Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

T Takeichi

Showing results (41-50 of 69) with videos related to

Pageof 7
Sort By:
[Rinsho Ketsueki] the Japanese Journal of Clinical Hematology|June 1, 1984
[Decreases in plasma antithrombin III, fibrinogen, factor IX, X and XI, fibronectin and thyroxine binding globulin during therapy with L-asparaginase, vincristine and prednisolone in a patient with CML blastic crisis]H Nishino, S Miura, Y Hirai, et al.
Clinical and Experimental Dermatology|April 10, 2019
A case of pustular psoriasis possibly precipitated by periodic oestrogen/gestagen therapy for Turner syndromeT Shiratori, T Takeichi, M Kono, et al.
The British Journal of Dermatology|August 18, 2019
A novel NCSTN missense mutation in the signal peptide domain causes hidradenitis suppurativa, which has features characteristic of an autoinflammatory keratinization diseaseT Takeichi, T Matsumoto, T Nomura, et al.
Nihon Hotetsu Shika Gakkai Zasshi|February 1, 1987
[Histopathological study of pulpal irritation of dental adhesive resin. Part 1. Panavia EX]T Matsuura, T Katsumata, T Matsuura, et al.
The British Journal of Dermatology|December 23, 2017
A novel IFIH1 mutation in the pincer domain underlies the clinical features of both Aicardi-Goutières and Singleton-Merten syndromes in a single patientT Takeichi, C Katayama, T Tanaka, et al.
International Journal of Hematology|October 20, 2000
No increased risk of thrombosis in heterozygous congenital dysplasminogenemiaT Shigekiyo, M Kanazuka, K Aihara, et al.
[Rinsho Ketsueki] the Japanese Journal of Clinical Hematology|September 1, 1991
[IBL-type lymphadenopathy after infection of rubella virus]H Kondo, K Okagawa, T Takeichi, et al.
The British Journal of Dermatology|March 16, 2017
Autosomal dominant familial generalized pustular psoriasis caused by a CARD14 mutationT Takeichi, A Kobayashi, E Ogawa, et al.
The British Journal of Dermatology|June 3, 2015
Autosomal dominant diffuse nonepidermolytic palmoplantar keratoderma due to a recurrent mutation in aquaporin-5A Abdul-Wahab, T Takeichi, L Liu, et al.
The British Journal of Dermatology|June 1, 2018
Sterol profiles are valuable biomarkers for phenotype expression of Conradi-Hünermann-Happle syndrome with EBP mutationsT Takeichi, A Honda, Y Okuno, et al.
Pageof 7

Showing results (41-50 of 69) with videos related to

Sort By:
Pageof 7
[Rinsho Ketsueki] the Japanese Journal of Clinical Hematology|June 1, 1984
[Decreases in plasma antithrombin III, fibrinogen, factor IX, X and XI, fibronectin and thyroxine binding globulin during therapy with L-asparaginase, vincristine and prednisolone in a patient with CML blastic crisis]H Nishino, S Miura, Y Hirai, et al.
Clinical and Experimental Dermatology|April 10, 2019
A case of pustular psoriasis possibly precipitated by periodic oestrogen/gestagen therapy for Turner syndromeT Shiratori, T Takeichi, M Kono, et al.
The British Journal of Dermatology|August 18, 2019
A novel NCSTN missense mutation in the signal peptide domain causes hidradenitis suppurativa, which has features characteristic of an autoinflammatory keratinization diseaseT Takeichi, T Matsumoto, T Nomura, et al.
Nihon Hotetsu Shika Gakkai Zasshi|February 1, 1987
[Histopathological study of pulpal irritation of dental adhesive resin. Part 1. Panavia EX]T Matsuura, T Katsumata, T Matsuura, et al.
The British Journal of Dermatology|December 23, 2017
A novel IFIH1 mutation in the pincer domain underlies the clinical features of both Aicardi-Goutières and Singleton-Merten syndromes in a single patientT Takeichi, C Katayama, T Tanaka, et al.
International Journal of Hematology|October 20, 2000
No increased risk of thrombosis in heterozygous congenital dysplasminogenemiaT Shigekiyo, M Kanazuka, K Aihara, et al.
[Rinsho Ketsueki] the Japanese Journal of Clinical Hematology|September 1, 1991
[IBL-type lymphadenopathy after infection of rubella virus]H Kondo, K Okagawa, T Takeichi, et al.
The British Journal of Dermatology|March 16, 2017
Autosomal dominant familial generalized pustular psoriasis caused by a CARD14 mutationT Takeichi, A Kobayashi, E Ogawa, et al.
The British Journal of Dermatology|June 3, 2015
Autosomal dominant diffuse nonepidermolytic palmoplantar keratoderma due to a recurrent mutation in aquaporin-5A Abdul-Wahab, T Takeichi, L Liu, et al.
The British Journal of Dermatology|June 1, 2018
Sterol profiles are valuable biomarkers for phenotype expression of Conradi-Hünermann-Happle syndrome with EBP mutationsT Takeichi, A Honda, Y Okuno, et al.
Pageof 7