Neurodevelopmental outcomes in infants with birth weight ≤500 g at 3 years of age.
Inoue H, Ochiai M, Sakai Y, Yasuoka K, Tanaka K, Ichiyama M, Kurata H, Fujiyoshi J, Matsushita Y, Honjo S, Nonaka K, Taguchi T, Kato K, Ohga S, Neonatal Research Network of Japan:
Pediatrics 142(6). pii: e20174286. 2018.
A rightward saccade to an unexpected stimulus as a marker for lateralised visuospatial attention.
Sanefuji M, Yamashita H, Torio M, Katsuki D, Akamine S, Ishizaki Y, Kishimoto J, Sakai Y, Takada H, Yoshida K, Ohga S:
Sci Rep 8(1):7562, 2018.
Effective infliximab therapy for the early regression of coronary artery aneurysm in Kawasaki disease
Nagatomo Y, Muneuchi J, Nakashima Y, Nanishi E, Shirozu H, Watanabe M, Uike K, Nagata H, Hirata Y, Yamamura K, Takahashi Y, Okada S, Suzuki Y, Hasegawa S, Ohga S:
Int J Cardiol. 271:317-21, 2018.
Reappraising newborn screening for cobalamin C disorder.
Tocan V, Ohkubo K, Higashi K, Toda N, Kojima-Ishii K, Nishiyama K, Ishimura M, Takada H, Sakamoto O, Sasaki F, Yoshimura K, Hirose S, Ohga S:
Pediatr Neonatol. 2018 Aug;59(4):415-417. doi: 10.1016/j.pedneo.2017.11.002. Epub 2017 Nov 22.
Slow Elevation in Protein C Activity without a PROC Mutation in a Neonate with Intracranial Hemorrhage.
Uehara E, Nakao H, Tsumura Y, Nakadate H, Amari S, Fujinaga H, Tsutsumi Y, Kang D, Ohga S, Ishiguro A:
AJP Rep. 2018 Apr;8(2):e68-e70. doi: 10.1055/s-0038-1639614. Epub 2018 Apr 12.
Letter to 'Pregnancy and delivery outcomes from patients with repaired anomalous origin of the left coronary artery from the pulmonary artery'.
Yamamura K, Ohga S:
J Obstet Gynaecol Res. 2018 Aug;44(8):1498. doi: 10.1111/jog.13673. Epub 2018 May 10.
Streptococcus pyogenes-purpura fulminans as an invasive form of group A streptococcal infection.
Okuzono S, Ishimura M, Kanno S, Sonoda M, Kaku N, Motomura Y, Nishio H, Oba U, Hanada M, Fukushi JI, Urata M, Kang D, Takada H, Ohga S:
Ann Clin Microbiol Antimicrob. 2018 Jul 9;17(1):31. doi: 10.1186/s12941-018-0282-9.
A pediatric case with prostaglandin I2-associated thyrotoxicosis: Case report and the literature review.
Sonoda Y, Yamamura K, Ishii K, Ohkubo K, Ihara K, Sakai Y, Ohga S:
J Clin Res Pediatr Endocrinol 2018 Oct 16. doi: 10.4274/jcrpe.0169. [Epub ahead of print]
Immunoglobulin-Resistant Kawasaki Disease Associated with Human Parvovirus B19 Infection.
Iida Y, Hasegawa S, Korenaga Y, Okada S, Suzuki Y, Hirano R, Ohga S:
Bull Yamaguchi Med Sch, 65(1-2):21-25, 2018.
Cancer Management in Kabuki Syndrome: The First Case of Wilms Tumor and a Literature Review.
Teranishi H, Koga Y, Nakashima K, Morihana E, Ishii K, Sakai Y, Taguchi T, Oda Y, Miyake N, Matsumoto N, Ohga S:
J Pediatr Hematol Oncol 40(5):391-4, 2018.
A male case with CDKL5-associated encephalopathy manifesting transient methylmalonic acidemia.
Akamine S, Ishizaki Y, Sakai Y, Torisu H, Fukai R, Miyake N, Ohkubo K, Koga H, Sanefuji M, Sakata A, Kimura M, Yamaguchi S, Sakamoto O, Hara T, Saitsu H, Matsumoto N, Ohga S:
Eur J Med Genet 61(8): 451-4, 2018.
Posttransplant recipient-derived CD4+ T-cell lymphoproliferative disease in X-linked hyper-IgM syndrome.
Hagio Y, Shiraishi A, Ishimura M, Sonoda M, Eguchi K, Yamamoto H, Oda Y, Ohga S:
Pediatr Blood Cancer. 2018 Oct 30:e27529. doi: 10.1002/pbc.27529. [Epub ahead of print]
Radiotherapy for Langerhans cell histiocytosis with paraplegia: a rare oncologic emergency case report in infancy and literature review.
Nakashima K, Koga Y, Sakai Y, Takada H, Harimaya K, Taguchi T, Oda Y, Honda H, Ohga S:
Brain Dev 40:952-955, 2018.
Atypical erythroblastosis in a patient with Diamond-Blackfan anemia who developed del(20q) myelodysplasia.
Sonoda M, Ishimura M, Ichimiya Y, Terashi E, Eguchi K, Sakai Y, Takada H, Hama A, Kanno H, Toki T, Ito E, Ohga S:
Int J Hematol. 2018 Feb 23. doi: 10.1007/s12185-018-2424-4. [Epub ahead of print]
Nontuberculous mycobacteria-associated hemophagocytic lymphohistiocytosis in MonoMAC syndrome
Eguchi K, Ishimura M, Sonoda M, Ono H, Shiraishi A, Kanno S, Koga Y, Takada H, Ohga S:
Pediatr Blood Cancer. 2018 Mar 1. doi: 10.1002/pbc.27017. [Epub ahead of print]
Prolonged PR Interval at Birth Predicting the High Occurrence of Fatal Atrioventricular Block in Hypoplastic Left Heart Syndrome.
