研究業績

Publications 2006

  • Aramaki M, Hokuto I, Matsumoto T, Ishimoto H, Inoue M, Kimura T, Oikawa Y, Ikeda K, Yoshimura Y, Takahashi T, Kosaki K. Iridic and retinal coloboma associated with prenatal methimazole exposure. Am J Med Genet 2006;139.
  • Aramaki M, Udaka T, Kosaki R, Makita Y, Okamoto N, Yoshihashi H, Oki H, Nanao K, Moriyama N, Oku S, Hasegawa T, Takahashi T, Fukushima Y, Kawame H, Kosaki K. Phenotypic spectrum of CHARGE syndrome with CHD7 mutations. J Pediatr 2006;148:410-414.
  • Aramaki M, Udaka T, Torii C, Samejima H, Kosaki R, Takahashi T, Kosaki K. Comprehensive screening of CHD7 mutations among patients with CHARGE Syndrome using denaturing high-performance liquid chromatography. Genet Test (in press)
  • Bamba M, Jozaki K, Sugaya N, Tamai S, Ishihara J, Kori T, Shiro H, Takeuchi Y, Cho H, Nakao A, Okano Y, Kimura K, Komiyama O, Nonoyama M, Kobayashi I, Kato T, Sunakawa K. Prospective surveillance for atypical pathogens in children with community-acquired pneumonia in Japan. Journal of Infection and Chemotherapy 2006;12:36-41.
  • Batista CM, Kippin TE, Willaime-Morawek S, Shimabukuro KM, Akamatsu W, van der Kooy D. A Progressive and Cell Non-Autonomous Increase in Striatal Neural Stem Cells in the Huntingtonメs Disease R6/2 Mouse. J.Neurosci (in press)
  • Fujita H, Samejima H, Kitagawa N, Mitsuhashi T, Washio T, Yonemoto J, Tomita M, Takahashi T, Kosaki K. Genome-wide screening of dioxin-responsive genes in fetal brain: bioinformatic and experimental approaches. Congenit Anom (in press)
  • Fukami M, Kato F, Tajima T, Yokoya S, Ogata T. Transactivation function of a ~800 bp evolutionally conserved sequence at the SHOX 3' region: implication for the downstream enhancer. Am J Hum Genet 2006; 78:167-170.
  • Fukami M, Wada Y, Miyabayashi K, Nishino I, Hasegawa T, Camerino G, Kretz C, Buj-Bello A, Laporte J, Yamada G, Morohashi K, Ogata T. CXorf6 is a novel causative gene for hypospadias. Nat Genet (in press)
  • Fukuhara Y, Li XK, Kitazawa Y, Inagaki M, Matsuoka K, Kosuga M, Kosaki R, Shimazaki T, Endo H, Umezawa A, Okano H, Takahashi T, Okuyama T. Histopathological and behavioral improvement of murine mucopolysaccharidosis type VII by intracerebral transplantation of neural stem cells. Mol Ther 2006;13:548-555.
  • Goto M, Nishimura G, Nagai T, Yamazawa K, Ogata T. Familial Klippel-Feil anomaly and t(5;8)(q35.1;p21.1) translocation. Am J Med Genet 2006; A140:1013-1015.
  • Hasegawa K, Kobayashi R, Takada E, Ono A, Chiba N, Morozumi M, Iwata S, Sunakawa K, Ubukata K. Nationwide Surveillance for Bacterial Meningitis.: High prevalence of type b beta-lactamase-non-producing ampicillin-resistant Haemophilus influenzae in meningitis: the situation in Japan where Hib vaccine has not been introduced. J Antimicrob Chemother 2006;57:1077-1082.
  • Hasegawa K, Kobayashi R, Takada E, Ono A, Chiba N, Morozumi M, Iwata S, Sunakawa K, Ubukata K. High prevalence of type b β-lactamase-non-producing ampicillin-resistant Haemophilus influenzae in meningitis: the situation in Japan where Hib vaccine has not been introduced. J Antimicrob Chemother 2006;57:1077-1082.
  • Hirose Y, Nakashima E, Ohashi H, Mochizuki H, Bando Y, Ogata T, Adachi M, Toba E, Nishimura G, Ikegawa S. Identification of novel RMRP mutations and specific founder haplotypes in Japanese patients with cartilage-hair hypoplasia. J Hum Genet (in press)
  • Homma K, Hasegawa T, Nagai T, Adachi M, Horikawa R, Fujiwara I, Tajima T, Takeda R, Fukami M, Ogata T. Urine steroid hormone profile analysis in cytochrome P450 oxidereductase deficiency: Implication for the backdoor pathway to dihydrotestosterone. J Clin Endocrinol Metab 2006;91:2643-2649.
