Publications 2014 (Oct. 2013 – Sept. 2014)

  • Furuichi M, Imajo E, Sato Y, Tanno S, Kawada M, Sato S. Characteristics of Clostridium difficile colonization in Japanese children. J Infect Chemother. 2014;20:307-11
  • Yamada M (Masaki), Kamberos N, Grose C. Breakthrough varicella in a cancer patient with persistent varicella antibody after one varicella vaccination. J Pediatr. 2013;163:1511-1513
  • Shinjoh M, Iwata S, Yagihashi T, Sato Y, Akita H, Takahashi T, Sunakawa K. Recent trends in pediatric bacterial meningitis in Japan – A country where Haemophilus influenzae type b and Streptococcus pneumoniae conjugated vaccines have just been introduced. J Infect Chemother. 2014;20:477-83
  • Yui I, Fujino M, Sawada A, Nakayama T. Novel clinical features of recurrent human respiratory syncytial virus infections. J Med Virol. 2014;86:1629-1638
  • Iwata S, Nakata S, Ukae S, Koizumi Y, Morita Y, Kuroki H, Tanaka Y, Shizuya T, Schödel F, Brown ML, Lawrence J.: Efficacy and safety of pentavalent rotavirus vaccine in Japan: A randomized, double-blind, placebo-controlled, multicenter trial. Hum Vaccin Immunother. 2013;9:1626-1633
  • Takei T, Morozumi M, Ozaki H, Fujita H, Ubukata K, Kobayashi I, Kadota K, Miyamae T, Yokota S, Iwata S, Takahashi T. Clinical Features of Mycoplasma pneumoniae Infections in the 2010 Epidemic Season: Report of Two Cases with Unusual Presentations. Pediatr Neonatol. 2013;54:402-405
  • Jackson W, Yamada M (Masaki), Moninger T, Grose C. Visualization and quantitation of abundant macroautophagy in virus-infected cells by confocal three-dimensional fluorescence imaging.　J Virol Methods. 2013;193:244-250
  • Takeda K, Kawai T, Nakazawa Y, Komuro H, Shoji K, Morita K, Katsuta T, Yamamoto M, Miyairi I, Ohya Y, Ishiguro A, Onodera M. Augmentation of antitubercular therapy with IFNγ in a patient with dominant partial IFNγ receptor 1 deficiency. Clin Immunol. 2014;151:25-28
    Ikeno S, Suzuki MO, Muhsen M, Ishige M, Kobayashi-Ishihara M, Ohno S, Takeda M, Nakayama T, Morikawa Y, Terahara K, Okada S, Takeyama H, Tsunetsugu-Yokota Y. Sensitive detection of measles virus infection in the blood and tissues of humanized mouse by one-step quantitative RT-PCR. Front Microbiol. 2013;4:298
  • Kashiwagi Y, Miyata A, Kumagai T, Maehara K, Suzuki E, Nagai T, Ozaki T, Nishimura N, Okada K, Kawashima H, Nakayama T. Production of inflammatory cytokines in response to diphtheria-pertussis-tetanus (DPT), Haemophilus influenzae type b (Hib), and 7-valent pneumococcal (PCV7) vaccines. Human vaccine & Immunother. 2014;10:677-685
  • Kashiwagi Y, Maeda M, Kawashima H, Nakayama T. Inflammatory responses following intramuscular and subcutaneous immunization with aluminum-adjuvanted or non-adjuvanted vaccines. Vaccine. 2014; 32: 3393-3401
  • Yamaji Y, Nakayama T. Recombinant measles viruses expressing respiratory syncytial virus proteins induced virus-specific CTL responses in cotton rats. Vaccine. 2014; 32: 4529-4536
    　