Morihana E, Yamamura K, Sugitani Y, Kado H, Takahata Y, Nakano T, Nakashima Y, Fusazaki N, Ohga S:
Pediatr Cardiol. 2018 Apr;39(4):749-756. doi: 10.1007/s00246-018-1815-x. Epub 2018 Jan 19.
Effective shunt closure for pulmonary hypertension and liver dysfunction in congenital portosystemic venous shunt.
Uike K, Nagata H, Hirata Y, Yamamura K, Terashi E, Matsuura T, Morihana E, Ohkubo K, Ishii K, Sakai Y, Taguchi T, Ohga S:
Pediatr Pulmonol. 2018 Apr;53(4):505-511. doi: 10.1002/ppul.23944. Epub 2018 Jan 23.
Metabolic and immunological assessment of small-for-gestational-age children during one-year treatment with growth hormone: the clinical impact of apolipoproteins.
Kojima-Ishii K, Toda N, Okubo K, Tocan V, Ohyama N, Makimura M, Matsuo T, Ochiai M, Ohga S, Ihara K:
Endocr J. 2018 Apr 26;65(4):449-459. doi: 10.1507/endocrj.EJ17-0485. Epub 2018 Feb 20.
High incidence of progressive stenosis in aberrant left subclavian artery with right aortic arch.
Muraoka M, Nagata H, Hirata Y, Uike K, Terashi E, Morihana E, Ochiai M, Fujita Y, Kato K, Yamamura K, Ohga S:
Heart Vessels. 2018 Mar;33(3):309-315. doi: 10.1007/s00380-017-1056-6. Epub 2017 Sep 30.
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 TA, Nakahara T, Matsushita Y, Togao O, Hiwatashi A, Sanefuji M, Ishizaki Y, Torisu H, Saitsu H, Matsumoto N, Hara T, Sawa A, Kano S, Furue M, Kanba S, Shaw CA, Ohga S:
Epilepsia open 3(1):81-85, 2018.
Predictive indicators for the development of epilepsy after acute encephalopathy with biphasic seizures and late reduced diffusion.
Ichimiya Y, Kaku N, Sanefuji M, Torio M, Mizuguchi S, Motomura Y, Muraoka M, Lee S, Baba H, Sonoda Y, Ishizaki Y, Sasazuki M, Sakai Y, Maehara Y, Ohga S:
Epilepsy Res 143:70-74, 2018.
Diagnostic potential of stored dried blood spots for inborn errors of metabolism: a metabolic autopsy of medium-chain acyl-CoA dehydrogenase deficiency.
Kaku N, Ihara K, Hirata Y, Yamada K, Lee S, Kanemasa H, Motomura Y, Baba H, Tanaka T, Sakai Y, Maehara Y, Ohga S:
J Clin Pathol 71(10):885-889, 2018.
Burden of Human Metapneumovirus and Respiratory Syncytial Virus Infections in Asthmatic Children.
Furuta T, Hasegawa S, Mizutani M, Iwai T, Ohbuchi N, Kawano S, Tashiro N, Uchida M, Hasegawa M, Motoyama M, Sekino T, Nakatsuka K, Ichihara K, Shirabe K, Ohga S:
Pediatr Infect Dis J. 2018 Nov;37(11):1107-1111. doi: 10.1097/INF.0000000000002038.
Survey of Anticancer Drug Exposure to Attendant Families in Pediatric Medical Centers.
Noda Y, Koga Y, Ohta M, Miyazono M, Wakasugi Y, Funakoshi Y, Urabe Y, Kifune M, Ueda T, Oba U, Nakashima K, Souzaki R, Kinoshita Y, Taguchi T, Ohga S:
Gan To Kagaku Ryoho. 2018 Jun;45(6):945-948. Japanese.
Leucine-rich alpha-2 glycoprotein in the cerebrospinal fluid is a potential inflammatory biomarker for meningitis.
Chong PF, Sakai Y, Torisu H, Tanaka T, Furuno K, Mizuno Y, Ohga S, Hara T, Kira R:
J Neurol Sci 392:51-55, 2018.
Vascular pathomechanism in acute encephalopathy with biphasic seizures and late reduced diffusion.
Sanefuji M, Ichimiya Y, Kaku N, Sasazuki M, Yonemoto K, Torio M, Mizuguchi S, Motomura Y, Muraoka M, Lee S, Baba H, Ohkubo K, Sonoda Y, Ishizaki Y, Sakai Y, Ohga S:
J Neurol Sci 395:141-6, 2018.
Lipoteichoic acid anchor triggers Mincle to drive protective immunity against invasive group A Streptococcus infection.
Imai T, Matsumura T, Mayer-Lambertz S, Wells CA, Ishikawa E, Butcher SK, Barnett TC, Walker MJ, Imamura A, Ishida H, Ikebe T, Miyamoto T, Ato M, Ohga S, Lepenies B, van Sorge NM, Yamasaki S:
Proc Natl Acad Sci U S A 115(45): E10662-E10671, 2018
Thrombotic microangiopathy in a very young infant with mitral valvuloplasty.
Matsunaga Y., Ishimura M, Nagata H, Uike K, Kinjo T, Ochiai M, Yamamura K, Takada H, Tanoue Y, Hayakawa M, Matsumoto M, Hara T, Ohga S:
Pediatr Neonatol. 2018 pii: S1875-9572(17)30039-6. doi: 10.1016/j.pedneo.2018.02.002.
Fever and Skin Involvement at Diagnosis Predicting the Intractable Langerhans Cell Histiocytosis: 40 Case-Series in a Single Center.
