based ELISA for the detection of autoimmune antibodies in body fluid-the case of bullous pemphigoid

artículo científico publicado en 2014

Perifolliculitis capitis abscedens et suffodiens: eine Fallserie mit 66 Patienten und ein Vorschlag zur Klassifikation

scientific article published on 01 October 2018

Portable handheld diffuse reflectance spectroscopy system for clinical evaluation of skin: a pilot study in psoriasis patients

artículo científico publicado en 2016

Predictive phenotyping of inherited ichthyosis by next-generation DNA sequencing.

artículo científico publicado en 2016

Primary scarring alopecia: A retrospective study of 89 patients in Taiwan

artículo científico publicado en 2018

Prognostic Role of Tumoral PDL1 Expression and Peritumoral FoxP3+ Lymphocytes in Vulvar Melanomas.

artículo científico publicado en 2018

Progressive hyperpigmentation in a Taiwanese child due to an inborn error of vitamin B12 metabolism (cblJ).

artículo científico publicado en 2015

Pterygium and thinning of nails as an unusual manifestation in Clouston syndrome

artículo científico publicado en 2019

Recalcitrant extragenital giant condyloma acuminatum: A need for combination therapy

scientific article published on 18 March 2019

Semidominant GPNMB Mutations in Amyloidosis Cutis Dyschromica

artículo científico publicado en 2019

Spatial distribution of filament elasticity determines the migratory behaviors of a cell

artículo científico publicado en 2016

Successful treatment of recalcitrant pemphigus vulgaris and pemphigus vegetans with etanercept and carbon dioxide laser.

artículo científico publicado en 2005

Syndromic inherited poikiloderma due to a de novo mutation in FAM111B.

artículo científico publicado en 2016

Systematised naevus sebaceus resulting from post-zygotic mutation in HRAS

artículo científico publicado en 2015

The Medication Risk of Stevens-Johnson Syndrome and Toxic Epidermal Necrolysis in Asians: The Major Drug Causality and Comparison to the USA FDA Label.

artículo científico publicado en 2018

The Tension Biology of Wound Healing.

artículo científico publicado en 2017

Thumbnail-squeezing method: an effective method for assessing Demodex density in rosacea

scientific article published on 03 March 2020

Time Series Integrative Analysis of RNA Sequencing and MicroRNA Expression Data Reveals Key Biologic Wound Healing Pathways in Keloid-Prone Individuals

artículo científico publicado en 2018

Topical Betaxolol for Treating Relapsing Paronychia with Pyogenic Granuloma-Like Lesions Induced by Epidermal Growth Factor Receptor Inhibitors.

artículo científico publicado en 2018

Toward reliable retrieval of functional information of papillary dermis using spatially resolved diffuse reflectance spectroscopy.

artículo científico publicado en 2016

Treatment of hereditary epidermolysis bullosa: updates and future prospects.

artículo científico

[Primary human demodicosis. A disease sui generis]

artículo científico publicado en 2015

Lista de obras de Chao-Kai Hsu

"Spade sign" and inflammation/fibrosis limited to the upper and mid-dermis as the pathognomonic features of acne keloidalis

A new superficial needle-scraping method for assessing Demodex density in papulopustular rosacea

Adjuvant Radiotherapy After Keloid Excision: Preliminary Experience in Taiwan

Analysis of Taiwanese ichthyosis vulgaris families further demonstrates differences in FLG mutations between European and Asian populations.

Beneficial effect of ustekinumab in familial pityriasis rubra pilaris with a new missense mutation in CARD14.

Broadband absorption and reduced scattering spectra of in-vivo skin can be noninvasively determined using δ-P1 approximation based spectral analysis

Caveolin-1 Controls Hyperresponsiveness to Mechanical Stimuli and Fibrogenesis-Associated RUNX2 Activation in Keloid Fibroblasts

Central retinal vein occlusion and subsequent neovascular glaucoma after adalimumab treatment for psoriasis.

Clinicopathological study of Fox-Fordyce disease

Coagulation Factor XIII-A Subunit Missense Mutation in the Pathobiology of Autosomal Dominant Multiple Dermatofibromas

Congenital Anonychia and Uncombable Hair Syndrome: Coinheritance of Homozygous Mutations in RSPO4 and PADI3

Conjunctival geographic ulcer: an overlooked sign of herpes simplex virus infection

Dissecting folliculitis (dissecting cellulitis) of the scalp: a 66-patient case series and proposal of classification

Early intervention with high-dose steroid pulse therapy prolongs disease-free interval of severe alopecia areata: a retrospective study.

Ectodermal dysplasia-skin fragility syndrome resulting from a new atypical homozygous cryptic acceptor splice site mutation in PKP1.

Erythema multiforme, Stevens-Johnson syndrome, and toxic epidermal necrolysis: acute ocular manifestations, causes, and management

Erythema multiforme-like secondary syphilis in a HIV-positive bisexual man

Erythrokeratoderma Variabilis Caused by p.Gly45Glu in Connexin 31: Importance of the First Extracellular Loop Glycine Residue for Gap Junction Function.

