Hyperinsulinemic hypoglycemia in Beckwith-Wiedemann, Sotos, and Kabuki syndromes: A nationwide survey in Japan.
Toda N, Ihara K, Kojima-Ishii K, Ochiai M, Ohkubo K, Kawamoto Y, Kohno Y, Kumasaka S, Kawase A, Ueno Y, Futatani T, Miyazawa T, Nagaoki Y, Nakata S, Misaki M, Arai H, Kawai M, Sato M, Yada Y, Takahashi N, Komatsu A, Maki K, Watabe S, Sumida Y, Kuwashima M, Mizumoto H, Sato K, Hara T:
Am J Med Genet A 173(2):360-7, 2017
Clarithromycin plus intravenous immunoglobulin therapy can reduce the relapse rate of Kawasaki disease: a phase 2, Open-Label, Randomized Control Study.
Nanishi E, Nishio H, Takada H, Yamamura K, Fukazawa M, Furuno K, Mizuno Y, Saigo K, Kadoya R, Ohbuchi N, Onoe Y, Yamashita H, Nakayama H, Hara T, Ohno T, Takahashi Y, Hatae K, Harada T, Shimose T, Kishimoto J, Ohga S, Hara T:
J Am Heart Assoc. 6(7): e005370, 2017
Early Mortality and Morbidity of the Infants with Birth Weight of 500 grams or less in Japan
Inoue H, Ochiai M, Yasuoka K, Tanaka K, Kurata H, Fujiyoshi J, Matsushita Y, Suga S, Nonaka K, Taguchi T, Kato K, Ohga S, on behalf of the Neonatal Research Network of Japan (NRNJ):
J Pediatr 190:112-117, 2017
Calcineurin inhibitors exacerbate coronary arteritis via the MyD88 signaling pathway in a murine model of Kawasaki disease.
Murata K, Motomura Y, Tanaka T, Kanno S, Yano T, Onimaru M, Shimoyama A, Nishio H, Sakai Y, Oh-hora M, Hara H, Fukase K, Takada H, Masuda S, Ohga S, Yamasaki S, Hara T:
Clin Exp Immunol 190(1):54-67, 2017
Early-onset epileptic encephalopathy and severe developmental delay in an association with de novo double mutations in NF1 and MAGEL2.
Akamine S, Sagata N, Sakai Y, Kato T, Nakahara T, Matsushita Y, Togao O, Hiwatashi A, Sanefuji M, Ishizaki Y, Torisu H, Saitsu H, Matsumoto N, Hara T, Kanba S, Shaw CA, Ohga S:
Epilepsia Open 23;3(1):81-85, 2017
The efficacy of the direct clinical intervention for infectious diseases by a pediatric infectious disease specialist in the pediatric ward of a tertiary medical facility without a pediatric antimicrobial stewardship program.
Hoshina T, Yamamoto N, Ogawa M, Nakamoto T, Kusuhara K:
Eur J Clin Microbiol Infect Dis 36(8):1449-54, 2017
Diagnostic challenge of Diamond-Blackfan anemia in mothers and children by whole-exome sequencing.
Ichimura T, Yoshida K, Yosuke O, Yujiri T, Nagai K, Nishi M, Shiraishi Y, Hiroo U, Toki T, Azuma Y, Chiba K, Tanaka H,
Muramatsu H, Ogawa S, Tanizawa Y, Hara T, Kanno H, Kojima S, Miyano S, Ito E, Ogawa S, Ohga S:
Int J Hematol 05(4):515-520, 2017
The clinical presentation and genotype of protein C deficiency with double mutations
Inoue H, Terachi S, Uchiumi T, Sato T, Urata M, Ishimura M, Koga Y, Hotta T, Hara T, Kang D, Ohga S:
Pediatr Blood Cancer 64(7): doi: 10.1002/pbc.26404, 2017
DOCK8 Regulates Macrophage Migration through Cdc42 Activation and LRAP35a Interaction.
Shiraishi A, Uruno T, Sanematsu F, Ushijima M, Sakata D, Hara T, Fukui Y:
J Biol Chem 292:2191-2202, 2017
Clinical efficacy of cycling empirical antibiotic therapy for febrile neutropenia in pediatric cancer patients.
