Tatsuro Kondoh
Department of Pediatrics
Nagasaki University School of Medicine Nagasaki University
Nagasaki
Japan
Name/email consistency: high
- A Japanese case of oto-palato-digital syndrome type II: an apparent lack of phenotype-genotype correlation. Kondoh, T., Okamoto, N., Norimatsu, N., Uetani, M., Nishimura, G., Moriuchi, H. J. Hum. Genet. (2007)
- Genotype-phenotype correlation of 5p-syndrome: pitfall of diagnosis. Kondoh, T., Shimokawa, O., Harada, N., Doi, T., Yun, C., Gohda, Y., Kinoshita, F., Matsumoto, T., Moriuchi, H. J. Hum. Genet. (2005)
- Dramatic improvement in Down syndrome-associated cognitive impairment with donepezil. Kondoh, T., Amamoto, N., Doi, T., Hamada, H., Ogawa, Y., Nakashima, M., Sasaki, H., Aikawa, K., Tanaka, T., Aoki, M., Harada, J., Moriuchi, H. Ann. Pharmacother (2005)
- Hearing impairment, undescended testis, circumferential skin creases, and mental handicap (HITCH) syndrome: a case report. Kondoh, T., Eguchi, J., Hamasaki, Y., Doi, T., Kinoshita, E., Matsumoto, T., Abe, K., Ohtani, Y., Moriuchi, H. Am. J. Med. Genet. A (2004)
- A case of Schinzel-Giedion syndrome complicated with progressive severe gingival hyperplasia and progressive brain atrophy. Kondoh, T., Kamimura, N., Tsuru, A., Matsumoto, T., Matsuzaka, T., Moriuchi, H. Pediatr. Int (2001)
- Condition of microcephaly, growth retardation, joint contractures, atopic dermatitis, and mental retardation in two Japanese sisters: a new autosomal recessive MCA/MR syndrome?. Kondoh, T., Yamamoto, T., Kono, Y., Matsumoto, T., Sugawara, H., Matsumoto, N., Moriuchi, H. Am. J. Med. Genet. (2001)
- Severe cervical kyphosis in osteopathia striata with cranial sclerosis: case report. Kondoh, T., Yoshinaga, M., Matsumoto, T., Takayanagi, T., Uetani, M., Kubota, T., Nishimura, G., Moriuchi, H. Pediatr. Radiol (2001)
