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Shigeo Kure

Showing results (1-10 of 351) with videos related to

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Brain & Development|April 8, 2011
Two novel laboratory tests facilitating diagnosis of glycine encephalopathy (nonketotic hyperglycinemia)Shigeo Kure
Human Mutation|July 23, 2003
Detection of single nucleotide substitution by competitive allele-specific short oligonucleotide hybridization (CASSOH) with immunochromatographic stripYoichi Matsubara, Shigeo Kure
Clinical Medicine Insights. Circulatory, Respiratory and Pulmonary Medicine|October 30, 2015
Interstitial Lung Disease in Childhood: Clinical and Genetic AspectsHiroshi Kitazawa, Shigeo Kure
Journal of Human Genetics|December 4, 2018
Tetrahydrobipterin-responsive phenylalanine hydroxylase deficiencyShigeo Kure, Haruo Shintaku
No to Hattatsu = Brain and Development|April 18, 2014
[Pathology understanding of developmental disorders seen from the structure and functions of the genome]Shigeo Kure, Toshiyuki Yamamoto
Cardiology in the Young|June 21, 2016
An asymptomatic case of a single coronary artery in a 7-year-old girlHisao Yaoita, Masato Kimura, Shigeo Kure
Molecular Genetics and Metabolism|September 15, 2005
Atypical variants of nonketotic hyperglycinemiaArgirios Dinopoulos, Yoichi Matsubara, Shigeo Kure
Pediatric Pulmonology|January 19, 2016
ABCA3 mutations led to pulmonary fibrosis and emphysema with pulmonary hypertension in an 8-year-old girlChiharu Ota, Masato Kimura, Shigeo Kure
Pediatric Neurology|July 18, 2013
Head turning associated with involuntary gaze deviationYosuke Kakisaka, Naomi Hino-Fukuyo, Shigeo Kure
BMJ Case Reports|June 6, 2018
Asymptomatic left atrial appendage aneurysm (LAAA) with pericardial defect in a 1-year-old girlChiharu Ota, Masato Kimura, Masahiro Kitami, et al.
Pageof 36

Showing results (1-10 of 351) with videos related to

Sort By:
Pageof 36
Brain & Development|April 8, 2011
Two novel laboratory tests facilitating diagnosis of glycine encephalopathy (nonketotic hyperglycinemia)Shigeo Kure
Human Mutation|July 23, 2003
Detection of single nucleotide substitution by competitive allele-specific short oligonucleotide hybridization (CASSOH) with immunochromatographic stripYoichi Matsubara, Shigeo Kure
Clinical Medicine Insights. Circulatory, Respiratory and Pulmonary Medicine|October 30, 2015
Interstitial Lung Disease in Childhood: Clinical and Genetic AspectsHiroshi Kitazawa, Shigeo Kure
Journal of Human Genetics|December 4, 2018
Tetrahydrobipterin-responsive phenylalanine hydroxylase deficiencyShigeo Kure, Haruo Shintaku
No to Hattatsu = Brain and Development|April 18, 2014
[Pathology understanding of developmental disorders seen from the structure and functions of the genome]Shigeo Kure, Toshiyuki Yamamoto
Cardiology in the Young|June 21, 2016
An asymptomatic case of a single coronary artery in a 7-year-old girlHisao Yaoita, Masato Kimura, Shigeo Kure
Molecular Genetics and Metabolism|September 15, 2005
Atypical variants of nonketotic hyperglycinemiaArgirios Dinopoulos, Yoichi Matsubara, Shigeo Kure
Pediatric Pulmonology|January 19, 2016
ABCA3 mutations led to pulmonary fibrosis and emphysema with pulmonary hypertension in an 8-year-old girlChiharu Ota, Masato Kimura, Shigeo Kure
Pediatric Neurology|July 18, 2013
Head turning associated with involuntary gaze deviationYosuke Kakisaka, Naomi Hino-Fukuyo, Shigeo Kure
BMJ Case Reports|June 6, 2018
Asymptomatic left atrial appendage aneurysm (LAAA) with pericardial defect in a 1-year-old girlChiharu Ota, Masato Kimura, Masahiro Kitami, et al.
Pageof 36