Teranishi H, Koga Y, Nishio H, Kato W, Ono H, Kanno S, Nakashima K, Takada H:
J Infect Chemother 23(7):463-7, 2017
Intramuscular venous malformation in an infant masquerading as a recurrent gonarthritis.
Nanishi E, Hoshina T, Nishio H, Aman M, Sakamoto A, Ohga S, Hara T:
Pediatr Neonatol 58: 185-6, 2017
Resolution of Hydronephrosis in a Patient With Mucopolysaccharidosis Type II With Enzyme Replacement Therapy.
Nishiyama K, Imai T, Ohkubo K, Sanefuji M, Takada H:
Urology 101:163-5, 2017
Toxic epidermal necrolysis in a child 6 months post-hematopoietic stem cell transplantation.
Oba U, Yamada H, Suenobu SI, Nakamura Y, Ito A, Hatano Y, Itonaga N, Ohshima K, Koga Y, Ohga S, Ihara K:
Pediatr Transplant 21(5), 2017
A childhood-onset intestinal toxemia botulism during chemotherapy for relapsed acute leukemia.
Ohyama N, Torio M, Nakashima K, Koga Y, Kanno S, Nishio H, Sasazuki M, Kato H, Asakura H, Akamine S, Ishizaki Y, Sanefuji M, Sakai Y, Ohga S:
Ann Clin Microbiol Antimicrob 16(1):61, 2017
Transient Hemi-Lower Limb Ischemia in the Newborn: Arterial Thrombosis or Persistent Sciatic Artery?
Kirino M, Ochiai M, Ichiyama M, Inoue H, Kusuda T, Kinjo T, Ishimura M, Ohga S:
AJP Rep. 7(1):e13-e16, 2017
Disappearance of basal ganglia lesions in T1-weighted magnetic resonance images after the ligation of congenital portosystemic venous shunt.
Takemoto R, Yamamura K, Nagata H, Kawaguchi N, Sakai Y, Matsuura T, Tomoaki T, Ohga S:
Pediatr Neonatol 58:465-6, 2017
Activated phosphoinositide 3-kinase δ syndrome presenting with gut-associated T-cell lymphoproliferative disease.
Teranishi H, Ishimura M, Koga Y, Eguchi K, Sonoda M, Kobayashi T, Shiraishi S, Nakashima K, Ikegami K, Aman M, Yamamoto H, Takada H, Ohga S:
Rinsho Ketsueki 58(1):20-5, 2017
Severe Hemolytic Anemia Following Intravenous Immunoglobulin in an Infant With Kawasaki Disease.
Tocan V, Inaba A, Kurano T, Sonoda M, Soebijanto K, Nakayama H:
J Pediatr Hematol Oncol. 39(2):e100-e102, 2017
Silent Progression of Coronary Artery Thrombosis in a Pregnant Woman With Anomalous Origin of Left Coronary Artery From the Pulmonary Artery.
Yamamura K, Sakamoto I, Yamasaki Y, Fujiwara A, Nagao M, Takada H:
Circ J. 25;81(8):1236-1237, 2017
Successful Liver Transplantation for Transient Abnormal Myelopoiesis-Associated Liver Failure.
Yasuoka K, Inoue H, Tanaka K, Fujiyoshi J, Matsushita Y, Ochiai M, Koga Y, Matsuura T, Taguchi T, Ohga S:
Neonatology 112(2):159-62, 2017
Clinical Significance of WT1 mRNA Levels in Japanese Acute Lymphoblastic Leukemia Patients.
Hashii Y, Kosaka Y, Watanabe K, Kato K, Imaizumi M, Kaneko T, Sunami S, Watanabe A, Hiramatsu H, Koga Y, Hirayama M, Nakao T, Hata T, Uchida N, Ishiyama K, Mitani K, Hidaka M, Kitamura K, Tsunemine H, Ueda Y, Mugitani A, Usuki K, Kanda Y, Miyazaki Y, Imai K, Naoe T, Koh K, Sugiyama H, Horibe K:
J Leuk Dec 5(4): 243, 2017
Regional differences in infant 25-Hydroxyvitamin D: Pilot study of the Japan Environment and Children's Study.