  • Hoshii S, Wada N, Honda M. A survey of peritonitis and exit-site and/or tunnel infections in Japanese children on PD. Pediatr Nephrol 2006;21:828-834.
  • Hososaka Y, Hanaki H, Yanagisawa C, Yamaguchi Y, Matsui H, Nakae T, Iwata S, Hayashi I, Sunakawa K. Nosocomial infection of beta-lactam antibiotic-induced vancomycin-resistant Staphylococcus aureus (BIVR). J Infect Chemother 2006;12:181-184.
  • Ikeda K, Hayashida S, Hokuto I, Kusuda S, Nishida H. Recent short-term outcomes of ultrapremature infants born at 22-23 weeks' gestation and infants born weighing less than 500 grams in Japan . NeoReviews (in press)
  • Inagaki K, Suzuki T, Ito S, Suzuki N, Adachi K, Okuyama T, Nakata Y, Shimizu H, Matsuura H, Oono T, Iwamatsu H, Kono M, Tomita Y. Oculocutaneous albinism type 4: six novel mutations in the membrane-associated transporter protein gene and their phenotypes. Pigment Cell Res 2006;19:451-453.
  • Inagaki M, Mori T, Tsunematsu Y, Ambo H, Kawai Y. Use of recombinant activated factor VII to control bleeding in a young child with qualitative platelet disorder: a case report. Blood Coagul Fibrinolysis 2006;17:317-322.
  • Inokuchi M, Hasegawa T, Anzo M, Matsuo N. Standardized Centile Curves of Body Mass Index for Japanese Children and Adolescents Based on the 1978-1981 National Survey Data. Ann Hum Biol (in press)
  • Inokuchi M, Matsuo N, Anzo M, Takayama JI, Hasegawa T. Age dependent percentile for waist circumference for Japanese children based on the 1992-1994 cross-sectional national survey data. Eur J Pediatr (in press)
  • Ishikura K, Ikeda M, Hamasaki Y, Hataya H, Shishido S, Asanuma H, Nishimura G, Hiramoto R, Honda M. Posterior Reversible Encephalopathy Syndrome in Children:Its High Prevalence and More Extensive Imaging Findings. AJKD 2006;48:231-238.
  • Ishikura K, Kamimaki I, Hamasaki Y, Hataya H, Ikeda M, Honda M. QUIZ PAGE(What is the cause of the increase in kidney size?). AJKD 2006;47:xxxvii.
  • Itoh T, Shirahama S, Nakashima E, Maeda K, Haga N, Kitoh H, Kosaki R, Ohashi H, Nishimura G, Ikegawa S. Comprehensive screening of multiple epiphyseal dysplasia mutations in Japanese population. Am J Med Genet 2006;140:1280-1284.
  • Izumi K, Kosaki K, Benirschke K, Jones K. Umbilical cord length in urinary tract abnormalities associated with oligohydramnios: Evidence regarding developmental pathogenesis. Fetal Pediatr Pathol (in press)
  • Izumi K, Yahagi N, Fujii Y, Higuchi M, Kosaki R, Naito Y, Nishimura G, Hosokai N, Takahashi T, Kosaki K. Cleidocranial dysplasia plus vascular anomalies with 6p21.2 microdeletion spanning RUNX2 and VEGF. Am J Med Genet 2006;140:398-401.
  • Kamada M, Nagai T, Kumagai T, Igarashi M, Ihara T, Okafuji T, Ochiai H, Sakiyama H, Shimomura K, Suzuki E, Torigoe S, Miyazaki C, Miyata A, Yuri K, Ito Y, Nakayama T, Kase T, Okuno Y. Efficacy of inactivated influenza vaccine in alleviating the febrile illness of culture-confirmed influenza in children in the 2000-2001 influenza season. Vaccine 2006;24:3618-3623.
  • Kato S, Hanabusa H, Kaneko S, Takakuwa K, Suzuki M, Kuji N, Jinno M, Tanaka R, Kojima K, Iwashita M, Yoshimura Y, Tanaka K. Complete removal of HIV-1 RNA and proviral DNA from semen by the swim-up method: assisted reproduction technique using spermatozoa free from HIV-1. AIDS 2006;20:967-973.
