List of works - Nobuo Kanazawa

A Case of Blau Syndrome with NOD2 E383K Mutation.

scientific article published on 24 June 2016

A Case of Hailey-Hailey Disease with a Novel Nonsense Mutation in the ATP2C1 Gene

scientific article published on 25 August 2017

A Japanese Family with Congenital Erythrocytosis Caused by Haemoglobin Bethesda

scientific article published on 15 September 2015

A case of neonatal-onset autoinflammatory syndrome with a de novo PSMB9 mutation resembling Nakajo-Nishimura syndrome

scientific article published on 28 September 2015

A new infant case of Nakajo-Nishimura syndrome with a genetic mutation in the immunoproteasome subunit: an overlapping entity with JMP and CANDLE syndrome related to PSMB8 mutations.

scientific article published on 8 August 2013

Anticomplement therapy in bullous pemphigoid

scientific article published on 21 July 2019

Atypical fibroxanthoma-a diagnosis of exclusion!

scientific article published on 15 January 2013

Autoimmunity versus autoinflammation from the 2nd JSID-Asia-Oceania-Forum, Wakayama, Japan, 5th December, 2010

scientific article published on 14 May 2011

Autoimmunity versus autoinflammation--friend or foe?

scientific article published on 09 July 2014

Beneficial effect of methotrexate on a child case of Nakajo-Nishimura syndrome

scientific article published on 06 May 2019

Calumenin, a Ca2+-binding Protein Retained in the Endoplasmic Reticulum with a Novel Carboxyl-terminal Sequence, HDEF ⬇️

scientific article published on July 18, 1997

Cancer, infection and disturbances of the integrity of tissue homeostasis: the most significant triggers for molecular mimicry and autoimmunity in dermatology?

scientific article published on 01 July 2014

Case of Legionella pneumophila pneumonia (legionellosis) developed in a psoriatic arthritis patient receiving adalimumab.

scientific article

Cutaneous polyarteritis nodosa: revisiting its definition and diagnostic criteria

scientific article published on 19 September 2008

Dendritic cell immunoreceptors: C-type lectin receptors for pattern-recognition and signaling on antigen-presenting cells.

scientific article published on 13 October 2006

Depletion of Epidermal Langerhans Cells in the Skin Lesions of Pellagra Patients.

scientific article published on 28 February 2017

Difference in distribution of malignant melanoma and melanocytic nevus in the palm and finger

scientific article published on 01 January 2019

Distribution analysis of infantile hemangioma or capillary malformation on the head and face in Japanese patients

scientific article published on 16 August 2019

Early-onset sarcoidosis and CARD15 mutations with constitutive nuclear factor-kappaB activation: common genetic etiology with Blau syndrome

scientific article published on 30 September 2004

Effective treatment of intractable skin ulcers using allogeneic cultured dermal substitutes in patients with systemic lupus erythematosus

scientific article published on 07 August 2009

Effects of sarpogrelate hydrochloride on skin ulcers and quality of life in patients with systemic sclerosis.

scientific article

Efficacy of 0.1% adapalene in a non-inflammatory Kyoto Rhino Rat acne model

scientific article published on 15 August 2014

Expression of prostate-specific antigen and androgen receptor in extramammary Paget's disease and carcinoma

scientific article published on 30 November 2006

Fractalkine and macrophage-derived chemokine: T cell-attracting chemokines expressed in T cell area dendritic cells.

scientific article published on June 1999

Genotyping of Trichophyton tonsurans isolate from a Japanese boy reveals infection in the USA.

scientific article published on 19 February 2009

HLA-DQ and RBFOX1 as susceptibility genes for an outbreak of hydrolyzed wheat allergy

scientific article published on 10 July 2019

Hereditary disorders presenting with urticaria

scientific article published on 26 September 2013

Identification of 736T>A mutation of lipase H in Japanese siblings with autosomal recessive woolly hair

scientific article published on 01 February 2011

Identification of a novel CCDC22 mutation in a patient with severe Epstein-Barr virus-associated hemophagocytic lymphohistiocytosis and aggressive natural killer cell leukemia

scientific article published on 31 January 2019

Influence of chemical peeling on the skin stress response system.