Ayabe T, Yamamoto-Hanada K, Mezawa H, Konishi M, Ishitsuka K, Saito M, Fukami M, Michikawa T, Yamazaki S, Senju A, Kusuhara K, Kawamoto T, Sanefuji M, Kato K, Oda M, Mitsubuchi H, Katoh T, Monden Y, Mise N, Kayama F, Saito H, Ohya Y:
Pediatr Int 60(1):30-34, 2017
Pulmonary inflammation and cytokine dynamics of bronchoalveolar lavage fluid from a mouse model of bronchial asthma during A(H1N1)pdm09 infection.
Fujimoto Y, Hasegawa S, Matsushigea T, Wakiguchi H, Nakamura T, Hasegawa H, Nakajima N, Ainai A, Oga A, Itoh H, ShirabeK, Toda S, Atsutae R, Morishima T, Ohga S:
Sci Rep 22;7(1):9128, 2017
Difference of the change of the hospitalization for pneumonia in children between Japanese secondary and tertiary medical facilities after the introduction of pneumococcal conjugate vaccine.
Haro K, Ogawa M, Hoshina T, Kojiro M, Kusuhara K:
Jpn J Infect Dis 70(3):270-4, 2017
CD57+ CTL degranulation assay provides sensitive and specific detection of FHL3 patients.
Hori M, Yasumi T, Shimodera S, Shibata H, Hiejima E, Izawa K, Oda H, Ishimura M, Nakano N, Shirakawa R, Nishikomori R, Takada H, Horiuchi H, Ohara O, Ishii E, Heike T:
J Clin Immunol 37(1):92-99, 2017
Abnormal hematopoiesis and autoimmunity in human subjects with germline IKZF1 mutations.
Hoshino A, Okada S, Yoshida K, Nishida N, Okuno Y, Ueno H, Yamashita M, Okano T, Tsumura M, Nishimura S, Sakata S, Kobayashi M, Nakamura H, Kamizono J, Mitsui-Sekinaka K, Ichimura T, Ohga S, Nakazawa Y, Takagi M, Imai K, Shiraishi Y, Chiba K, Tanaka H, Miyano S, Ogawa S, Kojima S, Nonoyama S, Morio T, Kanegane H:
J Aller Clin Immunol 140(1):223-231, 2017
Efficacy of periodic surveillance culture in a neonatal intensive care unit in the presumption of causative pathogens of late-onset bacterial infection.
Ichikawa S, Hoshina T, Kinjo T, Araki S, Kusuhara K:
Am J Infect Control 45(3): 251-4, 2017
Exome sequencing identified RPS15A as a novel causative gene for Diamond-Blackfan anemia.
Ikeda F, Yoshida K, Toki T, Uechi T, Ishida S, Nakajima Y, Sasahara Y, Okuno Y,Kanezaki R, Terui K, Kamio T, Kobayashi A, Fujita T, Sato-Otsubo A, Shiraishi Y, Tanaka H, Chiba K, Muramatsu H, Kanno H, Ohga S, Ohara A, Kojima S, Kenmochi N, Miyano S, Ogawa S, Ito E:
Hematologica 102:e93-96, 2017
Mutations in genes encoding polycomb repressive complex 2 subunits cause Weaver syndrome.
Imagawa E, Higashimoto K, Sakai Y, Numakura C, Okamoto N, Matsunaga S, Ryo A, Sato Y, Sanefuji M, Ihara K, Takada Y, Nishimura G, Saitsu H, Mizuguchi T, Miyatake S, Nakashima M, Miyake N, Soejima H, Matsumoto N:
Hum Mutat 38: 637-648, 2017
High mobility group box 1 enhances hyperthermia-induced seizures and secondary epilepsy associated with prolonged hyperthermia-induced seizures in developing rats.
Ito M, Takahashi H, Yano H, Shimizu Y, Yano Y, Ishizaki Y, Tanaka J, Ishii E, Fukuda M:
Metab Brain Dis 32:2095-2104, 2017
Alanine-scanning mutagenesis of human signal transducer and activator of transcription 1 to estimate loss- or gain-of-function variants.
