Hiroshi Kitoh

Publication Activity (10 Years)

Years Active: 2016-2024
Publications (10 Years): 10

Top Topics

Total Knee Arthroplasty

Prognostic Factors

Top Venues

Molecular genetics & genomic medicine

Pediatric radiology

JBJS case connector

This page only lists publications with an associated author ORCID identifier.

Publications

Kenta Sawamura, Takashi Hamajima, Hiroshi Kitoh
Improvement of Fibrous Dysplasia After Burosumab Therapy in a Pediatric Patient with McCune-Albright Syndrome: A Case Report. JBJS case connector 14 (3) (2024)
Hiroshi Kitoh, Masaki Matsushita, Kenichi Mishima, Yasunari Kamiya, Kenta Sawamura
Disease-specific complications and multidisciplinary interventions in achondroplasia. Journal of bone and mineral metabolism 40 (2) (2022)
Kenta Sawamura, Hiroshi Kitoh, Hiroshi Kaneko, Akiko Kitamura, Tadashi Hattori
Prognostic factors for mobility in children with osteogenesis imperfecta. Medicine 101 (36) (2022)
Kenta Sawamura, Hiroshi Kitoh, Hiroshi Kaneko, Akiko Kitamura, Tadashi Hattori
Appropriate Surgical Timing of Salter Innominate Osteotomy for Residual Acetabular Dysplasia in Children. Journal of pediatric orthopedics 42 (10) (2022)
Hiroshi Kitoh
Clinical Aspects and Current Therapeutic Approaches for FOP. Biomedicines 8 (9) (2020)
Hiroshi Kitoh, Masaki Matsushita, Kenichi Mishima, Tadashi Nagata, Yasunari Kamiya, Kohei Ueda, Yachiyo Kuwatsuka, Hiroshi Morikawa, Yasuhiro Nakai, Naoki Ishiguro
Pharmacokinetics and safety after once and twice a day doses of meclizine hydrochloride administered to children with achondroplasia. PloS one 15 (4) (2020)
Kenichi Mishima, Atsushi Fujita, Seiji Mizuno, Masaki Matsushita, Tadashi Nagata, Yasunari Kamiya, Noriko Miyake, Naomichi Matsumoto, Shiro Imagama, Hiroshi Kitoh
Legg-Calvé-Perthes disease in a patient with Bardet-Biedl syndrome: A case report of a novel MKKS/BBS6 mutation. Clinical case reports 8 (12) (2020)
Tadashi Nagata, Masaki Matsushita, Kenichi Mishima, Yasunari Kamiya, Kohji Kato, Miho Toyama, Tomoo Ogi, Naoki Ishiguro, Hiroshi Kitoh
Severe achondroplasia due to two de novo variants in the transmembrane domain of FGFR3 on the same allele: A case report. Molecular genetics & genomic medicine 8 (3) (2020)
Kenichi Mishima, Hiroshi Kitoh, Masaki Matsushita, Tadashi Nagata, Yasunari Kamiya, Naoki Ishiguro
Extensive Bone Lengthening for a Patient with Linear Morphea. Case reports in orthopedics 2018 (2018)
Sachi Hasegawa, Teresa Victoria, Hülya Kayserili, Elaine Zackai, Gen Nishimura, Nobuhiko Haga, Yasuharu Nakashima, Osamu Miyazaki, Hiroshi Kitoh
Characteristic calcaneal ossification: an additional early radiographic finding in infants with fibrodysplasia ossificans progressiva. Pediatric radiology 46 (11) (2016)