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American Journal of Medical Genetics. Part A|July 3, 2003
EEC syndrome type 3 with a heterozygous germline mutation in the P63 gene and B cell lymphomaKeiko Akahoshi, Satoru Sakazume, Kenjiro Kosaki, et al.
The British Journal of Oral & Maxillofacial Surgery|May 18, 2005
Taste after reduction of the tongue in Beckwith-Wiedemann syndromeKensuke Matsune, Katsumi Miyoshi, Rika Kosaki, et al.
Clinical Pediatric Endocrinology : Case Reports and Clinical Investigations : Official Journal of the Japanese Society for Pediatric Endocrinology|July 21, 2021
20p11.23-p11.21 deletion in a child with hyperinsulinemic hypoglycemia and GH deficiency: A case reportDaisuke Sugawara, Misa Matsuura, Hiroaki Sato, et al.
European Journal of Obstetrics, Gynecology, and Reproductive Biology|June 2, 2009
Decreasing margins to the uterine serosa as a method for increasing the volume of fibroids ablated with magnetic resonance-guided focused ultrasound surgeryYutaka Morita, Sawako Takeuchi, Hiromi Hikida, et al.
Human Genetics|September 29, 2005
A type II collagen mutation also results in oto-spondylo-megaepiphyseal dysplasiaYoshinari Miyamoto, Eiji Nakashima, Hisatada Hiraoka, et al.
Congenital Anomalies|May 21, 2005
Refining chromosomal region critical for Down syndrome-related heart defects with a case of cryptic 21q22.2 duplicationRika Kosaki, Kenjiro Kosaki, Kazushige Matsushima, et al.
Human Genome Variation|October 28, 2025
Biallelic CPAMD8 variants in a patient with ectopia lentis associated with extraocular systemic features reminiscent of Marfan syndromeDaiju Oba, Mariko Sagara, Sayuri Oda, et al.
JACC. Case Reports|October 17, 2025
Artificial Intelligence-Driven High-Resolution Coronary CT Angiography for PCI Planning in Severe Coronary CalcificationHirofumi Ohashi, Hirohiko Ando, Masanobu Fujimoto, et al.
Clinical Case Reports|November 21, 2024
Rheocarna Effectively Treats Oral Medicinal Therapy-Resistant Cutaneous Symptoms and Renal Failure Induced by Cholesterol Crystal EmbolismAkinori Satake, Takahiro Tokuda, Hirofumi Ohashi, et al.
American Journal of Medical Genetics. Part A|September 15, 2005
Ehlers-Danlos syndrome type VIB with characteristic facies, decreased curvatures of the spinal column, and joint contractures in two unrelated girlsTomoki Kosho, Jun Takahashi, Hirofumi Ohashi, et al.
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