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Brain & Development
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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 strip
Yoichi Matsubara, Shigeo Kure
Clinical Medicine Insights. Circulatory, Respiratory and Pulmonary Medicine
|
October 30, 2015
Interstitial Lung Disease in Childhood: Clinical and Genetic Aspects
Hiroshi Kitazawa, Shigeo Kure
Journal of Human Genetics
|
December 4, 2018
Tetrahydrobipterin-responsive phenylalanine hydroxylase deficiency
Shigeo 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 girl
Hisao Yaoita, Masato Kimura, Shigeo Kure
Molecular Genetics and Metabolism
|
September 15, 2005
Atypical variants of nonketotic hyperglycinemia
Argirios 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 girl
Chiharu Ota, Masato Kimura, Shigeo Kure
Pediatric Neurology
|
July 18, 2013
Head turning associated with involuntary gaze deviation
Yosuke 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 girl
Chiharu Ota, Masato Kimura, Masahiro Kitami, et al.
Page
of 36
Search research articles
Search
Showing results (1-10 of 351) with videos related to
Sort By:
Page
of 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 strip
Yoichi Matsubara, Shigeo Kure
Clinical Medicine Insights. Circulatory, Respiratory and Pulmonary Medicine
|
October 30, 2015
Interstitial Lung Disease in Childhood: Clinical and Genetic Aspects
Hiroshi Kitazawa, Shigeo Kure
Journal of Human Genetics
|
December 4, 2018
Tetrahydrobipterin-responsive phenylalanine hydroxylase deficiency
Shigeo 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 girl
Hisao Yaoita, Masato Kimura, Shigeo Kure
Molecular Genetics and Metabolism
|
September 15, 2005
Atypical variants of nonketotic hyperglycinemia
Argirios 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 girl
Chiharu Ota, Masato Kimura, Shigeo Kure
Pediatric Neurology
|
July 18, 2013
Head turning associated with involuntary gaze deviation
Yosuke 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 girl
Chiharu Ota, Masato Kimura, Masahiro Kitami, et al.
Page
of 36