各診療班の紹介
 
業績集 欧文
 
2010
 
 
A 欧 文
A-a
  1. S Dateki, K Kosaka, K Hasegawa, H Tanaka, N Azuma, S Yokoya, K Muroya,M Adachi, T Tajima, K Motomura, E Kinoshita, H Moriuchi, N Sato, M Fukami, T Ogata: Heterozygous Orthodenticle Homeobox 2 Mutations Are Associated with Variable Pituitary phenotype. J Clin Endocr Metab 95(2):756-764,2010(IF:6.202)*
  2. K Nakashima, K Ikeda, S Nishimura, Y Shibata, H Motomura, T Ohno, M Zaitsu, T Hara, Y Hamasaki, H Moriuchi: The Uteroglobin Gene G38A Polymorphism Is Not Associated with Kawasaki Disease. Acta Medica Nagasakiensia54(3): 53-58, 2010
  3. M Kawatani, A Nakai, T Okuno, R Kobata, M Moriuchi, H Moriuchi, H Tsukahara, M Mayumi: Detection of cytomegalovirus in preserved umbilical cord from a boy with autistic disorder. Pediatr Int52(2):304-307,2010(IF:0.707) *
  4. M Tagawa, T Minematsu, H Masuzaki, T Ishimura, H Moriuchi: Seroepidemiological survey of cytomegalovirus infection among pregnant women in Nagasaki, Japan. Pediatr Int52(3):459-462,2010(IF:0.707) *
  5. T Taga, Y Shimomura, Y Horikoshi, A Ogawa, M Itoh, M Okada, J Ueyama, T Higa, A Watanabe, H Kanegane, A Iwai, Y Saiwakawa, K Kogawa, J Yamanaka, and M Tsurusawa: Continuous and High-Dose Cytarabine Combined Chemotherapy in Children with Down Syndrome and Acute Myeloid Leukemia: Report from the Japanese Children's Cancer and Leukemia Study Group(JCCLSG)AML 9805 Down Study. Pediatr Blood Cancer, 2010. dec30 (IF:2.134) *
  6. S Dateki, M Fukami, A Uematsu, M Kaji, M Iso, M Ono, M Mizota, S Yokoya, K Motomura, E Kinoshita, H Moriuchi and T Ogata: Mutation and Gene Copy Number Analyses of Six Pituitary Transcription Factor Genes in 71 Patients with Combined Pituitary Hormone Deficiency: Identification of a Single Patient with LHX4 Deletion. J Clin Endocr Metab95(8): 4043-4047, 2010 (IF:6.202) *
  7. Y Funakoshi, A Nazneen, Y Nakashima, K Nakashima, M Okada, T Taguchi, H Moriuchi. Possible involvement of G-CSF in IgA nephropathy developing in an allogeneic peripheral blood SCT donor. Bone Marrow Transpl45(9): 1477-1478, 2010 (IF:2.998) *
  8. M Oikawa, H Kuniba, T Kondoh, A Kinoshita, T Nagayasu, N Niikawa, K Yoshiura: Familial brain arteriovenous malformation maps to 5p13-q14, 15q11-q13 or 18p11: Linkage analysis. Eur J Med Genet53(5): 244-249, 2010 (IF:1.568) *
 
長崎大学小児科学教室
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