Kagawa R, Fujiki R, Tsumura M, Sakata S, Nishimura S, Itan Y, Kong XF, Kato Z, Ohnishi H, Hirata O, Saito S, Ikeda M, El Baghdadi J, Bousfiha A, Fujiwara K, Oleastro M, Yancoski J, Perez L, Danielian S, Ailal F, Takada H, Hara T, Puel A, Boisson-Dupuis S, Bustamante J, Casanova JL, Ohara O, Okada S, Kobayashi M:
J Allergy Clin Immunol. 140(1):232-241, 2017
Effectiveness of an early switch from intravenous to oral antimicrobial therapy for community-acquired lower respiratory tract infection in patients with severe motor intellectual disabilities.
Kawamura M, Hoshina T, Ogawa M, Nakamoto T, Kusuhara K:
J Infect Chemother 2017, in press.
Outcome differences between children and adolescents and young adults with non-Hodgkin lymphoma following stem cell transplantation.
Kobayashi R, Mitsui T, Fujita N, Osumi T, Aoki T, Aoki K, Suzuki R, Fukuda T, Miyamoto T, Kato K, Nakamae H, Goto H, Eto T, Inoue M, Mori T, Terui K, Onizuka M, Koh K, Koga Y, Ichinohe T, Sawada A, Atsuta Y, Suzumiya J:
Int J Hematol 105(3):369-76, 2017
Targeting the Hippo signalling pathway for cancer treatment.
Nakatani K, Maehama T, Nishio M, Goto H, Kato W, Omori H, Miyachi Y, Togashi H, Shimono Y, Suzuki A:
J Biochem 1;161(3):237-244, 2017
Long-term outcomes of 95 children with moderate aplastic anemia treated with horse antithymocyte globulin and cyclosporine
Nishikawa E, Yagasaki H, Hama A, Yabe H, Ohara A, Kosaka Y, Kudo K, Kobayashi R, Ohga S, Morimoto A, Watanabe KI,Yoshida N, Muramatsu H, Takahashi Y, Kojima S:
Pediatr Blood Cancer 64(5). doi: 10.1002/pbc.26305, 2017
Hippo vs. Crab: tissue-specific functions of the mammalian Hippo pathway.
Nishio M, Maehama T, Goto H, Nakatani K, Kato W, Omori H, Miyachi Y, Togashi H, Shimono Y, Suzuki A:
Genes Cells 22(1):6-31, 2017
Distinct distribution of immunocytes in a retropharyngeal lymphadenopathy associated with Kawasaki disease: a case study compared with tonsillitis
Okada S, Kobayashi-Fujiwara Y, Oga A, Furuta T, Ikemoto K, Fujii H, Sakata Y, Suzuki Y, Hasegawa S, Kusuda T, Itoh H, Yamashita H, Ohga S:
Cardiology 137(4):237-243, 2017
Distinctive cytokine profile between acute focal bacterial nephritis and acute pyelonephritis in children
Mizutani M, Hasegawa S, Matsushige T, Ohta N, Kittaka S, Hoshide M, Kusuda T, Takahashi K, Ichihara K, Ohga S:
Cytokine 99:24-29, 2017
Maternal sleep and small for gestational age infants in the Japan Environment and Children's Study: a cohort study.
Morokuma S, Shimokawa M, Kato K, Sanefuji M, Shibata E, Tsuji M, Senju A, Kawamoto T, Kusuhara K; Japan Environment ∧ Children’s Study Group:
BMC Res Notes 10:394, 2017
Dysregulated gene expressions of MEX3D, FOS and BCL2 in human induced-neuronal (iN) cells from NF1 patients: a pilot study.
Sagata N, Kato TA, Kano S, Ohgidani M, Shimokawa N, Sato-Kasai M, Hayakawa K, Kuwano N, Wilson AM, Ishizuka K, Kato S, Nakahara T, Nakahara-Kido M, Setoyama D, Sakai Y, Ohga S, Furue M, Sawa A, Kanba S:
Sci Rep 7:13905, 2017
Clinical characteristics of type A acute aortic dissection with symptom of the central nervous system.