Kobayashi T, Koga Y, Ishimura M, Nakashima K, Kato W, Ono H, Sonoda M, Eguchi K, Fukano R, Honjo S, Oda Y, Ohga S:
J Pediatr Hematol Oncol. 2018 Apr;40(3):e148-e153. doi: 10.1097/MPH.0000000000001080.
A male case with CDKL5-associated encephalopathy manifesting transient methylmalonic acidemia.
Akamine S, Ishizaki Y, Sakai Y, Torisu H, Fukai R, Miyake N, Ohkubo K, Koga H, Sanefuji M, Sakata A, Kimura M, Yamaguchi S, Sakamoto O, Hara T, Saitsu H, Matsumoto N, Ohga S:
Eur J Med Genet 61(8): 451-4, 2018.
Posttransplant recipient-derived CD4+ T-cell lymphoproliferative disease in X-linked hyper-IgM syndrome.
Hagio Y, Shiraishi A, Ishimura M, Sonoda M, Eguchi K, Yamamoto H, Oda Y, Ohga S:
Pediatr Blood Cancer. 2018 Oct 30:e27529. doi: 10.1002/pbc.27529. [Epub ahead of print]
Nontuberculous mycobacteria-associated hemophagocytic lymphohistiocytosis in MonoMAC syndrome
Eguchi K, Ishimura M, Sonoda M, Ono H, Shiraishi A, Kanno S, Koga Y, Takada H, Ohga S:
Pediatr Blood Cancer. 2018 Mar 1. doi: 10.1002/pbc.27017. [Epub ahead of print]
Clinical features of acute flaccid myelitis temporally associated with an enterovirus D68 outbreak: results of a nationwide survey of acute flaccid paralysis in Japan, August-December 2015.
Chong PF, Kira R, Mori H, Okumura A, Torisu H, Yasumoto S, Shimizu H, Fujimoto T, Hanaoka N, Kusunoki S, Takahashi T, Oishi K, Tanaka-Taya K; Acute Flaccid Myelitis Collaborative Study Investigators:
Clin Infect Dis 66:653-664, 2018
Mulberries in the urine: a tell-tale sign of Fabry disease.
Chong PF, Nakamura K, Kira R::
J Inherit Metab Dis 41:745-746, 2018
Deletions of SCN2A and SCN3A genes in a patient with West syndrome and autistic spectrum disorder.
Chong PF, Saitsu H, Sakai Y, Imagi T, Nakamura R, Matsukura M, Matsumoto N, Kira R:
Seizure 60:91-93, 2018
Treatment and outcome of adult-onset neuroblastoma.
Suzuki M, Kushner BH, Kramer K, Basu EM, Roberts SS, Hammond WJ, LaQuaglia MP, Wolden SL, Cheung NV, Modak S:
Int J Cancer 143(5):1249-1258, 2018
The effect of interim FDG-PET-guided response-adapted therapy in pediatric patients with Hodgkin's lymphoma (HL-14): Protocol for a phase II study.
Koga Y, Baba S, Fukano R, Nakamura K, Soejima T, Maeda N, Sunami S, Ueyama J, Mitsui T, Mori T, Osumi T, Sekimizu M, Ohki K, Tanaka F, Kamei M, Fujita N, Mori T, Saito A, Kada A, Kobayashi R:
Acta Med Okayama 72(4): 437-440, 2018
Nontuberculous mycobacteria-associated hemophagocytic lymphohistiocytosis in MonoMAC syndrome
Eguchi K, Ishimura M, Sonoda M, Ono H, Shiraishi A, Kanno S, Koga Y, Takada H, Ohga S:
Pediatr Blood Cancer 65(7):e27017, 2018
Klebsiella pneumoniae-associated septic pulmonary emboli in a healthy child.
Kano Z, Onoyama S, Tsuji M, Tezuka J, Furuno K:
Pediatr Int. 2018; 13583
Optimal doses of H1 antihistamines do not increase susceptibility to febrile convulsions in children.
Yonemoto K, Okanari K, Koga H
Pediatr Neurol 2018;87:42-47.
Relationship between birth weight to placental weight ratio and major congenital anomalies in Japan.
Takemoto R, Anami A, Koga H.
PLoS One 2018;13:e0206002.
Increased pituitary volume in children after Fontan operation: Congestion in the other portal circulation.
Muneuchi J, Nagatomo Y, Okada S, Iida C, Shirozu H, Sugitani Y, Watanabe M.
J Pediatr. 2018;193:249-251.
Ventricular efficiency in pregnant women with congenital heart disease
Muneuchi J, Yamasaki K, Watanabe M, Fukumitsu A, Kawakami T, Nakahara H, Joo K.
Int J Cardiol 2018;261:58-61.
Absence of exertional oscillatory ventilation during exercise related to late adverse outcome in Fontan patients
Muneuchi J, Watanabe M.
Pediatr Cardiol 2018;39(3):640-641.
Electrocardiogram in a patient with Paragonimiasis westermani-triggered Takotsubo syndrome.
Muneuchi J.
Paediatr Int Child Health. 2018 May 18:1-2.
infiltrate the destructed mitral tissue in Kawasaki disease.
Sugitani Y, Furuno K, Sueishi K, Hara T. Macrophages and cytotoxic T cells
BMJ Case Rep. 2018 Feb 2;2018.
Coronary sinus orifice atresia in tricuspid atresia
Shirozu H, Muneuchi J, Nagatomo Y, Watanabe M, Okada S, Iida C, Ochiai Y.
Journal of Pediatric Cardiology and Cardiac Surgery 2018;2(2): 84-86
Infantile hypophosphatasia combined with vitamin B6-responsive seizures and reticular formation lesions on magnetic resonance imaging: A case report.