    Kumagai T, Yoshikawa T, Shiraki K, Yoshida M, Nakayama T, Ihira M, Asano Y. Virus specific cell-mediated immunity may play a role in controlling reactivated human herpes virus 6B in patients under measles induced immunosuppression. J Med Virol. 2014;86: 658-665
  • Chiba N, Morozumi M, Shouji M, Wajima T, Iwata S, Ubukata K. Invasive Pneumococcal Diseases Surveillance Study Group.: Changes in capsule and drug resistance of Pneumococci after introduction of PCV7, Japan, 2010-2013. Emerg Infect Dis. 2014;20:1132-1139
  • Morita A, Kamei S, Minami M, Yoshida K, Kawabata S, Kuroda H, Suzuki Y, Araki N, Iwasaki Y, Kobayashi R, Hayashi N, Hirayama T, Ochiai J, Ueda M, Yamagishi Y, Niwa J, Shindo K, Fukushima Y, Takita T, Sato T, Sato S, Mikamo H, Iwata S. Open-label study to evaluate the pharmacodynamics, clinical efficacy, and safety of meropenem for adult bacterial meningitis in Japan. J Infect Chemother. 2014;20:535-540
  • Namkoong H, Kameyama Y, Yasuda H, Nakayama S, Kaneko H, Kawashima C, Terajima T, Maezawa K, Hayashi T, Sandoh M, Ishii M, Tasaka S, Kanayama A, Kobayashi I, Betsuyaku T, Kizu J, Iwata S, Sato Y, Hasegawa N. The efficacy, safety, and pharmacokinetics of biapenem administered thrice daily for the treatment of pneumonia in the elderly. J Infect Chemother. 2014;20:356-360
  • Kawajiri H, Aeba R, Takaki H, Yozu R, Iwata S. Negative pressure therapy for post-sternotomy wound infections in young children. Interact Cardiovasc Thorac Surg. 2014;19:102-106
  • Morozumi M, Shimizu H, Matsushima Y, Mitamura K, Tajima T, Iwata S, Ubukata K. Evaluation of new immunochromatographic assay kit for adenovirus detection in throat swab: comparison with culture and real-time PCR results. J Infect Chemother. 2014;20:303-306
  • Wajima T, Morozumi M, Chiba N, Shouji M, Iwata S, Sakata H, Ubukata K. Associations of macrolide and fluoroquinolone resistance with molecular typing in Streptococcus pyogenes from invasive infections, 2010-2012. Int J Antimicrob Agents. 2013;42:447-449
  • Morozumi M, Wajima T, Kuwata Y, Chiba N, Sunaoshi K, Sugita K, Sakata H, Iwata S, Ubukata K. Associations between capsular serotype, multilocus sequence type, and macrolide resistance in Streptococcus agalactiae isolates from Japanese infants with invasive infections. Epidemiol Infect. 2014;142:812-819
  • Karigane D, Takaya S, Seki Y, Mastumoto Y, Onose A, Kosakai A, Sugaya N, Mori T. Cytomegalovirus enteritis in immunocompetent subjects: a case report and review of the literature. J Infect chemother. 2014;20:325-329
  • Fukushima H, Mitsuhashi T, Oto T, Sano Y, Fukushima-Kusano K, Goto K, Okazaki M, Date H, Kojima Y, Yamagishi H, Takahashi T. Successful lung transplantation in a case with diffuse pulmonary arteriovenous malformations and hereditary hemorrhagic telangiectasia. Am J Transplant. 2013;13:3278-3281
  • Kojima K, Sato A, Yamashita Y, Ishihara J, Aoyagi H, Okishige K. Young athlete with sudden cardiac arrest treated with therapeutic hypothermia. Pediatr Int. 2013;55:e123-e125
  • Sallam K, Kodo K, Wu JC. Modeling inherited cardiac disorders. Circ J. 2014;78:784-94