scientific article published on July 2012

Influence of trichloroacetic acid peeling on the skin stress response system.

scientific article

Intractable leg ulcers in Blau syndrome

scientific article published on 11 March 2016

Involvement of FcɛR1α immunopositive cells in alopecia areata with atopic dermatitis and a high titer of serum immunoglobulin E

scientific article published on 01 July 2014

Is CANDLE the best nomenclature?

scientific article published on 5 August 2014

Lupus erythematosus tumidus in Japan: a case report and a review of the literature.

scientific article published on 27 June 2009

Mast cells and histamine metabolism in skin lesions from MRL/MP-lpr/lpr mice

scientific article published on 20 January 2009

Molecular cloning of human dectin-2.

scientific article published in June 2004

Molecular cloning, characterization, and chromosomal localization of FKBP23, a novel FK506-binding protein with Ca2+-binding ability

scientific journal article

Monogenic early-onset sarcoidosis is no longer a variant of "idiopathic" sarcoidosis.

scientific article

Multiple courses of pulse corticosteroid therapy for alopecia areata.

scientific article

Nakajo-Nishimura syndrome

scientific article

No involvement of non-synonymous TLR2 polymorphisms in Japanese leprosy patients

scientific article published on 25 December 2008

Novel IL36RN mutation in a Japanese case of early onset generalized pustular psoriasis.

scientific article

Novel PSTPIP1 gene mutation in pyoderma gangrenosum, acne and suppurative hidradenitis syndrome.

scientific article published on 25 March 2018

Novel compound heterozygous DNA ligase IV mutations in an adolescent with a slowly-progressing radiosensitive-severe combined immunodeficiency

scientific article published on 11 July 2015

Pachyonychia congenita in Japan: report of familial cases with a recurrent KRT16 mutation

scientific article published on 01 January 2014

Pediatric pustular psoriasis with Turner's syndrome

scientific article published on 21 September 2015

Peripheral blood eosinophilia is associated with the presence of skin ulcers in patients with systemic sclerosis

scientific article published on 04 February 2019

Pluripotent Stem Cell Model of Nakajo-Nishimura Syndrome Untangles Proinflammatory Pathways Mediated by Oxidative Stress.

scientific article

Preliminary study of etidronate for prevention of corticosteroid-induced osteoporosis caused by oral glucocorticoid therapy

scientific article published on 01 March 2011

Prognostic factors of daily blood examination for advanced melanoma patients treated with nivolumab

scientific article published on 29 August 2018

Proteasome assembly defect due to a proteasome subunit beta type 8 (PSMB8) mutation causes the autoinflammatory disorder, Nakajo-Nishimura syndrome.

scientific article

Psoriatic arthritis induced by anti-programmed death 1 antibody pembrolizumab

scientific article published on 02 August 2019

Race differences in immunogenetic features and photosensitivity of cutaneous lupus erythematosus from the aspect of Japanese studies

scientific article published on 01 September 2009

Rare hereditary autoinflammatory disorders: towards an understanding of critical in vivo inflammatory pathways.

scientific article published on 18 January 2012

Repeated hyperhidrosis and chilblain-like swelling with ulceration of the fingers and toes in hereditary sensory and autonomic neuropathy type II

scientific article published on 27 April 2018

Role of the NOD2 genotype in the clinical phenotype of Blau syndrome and early-onset sarcoidosis.

scientific article

Sarcoidosis and molecular mimicry--important etiopathogenetic aspects: current state and future directions

scientific article published on 14 April 2012

Severe ulceration with impaired induction of growth factors and cytokines in keratinocytes after trichloroacetic acid application on TRPV1-deficient mice.

scientific article

Severer lupus erythematosus-like skin lesions in MRL/lpr mice with homozygous Kitwsh/wsh mutation

scientific article published on 11 July 2017

Signaling and immune regulatory role of the dendritic cell immunoreceptor (DCIR) family lectins: DCIR, DCAR, dectin-2 and BDCA-2.

