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Prader-Willi syndrome in a child with XYY.
Honma A, Ishii R, Ito A, Kato M, Saitoh S, Hayasaka K. Honma A, et al. Among authors: ishii r. J Hum Genet. 1999;44(6):412-3. doi: 10.1007/s100380050189. J Hum Genet. 1999. PMID: 10570915
Brainstem lesion in Aicardi-Goutières syndrome.
Kato M, Ishii R, Honma A, Ikeda H, Hayasaka K. Kato M, et al. Among authors: ishii r. Pediatr Neurol. 1998 Aug;19(2):145-7. doi: 10.1016/s0887-8994(98)00025-3. Pediatr Neurol. 1998. PMID: 9744637
Multiple sulphatase deficiency and carotenaemia.
Homma A, Ikeda H, Ishii R, Sukegawa K, Hayasaka K. Homma A, et al. Among authors: ishii r. J Inherit Metab Dis. 1996;19(1):88-9. doi: 10.1007/BF01799355. J Inherit Metab Dis. 1996. PMID: 8830185 No abstract available.
A case of adult type 1 Gaucher disease complicated by temporal intestinal hemorrhage.
Ito J, Saito T, Numakura C, Iwaba A, Sugahara S, Ishii R, Sato C, Haga H, Okumoto K, Nishise Y, Watanabe H, Ida H, Hayasaka K, Togashi H, Kawata S, Ueno Y. Ito J, et al. Among authors: ishii r. Case Rep Gastroenterol. 2013 Aug 16;7(2):340-6. doi: 10.1159/000354725. eCollection 2013. Case Rep Gastroenterol. 2013. PMID: 24019767 Free PMC article.
[Case of chronic type C hepatitis complicated with idiopathic thrombocytopenic purpura that was successfully treated by interferon therapy].
Karasawa T, Togashi H, Tajima K, Suzuki A, Onodera S, Haga H, Ishii R, Misawa K, Sanjo M, Okumoto K, Nishise Y, Ito J, Sugahara K, Saito K, Saito T, Kawata S. Karasawa T, et al. Among authors: ishii r. Nihon Shokakibyo Gakkai Zasshi. 2009 Mar;106(3):405-10. Nihon Shokakibyo Gakkai Zasshi. 2009. PMID: 19262055 Japanese.
921 results