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Genetic analysis of the ferrochelatase gene in eight Japanese patients from seven families with erythropoietic protoporphyria

Journal of dermatology, 2006-09, Vol.33 (9), p.603-608

2006

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Early onset sarcoidosis masquerading as juvenile rheumatoid arthritis

Journal of the American Academy of Dermatology, 2000-11, Vol.43 (5), p.969-971

2000

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A Novel Point Mutation in the Keratin 17 Gene in a Japanese Case of Pachyonychia Congenita Type 2

Journal of investigative dermatology, 2002-03, Vol.118 (3), p.545-547

2002

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Early onset sarcoidosis masquerading as juvenile rheumatoid arthritis

Journal of the American Academy of Dermatology, 2000-11, Vol.43 (5), p.969-971

2000

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Analyses of the transglutaminase 1 gene mutation and ultrastructural characteristics in a Japanese patient with lamellar ichthyosis

Journal of dermatological science, 2000-11, Vol.24 (2), p.119-125

2000

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Novel mutations in GJB2 encoding connexin-26 in Japanese patients with keratitis-ichthyosis-deafness syndrome

British journal of dermatology (1951), 2003-04, Vol.148 (4), p.649-653

2003

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Histopathologic and Ultrastructural Studies of Angiokeratoma Corporis Diffusum in Kanzaki Disease

Journal of dermatology, 1995-01, Vol.22 (1), p.10-18

1995

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Failure to detect paramyxovirus RNA in the skin of connective tissue disease

Journal of dermatological science, 1996, Vol.11 (1), p.70-75

1996

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Two patients with severe corneal disease in KID syndrome

American journal of ophthalmology, 2004, Vol.137 (1), p.181-183

2004

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Mutations in the ED1 gene in Japanese families with X-linked hypohidrotic ectodermal dysplasia

Experimental Dermatology, 2003-08, Vol.12 (4), p.518-522

2003

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Expression of Adrenomedullin, a Hypotensive Peptide, in the Trophoblast Giant Cells at the Embryo Implantation Site in Mouse

Developmental biology, 1998-11, Vol.203 (2), p.264-275

1998

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Genome-Wide Mapping of Unselected Transcripts From Extraembryonic Tissue of 7.5-Day Mouse Embryos Reveals Enrichment in the t-Complex and Under-Representation on the X Chromosome

Human molecular genetics, 1998-11, Vol.7 (12), p.1967-1978

1998

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ORIGINAL ARTICLE: Genetic analysis of the ferrochelatase gene in eight Japanese patients from seven families with erythropoietic protoporphyria

Journal of dermatology, 2006-09, Vol.33 (9), p.603-608

2006

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Estrogen dermatitis: a dendritic-cell-mediated allergic condition

Dermatology (Basel), 2003-01, Vol.207 (3), p.265

2003

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Curved nail of the fourth toe

Journal of the American Academy of Dermatology, 1999, Vol.40 (1), p.124-125

1999

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A frameshift mutation of the ED1 gene in sibling cases with X-linked hypohidrotic ectodermal dysplasia

Dermatology (Basel), 2003-01, Vol.207 (2), p.178

2003

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A Novel Point Mutation Affecting the Tyrosine Kinase Domain of the TRKA Gene in a Family with Congenital Insensitivity to Pain with Anhidrosis

Journal of investigative dermatology, 1999-05, Vol.112 (5), p.810-814

1999

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A Novel a(- 4)-to-g Acceptor Splice Site Mutation Leads to Three Bases Insertion in Ferrochelatase mRNA in a Patient with Erythropoietic Protoporphyria

Journal of investigative dermatology, 2001-07, Vol.117 (1), p.159-161

2001

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A Novel Point Mutation of the EDA Gene in a Japanese Family with Anhidrotic Ectodermal Dysplasia

Journal of investigative dermatology, 1998-12, Vol.111 (6), p.1246-1247

1998

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A case of symptomatic heterozygous female Fabry's disease without detectable mutation in the alpha-galactosidase gene