  • Huber BC, Ransohoff JD, Ransohoff KJ, Riegler J, Ebert A, Kodo K, Gong Y, Sanchez-Freire V, Dey D, Kooreman NG, Diecke S, Zhang WY, Odegaard J, Hu S, Gold JD, 　Robbins RC, Wu JC. Costimulation-adhesion blockade is superior to cyclosporine A and prednisone immunosuppressive therapy for preventing rejection of differentiated human embryonic stem cells following transplantation. Stem Cells. 2013;31:2354-63
  • Yasuhara J, Yamada Y, Hara K, Suhara R, Hattori Y, Yamaguchi T, Mizuno Y, Kizu R, Bamba M. Primary ciliary dyskinesia diagnosed on nasal mucosal biopsy in two newborns. Pediatr Int. 2014;56:258-261
  • Mitani Y, Ohta K, Ichida F, Nii M, Arakaki Y, Ushinohama H, Takahashi T(Tsutomu), Ohashi H, Yodoya N, Fujii E, Ishikura K, Tateno S, Sato S, Suzuki T, Higaki T, Iwamoto M, Yoshinaga M, Nagashima M, Sumitomo N. Circumstances and outcomes of out-of-hospital cardiac arrest in elementary and middle school students in the era of public-access defibrillation. Circ J. 2014;78:701-707
  • Muraoka N, Yamakawa H, Miyamoto K, Sadahiro T, Umei T, Isomi M, Nakashima H, Akiyama M, Wada R, Inagawa K, Nishiyama T, Kaneda R, Fukuda T, Takeda S, Tohyama S, Hashimoto H, Kawamura Y, Goshima N, Aeba R, Yamagishi H, Fukuda K, Ieda M. MiR-133 promotes cardiac reprogramming by directly repressing Snai1 and silencing fibroblast signatures. EMBO J. 2014;33:1565-1581
  • Yamagishi H. Lessons from Heart Development to Regeneration. In: Cardiac Regeneration using ES and iPS Cells (eds) Fukuda K, Yuasa S. Science Publishers, Florida, 2013, p.59-83
  • Yamagishi H, Yamagishi C. Embryology. In: Cardiac CT and MR for Adult Congenital Heart Disease (ed) Saremi F. Springer, 2014, p.7-21
  • Stoppa-Vaucher S, Ayabe T, Paquette J, Patey N, Francoeur D, Vuissoz JM, Deladoëy J, Samuels M, Ogata T, Deal C. 46,XY gonadal dysgenesis: new SRY point mutation in two siblings with paternal germ line mosaicism. Clin Genet. 2012;82:505-513
  • Fukami M, Shozu M, Ogata T. Molecular bases and phenotypic determinations of aromatase excess syndrome. Int J Endocrinol. 2012;2012: 584807

    Fukami M, Tsuchiya T, Vollbach H, Brown KA, Abe S, Ohtsu S, Wabitsch M, Burger H, Simpson ER, Umezawa A, Shihara D, Nakabayashi K, Bulun SE, Shozu M, Ogata T. Genomic Basis of Aromatase Excess Syndrome: Recombination- and Replication-Mediated Rearrangements Leading to CYP19A1 Overexpression. J Clin Endocrinol Metab. 2013;98:E2013-2021
  • Uchida K, Matsuo N, Hori N, Hasegawa T, Takahashi T. Spousal choice by height in as urban middle-class Japanese population. Hum Biol. 2013;85:619-621
  • Takagi M, Sato S, Hara K, Tani C, Miyazaki O, Nishiura G, Hasegawa T. A recurrent mutation in the 5′-UTR of IFITM5 causes osteogenesis imperfecta type V with broad phenotypic spectrum. Am J Med Genet A. 2013;161A:1980-1982
  • Takagi M, Sasaki G, Mitsui T, Honda M, Tanaka Y, Hasegawa T. A 2.0 Mb microdeletion in proximal chro
    mosome 14q12, involving regulatory elements of FOXG1, with the coding region of FOXG1 being unaffected, results in severe developmental delay, microcephaly, and hypoplasia of the corpus callosum. Eur J Med Genet. 2013;56:526-528
