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Jinrui Idengaku Zasshi. the Japanese Journal of Human Genetics|September 1, 1984
Biochemical heterogeneity of ornithine carbamoyl transferase(OCT) in patients with OCT deficiencyI Matsuda, N Nagata, K Ohyanagi, et al.
Journal of Biochemistry|December 1, 1984
Histamine metabolism in patients with histidinemia: determination of urinary levels of histamine, N tau-methylhistamine, imidazole acetic acid, and its conjugate(s)I Imamura, T Watanabe, Y Hase, et al.
Acta Paediatrica Japonica : Overseas Edition|December 1, 1988
Neonatal hypothyroid screening using enzymeimmunoassay of thyrotropin--comparison with radioimmunoassayS Kusuda, T Tsuruhara, Y Hase, et al.
Journal of Inherited Metabolic Disease|January 1, 1994
Prenatal diagnosis of 6-pyruvoyl tetrahydropterin synthase deficiency in seven subjectsH Shintaku, K J Hsiao, T T Liu, et al.
Journal of Inherited Metabolic Disease|January 1, 1988
Immunochemical evidence of pyruvate dehydrogenase (E1) deficiencyA Kitano, I Akaboshi, F Endo, et al.
Basal Facts|January 1, 1986
A template therapy approach for non-specific complaintsK Maehara, S Sato, F Takada, et al.
Clinical Genetics|December 1, 1996
Partial deletion of the long arm of chromosome 11: ten Japanese childrenJ Ono, T Hasegawa, S Sugama, et al.
The Journal of Clinical Endocrinology and Metabolism|November 1, 1978
A new method of paired thyrotropin assay as a screening test for neonatal hypothyroidismK Miyai, T Oura, M Kawashima, et al.
American Journal of Human Genetics|August 1, 1989
Polymorphic DNA haplotypes at the phenylalanine hydroxylase (PAH) locus in Asian families with phenylketonuria (PKU)S P Daiger, L Reed, S S Huang, et al.
Neuropathology and Applied Neurobiology|April 5, 2019
Carotid artery disease in post-stroke survivors and effects of enriched environment on stroke pathology in a mouse model of carotid artery stenosisY Hase, T M Polvikoski, M Ihara, et al.
Pageof 5

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

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 50 results.
Jinrui Idengaku Zasshi. the Japanese Journal of Human Genetics|September 1, 1984
Biochemical heterogeneity of ornithine carbamoyl transferase(OCT) in patients with OCT deficiencyI Matsuda, N Nagata, K Ohyanagi, et al.
Journal of Biochemistry|December 1, 1984
Histamine metabolism in patients with histidinemia: determination of urinary levels of histamine, N tau-methylhistamine, imidazole acetic acid, and its conjugate(s)I Imamura, T Watanabe, Y Hase, et al.
Acta Paediatrica Japonica : Overseas Edition|December 1, 1988
Neonatal hypothyroid screening using enzymeimmunoassay of thyrotropin--comparison with radioimmunoassayS Kusuda, T Tsuruhara, Y Hase, et al.
Journal of Inherited Metabolic Disease|January 1, 1994
Prenatal diagnosis of 6-pyruvoyl tetrahydropterin synthase deficiency in seven subjectsH Shintaku, K J Hsiao, T T Liu, et al.
Journal of Inherited Metabolic Disease|January 1, 1988
Immunochemical evidence of pyruvate dehydrogenase (E1) deficiencyA Kitano, I Akaboshi, F Endo, et al.
Basal Facts|January 1, 1986
A template therapy approach for non-specific complaintsK Maehara, S Sato, F Takada, et al.
Clinical Genetics|December 1, 1996
Partial deletion of the long arm of chromosome 11: ten Japanese childrenJ Ono, T Hasegawa, S Sugama, et al.
The Journal of Clinical Endocrinology and Metabolism|November 1, 1978
A new method of paired thyrotropin assay as a screening test for neonatal hypothyroidismK Miyai, T Oura, M Kawashima, et al.
American Journal of Human Genetics|August 1, 1989
Polymorphic DNA haplotypes at the phenylalanine hydroxylase (PAH) locus in Asian families with phenylketonuria (PKU)S P Daiger, L Reed, S S Huang, et al.
Neuropathology and Applied Neurobiology|April 5, 2019
Carotid artery disease in post-stroke survivors and effects of enriched environment on stroke pathology in a mouse model of carotid artery stenosisY Hase, T M Polvikoski, M Ihara, et al.
Pageof 5