各診療班の紹介
 
業績集 欧文
 
2008
 
 
A 欧 文
A-a
  1. Dateki S, Fukami M, Sato N, Muroya K, Adachi M, Ogata T: OTX2mutation in a patient with anophthalmia, short stature, and partial growth hormone deficiency: functional studies using the IRBP, HESX1, and POU1F1 promoters. J Clin Endocrinol Metab. 2008 Oct;93(10):3697-702,2008(IF:6.325)*
  2. Kuniba H, Tsuda M, Nakashima M, Miura S, Miyake N, Kondoh T, Matsumoto T, Moriuchi H, Ohashi H, Kurosawa K, Tonoki H, Nagai T, Okamoto N, Kato M, Fukushima Y, Naritomi K, Matsumoto N, Kinoshita A, Yoshiura KI, Niikawa N.:Lack of C20orf133 and FLRT3 mutations in 43 patients with Kabuki syndrome in Japan.J Med Genet. 45(7):479-80,2008 (IF 5.713)*○◎◇.
  3. Soyama A, Eguchi S, TakatsukiM, Ichikawa T, Moriuchi M, Moriuchi H, Nagamura T, Tajima Y, Kanematsu T: Human T-cell leukemia virus type I- associated myelopathy following living-donor liver transplantation. Liver Transplant 14(5):647-650,2008 (IF4.085)*
  4. Fukuoka H, Moriuchi M, Yano H, Nagayasu T, Moriuchi H.: No association of mousemammary tumorvirus-relatedretrovirus with Japanesecases of breast cancer. J Med Virol.80(8):1447-51.2008 (IF: 2.576) *◎
  5. Kuniba H, Pooh RK, Sasaki K, Shimokawa O, Harada N, Kondoh T, Egashira M, Moriuchi H, Yoshiura K, Niikawa N.: Prenatal diagnosis of Costello syndrome using 3D ultrasonography amniocentesis confirmation of the rare HRAS mutation G12D. Am J Med Genet A. 18:785-787.2008 (IF 2.555) *
  6. Nishitani S, Miyamura T, Tagawa M, Sumi M, Takase R, Doi H, Moriuchi H, Shinohara K.: The calming effect of a maternal breast milk odor on the human newborn infant.Neurosci Res. 63(1):66-71. 2008 (IF 2.473)*◎
  7. Muraoka I, Ohno Y, Kamitamari A, Okada M, Moriuchi H, Kanematsu T.: Congenitaloccurrence of solitaryinfantilemyofibromatosis of the spleen.J Pediatr Surg. 43(1):227-30,2008 (IF 1.557)*
  8. Naganuma M, Tominaga N, Miyamura T, Soda A, Moriuchi M, Moriuchi H.: TT virusprevalence, viralloads and genotypic variability in saliva from healthy Japanese children.Acta Paediatr. 97(12):1686-90, 2008 (IF 1.517) *○◎
  9. Tominaga N, Takahira S, Taguchi T, Imagawa T, Yokota S, Moriuchi H.: Acutepancreatitis associated with systemic lupus erythematosus: Successful treatment with plasmapheresis followed by aggressive immunosuppressive therapy. Pediatr Int. 50(1):109-11, 2008 (IF 0.677) *
  10. Egashira M, Kondoh T, Kawara H, Motomura H, Tagawa M, Harada N, Moriuchi H.: Mirrorduplication of chromosome21 with completephenotype of Down syndrome.Pediatr Int. 50(4):597-599, 2008 (IF 0.677) *
 
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