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G Takada

Showing results (151-160 of 201) with videos related to

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The Tohoku Journal of Experimental Medicine|August 1, 1997
Changes in left ventricular diastolic filling patterns before and after the closure of the ductus arteriosus in very-low-birth weight infantsM Tamura, K Harada, Y Takahashi, et al.
Therapeutic Apheresis : Official Journal of the International Society for Apheresis and the Japanese Society for Apheresis|December 23, 1999
Evaluation of efficacy in platelet collection by the Haemonetics Component Collection SystemS Omokawa, G Takada, E Watanabe, et al.
Pediatric Cardiology|July 1, 1993
Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS) decrease in diastolic left ventricular function assessed by echocardiographyY Suzuki, K Harada, Y Miura, et al.
Annals of Neurology|January 23, 1999
Acute cerebellitis caused by Coxiella burnetiiY Sawaishi, I Takahashi, Y Hirayama, et al.
American Journal of Human Genetics|June 23, 1998
Evidence for linkage of human primary systemic carnitine deficiency with D5S436: a novel gene locus on chromosome 5qY Shoji, A Koizumi, T Kayo, et al.
Digestive Diseases and Sciences|March 25, 1998
Idiopathic neonatal hepatitis presenting as neonatal hepatic siderosis and steatosisY Tazawa, D Abukawa, S Maisawa, et al.
European Heart Journal|December 1, 1995
Morphological change of the 5th aortic arch with tetralogy of Fallot and pulmonary atresia: echocardiographic and angiographic findingsS Kishkurno, M Harada, M Tamura, et al.
Journal of Bioscience and Bioengineering|October 20, 2005
Production of D-lyxose from D-glucose by microbial and enzymatic reactionsZ Ahmed, H Sasahara, S H Bhuiyan, et al.
Journal of Inherited Metabolic Disease|January 1, 1994
Molecular and population genetics of phenylketonuria in Orientals: correlation between phenotype and genotypeY Okano, Y Hase, D H Lee, et al.
Pediatric Neurology|May 1, 1997
Cranial computed tomography scans of premature babies predict their eventual learning disabilitiesA Ishida, W Nakajima, H Arai, et al.
Pageof 21

Showing results (151-160 of 201) with videos related to

Sort By:
Pageof 21
The Tohoku Journal of Experimental Medicine|August 1, 1997
Changes in left ventricular diastolic filling patterns before and after the closure of the ductus arteriosus in very-low-birth weight infantsM Tamura, K Harada, Y Takahashi, et al.
Therapeutic Apheresis : Official Journal of the International Society for Apheresis and the Japanese Society for Apheresis|December 23, 1999
Evaluation of efficacy in platelet collection by the Haemonetics Component Collection SystemS Omokawa, G Takada, E Watanabe, et al.
Pediatric Cardiology|July 1, 1993
Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS) decrease in diastolic left ventricular function assessed by echocardiographyY Suzuki, K Harada, Y Miura, et al.
Annals of Neurology|January 23, 1999
Acute cerebellitis caused by Coxiella burnetiiY Sawaishi, I Takahashi, Y Hirayama, et al.
American Journal of Human Genetics|June 23, 1998
Evidence for linkage of human primary systemic carnitine deficiency with D5S436: a novel gene locus on chromosome 5qY Shoji, A Koizumi, T Kayo, et al.
Digestive Diseases and Sciences|March 25, 1998
Idiopathic neonatal hepatitis presenting as neonatal hepatic siderosis and steatosisY Tazawa, D Abukawa, S Maisawa, et al.
European Heart Journal|December 1, 1995
Morphological change of the 5th aortic arch with tetralogy of Fallot and pulmonary atresia: echocardiographic and angiographic findingsS Kishkurno, M Harada, M Tamura, et al.
Journal of Bioscience and Bioengineering|October 20, 2005
Production of D-lyxose from D-glucose by microbial and enzymatic reactionsZ Ahmed, H Sasahara, S H Bhuiyan, et al.
Journal of Inherited Metabolic Disease|January 1, 1994
Molecular and population genetics of phenylketonuria in Orientals: correlation between phenotype and genotypeY Okano, Y Hase, D H Lee, et al.
Pediatric Neurology|May 1, 1997
Cranial computed tomography scans of premature babies predict their eventual learning disabilitiesA Ishida, W Nakajima, H Arai, et al.
Pageof 21