Shono Y, Akahoshi T, Mezuki S, Momii K, Kaku N, Maki J, Tokuda K, Ago T, Kitazono T, Maehara Y:
Am J Emerg Med 35(12):1836-8, 2017
Comparative study on three different methods for arm-span measurement: the Japan environment and Children's study pilot.
Tsuji M, Ayabe T, Tanaka R, Senju A, Shibata E, Araki S, Morokuma S, Sanefuji M, Kusuhara K, Kawamoto T:
Environ Health Prev Med 22:28, 2017.
A heterozygous dominant-negative mutation in the coiled-coil domain of STAT1 is the cause of autosomal-dominant mendelian susceptibility to Mycobacterial disease.
Ueki M, Yamada M, Ito K, Tozawa Y, Morino S, Horikoshi Y, Takada H, Abdrabou SSMA, Takezaki S, Kobayashi I, Ariga T:
J Clin Immunol 174:24-31, 2017
Comprehensive screening for monogenic diabetes in 89 Japanese children with insulin-requiring antibody-negative type 1 diabetes.
Ushijima K, Fukami M, Ayabe T, Narumi S, Okuno M, Nakamura A, Takahashi T, Ihara K, Ohkubo K, Tachikawa E, Nakayama S, Arai J, Kikuchi N, Kikuchi T, Kawamura T, Urakami T, Hata K, Nakabayashi K, Matsubara Y, Amemiya S, Ogata T, Yokota I, Sugihara S; Japanese Study Group of Insulin Therapy for Childhood and Adolescent Diabetes:
Pediatr Diabetes 0:1-8, 2017
Evaluation of Teicoplanin Trough Values After the Recommended Loading Dose in Children With Associated Safety Analysis.
Yamada T, Kubota T, Yonezawa M, Nishio H, Kanno S, Yano T, Kobayashi D, Egashira N, Takada H, Hara T, Masuda S:
Pediatr Infect Dis J 36(4): 398-400, 2017
Histopathological and Genetic Review of Phosphaturic Mesenchymal Tumours, Mixed Connective Tissue Variant
Yamada Y, Kinoshita I, Kenichi K, Yamamoto H, Iwasaki T, Otsuka H, Yoshimoto M, Ishihara S, Toda Y, Kuma Y, Setsu N, Koga Y, Honda Y, Inoue T, Yanai H, Yamashita K, Ito I, Takahashi M, Ohga S, Furue M, Nakashima Y, Oda Y:
Histopathology 2017 (in press)
Long-term safety and efficacy of canakinumab in cryopyrin-associated periodic syndrome: results from an open-label, phase III
Yokota S, Imagawa T, Nishikomori R, Takada H, Abrams K, Lheritier K, Heike T, Hara T:
pivotal study in Japanese patients. Clin Exp Rheumatol 35 Suppl 108(6):19-26, 2017
Successful resolution of Epstein–Barr virus-associated hemophagocytic lymphohistiocytosis during the treatment course of acute lymphoblastic leukemia.
Harada M, Honda Y, Hoshina T, Ohga S, Ohshima K, Kusuhara K:
Pediatr Neonatol 58: 555-7, 2017
Distinct Distribution of Immunocytes in a Retropharyngeal Lymphadenopathy Associated with Kawasaki Disease: A Case Study Compared with Tonsillitis.
Okada S, Kobayashi-Fujiwara Y, Oga A, Furuta T, Ikemoto K, Fujii H, Sakata Y, Suzuki Y, Hasegawa S, Kusuda T, Itoh H, Yamashita H, Ohga S.
Cardiology. 137(4):237-43, 2017
An infant case with hydrocephalus as the initial manifestation of Mycoplasma hominis-associated meningitis.
Taku K, Hoshina T, Haro K, Ichikawa S, Kinjo T, Takahashi M, Akiba D, Fukuda K, Kusuhara K:
J Infect Chemother 23: 713-6, 2017
Lymphoma Committee and Japanese Pediatric Leukemia/Lymphoma Study Group: Pediatric follicular lymphoma in Japan.
Kobayashi R, Tanaka F, Nakazawa A, Ueyama JI, Sunami S, Mitsui T, Koga Y, Mori T, Osumi T, Fukano R, Ohki K, Sekimizu M, Fujita N, Kamei M, Mori T:
Int J Hematol 105(6):849-53, 2017