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Rinsho Shinkeigaku = Clinical Neurology|November 1, 1994
[A familial Charcot-Marie-Tooth disease type 1B (CMTD1B) manifesting a new mutation of myelin P0 gene]Y Mitsui, T Matsui, Y Nakamura, et al.Rinsho Shinkeigaku = Clinical Neurology|June 1, 1994
[A family of hereditary motor and sensory neuropathy type I with a new type of myelin P0 mutation]A Ohnishi, K Ohnari, T Hashimoto, et al.Thrombosis and Haemostasis|May 1, 1997
Defective signal transduction through the thromboxane A2 receptor in a patient with a mild bleeding disorder: deficiency of the inositol 1,4,5-triphosphate formation despite normal G-protein activationT Mitsui, S Yokoyama, Y Shimizu, et al.Hormone and Metabolic Research = Hormon- Und Stoffwechselforschung = Hormones Et Metabolisme|December 3, 2008
Overexpression of protein kinase C-delta plays a crucial role in interleukin-6-producing pheochromocytoma presenting with acute inflammatory syndrome: a case reportH Tokuda, T Hosoi, K Hayasaka, et al.Journal of Viral Hepatitis|January 4, 2014
Chronic hepatitis E: a review of the literatureS Fujiwara, Y Yokokawa, K Morino, et al.Journal of Inherited Metabolic Disease|March 28, 2002
Severe hypoglycaemia in a patient with glycogen storage disease type III induced by infectious mononucleosisT Kimura, H Ikeda, M Kato, et al.No to Shinkei = Brain and Nerve|July 1, 1995
[Abnormality of PMP-22 gene in Japanese patients with Charcot-Marie-Tooth disease--comparison between Southern blot and polymerase chain reaction analysis in the detection of PMP-22 gene duplication]M Yamamoto, G Sobue, K Kumazawa, et al.American Journal of Medical Genetics|December 30, 1996
New form of platyspondylic lethal chondrodysplasiaK Akaba, G Nishimura, M Hashimoto, et al.Skeletal Radiology|May 21, 1998
Spondyloepiphyseal dysplasia with accumulation of glycoprotein in the chondrocytes: spondyloepiphyseal dysplasia, Stanescu typeG Nishimura, Y Saitoh, S Okuzumi, et al.The Japanese Journal of Human Genetics|December 1, 1992
Localization of PMP-22 gene (candidate gene for the Charcot-Marie-Tooth disease 1A) to band 17p11.2 by direct R-banding fluorescence in situ hybridizationE Takahashi, O Takeda, M Himoro, et al.Pageof 35