Fukazawa M, Tezuka J, Sasazuki M, Masumoto N, Baba H, Doi T, Tsutsumi Y, Mizuno Y, Mihara F, Nakayama H:
Brain Dev. 40(2):140-144, 2018
Prednisolone for pulmonary hemorrhage after Fontan procedure.
Toyomura D, Kodama Y, Tezuka J, Sagawa K, Ishikawa S:
Pediatr Int. 60(3):294-295, 2018
Ocular findings in a case of Pierson syndrome with a novel mutation in laminin ß2 gene.
Arima M, Tsukamoto S, Akiyama R, Nishiyama K, Kohno RI, Tachibana T, Hayashida A, Murayama M, Hisatomi T, Nozu K, Iijima K, Ohga S, Sonoda KH:
J AAPOS. 2018 Oct;22(5):401-403.e1. doi: 10.1016/j.jaapos.2018.03.016. Epub 2018 Aug 16.
Pediatric ganglioglioma with an H3 K27M mutation arising from the cervical spinal cord.
Okuda T, Hata N, Suzuki SO, Yoshimoto K, Arimura K, Amemiya T, Akagi Y, Kuga D, Oba U, Koga Y, Ohga S, Iwaki T, Iihara K.
Neuropathology. 2018 Apr 19. doi: 10.1111/neup.12471.
Adalimumab for treatment of hemophagocytic syndrome following unrelated bone marrow transplantation in a boy with Behcet's disease and secondary myelodysplastic syndrome.
Noguchi M, Moritake H, Kamimura S, Sonoda M, Ishimura M, Inagaki J:
Bone Marrow Transplant. 2018;53:1214-1217.
Mitochondrial dysfunction in dopaminergic neurons differentiated from exfoliated deciduous tooth-derived pulp stem cells of a child with Rett syndrome.
Masuda K, Hirofuji Y, Hirofuji S, Kato H, Yamaza H, Sato H, Takayama F, Torio M, Sakai Y, Ohga S, Taguchi T, Nonaka K:
Biochem Biophys Res Commun 2018 (in press).
The Japanese Immune Tolerance Induction (J-ITI) study in hemophilia patients with inhibitor; outcomes and successful predictors of ITI treatment.
Nogami K, Taki M, Matsushita T, Ohga S, Hanabusa H, Oka T, Horikoshi Y, Amano K, Shima M:
Hemophilia 2018 Sep;24(5):e328-e337
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 72(3):460-471, 2018.
Integrative analyses of de novo mutations provide deeper biological insights into autism spectrum disorder.
Takata A, Miyake N, Tsurusaki Y, Fukai R, Miyatake S, Koshimizu E, Kushima I, Okada T, Morikawa M, Uno Y, Ishizuka K, Nakamura K, Tsujii M, Yoshikawa T, Toyota T, Okamoto N, Hiraki Y, Hashimoto R, Yasuda Y, Saitoh S, Ohashi K, Sakai Y, Ohga S, Hara T, Kato M, Nakamura K, Ito A, Seiwa C, Shirahata E, Osaka H, Matsumoto A, Takeshita S, Tohyama J, Saikusa T, Matsuishi T, Nakamura T, Tsuboi T, Kato T, Suzuki T, Saitsu H, Nakashima M, Mizuguchi T, Tanaka F, Mori N, Ozaki N, Matsumoto N:
Cell Rep 22(3):734-747, 2018.
Mitochondrial dysfunction in dopaminergic neurons differentiated from exfoliated deciduous tooth-derived pulp stem cells of a child with Rett syndrome.
Hirofuji S, Hirofuji Y, Kato H, Masuda K, Yamaza H, Sato H, Takayama F, Torio M, Sakai Y, Ohga S, Taguchi T, Nonaka K:
Biochem Biophys Res Commun 498(4): 898-904, 2018.
The efficacy of serum brain natriuretic peptide for the early detection of portopulmonary hypertension in biliary atresia patients before liver transplantation.
Yoshimaru K, Matsuura T, Takahashi Y, Yanagi Y, Nagata H, Ohga S, Taguchi T:
Pediatr Transplant. 2018 Aug;22(5):e13203. doi: 10.1111/petr.13203. Epub 2018 May 7.
Lysosomal membrane permeabilization causes secretion of IL-1β in human vascular smooth muscle cells.
Ono H, Ohta R, Kawasaki Y, Niwa A, Takada H, Nakahata T, Ohga S, Saito MK:
Inflamm Res 67(10):879-889, 2018.
Medical equipment deployment in pediatric emergency prehospital medical units in Japan.
Kaku N, Nitta M, Muguruma M, Hirata Y, Tsukahara K, Knaup E, Nosaka N, Enomoto Y.
Pediatr Int 2018 Jan;60(1):93-95.
De Novo Mutations Activating Germline TP53 in an Inherited Bone-Marrow-Failure Syndrome.
Toki T, Yoshida K, Wang R, Nakamura S, Maekawa T, Goi K, Katoh MC, Mizuno S, Sugiyama F, Kanezaki R, Uechi T, Nakajima Y, Sato Y, Okuno Y, Sato-Otsubo A, Shiozawa Y, Kataoka K, Shiraishi Y, Sanada M, Chiba K, Tanaka H, Terui K, Sato T, Kamio T, Sakaguchi H, Ohga S, Kuramitsu M, Hamaguchi I, Ohara A, Kanno H, Miyano S, Kojima S, Ishiguro A, Sugita K, Kenmochi N, Takahashi S, Eto K, Ogawa S, Ito E:
Am J Hum Genet. 2018 Sep 6;103(3):440-447. doi: 10.1016/j.ajhg.2018.07.020. Epub 2018 Aug 23.
Complement activation associated with ADAMTS13 deficiency may contribute to the characteristic glomerular manifestations in Upshaw-Schulman syndrome.
