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The British Journal of Dermatology
|
September 20, 2016
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
T Takeichi, K Tanahashi, T Taki, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV
|
December 20, 2021
Epithelioid cell granuloma formation in CARD14-associated papulosquamous eruptions
T Takeichi, K Ikeda, Y Muro, et al.
Nihon Ketsueki Gakkai Zasshi : Journal of Japan Haematological Society
|
May 1, 1988
[Inhibitory mechanism of plasma fibronectin on aggregation of elastase-treated platelet]
H Azuma, A Shirakami, T Shigekiyo, et al.
[Rinsho Ketsueki] the Japanese Journal of Clinical Hematology
|
February 1, 1984
[A case of elliptocytosis associated with defective neutrophil chemotaxis, B lymphocytopenia and hyperimmunoglobulinemia E]
H Nishino, T Takeichi, M Kosaka, et al.
The British Journal of Dermatology
|
November 10, 2018
Acrodermatitis continua of Hallopeau with dense infiltration of IgG4-positive cells in the lesional dermis
M Ogawa-Momohara, Y Muro, M Nakaguro, et al.
The British Journal of Dermatology
|
March 21, 2012
A novel IL36RN/IL1F5 homozygous nonsense mutation, p.Arg10X, in a Japanese patient with adult-onset generalized pustular psoriasis
K Sugiura, T Takeichi, M Kono, et al.
Revue Europeenne D'Etudes Cliniques Et Biologiques. European Journal of Clinical and Biological Research
|
April 1, 1970
Antigenic variant (WFT-2N) of a transplantable rat tumor induced by Friend virus
H Kobayashi, T Shirai, T Takeichi, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV
|
October 12, 2020
Cutaneous extramedullary hematopoiesis in a patient with secondary myelofibrosis due to MPL gene mutation
Y Murase, T Takeichi, K Tanahashi, et al.
Lancet (London, England)
|
March 1, 1986
Plasma fibronectin deficiency in eight members of one family
A Shirakami, T Shigekiyo, Y Hirai, et al.
Clinical and Experimental Dermatology
|
September 5, 2015
Intrafamilial phenotypic heterogeneity of epidermolytic ichthyosis associated with a new missense mutation in keratin 10
A Abdul-Wahab, T Takeichi, L Liu, et al.
Page
of 7
Search research articles
Search
Showing results (21-30 of 69) with videos related to
Sort By:
Page
of 7
The British Journal of Dermatology
|
September 20, 2016
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
T Takeichi, K Tanahashi, T Taki, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV
|
December 20, 2021
Epithelioid cell granuloma formation in CARD14-associated papulosquamous eruptions
T Takeichi, K Ikeda, Y Muro, et al.
Nihon Ketsueki Gakkai Zasshi : Journal of Japan Haematological Society
|
May 1, 1988
[Inhibitory mechanism of plasma fibronectin on aggregation of elastase-treated platelet]
H Azuma, A Shirakami, T Shigekiyo, et al.
[Rinsho Ketsueki] the Japanese Journal of Clinical Hematology
|
February 1, 1984
[A case of elliptocytosis associated with defective neutrophil chemotaxis, B lymphocytopenia and hyperimmunoglobulinemia E]
H Nishino, T Takeichi, M Kosaka, et al.
The British Journal of Dermatology
|
November 10, 2018
Acrodermatitis continua of Hallopeau with dense infiltration of IgG4-positive cells in the lesional dermis
M Ogawa-Momohara, Y Muro, M Nakaguro, et al.
The British Journal of Dermatology
|
March 21, 2012
A novel IL36RN/IL1F5 homozygous nonsense mutation, p.Arg10X, in a Japanese patient with adult-onset generalized pustular psoriasis
K Sugiura, T Takeichi, M Kono, et al.
Revue Europeenne D'Etudes Cliniques Et Biologiques. European Journal of Clinical and Biological Research
|
April 1, 1970
Antigenic variant (WFT-2N) of a transplantable rat tumor induced by Friend virus
H Kobayashi, T Shirai, T Takeichi, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV
|
October 12, 2020
Cutaneous extramedullary hematopoiesis in a patient with secondary myelofibrosis due to MPL gene mutation
Y Murase, T Takeichi, K Tanahashi, et al.
Lancet (London, England)
|
March 1, 1986
Plasma fibronectin deficiency in eight members of one family
A Shirakami, T Shigekiyo, Y Hirai, et al.
Clinical and Experimental Dermatology
|
September 5, 2015
Intrafamilial phenotypic heterogeneity of epidermolytic ichthyosis associated with a new missense mutation in keratin 10
A Abdul-Wahab, T Takeichi, L Liu, et al.
Page
of 7