List of works - Michihiro Kono

A case of pustular psoriasis possibly precipitated by periodic oestrogen/gestagen therapy for Turner syndrome

scientific article published on 15 May 2019

A novel IFIH1 mutation in the pincer domain underlies the clinical features of both Aicardi-Goutières and Singleton-Merten syndromes in a single patient.

scientific article published on 5 August 2017

A novel NCSTN missense mutation in the signal peptide domain causes hidradenitis suppurativa, which has features characteristic of an autoinflammatory keratinization disease

scientific article published on 13 October 2019

A patient with bullous pemphigoid with mucosal involvement serologically positive for anti-BP230 autoantibodies only

scientific article published on 01 September 2019

Acrodermatitis continua of Hallopeau with dense infiltration of IgG -positive cells in the lesional dermis

scientific article published on 27 December 2018

Antiphospholipid antibody-positive Sjögren's syndrome with leg ulcers

scientific article published on 19 July 2019

Atopic dermatitis without serum immunoglobulin E elevation or loss-of-function filaggrin gene mutation in a patient with X-linked agammaglobulinemia

scientific article published on 27 November 2019

Autosomal dominant familial generalized pustular psoriasis caused by a CARD14 mutation

scientific article published on 10 March 2017

Autosomal dominant progressive hyperpigmentation and lentigines in a Japanese pedigree due to a missense mutation near the C-terminus of KIT

scientific article published on 25 September 2018

Bilateral striatal necrosis and dyschromatosis symmetrica hereditaria: A-I editing efficiency of ADAR1 mutants and phenotype expression

scientific article published on 29 May 2018

Case of mild X-linked ichthyosis complicated with paroxysmal supraventricular tachycardia and anemia

scientific article published on 22 March 2018

Deficient stratum corneum intercellular lipid in a Japanese patient with lamellar ichthyosis with a homozygous deletion mutation in SDR9C7.

scientific article published on 23 January 2017

Dermoscopic features of endocrine mucin-producing sweat gland carcinoma.

scientific article published on 27 November 2017

Drug-induced acute eosinophilic pneumonia due to hydroxychloroquine in a chilblain lupus patient

scientific article published on 03 May 2019

Filaggrin gene mutations may influence the persistence of food allergies in Japanese primary school children.

scientific article published on 25 January 2018

Frequent FOXA1-Activating Mutations in Extramammary Paget's Disease

scientific article published on 29 March 2020

Highly variable clinical feature and course of aggressive digital papillary adenocarcinoma

scientific article

Hyaline vascular-type unicentric Castleman disease presenting as a subcutaneous nodule in a child

scientific article published on 29 August 2018

Image Gallery: Unilaterally dominant acrokeratoelastoidosis (punctate palmoplantar keratoderma type 3).

scientific article

Mild case of Hailey-Hailey disease caused by a novel ATP2C1 mutation.

scientific article

Multiple pebble-like ectopic nails as a subsequent complication of phenol cauterization treatment for onychocryptosis

scientific article published on 30 January 2019

Mutational analysis of 29 patients with autosomal-recessive woolly hair and hypotrichosis: LIPH mutations are extremely predominant in autosomal-recessive woolly hair and hypotrichosis in Japan

scientific article published on 19 September 2016

Pathogenesis of a variant in the 5' untranslated region of ADAR1 in dyschromatosis symmetrica hereditaria

scientific article published on 11 January 2020

Sterol profiles are valuable biomarkers for phenotype expression of Conradi-Hünermann-Happle syndrome with EBP mutations

scientific article published on 06 August 2018

Subacute cutaneous lupus erythematosus with melanocyte elimination induced by pembrolizumab

scientific article published on 15 March 2020

Successful secukinumab treatment of recalcitrant juvenile generalized pustular psoriasis

scientific article published on 06 January 2020

Unilateral case of multiple minute digitate hyperkeratosis

scientific article published on 28 January 2019

List of works by Michihiro Kono

A case of pustular psoriasis possibly precipitated by periodic oestrogen/gestagen therapy for Turner syndrome

A novel IFIH1 mutation in the pincer domain underlies the clinical features of both Aicardi-Goutières and Singleton-Merten syndromes in a single patient.

A novel NCSTN missense mutation in the signal peptide domain causes hidradenitis suppurativa, which has features characteristic of an autoinflammatory keratinization disease

A patient with bullous pemphigoid with mucosal involvement serologically positive for anti-BP230 autoantibodies only

Acrodermatitis continua of Hallopeau with dense infiltration of IgG -positive cells in the lesional dermis

Antiphospholipid antibody-positive Sjögren's syndrome with leg ulcers

Atopic dermatitis without serum immunoglobulin E elevation or loss-of-function filaggrin gene mutation in a patient with X-linked agammaglobulinemia

Autosomal dominant familial generalized pustular psoriasis caused by a CARD14 mutation

Autosomal dominant progressive hyperpigmentation and lentigines in a Japanese pedigree due to a missense mutation near the C-terminus of KIT

Bilateral striatal necrosis and dyschromatosis symmetrica hereditaria: A-I editing efficiency of ADAR1 mutants and phenotype expression

Case of mild X-linked ichthyosis complicated with paroxysmal supraventricular tachycardia and anemia

Deficient stratum corneum intercellular lipid in a Japanese patient with lamellar ichthyosis with a homozygous deletion mutation in SDR9C7.

Dermoscopic features of endocrine mucin-producing sweat gland carcinoma.

Drug-induced acute eosinophilic pneumonia due to hydroxychloroquine in a chilblain lupus patient

Filaggrin gene mutations may influence the persistence of food allergies in Japanese primary school children.

Frequent FOXA1-Activating Mutations in Extramammary Paget's Disease

Highly variable clinical feature and course of aggressive digital papillary adenocarcinoma

Hyaline vascular-type unicentric Castleman disease presenting as a subcutaneous nodule in a child

Image Gallery: Unilaterally dominant acrokeratoelastoidosis (punctate palmoplantar keratoderma type 3).

Mild case of Hailey-Hailey disease caused by a novel ATP2C1 mutation.

Multiple pebble-like ectopic nails as a subsequent complication of phenol cauterization treatment for onychocryptosis

Mutational analysis of 29 patients with autosomal-recessive woolly hair and hypotrichosis: LIPH mutations are extremely predominant in autosomal-recessive woolly hair and hypotrichosis in Japan

Pathogenesis of a variant in the 5' untranslated region of ADAR1 in dyschromatosis symmetrica hereditaria

Sterol profiles are valuable biomarkers for phenotype expression of Conradi-Hünermann-Happle syndrome with EBP mutations

Subacute cutaneous lupus erythematosus with melanocyte elimination induced by pembrolizumab

Successful secukinumab treatment of recalcitrant juvenile generalized pustular psoriasis

Unilateral case of multiple minute digitate hyperkeratosis