S. Yotsumoto

发表

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

T. Kanzaki, T. Hashiguchi, S. Yotsumoto, 2003, Experimental dermatology.

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

K. Matsunaga, H. Akamatsu, T. Kanzaki, 2003, The British journal of dermatology.

Improving Sun Protection Behaviour in Children: Study Design and Baseline Results of a Randomized Trial in Italian Elementary Schools

J. Utikal, C. Klemke, T. Waldmann, 2003, Dermatology.

A novel point mutation affecting the tyrosine kinase domain of the TRKA gene in a family with congenital insensitivity to pain with anhidrosis.

T. Saheki, K. Kobayashi, M. Setoyama, 1999, The Journal of investigative dermatology.

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

D. Mehregan, K. Hashimoto, D. Mehregan, 1998, Journal of cutaneous pathology.

A novel point mutation in the keratin 17 gene in a Japanese case of pachyonychia congenita type 2.

T. Saheki, Keiko Kobayashi, M. Setoyama, 2002, The Journal of investigative dermatology.

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

M. Akiyama, T. Saheki, K. Yoneda, 2000, Journal of dermatological science.

The beta subunit of the high‐affinity IgE receptor, a candidate for atopic dermatitis, is not imprinted

T. Kanzaki, S. Yotsumoto, M. S. Ko, 2000, The British journal of dermatology.

Anaplastic Large Cell Lymphoma, So‐called Ki‐1 Lymphoma: A Report of a Case of Long Course

T. Kanekura, M. Setoyama, S. Yotsumoto, 1991, The Journal of dermatology.

Ultrastructural immunocytochemical studies of blood group substances in human eccrine glands.

S. Tsuyama, M. Tashiro, S. Yotsumoto, 1990, The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society.

Selenium deficiency: report of a case

T. Kanekura, N. Maeno, T. Kanzaki, 2005, Clinical and experimental dermatology.

Two patients with severe corneal disease in KID syndrome.

S. Sonoda, E. Uchino, K. Sonoda, 2004, American journal of ophthalmology.

A Case of Chromomycosis with Tumor‐like Growth

T. Shimada, K. Fukumitsu, H. Hamada, 1996, The Journal of dermatology.

A case of follicular mucinosis treated successfully with minocycline

T. Kanzaki, S. Yotsumoto, H. Uchimiya, 2000, The British journal of dermatology.

A new case of α‐N‐acetylgalactosaminidase deficiency with angiokeratoma corporis diffusum, with Ménière's syndrome and without mental retardation

Y. Hirabayashi, Y. Nagatsuka, R. Abe, 2001, The British journal of dermatology.

Histopathologic and Ultrastructural Studies of Angiokeratoma Corporis Diffusum in Kanzaki Disease

S. Yotsumoto, M. Yokota, M. Koji, 1995, The Journal of dermatology.

Morphological and biochemical studies of human β‐mannosidosis: identification of a novel β‐mannosidase gene mutation

T. Kanzaki, T. Hashiguchi, S. Yotsumoto, 2003, The British journal of dermatology.

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.

J. Eppig, M. Ko, Xuepeng Wang, 1998, Human molecular genetics.

Expression of adrenomedullin, a hypotensive peptide, in the trophoblast giant cells at the embryo implantation site in mouse.

M. Ko, H. Nakashima, C. Cui, 1998, Developmental biology.

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

H. Fujiwara, K. Hashimoto, S. Yotsumoto, 1996, Journal of dermatological science.

Estrogen Dermatitis: A Dendritic-Cell-Mediated Allergic Condition

T. Kanekura, T. Kanzaki, T. Hashiguchi, 2003, Dermatology.

A Frameshift Mutation of the ED1 Gene in Sibling Cases with X-Linked Hypohidrotic Ectodermal Dysplasia

Koichiro Nakamura, F. Kaneko, T. Kanzaki, 2003, Dermatology.

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

T. Kanekura, T. Kanzaki, S. Yotsumoto, 2006, The Journal of dermatology.

A novel A(-4)-to-G acceptor splice site mutation leads to three bases insertion in ferrochelatase mRNA in a patient with erythropoietic protoporphyria.

T. Saheki, S. Taketani, K. Kobayashi, 2001, The Journal of investigative dermatology.

Cloning and expression analyses of mouse dystroglycan gene: specific expression in maternal decidua at the peri-implantation stage.

M. Ko, J. Horton, S. Yotsumoto, 1996, Human molecular genetics.

Virilizing adrenal adenoma stimulated by dexamethasone in a middle-aged woman.

T. Aizawa, T. Yamada, S. Yotsumoto, 1979, The Journal of clinical endocrinology and metabolism.

Chronic lupoid leishmaniasis. Evaluation by polymerase chain reaction.

D. Mehregan, H. Fujiwara, D. Mehregan, 1996, Archives of dermatology.

Chronic lupoid leishmaniasis : evaluation by polymerase chain reaction

D. Mehregan, A. Momeni, H. Fujiwara, 1996 .

A novel point mutation of the EDA gene in a Japanese family with anhidrotic ectodermal dysplasia.

T. Saheki, K. Kobayashi, T. Kanzaki, 1998, The Journal of investigative dermatology.

A Case of Symptomatic Heterozygous Female Fabry’s Disease without Detectable Mutation in the Alpha-Galactosidase Gene

S. Hamaguchi, T. Kanzaki, S. Yotsumoto, 2000, Dermatology.

Ultracytochemistry of glycoconjugates in rat Brunner's gland with labeled lectins.

S. Tsuyama, M. Tashiro, S. Yotsumoto, 1990, Journal of electron microscopy.

Early onset sarcoidosis masquerading as juvenile rheumatoid arthritis.

K. Miyata, S. Takei, T. Kanzaki, 2000, Journal of the American Academy of Dermatology.

Curved nail of the fourth toe.

T. Kanzaki, S. Yotsumoto, 1999, Journal of the American Academy of Dermatology.