Itami H, Hara S, Matsumoto M, Imamura S, Kanai R, Nishiyama K, Ishimura M, Ohga S, Yoshida M, Tanaka R, Ogawa Y, Asada Y, Sekita-Hatakeyama Y, Hatakeyama K, Ohbayashi C:
Thromb Res. 2018 Oct;170:148-155. doi: 10.1016/j.thromres.2018.08.020. Epub 2018 Sep 1.
Impaired neurite development associated with mitochondrial dysfunction in dopaminergic neurons differentiated from exfoliated deciduous tooth-derived pulp stem cells of children with autism spectrum disorder.
Nguyen HTN, Kato H, Masuda K, Yamaza H, Hirofuji Y, Sato H, Phama T, Takayama F, Sakai Y,Ohga S, Taguchi T, Nonaka K:
Biochem Biophys Rep 16:24-31, 2018.
Early canakinumab therapy for the sensorineural deafness in a family with Muckle-Wells syndrome due to a novel mutation of NLRP3 gene.
Iida Y, Wakiguchi H, Okazaki F, Nakamura T, Yasudo H, Kubo M, Sugahara K, Yamashita H, Suehiro Y, Okayama N, Hashimoto K, Iwamoto N, Kawakami A, Aoki Y, Takada H, Ohga S, Hasegawa S:
Clin Rheumatol. 2018 Oct 18. doi: 10.1007/s10067-018-4331-8. [Epub ahead of print]
Non-reassuring foetal status and neonatal irritability in the Japan Environment and Children's Study: A cohort study.
Morokuma S, Michikawa T, Kato K, Sanefuji M, Shibata E, Tsuji M, Senju A, Kawamoto T, Ohga S, Kusuhara K:
Sci Rep 8(1):15853, 2018.
Optimal protein intake during pregnancy for reducing the risk of fetal growth restriction: the Japan Environment and Children's Study.
Morisaki N, Nagata C, Yasuo S, Morokuma S, Kato K, Sanefuji M, Shibata E, Tsuji M, Senju A, Kawamoto T, Ohga S, Kusuhara K; Japan Environment and Children’s Study Group:
Br J Nutr. 2018 Dec;120(12):1432-1440. doi: 10.1017/S000711451800291X. Epub 2018 Nov 5.
Complement activation associated with ADAMTS13 deficiency may contribute to the characteristic glomerular manifestations in Upshaw-Schulman syndrome.
Itami H, Hara S, Matsumoto M, Imamura S, Kanai R, Nishiyama K, Ishimura M, Ohga S, Yoshida M, Tanaka R, Ogawa Y, Asada Y, Sekita-Hatakeyama Y, Hatakeyama K, Ohbayashi C:
Thromb Res. 2018 Sep 1;170:148-155. doi: 10.1016/j.thromres.2018.08.020.
Hematopoietic stem cell transplantation for progressive combined immunodeficiency and lymphoproliferation in patients with activated phosphatidylinositol-3-OH kinase δ syndrome type 1.
Okano T, Imai K, Tsujita Y, Mitsuiki N, Yoshida K, Kamae C, Honma K, Mitsui-Sekinaka K, Sekinaka Y, Kato T, Hanabusa K, Endo E, Takashima T, Hiroki H, Yeh TW, Tanaka K, Nagahori M, Tsuge I, Bando Y, Iwasaki F, Shikama Y, Inoue M, Kimoto T, Moriguchi N, Yuza Y, Kaneko T, Suzuki K, Matsubara T, Maruo Y, Kunitsu T, Waragai T, Sano H, Hashimoto Y, Tasaki K, Suzuki O, Shirakawa T, Kato M, Uchiyama T, Ishimura M, Tauchi T, Yagasaki H, Jou ST, Yu HH, Kanegane H, Kracker S, Durandy A, Kojima D, Muramatsu H, Wada T, Inoue Y, Takada H, Kojima S, Ogawa S, Ohara O, Nonoyama S, Morio T:
J Allergy Clin Immunol. 2018 May 18. pii: S0091-6749(18)30707-3. doi: 10.1016/j.jaci.2018.04.032. [Epub ahead of print]
Slow Elevation in Protein C Activity without a PROC Mutation in a Neonate with Intracranial Hemorrhage.
Uehara E, Nakao H, Tsumura Y, Nakadate H, Amari S, Fujinaga H, Tsutsumi Y, Kang D, Ohga S, Ishiguro A:
AJP Rep. 2018 Apr;8(2):e68-e70. doi: 10.1055/s-0038-1639614. Epub 2018 Apr 12.
Ocular findings in a case of Pierson syndrome with a novel mutation in laminin ß2 gene.
Arima M, Tsukamoto S, Akiyama R, Nishiyama K, Kohno RI, Tachibana T, Hayashida A, Murayama M, Hisatomi T, Nozu K, Iijima K, Ohga S, Sonoda KH:
J AAPOS. 2018 Oct;22(5):401-403.e1. doi: 10.1016/j.jaapos.2018.03.016. Epub 2018 Aug 16.
Adalimumab for treatment of hemophagocytic syndrome following unrelated bone marrow transplantation in a boy with Behcet's disease and secondary myelodysplastic syndrome.
Noguchi M, Moritake H, Kamimura S, Sonoda M, Ishimura M, Inagaki J:
Bone Marrow Transplant. 2018;53:1214-1217.
Clinical and genetic characteristics in patients with Gitelman syndrome.
Fujimura J, Nozu K, Yamamura T, Minamikawa S, Nakanishi K, Horinouchi T, Nagano C, Sakakibara N, Nakanishi K, Shima Y, Miyako K, Nozu Y, Morisada N, Nagase H, Ninchoji T, Kaito H, Iijima K:
Kidney Int Rep 2018 https://doi.org/10.1016/j.ekir.2018.09.015
Mitochondrial dysfunction in dopaminergic neurons differentiated from exfoliated deciduous tooth-derived pulp stem cells of a child with Rett syndrome.
