Search research articles
Contact Us
Filters
Showing results (21-30 of 162) with videos related to
Page
of 17
Sort By:
Journal of Pediatric Hematology/Oncology
|
June 5, 2010
Non-hodgkin lymphoma in a patient with cardiofaciocutaneous syndrome
Akira Ohtake, Yoko Aoki, Yuka Saito, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society
|
April 20, 2011
Fatal case of mitochondrial DNA depletion with severe asphyxia in a newborn
Yuya Nakano, Kei Murayama, Tomkoko Tsuruoka, et al.
Brain & Development
|
May 13, 2015
Reply to the letter: "The diagnostic value of MRI in pediatric chronic inflammatory demyelinating polyradiculoneuropathy"
Yuichi Abe, Hiroshi Terashima, Hideki Hoshino, et al.
Molecular Genetics and Metabolism Reports
|
February 25, 2025
A girl with intragenic variants in <i>MARS2</i> and a chondrodysplasia phenotype
Hiroyuki Iijima, Yuko Tsujioka, Yoshiyuki Tsutsumi, et al.
Biomolecules
|
August 29, 2024
Decidualized Endometrial Stromal Cells Promote Mitochondrial Beta-Oxidation to Produce the Octanoic Acid Required for Implantation
Yumi Mizuno, Shunsuke Tamaru, Hideno Tochigi, et al.
Molecular Genetics and Metabolism Reports
|
December 6, 2023
Enhanced osteoblastic differentiation of parietal bone in a novel murine model of mucopolysaccharidosis type II
Narutoshi Yamazaki, Mari Ohira, Shuji Takada, et al.
Molecular Genetics and Metabolism Reports
|
April 10, 2025
Corrigendum to "Enhanced osteoblastic differentiation of parietal bone in a novel murine model of mucopolysaccharidosis type II" [Molecular Genetics and Metabolism Reports Vol. 37, December 2023, 101021]
Narutoshi Yamazaki, Mari Ohira, Shuji Takada, et al.
Journal of Human Genetics
|
July 12, 2002
Expression analysis of two mutations in carnitine palmitoyltransferase IA deficiency
Emi Ogawa, Masaki Kanazawa, Shigenori Yamamoto, et al.
Brain & Development
|
February 18, 2015
Characteristic MRI features of chronic inflammatory demyelinating polyradiculoneuropathy
Yuichi Abe, Hiroshi Terashima, Hideki Hoshino, et al.
Eneurologicalsci
|
November 29, 2021
A Japanese family with P102L Gerstmann-Sträussler-Scheinker disease with a variant Creutzfeldt-Jakob disease-like phenotype among the siblings: A case report
Kazumichi Ota, Yoshihiko Nakazato, Ryu Yokoyama, et al.
Page
of 17
Search research articles
Search
Showing results (21-30 of 162) with videos related to
Sort By:
Page
of 17
Journal of Pediatric Hematology/Oncology
|
June 5, 2010
Non-hodgkin lymphoma in a patient with cardiofaciocutaneous syndrome
Akira Ohtake, Yoko Aoki, Yuka Saito, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society
|
April 20, 2011
Fatal case of mitochondrial DNA depletion with severe asphyxia in a newborn
Yuya Nakano, Kei Murayama, Tomkoko Tsuruoka, et al.
Brain & Development
|
May 13, 2015
Reply to the letter: "The diagnostic value of MRI in pediatric chronic inflammatory demyelinating polyradiculoneuropathy"
Yuichi Abe, Hiroshi Terashima, Hideki Hoshino, et al.
Molecular Genetics and Metabolism Reports
|
February 25, 2025
A girl with intragenic variants in <i>MARS2</i> and a chondrodysplasia phenotype
Hiroyuki Iijima, Yuko Tsujioka, Yoshiyuki Tsutsumi, et al.
Biomolecules
|
August 29, 2024
Decidualized Endometrial Stromal Cells Promote Mitochondrial Beta-Oxidation to Produce the Octanoic Acid Required for Implantation
Yumi Mizuno, Shunsuke Tamaru, Hideno Tochigi, et al.
Molecular Genetics and Metabolism Reports
|
December 6, 2023
Enhanced osteoblastic differentiation of parietal bone in a novel murine model of mucopolysaccharidosis type II
Narutoshi Yamazaki, Mari Ohira, Shuji Takada, et al.
Molecular Genetics and Metabolism Reports
|
April 10, 2025
Corrigendum to "Enhanced osteoblastic differentiation of parietal bone in a novel murine model of mucopolysaccharidosis type II" [Molecular Genetics and Metabolism Reports Vol. 37, December 2023, 101021]
Narutoshi Yamazaki, Mari Ohira, Shuji Takada, et al.
Journal of Human Genetics
|
July 12, 2002
Expression analysis of two mutations in carnitine palmitoyltransferase IA deficiency
Emi Ogawa, Masaki Kanazawa, Shigenori Yamamoto, et al.
Brain & Development
|
February 18, 2015
Characteristic MRI features of chronic inflammatory demyelinating polyradiculoneuropathy
Yuichi Abe, Hiroshi Terashima, Hideki Hoshino, et al.
Eneurologicalsci
|
November 29, 2021
A Japanese family with P102L Gerstmann-Sträussler-Scheinker disease with a variant Creutzfeldt-Jakob disease-like phenotype among the siblings: A case report
Kazumichi Ota, Yoshihiko Nakazato, Ryu Yokoyama, et al.
Page
of 17