  • Matsumura T, Imamichi Y, Mizutani T, Ju Y, Yazawa T, Kawabe S, Kanno M, Ayabe T, Katsumata N, Fukami M, Inatani M, Akagi Y, Umezawa A, Ogata T, Miyamoto K. Human glutathione S-transferase A (GSTA) family genes are regulated by steroidogenic factor 1 (SF-1) and are involved in steroidogenesis. FASEB J. 2013;27:3198-3208
  • Vasques GA, Amano N, Quedas EPS, Docko AJ, Funari MF, Nishi MY, Arnhold IJP, Hasegawa T, Jorge AA. Heterozygous mutations in natriuretic peptide receptor-B gene (NPR2) as a cause of idiopathis short stature. J Clin Endocrinol Metab. 2013;98:E1636-1644
  • Sekii K, Itoh H, Ogata T, Iwashima S. Possible contribution of fetal size and gestational age to myocardial tissue: Doppler velocities in preterm fetuses. Eur J Obstet Gynecol Reprod Biol. 2013;167:121
  • Sugiura H, Kouwaki M, Kato T, Ogata T, Sakamoto R, Ieshima A, Yokochi K. Magnetic resonance imaging in neonates with total asphyxia. Brain Dev. 2013;35:53-60
  • Nishina-Uchida N, Fukuzawa R, Numakura C, Suwanai A, Hasegawa T, Hasegawa Y. Characteristic testicular histology is useful for the identification of NR5A1 gene mutation in prepubertal 46,XY patients. Hor Res Paediatr. 2013;80:119-128
  • Hayashi M, Kataoka Y, Sugimura Y, Kato F, Fukami M, Ogata T, Homma K, Hasegawa T, Oiso Y, Sasano H, Tanaka H. A 68-year-old phenotypically male patient with 21-hydroxylase deficiency and concomitant adrenocortical neoplasm producing testosterone and cortisol. Tohoku J Exp Med. 2013;231:75-84
  • Kato F, Hamajima T, Hasegawa T, Amano N, Horikawa R, Nishimura G, Nakashima S, Fuke T, Sano S, Fukami M, Ogata T. IMAGe syndrome: clinical and genetic implications based on investigations in three Japanese patients. Clin Endocrinol. 2013;80:706-713
  • Kondo E, Nakamura A, Homma K, Hasegawa T, Yamaguchi T, Narugami T, Aoyagi H, Ishizu K, Tajima T. Two novel mutations of the CYP11B2 gene in a Japanese patient with aldosterone deficiency type 1. Endocrine J. 2013;60:51-55
  • Hamasaki H, Mukaino T, Kaneko H, Mitsui T, Moriyama S, Hasegawa T, Yanai H. Pseudopseudohypoparathyroidism with a novel mutation in the GNAS gene showing thin bones of extremities and ossification of enthuses. J Endocrinol Metab. 2013;3:150-152
  • Adachi M, Asakura Y, Muroya K, Goto H, Kigasawa H. Abnormal adipose tissue distribution with unfavorable metabolic profile in five children following hematopoietic stem cell transplantation: a new etiology for acquired partial lipodystrophy. Clin Pediatr Endocrinol. 2013;22:53-64
  • Adachi M, Tajima T, Muroya K, Asakura Y. Classic Bartter syndrome complicated with profound growth hormone deficiency: a case report. J Med Case Rep. 2013;7:283
  • Nakashima S, Watanabe Y, Okada J, Ono H, Nagata E, Fukami M, Ogata T. Critical role of Yp inversion in PRKX/PRKY-mediated Xp;Yp translocation in a patient with 45,X testicular disorder of sex development. Endocr J. 2013;60:1329-34