Hirofuji S, Hirofuji Y, Kato H, Masuda K, Yamaza H, Sato H, Takayama F, Torio M, Sakai Y, Ohga S, Taguchi T, Nonaka K:
Biochem Biophys Res Commun 498(4): 898-904, 2018
K; Japan Environment and Children’s Study Group.
Morisaki N, Nagata C, Yasuo S, Morokuma S, Kato K, Sanefuji M, Shibata E, Tsuji M, Senju A, Kawamoto T, Ohga S, Kusuhara
Br J Nutr 120(12):1432-1440, 2018.
Non-reassuring foetal status and neonatal irritability in the Japan Environment and Children's Study: A cohort study.
Morokuma S, Michikawa T, Kato K, Sanefuji M, Shibata E, Tsuji M, Senju A, Kawamoto T, Ohga S, Kusuhara K:
Sci Rep 8(1):15853, 2018.
Factors associated with occupation changes after pregnancy/delivery: result from Japan Environment & Children's pilot study.
Suga R, Tsuji M, Tanaka R, Shibata E, Tanaka M, Senju A, Araki S, Morokuma S, Sanefuji M, Oda M, Mise N, Baba Y, Hayama-Terada M, Kusuhara K, Mitsubuchi H, Katoh T, Kawamoto T:
BMC Womens Health 18(1):86, 2018.
Variation in Men's Dietary Intake Between Occupations, Based on Data From the Japan Environment and Children's Study.
Tanaka R, Tsuji M, Asakura K, Senju A, Shibata E, Kusuhara K, Morokuma S, Sanefuji M, Kawamoto T; Japan Environment and Children’s Study Group:
Am J Mens Health. 12(5):1621-1634, 2018.
The association between whole blood concentrations of heavy metals in pregnant women and premature births: The Japan Environment and Children's Study (JECS).
Tsuji M, Shibata E, Morokuma S, Tanaka R, Senju A, Araki S, Sanefuji M, Koriyama C, Yamamoto M, Ishihara Y, Kusuhara K, Kawamoto T; Japan Environment & Children's Study Group:
Environ Res 166, 562-569, 2018
Prognostic factors in patients with miliary tuberculosis.
Wakamatsu K, Nagata N, Kumazoe H, Honjyo S, Hara M, Nagaoka A, Noda N, Okamura K, Kawatoko K, Ose M, Yamada E, Akasaki T, Maki S, Ise S, Izumi M, Kawasaki M:
J Clin Tuberc Other Mycobact Dis 12: 66–72, 2018
Novel A178P mutation in SLC16A2 in a patient with Allan-Herndon-Dudley syndrome.
Yamamoto T, Lu Y, Nakamura R, Shimojima K, Kira R:
Congenit Anom 58:143-144, 2018
Impact of low-dose irradiation and in vivo T-cell depletion on hematopoietic stem cell transplantation for non-malignant diseases using fludarabine-based reduced-intensity conditioning.
Umeda K, Yabe H, Kato K, Imai K, Kobayashi M, Takahashi Y, Yoshida N, Sato M, Sasahara Y, Kato K, Adachi S, Koga Y, Okada K, Inoue M, Hashii Y, Atsuta Y, Morio T; Inherited Disease Working Group of the Japan Society for Hematopoietic Cell Transplantation:
Bone Marrow Transplant 2018 Dec 7. doi: 10.1038/s41409-018-0418-8. [Epub ahead of print]
Clinical characteristics of pediatric patients with myeloid sarcoma without bone marrow involvement in Japan.
Taga T, Imamura T, Nakashima K, Maeda N, Watanabe A, Miyajima Y, Sakaguchi S, Sano H, Hasegawa D, Kawasaki H, Adachi S, Takagi M, Koh K, Manabe A, Taki T, Ishida Y:
Int J Hematol 108(4):438-442, 2018
The influence of sarcopenia on high-risk neuroblastoma.
Kawakubo N, Kinoshita Y, Souzaki R, Koga Y, Oba U, Ohga S, Taguchi T:
J Surg Res, 2018 in press
Phase I clinical study of brentuximab vedotin (SGN-35) involving children with recurrent or refractory CD30-positive Hodgkin's lymphoma or systemic anaplastic large cell lymphoma: rationale, design and methods of BV-HLALCL study: study protocol.
Sekimizu M, Iguchi A, Mori T, Koga Y, Kada A, Saito AM, Horibe K:
BMC Cancer 18(1):122, 2018
A Phase I/II Study of Crizotinib for Recurrent or Refractory Anaplastic Lymphoma Kinase-Positive Anaplastic Large Cell Lymphoma and a Phase I Study of Crizotinib for Recurrent or Refractory Neuroblastoma : Study Protocol for a Multicenter Single-arm Open-label Trial.
Sekimizu M, Osumi T, Fukano R, Koga Y, Kada A, Saito AM, Mori T:
Acta Med Okayama 72(4):431-436, 2018
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 72(3):460-471, 2018
Adachi S. Risk-stratified therapy for children with FLT3-ITD positive acute myeloid leukemia: Results from the JPLSG AML-05 study.
Shimada A, Iijima-Yamashita Y, Tawa A, Tomizawa D, Yamada M, Shiba N, Watanabe T, Taga T, Iwamoto S, Terui K, Moritake H, Kinoshita A, Takahashi H, Nakayama H, Koh K, Goto H, Kosaka Y, Saito AM, Kiyokawa N, Horibe K, Hara Y, Oki K, Hayashi Y, Tanaka S:
Int J Hematol 107(5):586-595, 2018
Pediatric ganglioglioma with an H3 K27M mutation arising from the cervical spinal cord.
