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T Takeichi

Showing results (51-60 of 69) with videos related to

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[Rinsho Ketsueki] the Japanese Journal of Clinical Hematology|May 1, 1985
[Dysfibrinogenemia and nephrotic syndrome: a case report]T Shigekiyo, A Shirakami, S Kawauchi, et al.
Nihon Naika Gakkai Zasshi. the Journal of the Japanese Society of Internal Medicine|July 10, 1997
[A case of non-insulin-dependent diabetes mellitus with deficiency of cholesteryl ester transfer protein]K Kuriihara, M Miyata, Y Kanesaki, et al.
Hormone and Metabolic Research = Hormon- Und Stoffwechselforschung = Hormones Et Metabolisme|May 1, 1986
Changes in plasma fibronectin levels in thyroid diseasesA Shirakami, Y Hirai, T Takeichi, et al.
The British Journal of Dermatology|April 4, 2017
Granulocyte and monocyte apheresis can control juvenile generalized pustular psoriasis with mutation of IL36RNY Koike, M Okubo, T Kiyohara, et al.
The Japanese Journal of Antibiotics|April 1, 1987
[Clinical study on effects of cefmetazole on severe infections accompanied by hematologic diseases]A Shirakami, T Ohara, T Takeichi, et al.
The British Journal of Dermatology|January 24, 2017
Deficient stratum corneum intercellular lipid in a Japanese patient with lamellar ichthyosis with a homozygous deletion mutation in SDR9C7T Takeichi, T Nomura, H Takama, et al.
The British Journal of Dermatology|October 14, 2014
Whole-exome sequencing diagnosis of two autosomal recessive disorders in one familyT Takeichi, A Nanda, S Aristodemou, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|October 17, 2021
Mutations in SAM syndrome and palmoplantar keratoderma patients suggest genotype/phenotype correlations in DSG1 mutationsS Takeuchi, T Takeichi, Y Koike, et al.
The British Journal of Dermatology|May 1, 2018
Two cases of generalized pustular psoriasis complicated by IgG4-related diseaseH Miyazawa, Y Fujita, H Iwata, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|December 22, 2020
MEDNIK-like syndrome due to compound heterozygous mutations in AP1B1Y Ito, T Takeichi, S Igari, et al.
Pageof 7

Showing results (51-60 of 69) with videos related to

Sort By:
Pageof 7
[Rinsho Ketsueki] the Japanese Journal of Clinical Hematology|May 1, 1985
[Dysfibrinogenemia and nephrotic syndrome: a case report]T Shigekiyo, A Shirakami, S Kawauchi, et al.
Nihon Naika Gakkai Zasshi. the Journal of the Japanese Society of Internal Medicine|July 10, 1997
[A case of non-insulin-dependent diabetes mellitus with deficiency of cholesteryl ester transfer protein]K Kuriihara, M Miyata, Y Kanesaki, et al.
Hormone and Metabolic Research = Hormon- Und Stoffwechselforschung = Hormones Et Metabolisme|May 1, 1986
Changes in plasma fibronectin levels in thyroid diseasesA Shirakami, Y Hirai, T Takeichi, et al.
The British Journal of Dermatology|April 4, 2017
Granulocyte and monocyte apheresis can control juvenile generalized pustular psoriasis with mutation of IL36RNY Koike, M Okubo, T Kiyohara, et al.
The Japanese Journal of Antibiotics|April 1, 1987
[Clinical study on effects of cefmetazole on severe infections accompanied by hematologic diseases]A Shirakami, T Ohara, T Takeichi, et al.
The British Journal of Dermatology|January 24, 2017
Deficient stratum corneum intercellular lipid in a Japanese patient with lamellar ichthyosis with a homozygous deletion mutation in SDR9C7T Takeichi, T Nomura, H Takama, et al.
The British Journal of Dermatology|October 14, 2014
Whole-exome sequencing diagnosis of two autosomal recessive disorders in one familyT Takeichi, A Nanda, S Aristodemou, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|October 17, 2021
Mutations in SAM syndrome and palmoplantar keratoderma patients suggest genotype/phenotype correlations in DSG1 mutationsS Takeuchi, T Takeichi, Y Koike, et al.
The British Journal of Dermatology|May 1, 2018
Two cases of generalized pustular psoriasis complicated by IgG4-related diseaseH Miyazawa, Y Fujita, H Iwata, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|December 22, 2020
MEDNIK-like syndrome due to compound heterozygous mutations in AP1B1Y Ito, T Takeichi, S Igari, et al.
Pageof 7