  • Matsumoto T, Miyakoshi K, Saisho Y, Ishii T, Ikenoue S, Kasuga Y, Kadohira I, Sato S, Momotani N, Minegishi K, Yoshimura Y. Antenatal management of recurrent fetal goitrous hyperthyroidism associated with fetal cardiac failure in a pregnant woman with persistent high levels of thyroid-stimulating hormone receptor antibody after ablative therapy. Endocr J. 2013;60:1281-1287
  • Rapaport R, Saenger P, Schmidt H, Hasegawa Y, Colle M, Loche S, Marcantonio S, Bonfig W, Zabransky M, Lifshitz F.Validation and ease of use of a new pen device for self-administration of recombinant human growth hormone: results from a two-center usability study. Medical devices. 2013;6:141-146
  • Miyake N, Koshimizu E, Okamoto N, Mizuno S, Ogata T, Nagai T, Kosho T, Ohashi H, Kato M, Sasaki G, Mabe H, Watanabe Y, Yoshino M, Matsuishi T, Takanashi J, Shotelersuk V, Tekin M, Ochi N, Kubota M, Ito N, Ihara K, Hara T, Tonoki H, Ohta T, Saito K, Matsuo M, Urano M, Enokizono T, Sato A, Tanaka H, Ogawa A, Fujita T, Hiraki Y, Kitanaka S, Matsubara Y, Makita T, Taguri M, Nakashima M, Tsurusaki Y, Saitsu H, Yoshiura K, Matsumoto N, Niikawa N: MLL2 and KDM6A mutations in patients with Kabuki syndrome. Am J Med Genet A. 2013;161: 2234-2243
  • Ohishi A, Ueno D, Ogata T: Glucose-6-phosphate dehydrogenase deficiency and adrenal hemorrhage in a Filipino neonate with hyperbilirubinemia. AJP Rep. 2013;3: 5-8
  • Igarashi M, Dung VC, Suzuki E, Ida S, Nakacho M, Nakabayashi K, Mizuno K, Hayashi Y, Kohri K, Kojima Y, Ogata T, Fukami M. Cryptic genomic rearrangements in three patients with 46,XY disorders of sex development. PLoS One. 2013;8:e68194
  • Fujisawa Y, Yamaguchi R, Nagata E, Satake E, Sano S, Matsushita R, Kitsuta K, Nakashima S, Nakanishi T, Nakagawa Y, Ogata T. The lipid fraction of human milk initiates adipocyte differentiation in 3T3-L1 cells. Early Hum Dev. 2013;89:713-719.
  • Fujisawa Y, Yamaguchi R, Satake E, Ohtaka K, Nakanishi T, Ozono K, Ogata T: Identification of AP2S1 Mutation and Effects of Low Calcium Formula in an Infant with Hypercalcemia and Hypercalciuria. J Clin Endocrinol Metab. 2013;98:E2022-2027
  • Matsubara K, Ogata T. Advanced maternal age at childbirth and the development of uniparental disomy. A commentary on the proportion of uniparental disomy is increased in Prader-Willi syndrome due to an advanced maternal childbearing age in Korea. J Hum Genet. 2013;58: 118-119
  • Fukami M, Suzuki J, Nakabayashi K, Tsunasima R, Ogata T, Shozu M, Noguchi S. Lack of Genomic Rearrangements Involving the Aromatase Gene CYP19A1 Breast Cancer. Breast Cancer. 2014;21:382-385
  • Kuwahara E, Asakura K, Nishiwaki Y, Komatsu H, Nakawaza A, Ushiku H, Maejima F, Nishigaki Y, Hasegawa T, Okamura T, Takebayashi T. Steeper increases in body-mass index during childhood correlate with blood pressure elevation in adolescence: a long-term follow-up study in a Japanese community. Hypertension Res. 2014;37:179-184
  • Sato T, Muroya K, Hanakawa J, Asakura Y, Aida N, Tomiyasu M, Tajima G, Hasegawa T, Adachi M. Neonatal case of classic maple syrup urine disease: Usefulness of 1H-MRS in early diagnosis. Pediatr Int. 2014;56:112-115
