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Hiroshi Kitoh

Showing results (111-120 of 133) with videos related to

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JBMR Plus|March 28, 2024
Long-term oral meclozine administration improves survival rate and spinal canal stenosis during postnatal growth in a mouse model of achondroplasia in both sexesHiroto Funahashi, Masaki Matsushita, Ryusaku Esaki, et al.
American Journal of Medical Genetics. Part A|May 13, 2006
Comprehensive screening of multiple epiphyseal dysplasia mutations in Japanese populationTaichi Itoh, Shuya Shirahama, Eiji Nakashima, et al.
Clinical Pediatric Endocrinology : Case Reports and Clinical Investigations : Official Journal of the Japanese Society for Pediatric Endocrinology|January 10, 2022
Inconvenience and adaptation in Japanese adult achondroplasia and hypochondroplasia: A cross-sectional studyAkiko Ajimi, Masaki Matsushita, Kenichi Mishima, et al.
Plos One|July 10, 2023
Phase 1b study on the repurposing of meclizine hydrochloride for children with achondroplasiaMasaki Matsushita, Hiroshi Kitoh, Kenichi Mishima, et al.
Human Mutation|May 17, 2005
The phenotypic spectrum of COL2A1 mutationsGen Nishimura, Nobuhiko Haga, Hiroshi Kitoh, et al.
Human Mutation|October 2, 2004
Novel and recurrent mutations clustered in the von Willebrand factor A domain of MATN3 in multiple epiphyseal dysplasiaAkihiko Mabuchi, Nobuhiko Haga, Koichi Maeda, et al.
Orphanet Journal of Rare Diseases|October 18, 2013
Perhexiline maleate in the treatment of fibrodysplasia ossificans progressiva: an open-labeled clinical trialHiroshi Kitoh, Masataka Achiwa, Hiroshi Kaneko, et al.
Calcified Tissue International|December 1, 2025
Efficacy and Safety of Oral Meclizine for Growth Promotion in Children with Achondroplasia: A Phase 2 Clinical TrialMasaki Matsushita, Hiroshi Kitoh, Takuo Kubota, et al.
Calcified Tissue International|May 13, 2026
Correction to: Efficacy and Safety of Oral Meclizine for Growth Promotion in Children with Achondroplasia: A Phase 2 Clinical TrialMasaki Matsushita, Hiroshi Kitoh, Takuo Kubota, et al.
Mutagenesis|July 30, 2015
Characterisation of novel RUNX2 mutation with alanine tract expansion from Japanese cleidocranial dysplasia patientAkio Shibata, Junichiro Machida, Seishi Yamaguchi, et al.
Pageof 14

Showing results (111-120 of 133) with videos related to

Sort By:
Pageof 14
JBMR Plus|March 28, 2024
Long-term oral meclozine administration improves survival rate and spinal canal stenosis during postnatal growth in a mouse model of achondroplasia in both sexesHiroto Funahashi, Masaki Matsushita, Ryusaku Esaki, et al.
American Journal of Medical Genetics. Part A|May 13, 2006
Comprehensive screening of multiple epiphyseal dysplasia mutations in Japanese populationTaichi Itoh, Shuya Shirahama, Eiji Nakashima, et al.
Clinical Pediatric Endocrinology : Case Reports and Clinical Investigations : Official Journal of the Japanese Society for Pediatric Endocrinology|January 10, 2022
Inconvenience and adaptation in Japanese adult achondroplasia and hypochondroplasia: A cross-sectional studyAkiko Ajimi, Masaki Matsushita, Kenichi Mishima, et al.
Plos One|July 10, 2023
Phase 1b study on the repurposing of meclizine hydrochloride for children with achondroplasiaMasaki Matsushita, Hiroshi Kitoh, Kenichi Mishima, et al.
Human Mutation|May 17, 2005
The phenotypic spectrum of COL2A1 mutationsGen Nishimura, Nobuhiko Haga, Hiroshi Kitoh, et al.
Human Mutation|October 2, 2004
Novel and recurrent mutations clustered in the von Willebrand factor A domain of MATN3 in multiple epiphyseal dysplasiaAkihiko Mabuchi, Nobuhiko Haga, Koichi Maeda, et al.
Orphanet Journal of Rare Diseases|October 18, 2013
Perhexiline maleate in the treatment of fibrodysplasia ossificans progressiva: an open-labeled clinical trialHiroshi Kitoh, Masataka Achiwa, Hiroshi Kaneko, et al.
Calcified Tissue International|December 1, 2025
Efficacy and Safety of Oral Meclizine for Growth Promotion in Children with Achondroplasia: A Phase 2 Clinical TrialMasaki Matsushita, Hiroshi Kitoh, Takuo Kubota, et al.
Calcified Tissue International|May 13, 2026
Correction to: Efficacy and Safety of Oral Meclizine for Growth Promotion in Children with Achondroplasia: A Phase 2 Clinical TrialMasaki Matsushita, Hiroshi Kitoh, Takuo Kubota, et al.
Mutagenesis|July 30, 2015
Characterisation of novel RUNX2 mutation with alanine tract expansion from Japanese cleidocranial dysplasia patientAkio Shibata, Junichiro Machida, Seishi Yamaguchi, et al.
Pageof 14