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G Takada

Showing results (181-190 of 201) with videos related to

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American Heart Journal|February 1, 1993
Deletion of mitochondrial DNA in a patient with conduction blockW Sato, M Tanaka, S Sugiyama, et al.
American Heart Journal|June 1, 1994
Chylothorax, splenic lymphangiomatosis, and consumptive coagulopathy after surgical treatment of primary chylopericardiumK Harada, T Ito, T Shiota, et al.
Human Pathology|October 1, 1993
A case of fatal infectious mononucleosis presenting with fulminant hepatic failure associated with an extensive CD8-positive lymphocyte infiltration in the liverY Tazawa, F Nishinomiya, H Noguchi, et al.
American Heart Journal|October 1, 1994
Cardiomyopathy and angiopathy in patients with mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodesW Sato, M Tanaka, S Sugiyama, et al.
Therapeutic Apheresis : Official Journal of the International Society for Apheresis and the Japanese Society for Apheresis|March 22, 2001
Status of platelet collection and platelet transfusionS Omokawa, T Notoya, M Kumagai, et al.
Biochemical and Biophysical Research Communications|July 31, 1990
Multiple mitochondrial DNA deletions exist in cardiomyocytes of patients with hypertrophic or dilated cardiomyopathyT Ozawa, M Tanaka, S Sugiyama, et al.
Journal of Inherited Metabolic Disease|December 31, 1998
Mutational analyses in four Japanese families with X-linked liver phosphorylase kinase deficiency type 1H Hirono, Y Shoji, T Takahashi, et al.
Gan No Rinsho. Japan Journal of Cancer Clinics|February 1, 1990
[A case of malignant neuroepithelioma in the retroperitoneum]T Hara, S Matsuge, S Yamazaki, et al.
Acta Paediatrica Japonica : Overseas Edition|May 15, 1998
Neonatal intrahepatic cholestasis with hepatic siderosis and steatosisY Tazawa, F Nishinomiya, D Abukawa, et al.
Nature Genetics|November 1, 1993
De novo mutation of the myelin P0 gene in Dejerine-Sottas disease (hereditary motor and sensory neuropathy type III)K Hayasaka, M Himoro, Y Sawaishi, et al.
Pageof 21

Showing results (181-190 of 201) with videos related to

Sort By:
Pageof 21
American Heart Journal|February 1, 1993
Deletion of mitochondrial DNA in a patient with conduction blockW Sato, M Tanaka, S Sugiyama, et al.
American Heart Journal|June 1, 1994
Chylothorax, splenic lymphangiomatosis, and consumptive coagulopathy after surgical treatment of primary chylopericardiumK Harada, T Ito, T Shiota, et al.
Human Pathology|October 1, 1993
A case of fatal infectious mononucleosis presenting with fulminant hepatic failure associated with an extensive CD8-positive lymphocyte infiltration in the liverY Tazawa, F Nishinomiya, H Noguchi, et al.
American Heart Journal|October 1, 1994
Cardiomyopathy and angiopathy in patients with mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodesW Sato, M Tanaka, S Sugiyama, et al.
Therapeutic Apheresis : Official Journal of the International Society for Apheresis and the Japanese Society for Apheresis|March 22, 2001
Status of platelet collection and platelet transfusionS Omokawa, T Notoya, M Kumagai, et al.
Biochemical and Biophysical Research Communications|July 31, 1990
Multiple mitochondrial DNA deletions exist in cardiomyocytes of patients with hypertrophic or dilated cardiomyopathyT Ozawa, M Tanaka, S Sugiyama, et al.
Journal of Inherited Metabolic Disease|December 31, 1998
Mutational analyses in four Japanese families with X-linked liver phosphorylase kinase deficiency type 1H Hirono, Y Shoji, T Takahashi, et al.
Gan No Rinsho. Japan Journal of Cancer Clinics|February 1, 1990
[A case of malignant neuroepithelioma in the retroperitoneum]T Hara, S Matsuge, S Yamazaki, et al.
Acta Paediatrica Japonica : Overseas Edition|May 15, 1998
Neonatal intrahepatic cholestasis with hepatic siderosis and steatosisY Tazawa, F Nishinomiya, D Abukawa, et al.
Nature Genetics|November 1, 1993
De novo mutation of the myelin P0 gene in Dejerine-Sottas disease (hereditary motor and sensory neuropathy type III)K Hayasaka, M Himoro, Y Sawaishi, et al.
Pageof 21