  • Takagi M, Narumi S, Asakura Y, Muroya K, Hasegawa Y, Adachi M, Hasegawa T. A novel mutation in SOX2 causes hypogonadotropic hypogonadism with mild ocular malformation. Hor Res Paediatr. 2014;81:133-138
  • Iwasaki Y, Suganami T, Hachiya R, Shirakawa I, Kim-Saijo M, Tanaka M, Hamaguchi M, Takai-Igarashi T, Nakai M, Miyamoto Y, Ogawa Y. Activating transcription factor 4 links metabolic stress to interleukin-6 expression in macrophages. Diabetes. 2014;63:152-161
  • Miyake Y, Tanaka K, Nishikawa T, Naruse M, Takayanagi R, Sasano H, Takeda Y, Shibata H, Sone M, Satoh F, Yamada M, Ueshiba H, Katabami T, Iwasaki Y, Tanaka H, Tanahashi Y, Suzuki S, Hasegawa T, Katsumata N, Tajima T, Yanase T. Prognosis of primary aldosteronism in Japan:results from a nationwide epidemiological study. Endocrine J. 2014;61:35-40
  • Inokuchi M, Matsuo N, Takayama JI, Hasegawa T. Trends in thin body stature among Japanese male adolescents, 2003 to 2012. Ann Hum Biol. 2014;41:277-281
  • Amano N, Mukai T, Iyo Y, Narumi S, Tanaka T, Yokoya S, Ogata T, Hasegawa T. Identification and functional characterization of two novel NPR2 mutations in Japanese patients with short stature. J Clin Endocrinol Metab. 2014;99:E713-F718
  • Suzuki J, Azuma N, Dateki S, Soneda S, Muroya K, Yamamoto Y, Saito R, Sano S, Nagai T, Wada H, Endo A, Urakami T, Ogata T, Fukami M. Mutation spectrum and phenotypic variation in nine patients with SOX2 abnormalities. J Hum Genet. 2014;59:353-356
  • Kitaoka T, Miyoshi Y, Namba N, Miura K, Kubota T, Ohata Y, Fujiwara M, Takagi M, Hasegawa T, Juppner H, Ozono K. Two Japanese familial cases of Caffey disease with and without the common COL1A1 mutation and normal bone density, and review of the literature. Eur J Pediatr. 2014;173:799-804
  • Sasaki G, Zubair M, Ishii T, Mitsui T, Hasegawa T, Auchus RJ. The contribution of serine 194 phosphorylation to steroidogenic acute regulatory protein function. Mol Endocrinol. 2014;28:1088-1096
    Tanaka T, Hasegawa T, Ozono K, Tanaka H, Kanzaki S, Yokoya S, Chihara K, Iwamoto N, Seino Y. Effect of growth hormone treatment on quality of life in Japanese children with growth horomone deficiency: An analysis from a prospective observational study. Clin Pediatr Endocrinol. 2014;23:83-92
  • Seki A, Jinno T, Suzuki E, Takayama S, Ogata T, Fukami M. Skeletal deformity associated with SHOX deficiency. Clin Pediatr Endocrinol. 2014;23:65-72
  • Fukami M, Miyado M, Nagasaki K, Shozu M, Ogata T. Aromatase excess syndrome: A rare autosomal dominant disorder leading to pre- or peri-pubertal onset gynecomastia. Pediatr Endocrinol Rev. 2014;11:298-305
  • Inui M, Miyado M, Igarashi M, Tamano M, Kubo A, Yamashita S, Asahara H, Fukami M, Takada S. Rapid generation of mouse models with defined point mutations by the CRISPR/Cas9 system. Sci Rep. 2014;4:5396
  • Shihara D, Miyado M, Nakabayashi K, Shozu M, Ogata T, Nagasaki K, Fukami M. Aromatase excess syndrome in a family with upstream deletion of CYP19A1. Clin Endocrinol. 2014;81:314-316
