H Kawai

Dysferlin mutations in Japanese Miyoshi myopathy

Takashi Takahashi, Masashi Aoki, M. Tateyama et al. · Neurology · 2003 · 78 citations

Radioimmunoassay for human myoglobin: methods and results in patients with skeletal muscle or myocardial disorders.

Keiko Miyoshi, Seiichi Saito, H Kawai et al. · Munich Personal RePEc Archive (Ludwig Maximilian University of Munich) · 1978 · 73 citations

HTLV‐I infection in patients with autoimmune thyroiditis (Hashimoto's thyroiditis)

H Kawai, Toshio Inui, Setsuko Kashiwagi et al. · Journal of Medical Virology · 1992 · 63 citations

Experimental glycerol myopathy: a histological study

H Kawai, Hiroshi Nishino, Kazuya Kusaka et al. · Acta Neuropathologica · 1990 · 46 citations

Experimental Glycerol Myopathy, Histopathology, Pathology +3

Adhalin gene mutations in patients with autosomal recessive childhood onset muscular dystrophy with adhalin deficiency.

H Kawai, M. Akaike, Takenori Endo et al. · Journal of Clinical Investigation · 1995 · 43 citations · Full text

Rare Diseases, Adhalin Gene Mutations, Developmental Biology +12