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Hiroshi Kitoh

Showing results (61-70 of 133) with videos related to

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Journal of Visualized Experiments : Jove|December 4, 2018
A Mouse Distraction Osteogenesis ModelMasahito Fujio, Yusuke Osawa, Masaki Matsushita, et al.
Bone Reports|October 11, 2022
Two children with hypophosphatasia with a heterozygous c.1559delT variant in the <i>ALPL</i> gene, the most common variant in Japanese populationsHiroshi Kitoh, Masako Izawa, Hiroshi Kaneko, et al.
Bone|September 30, 2004
Transplantation of marrow-derived mesenchymal stem cells and platelet-rich plasma during distraction osteogenesis--a preliminary result of three casesHiroshi Kitoh, Takahiko Kitakoji, Hiroki Tsuchiya, et al.
Journal of Pediatric Orthopedics. Part B|June 8, 2018
Changes in the range of motion of the lower limb joints during extensive tibial lengthening in achondroplasiaIzumi Kadono, Hiroshi Kitoh, Kenichi Mishima, et al.
Journal of Orthopaedic Science : Official Journal of the Japanese Orthopaedic Association|August 4, 2019
Lower limb pain following allogeneic hematopoietic stem cell transplantation in Japanese childrenKenichi Mishima, Hiroshi Kitoh, Masaki Matsushita, et al.
Molecular Syndromology|December 11, 2025
Out-of-Frame Transcript and in-Frame Deletion owing to a Novel Splice Mutation of <i>COL2A1</i> (c.1266+2T>A) in an Adult with Kniest Dysplasia: A Case ReportKenta Sawamura, Masaki Matsushita, Takaaki Okamoto, et al.
Case Reports in Genetics|December 25, 2024
Generalized Epileptic Seizures in Fibrodysplasia Ossificans Progressiva Harboring a Recurrent Heterozygous Variant of the <i>ACVR1</i> Gene (R206H)Kenichi Mishima, Hiroshi Kitoh, Anna Shiraki, et al.
Human Genetics|March 31, 2007
A recurrent mutation in type II collagen gene causes Legg-Calvé-Perthes disease in a Japanese familyYoshinari Miyamoto, Tatsuo Matsuda, Hiroshi Kitoh, et al.
Journal of Bone and Mineral Metabolism|April 6, 2013
A novel in-frame deletion of the RUNX2 gene causes a classic form of cleidocranial dysplasiaMasaki Matsushita, Hiroshi Kitoh, Hiroshi Kaneko, et al.
American Journal of Medical Genetics. Part A|September 17, 2013
A novel SOX9 H169Q mutation in a family with overlapping phenotype of mild campomelic dysplasia and small patella syndromeMasaki Matsushita, Hiroshi Kitoh, Hiroshi Kaneko, et al.
Pageof 14

Showing results (61-70 of 133) with videos related to

Sort By:
Pageof 14
Journal of Visualized Experiments : Jove|December 4, 2018
A Mouse Distraction Osteogenesis ModelMasahito Fujio, Yusuke Osawa, Masaki Matsushita, et al.
Bone Reports|October 11, 2022
Two children with hypophosphatasia with a heterozygous c.1559delT variant in the <i>ALPL</i> gene, the most common variant in Japanese populationsHiroshi Kitoh, Masako Izawa, Hiroshi Kaneko, et al.
Bone|September 30, 2004
Transplantation of marrow-derived mesenchymal stem cells and platelet-rich plasma during distraction osteogenesis--a preliminary result of three casesHiroshi Kitoh, Takahiko Kitakoji, Hiroki Tsuchiya, et al.
Journal of Pediatric Orthopedics. Part B|June 8, 2018
Changes in the range of motion of the lower limb joints during extensive tibial lengthening in achondroplasiaIzumi Kadono, Hiroshi Kitoh, Kenichi Mishima, et al.
Journal of Orthopaedic Science : Official Journal of the Japanese Orthopaedic Association|August 4, 2019
Lower limb pain following allogeneic hematopoietic stem cell transplantation in Japanese childrenKenichi Mishima, Hiroshi Kitoh, Masaki Matsushita, et al.
Molecular Syndromology|December 11, 2025
Out-of-Frame Transcript and in-Frame Deletion owing to a Novel Splice Mutation of <i>COL2A1</i> (c.1266+2T>A) in an Adult with Kniest Dysplasia: A Case ReportKenta Sawamura, Masaki Matsushita, Takaaki Okamoto, et al.
Case Reports in Genetics|December 25, 2024
Generalized Epileptic Seizures in Fibrodysplasia Ossificans Progressiva Harboring a Recurrent Heterozygous Variant of the <i>ACVR1</i> Gene (R206H)Kenichi Mishima, Hiroshi Kitoh, Anna Shiraki, et al.
Human Genetics|March 31, 2007
A recurrent mutation in type II collagen gene causes Legg-Calvé-Perthes disease in a Japanese familyYoshinari Miyamoto, Tatsuo Matsuda, Hiroshi Kitoh, et al.
Journal of Bone and Mineral Metabolism|April 6, 2013
A novel in-frame deletion of the RUNX2 gene causes a classic form of cleidocranial dysplasiaMasaki Matsushita, Hiroshi Kitoh, Hiroshi Kaneko, et al.
American Journal of Medical Genetics. Part A|September 17, 2013
A novel SOX9 H169Q mutation in a family with overlapping phenotype of mild campomelic dysplasia and small patella syndromeMasaki Matsushita, Hiroshi Kitoh, Hiroshi Kaneko, et al.
Pageof 14