  • Tsuchiya T, Shibata M, Numabe H, Jinno T, Nakabayashi K, Nishimura G, Nagai T, Ogata T, Fukami M. Compound heterozygous deletions in pseudoautosomal region 1 in an infant with mild manifestations of Langer mesomelic dysplasia. Am J Med Genet. 2014;164A:505-510
  • Nagasaki K, Asami T, Sato H, Ogawa Y, Kikuchi T, Saitoh A, Ogata T, Fukami M. Long term follow up study for a patient with Floating-Harbor syndrome due to a hotspot SRCAP mutation. Am J Med Genet A. 2014;164A:731-5
  • Suzuki E, Yatsuga S, Igarashi M, Miyado M, Nakabayashi K, Hayashi K, Hata K, Umezawa A, Yamada G, Ogata T, Fukami M. De Novo Frameshift Mutation in Fibroblast Growth Factor 8 in a Male Patient with Gonadotropin Deficiency. Horm Res Paediatr. 2014;81:139-144
  • Saito R, Yamamoto Y, Goto M, Araki S, Kubo K, Kawagoe R, Kawada Y, Kusuhara K, Igarashi M, Fukami M. Tamoxifen Treatment for Pubertal Gynecomastia in Two Siblings with Partial Androgen Insensitivity Syndrome. Horm Res Pediatr. 2014;81:211-216
  • Matsubara K, Kataoka N, Ogita S, Sano S, Ogata T, Fukami M, Katsumata N. Uniparental disomy of chromosome 8 leading to homozygosity of a CYP11B1 mutation in a patient with congenital adrenal hyperplasia: Implication for a rare etiology of an autosomal recessive disorder. Endocr J. 2014;61:629-33
  • Ogata T, Niihori T, Tanaka N, Kawai M, Nagashima T, Funayama R, Nakayama K, Nakashim S, Kato F, Fukami M, Aoki Y, Matsubara Y. TBX1 Mutation Identified by Exome Sequencing in a Japanese Family with 22q11.2 Deletion Syndrome-like Craniofacial Features and Hypocalcemia. PLoS One. 2014;9:e91598
  • Ohishi A, Nakashima S, Ogata T, Iijima S: Early vitamin K deficiency bleeding in a neonate associated with maternal Crohn’s disease. J Perinatol. 2014;34:636-639
  • Matsuo N, Ishii T, Takayama JI, Miwa M, Hasegawa T. Reference standard of penile size and prevalence of buried penis in Japanese newborn male infants. Endocrine J. 2014;61:849-853
  • Shozu M, Fukami M, Ogata T: Understanding the pathological manifestations of aromatase excess syndrome: lessons for the clinic. Exp Rev Endocrinol Metab. 2014 9:397-409
  • Kojima K, Brown EC, Matsuzaki N, Rothermel R, Fuerst D, Shah A, Mittal S, Sood S, Asano E. Gamma activity modulated by picture and auditory naming tasks: intracranial recording in patients with focal epilepsy. Clin Neurophysiol. 2013;124:1737-44
  • Kojima K, Brown EC, Matsuzaki N, Asano E. Animal category-preferential gamma-band responses in the lower- and higher-order visual areas: intracranial recording in children. Clin Neurophysiol. 2013;124:2368-77
  • Uematsu M, Matsuzaki N, Brown EC, Kojima K, Asano E. Human occipital cortices differentially exert saccadic suppression: Intracranial recording in children. Neuroimage. 2013;83:224-36
  • Miyakoshi M, Delorme A, Mullen T, Kojima K, Makeig S, Asano E. Automated detection of cross-frequency coupling in the electrocorticogram for clinical inspection. Conf Proc IEEE Eng Med Biol Soc. 2013;2013:3282-5
  • Cho-Hisamoto Y, Kojima K, Brown EC, Matsuzaki N, Asano E. Gamma activity modulated by naming of ambiguous and unambiguous images: Intracranial recording. Clin Neurophysiol. 2014 Apr 18. [Epub ahead of print]