Evanescent and persistent pruritic eruptions of adult-onset still disease: a clinical and pathologic study of 36 patients

Filaggrin: an emerging star in atopic march

Further evidence for genotype-phenotype disparity in Griscelli syndrome.

Genetic variants associated with phenytoin-related severe cutaneous adverse reactions

Good cosmesis of a large rhinophyma after carbon dioxide laser treatment

Granulomatous rosacea-like demodicidosis.

Higher body mass index is associated with greater severity of alopecia in men with male-pattern androgenetic alopecia in Taiwan: a cross-sectional study.

Homozygous acceptor splice site mutation in DSG1 disrupts plakoglobin localization and results in keratoderma and skin fragility.

Ichthyosis Prematurity Syndrome: From Fetus to Adulthood

Improved molecular diagnosis of the common recurrent intragenic deletion mutation in IKBKG in a Filipino family with incontinentia pigmenti.

Incontinentia pigmenti in a father and daughter

Insect bite-like reaction in association with chronic lymphocytic leukemia

Large Intragenic Deletion in DSTYK Underlies Autosomal-Recessive Complicated Spastic Paraparesis, SPG23.

Large, papillomatous and pedunculated nevus sebaceus

Late-onset comedonal Darier's disease caused by a recurrent ATP2A2 mutation

Lichen planus and lichenoid dermatoses: Clinical overview and molecular basis

Lichen planus and lichenoid dermatoses: Conventional and emerging therapeutic strategies

Linear lupus panniculitis of the scalp presenting as alopecia along Blaschko's lines: a distinct variant of lupus panniculitis in East Asians?

Lipodystrophia centrifugalis abdominalis infantilis: report of four cases

Mechanical coupling of cytoskeletal elasticity and force generation is crucial for understanding the migrating nature of keloid fibroblasts.

Mechanical forces in skin disorders.

Mechanobiological dysregulation of the epidermis and dermis in skin disorders and in degeneration ⬇️

Mutations in KLHL24 Add to the Molecular Heterogeneity of Epidermolysis Bullosa Simplex

Non-invasive evaluation of therapeutic response in keloid scar using diffuse reflectance spectroscopy

Noninvasive evaluation of collagen and hemoglobin contents and scattering property of in vivo keloid scars and normal skin using diffuse reflectance spectroscopy: pilot study.

Novel homozygous missense mutation in NT5C2 underlying hereditary spastic paraplegia SPG45.

Novel indel mutation of STS underlies a new phenotype of self-healing recessive X-linked ichthyosis

Novel p.Ala675Thr missense mutation in TRPV3 in Olmsted syndrome

PLACK syndrome resulting from a new homozygous insertion mutation in CAST.

Paper-based ELISA for the detection of autoimmune antibodies in body fluid-the case of bullous pemphigoid

Perifolliculitis capitis abscedens et suffodiens: eine Fallserie mit 66 Patienten und ein Vorschlag zur Klassifikation

Portable handheld diffuse reflectance spectroscopy system for clinical evaluation of skin: a pilot study in psoriasis patients

Predictive phenotyping of inherited ichthyosis by next-generation DNA sequencing.

Primary scarring alopecia: A retrospective study of 89 patients in Taiwan

Prognostic Role of Tumoral PDL1 Expression and Peritumoral FoxP3+ Lymphocytes in Vulvar Melanomas.

Progressive hyperpigmentation in a Taiwanese child due to an inborn error of vitamin B12 metabolism (cblJ).

Pterygium and thinning of nails as an unusual manifestation in Clouston syndrome

Recalcitrant extragenital giant condyloma acuminatum: A need for combination therapy

Semidominant GPNMB Mutations in Amyloidosis Cutis Dyschromica

Spatial distribution of filament elasticity determines the migratory behaviors of a cell

Successful treatment of recalcitrant pemphigus vulgaris and pemphigus vegetans with etanercept and carbon dioxide laser.

Syndromic inherited poikiloderma due to a de novo mutation in FAM111B.

Systematised naevus sebaceus resulting from post-zygotic mutation in HRAS

The Medication Risk of Stevens-Johnson Syndrome and Toxic Epidermal Necrolysis in Asians: The Major Drug Causality and Comparison to the USA FDA Label.

The Tension Biology of Wound Healing.

Thumbnail-squeezing method: an effective method for assessing Demodex density in rosacea

Time Series Integrative Analysis of RNA Sequencing and MicroRNA Expression Data Reveals Key Biologic Wound Healing Pathways in Keloid-Prone Individuals

Topical Betaxolol for Treating Relapsing Paronychia with Pyogenic Granuloma-Like Lesions Induced by Epidermal Growth Factor Receptor Inhibitors.

Toward reliable retrieval of functional information of papillary dermis using spatially resolved diffuse reflectance spectroscopy.

Treatment of hereditary epidermolysis bullosa: updates and future prospects.

[Primary human demodicosis. A disease sui generis]