  • Kobayashi S, Murayama S, Tatsuzawa O, Koinuma G, Kawasaki K, Kiyotani C, Kumagai M. X-linked severe combined immunodeficiency (X-SCID) with high blood levels of immunoglobulins and Aspergillus pneumonia successfully treated with micafangin followed by unrelated cord blood stem cell transplantation. Eur J Pediatr 2006;[Epub ahead of print].
  • Kohda E, Yamazaki H, Hisazumi H, Tutumi Y, Ogata T, Shiraga N. Imaging of congenital lipoid adrenal hyperplasia. Radiation Medicine 2006;24:217-219.
  • Komase K, Nakayama T, Iijima M, Miki K, Kawanishi R, Uejima H. The phosphoprotein of attenuated measles AIK-C vaccine strain contributes to its temperature-sensitive phenotype. Vaccine 2006;24:826-834.
  • Konno M, Baba S, Mikawa H, Hara K, Matsumoto F, Kaga K, Nishimura T, Kobayashi T, Furuya N, Moriyama H, Okamoto Y, Furukawa M, Yamanaka N, Matsushima T, Yoshizawa Y, Kohno S, Kobayashi K, Morikawa A, Koizumi S, Sunakawa K, Inoue M, Ubukata K. Study of upper respiratory tract bacterial flora: first report. Variations in upper respiratory tract bacterial flora in patients with acute upper respiratory tract infection and healthy subjects and variations by subject age. J Infect Chemother 2006;12:83-96.
  • Kosaki K, Takahashi D, Udaka T, Kosaki R, Matsumoto M, Ibe S, Isobe T, Tanaka Y, Takahashi T. Molecular Pathology of Shprintzen-Goldberg Syndrome. Am J Med Genet 2006;140:104-108.
  • Kosaki R, Hanai S, Kakishima H, Okada M, Hayashi S, Ito Y, Takahashi T, Kosaki K, Okuyama T. Discrepancies in cytogenetic results between amniocytes and postnatally obtained blood: trisomy 9 mosaicism. Congenit Anom 2006;46:115-117.
  • Kosaki R, Kamiishi A, Sugiyama R, Kawai M, Hasegawa T, Kosaki K. Hypothyroidism in Peters plus syndrome. Ophthalmic Genet 2006;27:67-69.
  • Kosaki R, Okuyama T, Tanaka T MO, Kosaki K. Monozygotic twins of Smith -Magenis syndrome. Am J Med Genet (in press)
  • Maeda J, Yamagishi H, McAnally J, Yamagishi C, Srivastava D. Tbx1 is regulated by forkhead proteins in the secondary heart field. Developmental Dynamics 2006;235:701-710.
  • Matsune K, Miyoshi K, Kosaki R, Ohashi H, Maeda T. Taste after reduction of the tongue in Beckwith-Wiedemann syndrome. Br J Oral Maxillofac Surg 2006;44:49-51.
  • Matsuyama T, Syoji K, Watanabe H, Shimizu M, Saotome Y, Nagao T, Matsuo N, Hase T, Tokimitsu I, Nakaya N. Effects of diacylglycerol oil on adiposity in obese children: initial communication. J Pediatr Endocrinol Metab 2006;19:795-804.
  • Matsuzaki Y, Xu Y, Ikegami M, Besnard V, Park KS , Hull WM, Wert SE, Whitsett JA. Stat3 is required for cytoprotection of the respiratory epithelium during adenoviral infection. J Immunol 2006;177:527-537.
  • Miyairi I, Byrne GI. Chlamydia and programmed cell death. Curr Opin Microbiol 2006;9:102-108.
  • Miyairi I, Causey KT, DeVincenzo JP, Buckingham SC. Group B streptococcal ventriculitis: a report of three cases and literature review. Pediatr Neurol 2006;34:395-399.
  • Miyairi I, Mahdi OS, Ouellette SP, Belland RJ, Byrne GI. Different Growth Rates of Chlamydia trachomatis Biovars Reflect Pathotype. J Infect Dis 2006;194:350-357.