scientific article published in January 2004

Steady state migratory RelB+ langerin+ dermal dendritic cells mediate peripheral induction of antigen-specific CD4+ CD25+ Foxp3+ regulatory T cells

scientific article

The cytosolic pattern-recognition receptor Nod2 and inflammatory granulomatous disorders

scientific article

The effect of hydroxychloroquine on lupus erythematosus-like skin lesions in MRL/lpr mice

scientific article published on 12 February 2016

The protective effects of ultraviolet A1 irradiation on spontaneous lupus erythematosus-like skin lesions in MRL/lpr mice

scientific article published on 26 April 2009

Ultrasonographic assessment reveals detailed distribution of synovial inflammation in Blau syndrome.

scientific article

WNK1/HSN2 founder mutation in patients with hereditary sensory and autonomic neuropathy: A Japanese cohort study.

scientific article

[Clinical features of Blau syndrome and early-onset sarcoidosis and associating CARD15/NOD2 gene mutations]

scientific article published on 01 April 2007

[Genetic involvement of bacterial sensor molecules in Japanese leprosy]

scientific article published on 01 September 2009

[Pathogenesis of cutaneous lupus erythematosus from LE-prone mice]

scientific article published on 01 January 2010

List of works by Nobuo Kanazawa

A Case of Blau Syndrome with NOD2 E383K Mutation.

A Case of Hailey-Hailey Disease with a Novel Nonsense Mutation in the ATP2C1 Gene

A Japanese Family with Congenital Erythrocytosis Caused by Haemoglobin Bethesda

A case of neonatal-onset autoinflammatory syndrome with a de novo PSMB9 mutation resembling Nakajo-Nishimura syndrome

A new infant case of Nakajo-Nishimura syndrome with a genetic mutation in the immunoproteasome subunit: an overlapping entity with JMP and CANDLE syndrome related to PSMB8 mutations.

Anticomplement therapy in bullous pemphigoid

Atypical fibroxanthoma-a diagnosis of exclusion!

Autoimmunity versus autoinflammation from the 2nd JSID-Asia-Oceania-Forum, Wakayama, Japan, 5th December, 2010

Autoimmunity versus autoinflammation--friend or foe?

Beneficial effect of methotrexate on a child case of Nakajo-Nishimura syndrome

Calumenin, a Ca2+-binding Protein Retained in the Endoplasmic Reticulum with a Novel Carboxyl-terminal Sequence, HDEF ⬇️

Cancer, infection and disturbances of the integrity of tissue homeostasis: the most significant triggers for molecular mimicry and autoimmunity in dermatology?

Case of Legionella pneumophila pneumonia (legionellosis) developed in a psoriatic arthritis patient receiving adalimumab.

Cutaneous polyarteritis nodosa: revisiting its definition and diagnostic criteria

Dendritic cell immunoreceptors: C-type lectin receptors for pattern-recognition and signaling on antigen-presenting cells.

Depletion of Epidermal Langerhans Cells in the Skin Lesions of Pellagra Patients.

Difference in distribution of malignant melanoma and melanocytic nevus in the palm and finger

Distribution analysis of infantile hemangioma or capillary malformation on the head and face in Japanese patients

Early-onset sarcoidosis and CARD15 mutations with constitutive nuclear factor-kappaB activation: common genetic etiology with Blau syndrome

Effective treatment of intractable skin ulcers using allogeneic cultured dermal substitutes in patients with systemic lupus erythematosus

Effects of sarpogrelate hydrochloride on skin ulcers and quality of life in patients with systemic sclerosis.

Efficacy of 0.1% adapalene in a non-inflammatory Kyoto Rhino Rat acne model

Expression of prostate-specific antigen and androgen receptor in extramammary Paget's disease and carcinoma

Fractalkine and macrophage-derived chemokine: T cell-attracting chemokines expressed in T cell area dendritic cells.

Genotyping of Trichophyton tonsurans isolate from a Japanese boy reveals infection in the USA.

HLA-DQ and RBFOX1 as susceptibility genes for an outbreak of hydrolyzed wheat allergy

Hereditary disorders presenting with urticaria

Identification of 736T>A mutation of lipase H in Japanese siblings with autosomal recessive woolly hair

Identification of a novel CCDC22 mutation in a patient with severe Epstein-Barr virus-associated hemophagocytic lymphohistiocytosis and aggressive natural killer cell leukemia

Influence of chemical peeling on the skin stress response system.

