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Akio Shibata

Showing results (11-20 of 33) with videos related to

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Medicine|December 23, 2022
Solitary fibrous tumor of male breast: A case report and literature reviewShun Kawaguchi, Keiichi Kinowaki, Nobuko Tamura, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society|June 21, 2013
Severe retinopathy of prematurity with retinal detachment in monozygotic twinsKazumichi Fujioka, Ichiro Morioka, Shigeru Honda, et al.
Human Genome Variation|January 26, 2018
WNT10A variants isolated from Japanese patients with congenital tooth agenesisJunichiro Machida, Hiroaki Goto, Tadashi Tatematsu, et al.
Breast Cancer (Tokyo, Japan)|April 5, 2023
High-accuracy prediction of axillary lymph node metastasis in invasive lobular carcinoma using focal cortical thickening on magnetic resonance imagingShun Kawaguchi, Keiichi Kinowaki, Nobuko Tamura, et al.
European Journal of Oral Sciences|December 17, 2013
Novel nonsense mutation in MSX1 in familial nonsyndromic oligodontia: subcellular localization and role of homeodomain/MH4Masashi Kimura, Junichiro Machida, Seishi Yamaguchi, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|January 27, 2009
Identification of N-acetyl Proline-Glycine-Proline (acPGP) in human serum of adults and newborns by liquid chromatography-tandem mass spectrometryAkio Shibata, Ichiro Morioka, Chitose Ashi, et al.
Plos One|August 8, 2014
Characterization of novel MSX1 mutations identified in Japanese patients with nonsyndromic tooth agenesisSeishi Yamaguchi, Junichiro Machida, Munefumi Kamamoto, et al.
Archives of Disease in Childhood|September 28, 2014
Incidence of short stature at 3 years of age in late preterm infants: a population-based studyMiwako Nagasaka, Ichiro Morioka, Tomoyuki Yokota, et al.
Human Genome Variation|April 16, 2016
A novel PITX2 mutation causing iris hypoplasiaMasashi Kimura, Yoshihito Tokita, Junichiro Machida, et al.
Plos One|June 2, 2015
An aberrant splice acceptor site due to a novel intronic nucleotide substitution in MSX1 gene is the cause of congenital tooth agenesis in a Japanese familyTadashi Tatematsu, Masashi Kimura, Mitsuko Nakashima, et al.
Pageof 4

Showing results (11-20 of 33) with videos related to

Sort By:
Pageof 4
Medicine|December 23, 2022
Solitary fibrous tumor of male breast: A case report and literature reviewShun Kawaguchi, Keiichi Kinowaki, Nobuko Tamura, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society|June 21, 2013
Severe retinopathy of prematurity with retinal detachment in monozygotic twinsKazumichi Fujioka, Ichiro Morioka, Shigeru Honda, et al.
Human Genome Variation|January 26, 2018
WNT10A variants isolated from Japanese patients with congenital tooth agenesisJunichiro Machida, Hiroaki Goto, Tadashi Tatematsu, et al.
Breast Cancer (Tokyo, Japan)|April 5, 2023
High-accuracy prediction of axillary lymph node metastasis in invasive lobular carcinoma using focal cortical thickening on magnetic resonance imagingShun Kawaguchi, Keiichi Kinowaki, Nobuko Tamura, et al.
European Journal of Oral Sciences|December 17, 2013
Novel nonsense mutation in MSX1 in familial nonsyndromic oligodontia: subcellular localization and role of homeodomain/MH4Masashi Kimura, Junichiro Machida, Seishi Yamaguchi, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|January 27, 2009
Identification of N-acetyl Proline-Glycine-Proline (acPGP) in human serum of adults and newborns by liquid chromatography-tandem mass spectrometryAkio Shibata, Ichiro Morioka, Chitose Ashi, et al.
Plos One|August 8, 2014
Characterization of novel MSX1 mutations identified in Japanese patients with nonsyndromic tooth agenesisSeishi Yamaguchi, Junichiro Machida, Munefumi Kamamoto, et al.
Archives of Disease in Childhood|September 28, 2014
Incidence of short stature at 3 years of age in late preterm infants: a population-based studyMiwako Nagasaka, Ichiro Morioka, Tomoyuki Yokota, et al.
Human Genome Variation|April 16, 2016
A novel PITX2 mutation causing iris hypoplasiaMasashi Kimura, Yoshihito Tokita, Junichiro Machida, et al.
Plos One|June 2, 2015
An aberrant splice acceptor site due to a novel intronic nucleotide substitution in MSX1 gene is the cause of congenital tooth agenesis in a Japanese familyTadashi Tatematsu, Masashi Kimura, Mitsuko Nakashima, et al.
Pageof 4