  • Miyamoto J, Asanuma, Nakai H, Hasegawa T, Nawata H, Hasegawa Y. Mutational analysis of androgen receptor genes (AR) in 46,XY patients with ambiguous genitalia and normal testosterone secretion: Endocrinological characteristics of three patients with AR mutations. Endocrine J (in press)
  • Mori N, Motegi Y, Shimamura Y, Ezaki T, Natsumeda T, Yonekawa T, Ota Y, Notomi T, Nakayama T. Development of a new method for diagnosis of rubella virus infection by reverse transcription-loop mediated isothermal amplification. J Clin Microbiol 2006;44:3268-3273.
  • Mori T, Takimoto T, Katano N, Kikuchi A, Tabuchi K, Kobayashi R, Ayukawa H, Kumagai MA, Horibe K, Tsurusawa M. Recurrent childhood anaplastic large cell lymphoma: a retrospective analysis of registered cases in Japan. Br J Haematol 2006;132:594-597.
  • Morimoto A, Ikushima S, Kinugawa N, Ishii E, Kohdera U, Sako M, Fujimoto J, Bessho F, Horibe K, Tsunematsu Y, Imashuku S, and JLCHSG. Improved outcome in the treatment of pediatric multifocal Langerhans cell histiocytosis: Results from the Japan Langerhans Cell Histiocytosis Study Group-96 protocol study. Cancer 2006;107:613-619.
  • Morozumi M, Ito A, Murayama SY, Hasegawa K, Kobayashi R, Iwata S, Kawamura N, Kuroki H, Nakayama E, Tajima T, Ubukata K. Assessment of real-time PCR for diagnosis of Mycoplasma pneumoniae pneumonia in pediatric patients. Can J Microbiol 2006;52:125-129.
  • Morozumi M, Nakayama E, Iwata S, Aoki Y, Hasegawa K, Kobayashi R, Chiba N, Tajima T, Ubukata K. Simultaneous detection of pathogens in clinical samples from patients with community-acquired pneumonia by real-time PCR with pathogen-specific molecular beacon probes. J Clin Microbiol 2006;44:1440-1446.
  • Murakani N, Tomita Y, Koga M, Takahashi E, Katada Y, Sakuta R, Nagai T. An adolescent with pharyngeal-cervical-brachial variant of Guillain-Barre syndrome and cytomegalovirus infection. Brain & Development 2006;28:269-271.
  • Nagai T, Obata K, Ogata T, Murakami N, Katada Y, Yoshino N, Sakazume S, Tomita Y, Niikawa N. Growth hormone therapy and scoliosis in patients with Pdare-Willi syndrome. Am J Med Genet 2006;A140:1623-1627.
  • Nagai T, Obata K, Yoshino A, Katada Y, Takahashi E, Murakami N, Sakuta R, Niikawa N. Cause of sudden, unexpected death of Prader-Willi syndrome patients with and without growth hormone treatment. Am J Med Genet 2006;136:45-48.
  • Nagai T, Okafuji T, Miyazaki C, Ito Y, Kamada M, Kumagai T, Yuri K, Sakiyama H, Miyata A, Ihara T, Ochiai H, Shimomura K, Suzuki E, Torigoe S, Igarashi M, Kase T, Okuno Y, Nakayama T. A comparative study of the incidence of aseptic meningitis in symptomatic natural mumps patients and monovalent mumps vaccine recipients in Japan . Vaccine (in press)
  • Nakama H, Ohsugi K, Otsuki T, Date I, Kosuga M, Okuyama T, Sakuragawa N. Encapsulation cell therapy for mucopolysaccharidosis type VII using genetically engineered immortalized human amniotic epithelial cells. Tohoku J Exp Med 2006;209:23-32.
  • Nakata Y, Tomkowicz B, Gewirtz AM, Ptasznik A. Integrin inhibition through Lyn-dependent cross talk from CXCR4 chemokine receptors in normal human CD34+ marrow cells. Blood 2006;107:4234-4239.
  • Nakayama T, Onoda K. Vaccine adverse events reported in post-marketing study of the Kitasato Institute from 1994 to 2004. Vaccine (in press)
  • Niu D, Huang J, Li H, Liu K, Wang S, Chen Y, Udaka T, Izumi K, Kosaki K. Paternal gonadal mosaicism of NIPBL mutation in a father of siblings with Cornelia de Lange syndrome. Prenat Diagn 2006:in press.
  • Ogata T. Genetics of human growth. Clin Pediatr Endocrinol 2006;15:45-53.
  • Ogata T, Fukami M. Clinical lessons from SHOX mutation research. International Growth Monitor 2006;16:2-6.