Dermatology (Basel), 2000-01, Vol.200 (3), p.262

2000

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Staining of eccrine and apocrine neoplasms and metastatic adenocarcinoma with IKH-4, a monoclonal antibody specific for the eccrine gland

Journal of cutaneous pathology, 1998-02, Vol.25 (2), p.100-105

1998

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Cloning and Expression Analyses of Mouse Dystroglycan Gene: Specific Expression in Maternal Decidua at the Peri-Implantation Stage

Human molecular genetics, 1996-09, Vol.5 (9), p.1259-1267

1996

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A novel point mutation affecting the tyrosine kinase domain of the nerve growth factor receptor gene, TRKA, in a family with congenital insensitivity to pain with anhidrosis

Journal of dermatological science, 1998-03, Vol.16, p.S144-S144

1998

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Molecular defect of ferrochelatase in five Japanese patients with erythropoietic protoporphyria

Journal of dermatological science, 1998-03, Vol.16, p.S149-S149

1998

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Basal cell carcinoma occurring in multiple familial trichoepithelioma: detection of loss of heterozygosity in chromosome 9q

Archives of dermatology (1960), 1997-05, Vol.133 (5), p.666

1997

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Genetic analysis of the ferrochelatase gene in eight Japanese patients from seven families with erythropoietic protoporphyria

Early onset sarcoidosis masquerading as juvenile rheumatoid arthritis

A Novel Point Mutation in the Keratin 17 Gene in a Japanese Case of Pachyonychia Congenita Type 2

Early onset sarcoidosis masquerading as juvenile rheumatoid arthritis

Analyses of the transglutaminase 1 gene mutation and ultrastructural characteristics in a Japanese patient with lamellar ichthyosis

Novel mutations in GJB2 encoding connexin-26 in Japanese patients with keratitis-ichthyosis-deafness syndrome

Histopathologic and Ultrastructural Studies of Angiokeratoma Corporis Diffusum in Kanzaki Disease

Failure to detect paramyxovirus RNA in the skin of connective tissue disease

Two patients with severe corneal disease in KID syndrome

Mutations in the ED1 gene in Japanese families with X-linked hypohidrotic ectodermal dysplasia

Expression of Adrenomedullin, a Hypotensive Peptide, in the Trophoblast Giant Cells at the Embryo Implantation Site in Mouse

Genome-Wide Mapping of Unselected Transcripts From Extraembryonic Tissue of 7.5-Day Mouse Embryos Reveals Enrichment in the t-Complex and Under-Representation on the X Chromosome

ORIGINAL ARTICLE: Genetic analysis of the ferrochelatase gene in eight Japanese patients from seven families with erythropoietic protoporphyria

Estrogen dermatitis: a dendritic-cell-mediated allergic condition

Curved nail of the fourth toe

A frameshift mutation of the ED1 gene in sibling cases with X-linked hypohidrotic ectodermal dysplasia

A Novel Point Mutation Affecting the Tyrosine Kinase Domain of the TRKA Gene in a Family with Congenital Insensitivity to Pain with Anhidrosis

A Novel a(- 4)-to-g Acceptor Splice Site Mutation Leads to Three Bases Insertion in Ferrochelatase mRNA in a Patient with Erythropoietic Protoporphyria

A Novel Point Mutation of the EDA Gene in a Japanese Family with Anhidrotic Ectodermal Dysplasia

A case of symptomatic heterozygous female Fabry's disease without detectable mutation in the alpha-galactosidase gene

Staining of eccrine and apocrine neoplasms and metastatic adenocarcinoma with IKH-4, a monoclonal antibody specific for the eccrine gland

Cloning and Expression Analyses of Mouse Dystroglycan Gene: Specific Expression in Maternal Decidua at the Peri-Implantation Stage

A novel point mutation affecting the tyrosine kinase domain of the nerve growth factor receptor gene, TRKA, in a family with congenital insensitivity to pain with anhidrosis

Molecular defect of ferrochelatase in five Japanese patients with erythropoietic protoporphyria

Basal cell carcinoma occurring in multiple familial trichoepithelioma: detection of loss of heterozygosity in chromosome 9q

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