  • Toyoda G, Brown EC, Matsuzaki N, Kojima K, Nishida M, Asano E. Electrocorticographic correlates of overt articulation of 44 English phonemes: intracranial recording in children with focal epilepsy. Clin Neurophysiol. 2014;125:1129-37
  • Mochida GH, Chugani H. Studying rare genetic disorders in child neurology–the need for an international network of collaboration. Dev Med Child Neurol. 2014;56:412
  • Hills LB, Masri A, Konno K, Kakegawa W, Lam AT, Lim-Melia E, Chandy N, Hill RS, Partlow JN, Al-Saffar M, Nasir R, Stoler JM, Barkovich AJ, Watanabe M, Yuzaki M, Mochida GH. Deletions in GRID2 lead to a recessive syndrome of cerebellar ataxia and tonic upgaze in humans. Neurology. 2013;81:1378-86
  • Reiff RE, Ali BR, Baron B, Yu TW, Ben-Salem S, Coulter ME, Schubert CR, Hill RS, Akawi NA, Al-Younes B, Kaya N, Evrony GD, Al-Saffar M, Felie JM, Partlow JN, Sunu CM, Schembri-Wismayer P, Alkuraya FS, Meyer BF, Walsh CA, Al-Gazali L, Mochida GH. METTL23, a transcriptional partner of GABPA, is essential for human cognition. Hum Mol Genet. 2014;23:3456-66
  • Zhang X, Ling J, Barcia G, Jing L, Wu J, Barry BJ, Mochida GH, Hill RS, Weimer JM, Stein Q, Poduri A, Partlow JN, Ville D, Dulac O, Yu TW, Lam AT, Servattalab S, Rodriguez J, Boddaert N, Munnich A, Colleaux L, Zon LI, Söll D, Walsh CA, Nabbout R. Mutations in QARS, encoding glutaminyl-tRNA synthetase, cause progressive microcephaly, cerebral-cerebellar atrophy, and intractable seizures. Am J Hum Genet. 2014;94:547-58
  • Matsuda S, Kakegawa W, Budisantoso T, Nomura T, Kohda K, Yuzaki M. Stargazin regulates AMPA receptor trafficking through adaptor protein complexes during long-term 　depression. Nat Commun. 2013;4:2759
  • He Q, NomuraT, Xu J, Contractor A. The developmental switch in GABA polarity is delayed in fragile X mice. J Neurosci. 2014;34:446-50
  • Takenouchi T, Sasaki A, Takahashi T. Multiple cerebral aneurysms after myxomatous stroke. Arch Dis Child. 2014;99:849
  • Sánchez Fernández I, Peters JM, An S, Bergin AM, Takeoka M, Rotenberg A, Kothare SV, Riviello JJ Jr, Loddenkemper T. Long-term response to high-dose diazepam treatment in continuous spikes and waves during sleep. Pediatr Neurol. 2013;49:163-170
  • Harini C, Singh K, Takeoka M, Parulkar I, Bergin AM, Loddenkemper T, Kothare SV. Predictors of seizure occurrence in children undergoing pre-surgical monitoring. Seizure. 2013;22:640-6
    Wintermark P, Lechpammer M, Warfield SK, Kosaras B, Takeoka M, Poduri A, Madsen JR, Bergin AM, Whalen S, Jensen FE. Perfusion Imaging of Focal Cortical Dysplasia Using Arterial Spin Labeling: Correlation With Histopathological Vascular Density. J Child Neurol. 2013;28:1474-1482
  • Taimouri V, Akhondi-Asl A, Tomas-Fernandez X, Peters JM, Prabhu SP, Poduri A, Takeoka M, Loddenkemper T, Bergin AM, Harini C, Madsen JR, Warfield SK. Electrode localization for planning surgical resection of the epileptogenic zone in pediatric epilepsy. Int J Comput Assist Radiol Surg. 2014;9:91-105
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