N. Koyama

发表

Frameshift mutations of the ARX gene in familial Ohtahara syndrome

K. Hayasaka, K. Miura, M. Kato, 2010, Epilepsia.

Asymptomatic C‐reactive protein elevation in neutropenic children

Y. Imanaka, H. Ikai, N. Sasaki, 2017, Pediatrics international : official journal of the Japan Pediatric Society.

Effects of pegylated interferon α-2a on hepatitis-C-virus-associated glomerulonephritis

N. Fujita, Tokio Sugiura, N. Koyama, 2009, Pediatric Nephrology.

Elevated platelet activating factor in the tracheal aspirate at birth and signs of intra-uterine inflammation in infants with neonatal pulmonary emphysema

Y. Ogawa, N. Koyama, 1999, European Journal of Pediatrics.

Increased platelet activating factor in the tracheal aspirates from neonates with patent ductus arteriosus.

Y. Ogawa, N. Koyama, Y. Itakura, 1993, Clinica chimica acta; international journal of clinical chemistry.

Biallelic COLGALT1 variants are associated with cerebral small vessel disease

K. Yokochi, M. Frith, H. Mori, 2018, Annals of neurology.

Phenotypic Spectrum of COL4A1 Mutations: Porencephaly to Schizencephaly

K. Yokochi, A. Kakita, H. Arai, 2013, Annals of neurology.

A fatal case of encephalopathy possibly associated with human metapneumovirus infection.

T. Yamashita, Miyabi Ito, H. Minagawa, 2007, Japanese journal of infectious diseases.

Granulocyte elastase α1‐proteinase inhibitor complex measurement in very low birthweight infants with severe intraventricular hemorrhage

Y. Ogawa, Taihei Tanaka, N. Koyama, 1993, Acta paediatrica Japonica : Overseas edition.

Acylcarnitine Profi les during Carnitine Loading and Fasting Tests in a Japanese Patient with Medium-Chain Acyl-CoA Dehydrogenase Defi ciency

H. Togari, I. Kato, Satoshi Suzuki, 2003 .

ANTENATAL ULTRASONOGRAPHIC APPEARANCE OF A CLOACAL ANOMALY

N. Koyama, Y. Ohno, Y. Arii, 2000, Obstetrics and gynecology.

Three novel mutations of the PAX6 gene in Japanese aniridia patients

S. Minoshima, N. Shimizu, M. Ohtsubo, 2007, Journal of Human Genetics.

Risk Factors for Early Death in Transient Myeloproliferative Disorder Without Phenotypic Features of Down Syndrome: A Case Report and Literature Review

Tomoaki Sasaki, M. Hirayama, E. Azuma, 2012, Journal of pediatric hematology/oncology.

A case of systemic aplasia cutis congenita: a newly recognized syndrome?

Matsuyoshi Maeda, N. Koyama, K. Goto, 2008, European Journal of Pediatrics.

Association of Neonatal Thrombocytopenia and Maternal Anti‐HLA Antibodies

H. Ohto, Y. Ogawa, Taihei Tanaka, 1991, Acta paediatrica Japonica : Overseas edition.

Effect of surfactant lavage in a rabbit model of meconium aspiration syndrome

Y. Ogawa, N. Koyama, H. Eguchi, 1994, Acta paediatrica Japonica : Overseas edition.

Cytokine Profiles Before and After Exchange Transfusion in a Neonate With Transient Myeloproliferative Disorder and Hepatic Fibrosis

H. Togari, T. Ninchoji, K. Aiba, 2010, Journal of pediatric hematology/oncology.

Acylcarnitine profiles during carnitine loading and fasting tests in a Japanese patient with medium-chain acyl-CoA dehydrogenase deficiency.

H. Togari, I. Kato, Satoshi Suzuki, 2007, The Tohoku journal of experimental medicine.

Single nucleotide polymorphisms in AGTR1, TFAP2B, and TRAF1 are not associated with the incidence of patent ductus arteriosus in Japanese preterm infants

S. Saitoh, Takenori Kato, Koichi Ito, 2016, Pediatrics international : official journal of the Japan Pediatric Society.

Echovirus Type 7 Virus-Associated Hemophagocytic Syndrome in a Neonate Successfully Treated With Intravenous Immunoglobulin Therapy: A Case Report

S. Saitoh, N. Koyama, T. Sugiura, 2019, Front. Pediatr..

Management of meconium‐related ileus in very low‐birthweight infants

T. Shinohara, N. Koyama, M. Tsuda, 2007, Pediatrics international : official journal of the Japan Pediatric Society.

DOOR syndrome concomitant with non-convulsive status epilepticus and hyperintense cerebellar cortex on T2-weighted imaging

K. Yokochi, N. Koyama, Takayasu Nomura, 2009, Brain and Development.

clinical features of late-onset circulatory dysfunction in premature infants

S. Fujimoto, H. Togari, Satoru Kobayashi, 2014 .

Late‐onset circulatory dysfunction of premature infants and late‐onset periventricular leukomalacia

S. Fujimoto, H. Togari, T. Okanishi, 2008, Pediatrics international : official journal of the Japan Pediatric Society.

Periventricular leukomalacia with late-onset circulatory dysfunction of premature infants: correlation with severity of magnetic resonance imaging findings and neurological outcomes.

S. Fujimoto, H. Togari, T. Okanishi, 2006, The Tohoku journal of experimental medicine.

GUIDELINES FOR PRE-TRANSFUSION COMPATIBILITY PROCEDURES IN BLOOD TRANSFUSION LABORATORIES IN JAPAN (3rd EDITION)

H. Yasuda, M. Uchikawa, J. Kitazawa, 2020, Japanese Journal of Transfusion and Cell Therapy.

Carnitine-Associated Encephalopathy Caused by Long-term Treatment With an Antibiotic Containing Pivalic Acid

Tetsuya Ito, N. Sugiyama, N. Koyama, 2007, Pediatrics.

Nemaline myopathy with KLHL40 mutation presenting as congenital totally locked-in state

K. Yokochi, I. Nishino, T. Kibe, 2015, Brain and Development.

Hypoxic ischemic encephalopathy in a case of intranuclear rod myopathy without any prenatal sentinel event

K. Yokochi, I. Nishino, N. Koyama, 2015, Brain and Development.

Surfactant Apoprotein A (SP‐A) in Tracheal Aspirates of Newborn Infants with RDS

Y. Ogawa, Taihei Tanaka, N. Koyama, 1991, Acta paediatrica Japonica : Overseas edition.

Neuropathology of infant with Pena-Shokeir I syndrome.

S. Itoyama, Y. Ogawa, N. Koyama, 1994, Pediatric neurology.

IgE-dependent mechanism and successful desensitization of erythritol allergy.

N. Kando, Komei Ito, I. Tsuge, 2016, Annals of allergy, asthma & immunology : official publication of the American College of Allergy, Asthma, & Immunology.

A case of anaphylaxis to erythritol diagnosed by CD203c expression-based basophil activation test.

M. Takeuchi, Komei Ito, Y. Kondo, 2013, Annals of allergy, asthma & immunology : official publication of the American College of Allergy, Asthma, & Immunology.

Pulmonary Surfactant Apoprotein‐A in Neonates with Different Respiratory Disorders

Y. Ogawa, Taihei Tanaka, N. Koyama, 1992, Acta paediatrica Japonica : Overseas edition.