  • Ogata T, Udaka T, Fujiwara I, Ogawa E, Sato N, Kosaki K. Kallmann syndrome phenotype in a female patient with CHARGE syndrome and CHD7 mutation. Endocrine J (in press)
  • Okada M, Fujimaru R, Morimoto N, Satomura K, Kaku Y, Tsuzuki K, Nozu K, Okuyama T, Iijima K. EYA1 and SIX1 gene mutations in Japanese patients with branchio-oto-renal (BOR) syndrome and related conditions. Pediatr Nephrol 2006;21:475-481.
  • Omori S, Hida M, Fujita H, Takahashi H, Tanimura S, Kohno M, Awazu M. Dysregulation of mitogen-activated protein kinases in murine polycystic kidney disease. J Am Soc Nephrol 2006;17:1604-1614.
  • Poduri A, Golja A, Takeoka M, Bourgeois BFD, Connolly L, Riviello JJ. Focal cortical malformations may show increased uptake on interictal FDG-PET. J Child Neurol (in press)
  • Rajab A, Yoo SY, Abdulgalil A, Kathiri S, Ahmed R, Mochida GH, Bodell A, Barkovich AJ, Walsh CA. An autosomal recessive form of spastic cerebral palsy (CP) with microcephaly and mental retardation. Am J Med Genet A 2006;140:1504-1510.
  • Sakai H, Visser R, Ikegawa S, Ito E, Numabe H, Watanabe Y, Mikami H, Kondoh T, Kitoh H, Sugiyama R, Okamoto N, Ogata T, Fodde R, Mizuno S, Takamura K, Egashira M, Sasaki N, Watanabe S, Nishimaki S, Takada F, Nagai T, Okada Y, Aoka Y, Yasuda K, Iwasa M, Kogaki S, Harada N, Mizuguchi T, Matsumoto N. Comprehensive genetic analysis of relevant four genes in 49 patients with Marfan syndrome or Marfan-related phenotypes. Am J Med Genet 2006;A140:1719-1725.
  • Sato N, Ohyama K, Fukami M, Okada M, Ogata T. Somatic and germline mutations of the fibroblast growth factor receptor 1 gene in a mother and the son: implication for apparently mutation negative Kallmann syndrome. J Clin Endocrinol Metab 2006;91:1415-1418.
  • Shimasaki N, Mori T, Samejima H, Sato R, Shimada H, Yahagi N, Torii C, Yoshihara H, Tanigawara Y, Takahashi T, Kosaki K. Effects of methylenetetrahydrofolate reductase and reduced folate carrier 1 polymorphisms on high-dose methotrexate-induced toxicities in children with acute lymphoblastic leukemia or lymphoma. J Pediatr Hematol Oncol 2006;28:64-68.
  • Shishido S, Sato H, Asanuma H, Shindo M, Hataya H, Ishikura K, Hamasaki Y, Goto M, Ikeda M, Honda M. Unexpectedly high prevalence of pretransplant abnormal glucose tolerance in pediatric kidney transplant recipients. Pediatric Transplantation 2006;10:67-73.
  • Sugawara W, Haruta M, F S, Watanabe N, Tsunematsu Y, Kikuta A, Kaneko Y. Promoter hypermethylation of the RASSF1A gene predicts the poor outcome of patients with hepatoblastoma. Pediatr Blood Cancer 2006;[Epub ahead of print].
  • Taguchi T, Takenouchi H, Matsui J, Tang WR, Itagaki M, Shiozawa Y, Suzuki K, Sakaguchi S, Ktagiri YU, Takahashi T, Okita H, Fujimoto J, Kiyokawa N. Involvement of insulin-like growth factor-I and insulin-like growth factor binding proteins in pro-B-cell development. Exp Hematol 2006;34:508-518.
  • Takeoka M, Riviello JJ. Sturge-Weber Syndrome. eMedicine 2006;WebMD.
  • Tsuji A, Hirasawa K, Manki S, Izumi K, Kobori K, Tsujimoto G. Side Effects of Salbutamol Sulfate Delivered through a Metered-Dose Inhaler in a 14-Year-Old Boy with Bronchial Asthoma. JMAJ 2006;49:81-83.
  • Uchino M, Ogawa Y, Kawai M, Shimada H, Kameyama K, Okamoto S, Dogru M, Tsubota K. Ocular complications in a child with acute graft-versus-host disease following cord blood stem cell transplantation: therapeutic challenges. Acta Ophthalmol Scand 2006;84:545-548.
