Kumi Shinahara

A case of recurrent myositis as the main manifestation of Behçet disease

Takeshi Ogose, Wataru Tamaki, Kumi Shinahara et al. · Pediatrics International · 2010 · 20 citations

Main Manifestation, Pathology, Recurrent Myositis +1

Single-strand conformation polymorphism analysis of the <i>FMR1</i> gene in autistic and mentally retarded children in Japan

Kumi Shinahara, Takahiko Saijo, Kenji Mori et al. · The Journal of Medical Investigation · 2004 · 11 citations · Full text

Genetics, Human Polymorphism, Molecular Biology +18

Three novel SURF-1 mutations in Japanese patients with Leigh syndrome

Yukiko Ogawa, Etsuo Naito, Michinori Ito et al. · Pediatric Neurology · 2002 · 10 citations

Genetic Disorder, Genetics, Molecular Biology +6

A Case of Recurrent Paroxysmal Cold Hemoglobinuria With the Different Temperature Thresholds of Donath-Landsteiner Antibodies

Takeshi Ogose, Yoshifumi Wakata, Masaya Kaneko et al. · Journal of Pediatric Hematology/Oncology · 2007 · 10 citations

Immunohematology, Immunology, Diagnosis +19