Okuda T, Hata N, Suzuki SO, Yoshimoto K, Arimura K, Amemiya T, Akagi Y, Kuga D, Oba U, Koga Y, Ohga S, Iwaki T, Iihara K:
Neuropathology Apr 19 [Epub ahead of print], 2018
Effectiveness of an early switch from intravenous to oral antimicrobial therapy for lower respiratory tract infection in patients with severe motor intellectual disabilities.
Kawamura M, Hoshina T, Ogawa M, Nakamoto T, Kusuhara K:
J Infect Chemother 24(1):40-44, 2018
The physiological variation in plasma presepsin levels during the early neonatal period.
Ishii M, Hoshina T, Ichikawa S, Shimizu D, Araki S, Kinjo T, Shibata E, Hachisuga T, Kusuhara K:
Tohoku J Exp Med 246(3):199-203, 2018
Utility of the Performance of Lumbar Puncture for Febrile Children with Status Epilepticus in the Bacterial Conjugate Vaccine Era.
Haro K, Igarashi R, Hoshina T, Kojiro M, Kusuhara K:
Pediatr Infect Dis J 37(10):963-966, 2018
Unexpected Ventriculitis complication of neonatal meningitis caused by Streptococcus gallolyticus subsp. pasteurianus: a case report.
Yamamura Y, Mihara Y, Nakatani K, Nishiguchi T, Ikebe T:
Jpn J Infect Dis 71:68-71, 2018
A pediatric case with parvovirus B19-associated uveitis without autoantibody formation.
Ito T, Hoshina T, Mizuki K, Fukuda T, Ishibashi S, Kusuhara K.
Nagoya J Med Sci 80:615-618, 2018
Kawasaki disease-related arthritis with synovial involvement.
Ito T, Hoshina T, Taku K, Kusuhara K:
Pediatr Int 2018 Oct. doi: 10.1111/ped.13721
Bullous artificial dermatitis due to aerosol sprays masquerading as fixed drug eruption.
Kudo K, Masuda A, Mizobe T, Kihara J, Onoyama S, Furuno K, Furue M:
J Dermatol. 2018 Dec. doi.org/10.1111/1346-8138.14729
Intelligence test at preschool-age predicts reading difficulty among school-aged very low birth weight infants in Japan
Takeuchi A, Ogino T, Koeda T, Oka M, Yorifuji T, Takayanagi T, Sato K, Sugino N, Bonno M, Nakamura M, Kageyama M.
Brain & Development 40: 735-742, 2018
Disharmonious Patterns of Heterotaxy and Isomerism: How Often Are the Classic Patterns Breached?
Yim D, Nagata H, Lam CZ, Grosse-Wortmann L, Seed M, Jaeggi E, Yoo SJ
Circ Cardiovasc Imaging doi: 10.1161/CIRCIMAGING.117.006917. 2018
The efficacy of serum brain natriuretic peptide for the early detection of portopulmonary hypertension in biliary atresia patients before liver transplantation.
Yoshimaru K, Matsuura T, Takahashi Y, Yanagi Y, Nagata H, Ohga S, Taguchi T.
Pediatr Transplant. 2018 Aug;22(5):e13203. doi: 10.1111/petr.13203. Epub 2018 May 7.
Patient-related factors influencing detectability of coronary arteries in 320-row CT angiography in infants with complex congenital heart disease
Yamasaki Y, Kawanami S, Kamitani T, Sagiyama K, Shin S, Hino T, Nagata H, Yabuuchi H, Nagao M, Honda H.
Int J Cardiovasc Imaging. 2018 Sep;34(9):1485-1491. doi: 10.1007/s10554-018-1363-8. Epub 2018 May 5.
Free-breathing 320-row computed tomographic angiography with low-tube voltage and hybrid iterative reconstruction in infants with complex congenital heart disease.
Yamasaki Y, Kawanami S, Kamitani T, Sagiyama K, Shin S, Hino T, Yamamura K, Yabuuchi H, Nagao M, Honda H.
Clin Imaging 50:147-156, 2018
Dynamic flow imaging using 320-detector row CT and motion coherence analysis in coronary aneurysms associated with Kawasaki disease.
Shimomiya Y, Nagao M, Yamasaki Y, Shirasaka T, Kondo M, Kojima T, Nishie A, Yamamura K, Honda H.
Cardiol Young 28(3):416-420, 2018
Association of Severity of Coronary Artery Aneurysms in Patients With Kawasaki Disease and Risk of Later Coronary Events.
Miura M, Kobayashi T, Kaneko T, Ayusawa M, Fukazawa R, Fukushima N, Fuse S, Hamaoka K, Hirono K, Kato T, Mitani Y, Sato S, Shimoyama S, Shiono J, Suda K, Suzuki H, Maeda J, Waki K; and The Z-score Project 2nd Stage Study Group, Kato H, Saji T, Yamagishi H, Ozeki A, Tomotsune M, Yoshida M, Akazawa Y, Aso K, Doi S, Fukasawa Y, Furuno K, Hayabuchi Y, Hayashi M, Honda T, Horita N, Ikeda K, Ishii M, Iwashima S, Kamada M, Kaneko M, Katyama H, Kawamura Y, Kitagawa A, Komori A, Kuraishi K, Masuda H, Matsuda S, Matsuzaki S, Mii S, Miyamoto T, Moritou Y, Motoki N, Nagumo K, Nakamura T, Nishihara E, Nomura Y, Ogata S, Ohashi H, Okumura K, Omori D, Sano T, Suganuma E, Takahashi T, Takatsuki S, Takeda A, Terai M, Toyono M, Watanabe K, Watanabe M, Yamamoto M, Yamamura K:
JAMA Pediatr. 2018 May 7;172(5)
Mode of death and predictors of mortality in adult Fontan survivors: A Japanese multicenter observational study.