  • Udaka T, Kurosawa K, Izumi K, Yoshida S, Tsukahara M, Okamoto N, Torii C, Kosaki R, Masuno M, Hosokai N, Takahashi T, Kosaki K. Screening for partial deletions of CREBBP locus in Rubinstein-Taybi Syndrome patients using multiplex PCR / Liquid chromatography. Genet Test (in press)
  • Udaka T, Okamoto N, Aramaki M, Torii C, Kosaki R, Hosokai N, Hayakawa T, Takahata N, Takahashi T, Kosaki K. An Alu retrotransposition-mediated deletion of CHD7 in a patient with CHARGE syndrome. Am J Med Genet (in press)
  • Torii C, Izumi K, Nakajima H, Takahashi T, Kosaki K. EFNB1 mutation at the ephrin ligand - ephrin receptor dimerization interface in a patient with craniofrontonasal syndrome. Congenit Anom (in press)
  • Uejima H, Nakayama T, Komase K. Passage in Vero cells alters the characteristics of measles AIK-C vaccine strain. Vaccine 2006;24:931-936.
  • Visser R, Hasegawa T, Niikawa N, Matsumoto N. Analysis of the NSD1 promoter region in patients with a Sotos syndrome phenotype. J Hum Genet 2006;51:15-20.
  • Wada Y, Okada M, Fukami M, Sasagawa I, Ogata T. Association of cryptorchidism with Gly146Ala polymorphism in the gene for steroidogenic factor-1. Fertility and Sterility 2006;85:787-790.
  • Watanabe H. Innovation in parent -infant psychotherapy in Japan :the infant reveasl family trauma in Maria Pozzi ed. Innovation in Infant Mental Health. London Karnac (in press)
  • Watanabe M, Yoshida R, Ueoka K, Aoki K, Sasagawa I, Hasegawa T, Sueoka K, Kamitsuji S, Kamatani N, Yoshimura Y, Ogata T. Haplotype analysis of the estrogen receptor a gene in male genital and reproductive abnormalities: implications for the susceptibility to estrogenic environmental endocrine disruptors. Hum Reprod (in press)
  • Watanabe N, Nakadate H, Haruta M, Sugawara W, Sasaki F, Tsunematsu Y, Kikuta A, Fukuzawa M, Okita H, Hata J, Soejima H, Kaneko Y. Association of 11q loss, trisomy 12, and possible 16q loss with loss of imprinting of insulin-like growth factor-II in Wilms tumor. Genes Chromosomes Cancer 2006;45:592-601.
  • Yabe H, Inoue H, Matsumoto M, Hamanoue S, Koike T, Ishiguro H, Koike H, Suzuki K, Kato S, Kojima S, Tsuchida M, Mori T, Adachi S, Tsuji K, Koike K, Morimoto A, Sako M, Yabe M. Allogeneic haematopoietic cell transplantation from alternative donors with a conditioning regimen of low-dose irradiation, fludarabine and cyclophosphamide in Fanconi anaemia. Br J Haematol 2006;134:208-212.
  • Yamagishi C, Yamagishi H, Maeda J, Tsuchihashi T, Ivey K, Hu T, Srivastava D. Sonic hedgehog is essential for first pharyngeal arch development. Pediatric Research 2006;59:349-354.
  • Yamazawa K, Kodo K, Maeda J, Omori S, Hida M, Mori T, Awazu M. Hyponatremia, hypophosphatemia, and hypouricemia in a girl with macrophage activation syndrome. Pediatrics (in press)
  • Yamazawa K, Wada Y, Sasagawa I, Aoki K, Ueoka K, Ogata T. Mutation and polymorphism analyses of INSL3 and LGR8/GREAT in 62 Japanese patients with cryptorchidism. Homr Res (in press)
  • Yoshikawa N, Honda M, Iijima K, Awazu M, Hattori S, Nakanishi K, Ito H. Steroid treatment in severe childhood IgA nephropathy: a randomized controlled trial. Clin J Am Soc Nephrol 2006;1:511-517.
  • Yoshino A, Honda M, Kanegane H, Obata K, Matsukura H, Sakazume S, Katada Y, Miyawaki T, Ueda Y, Nagai T. Membranoproliferative glomerulonephritis in a patient with X-linked agammaglobulinemia. Pediatr Nephrol 2006;21:36-38.