Influence of trichloroacetic acid peeling on the skin stress response system.

Intractable leg ulcers in Blau syndrome

Involvement of FcɛR1α immunopositive cells in alopecia areata with atopic dermatitis and a high titer of serum immunoglobulin E

Is CANDLE the best nomenclature?

Lupus erythematosus tumidus in Japan: a case report and a review of the literature.

Mast cells and histamine metabolism in skin lesions from MRL/MP-lpr/lpr mice

Molecular cloning of human dectin-2.

Molecular cloning, characterization, and chromosomal localization of FKBP23, a novel FK506-binding protein with Ca2+-binding ability

Monogenic early-onset sarcoidosis is no longer a variant of "idiopathic" sarcoidosis.

Multiple courses of pulse corticosteroid therapy for alopecia areata.

Nakajo-Nishimura syndrome

No involvement of non-synonymous TLR2 polymorphisms in Japanese leprosy patients

Novel IL36RN mutation in a Japanese case of early onset generalized pustular psoriasis.

Novel PSTPIP1 gene mutation in pyoderma gangrenosum, acne and suppurative hidradenitis syndrome.

Novel compound heterozygous DNA ligase IV mutations in an adolescent with a slowly-progressing radiosensitive-severe combined immunodeficiency

Pachyonychia congenita in Japan: report of familial cases with a recurrent KRT16 mutation

Pediatric pustular psoriasis with Turner's syndrome

Peripheral blood eosinophilia is associated with the presence of skin ulcers in patients with systemic sclerosis

Pluripotent Stem Cell Model of Nakajo-Nishimura Syndrome Untangles Proinflammatory Pathways Mediated by Oxidative Stress.

Preliminary study of etidronate for prevention of corticosteroid-induced osteoporosis caused by oral glucocorticoid therapy

Prognostic factors of daily blood examination for advanced melanoma patients treated with nivolumab

Proteasome assembly defect due to a proteasome subunit beta type 8 (PSMB8) mutation causes the autoinflammatory disorder, Nakajo-Nishimura syndrome.

Psoriatic arthritis induced by anti-programmed death 1 antibody pembrolizumab

Race differences in immunogenetic features and photosensitivity of cutaneous lupus erythematosus from the aspect of Japanese studies

Rare hereditary autoinflammatory disorders: towards an understanding of critical in vivo inflammatory pathways.

Repeated hyperhidrosis and chilblain-like swelling with ulceration of the fingers and toes in hereditary sensory and autonomic neuropathy type II

Role of the NOD2 genotype in the clinical phenotype of Blau syndrome and early-onset sarcoidosis.

Sarcoidosis and molecular mimicry--important etiopathogenetic aspects: current state and future directions

Severe ulceration with impaired induction of growth factors and cytokines in keratinocytes after trichloroacetic acid application on TRPV1-deficient mice.

Severer lupus erythematosus-like skin lesions in MRL/lpr mice with homozygous Kitwsh/wsh mutation

Signaling and immune regulatory role of the dendritic cell immunoreceptor (DCIR) family lectins: DCIR, DCAR, dectin-2 and BDCA-2.

Steady state migratory RelB+ langerin+ dermal dendritic cells mediate peripheral induction of antigen-specific CD4+ CD25+ Foxp3+ regulatory T cells

The cytosolic pattern-recognition receptor Nod2 and inflammatory granulomatous disorders

The effect of hydroxychloroquine on lupus erythematosus-like skin lesions in MRL/lpr mice

The protective effects of ultraviolet A1 irradiation on spontaneous lupus erythematosus-like skin lesions in MRL/lpr mice

Ultrasonographic assessment reveals detailed distribution of synovial inflammation in Blau syndrome.

WNK1/HSN2 founder mutation in patients with hereditary sensory and autonomic neuropathy: A Japanese cohort study.

[Clinical features of Blau syndrome and early-onset sarcoidosis and associating CARD15/NOD2 gene mutations]

[Genetic involvement of bacterial sensor molecules in Japanese leprosy]

[Pathogenesis of cutaneous lupus erythematosus from LE-prone mice]