Ohuchi H, Inai K, Nakamura M, Park IS, Watanabe M, Hiroshi O, Kim KS, Sakazaki H, Waki K, Yamagishi H, Yamamura K, Kuraishi K, Miura M, Nakai M, Nishimura K, Niwa K; JSACHD Fontan Investigators.
Int J Cardiol 2018 [Epub ahead of print]
Twin pregnancy complicated by total placenta previa in a Fontan palliated patient: A case report
Morita A, Kido S, Hachisuga M, Nagata H, Hidaka N, Kato K.
Case Rep Womens Health. 2018 Oct 26;20:e00085. doi: 10.1016/j.crwh.2018.e00085. eCollection 2018 Oct.
Successful treatment of protein-losing enteropathy and plastic bronchitis by biphasic cuirass ventilator in a patient with failing Fontan circulation.
Okada S, Muneuchi J, Nagatomo Y, Nonaka K, Iida C, Shirozu, H, Matsuoka R, Watanabe M, Joo K.
Int Heart J. 2018 Jul 31;59(4):873-876.
Transcatheter closure of a huge ductus arteriosus in a severely ill neonate.
Okada S, Muneuchi J, Nagatomo Y, Yokota C, Ohmura J, Yamamoto J, Watanabe M, Iida C, Shirouzu H, Takahashi Y.
Int Heart J. 2018 ;59(5):1161-1165.
Characterization of 3-dimensional mapping in Wolff-Parkinson-White syndrome with septal aneurysmal dyskinesis.
Okada S, Muneuchi J, Origuchi H.
Cardiol Young. 2018;28(1):168-170
Unique levoatriocardinal veins in neonates with hypoplastic left heart syndrome and intact atrial septum.
Iida C, Muneuchi J, Watanabe M.
Cardiol Young. 2018;28(1):150-152
Sutureless pericardial marsupialization for the repair of congenital right pulmonary veins atresia.
Ochiai Y, Ando Y, Tokunaga S, Muneuchi J.
Interact Cardiovasc Thorac Surg. 2018;27(1):151-152.
Bullous artificial dermatitis due to aerosol sprays masquerading as fixed drug eruption.
Kudo K, Masuda A, Mizobe T, Kihara J, Onoyama S, Furuno K, Furue M:
J Dermatol. in press
Complement activation associated with ADAMTS13 deficiency may contribute to the characteristic glomerular manifestations in Upshaw-Schulman syndrome.
Itami H, Hara S, Matsumoto M, Imamura S, Kanai R, Nishiyama K, Ishimura M, Ohga S, Yoshida M, Tanaka R, Ogawa Y, Asada Y, Sekita-Hatakeyama Y, Hatakeyama K, Ohbayashi C:
Thromb Res 170: 148-155, 2018
Detection of Splicing Abnormalities and Genotype-Phenotype Correlation in X-linked Alport Syndrome.
Horinouchi T, Nozu K, Yamamura T, Minamikawa S, Omori T, Nakanishi K, Fujimura J, Ashida A, Kitamura M, Kawano M, Shimabukuro W, Kitabayashi C, Imafuku A, Tamagaki K, Kamei K, Okamoto K, Fujinaga S, Oka M, Igarashi T, Miyazono A, Sawanobori E, Fujimaru R, Nakanishi K, Shima Y, Matsuo M, Ye MJ, Nozu Y, Morisada N, Kaito H, Iijima K:
J Am Soc Nephrol 29(8): 2244-2254, 2018
Strong Association of the HLA-DR/DQ Locus with Childhood Steroid-Sensitive Nephrotic Syndrome in the Japanese Population.
Jia X, Horinouchi T, Hitomi Y, Shono A, Khor SS, Omae Y, Kojima K, Kawai Y, Nagasaki M, Kaku Y, Okamoto T, Ohwada Y, Ohta K, Okuda Y, Fujimaru R, Hatae K, Kumagai N, Sawanobori E, Nakazato H, Ohtsuka Y, Nakanishi K, Shima Y, Tanaka R, Ashida A, Kamei K, Ishikura K, Nozu K, Tokunaga K, Iijima K：
J Am Soc Nephrol 29(8): 2189-2199, 2018
Combination therapy with or without warfarin and dipyridamole for severe childhood IgA nephropathy: an RCT.
Shima Y, Nakanishi K, Kaku Y, Ishikura K, Hataya H, Matsuyama T, Honda M, Sako M, Nozu K, Tanaka R, Iijima K, Yoshikawa N; Japanese Pediatric IgA Nephropathy Treatment Study Group：
Pediatr Nephrol 33: 2103-2112, 2018
Ocular findings in a case of Pierson syndrome with a novel mutation in laminin ß2 gene.
Arima M, Tsukamoto S, Akiyama R, Nishiyama K, Kohno RI, Tachibana T, Hayashida A, Murayama M, Hisatomi T, Nozu K, Iijima K, Ohga S, Sonoda KH:
J AAPOS 22(5): 401-403, 2018
Mitochondrial p32/C1qbp Is a Critical Regulator of Dendritic Cell Metabolism and Maturation.
Gotoh K, Morisaki T, Setoyama D, Sasaki K, Yagi M, Igami K, Mizuguchi S, Uchiumi T, Fukui Y, Kang D:
Cell Rep. 25:1800-1815, 2018
Accuracy of Reported Tidal Volume During Neonatal Ventilation With Airway Leak: A Lung Model Study.
Moon K, Takeuchi M, Tachibana K, Mizuguchi S, Hirano S:
Pediatr Crit Care Med. 2018 Oct 17. (in press)
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