J. Nakajima

发表

Nonalcoholic steatohepatitis and insulin resistance in children.

H. Kawashima, S. Nishimata, Mikage Arata, 2014, World journal of diabetes.

N. Arora, J. Kaushik, D. Dayal, 1873, Indian Pediatrics.

Reversible basal ganglia lesions in neuropsychiatric lupus: a report of three pediatric cases

T. Yoshio, H. Kawashima, Satoshi Sato, 2014, International journal of rheumatic diseases.

Efficacy of prolonged valganciclovir therapy for congenital cytomegalovirus infection

N. Inoue, Yu Ishida, Y. Kashiwagi, 2011, Journal of infection and chemotherapy : official journal of the Japan Society of Chemotherapy.

De novo EEF1A2 mutations in patients with characteristic facial features, intellectual disability, autistic behaviors and epilepsy

H. Arai, N. Matsumoto, N. Miyake, 2015, Clinical genetics.

Novel compound heterozygous DPH1 mutations in a patient with the unique clinical features of airway obstruction and external genital abnormalities

N. Matsumoto, N. Miyake, M. Nakashima, 2018, Journal of Human Genetics.

A novel homozygous YARS2 mutation causes severe myopathy, lactic acidosis, and sideroblastic anemia 2

N. Matsumoto, N. Miyake, Y. Tsurusaki, 2014, Journal of Human Genetics.

Novel FIG4 mutations in Yunis–Varon syndrome

N. Matsumoto, N. Miyake, Y. Tsurusaki, 2013, Journal of Human Genetics.

Dextro-Transposition of the Great Arteries in a Neonate with Ventricular Septal Defect and Pulmonary Stenosis Complicated by Premature Closure of the Ductus Arteriosus and Possible Pathophysiology of Both Defects

K. Tsuchiya, Tadashi Kawakami, J. Nakajima, 2012, Pediatric Cardiology.

Retinopathy in juvenile systemic lupus erythematosus successfully treated with plasma exchange

H. Kawashima, Satoshi Sato, J. Nakajima, 2015 .

Novel HPS6 mutations identified by whole-exome sequencing in two Japanese sisters with suspected ocular albinism

T. Ogata, N. Matsumoto, T. Nomura, 2016, Journal of Human Genetics.

Mother-Neonatal Intensive Care Unit – A New Model of Family Participatory Care ?

Kayo Mizutani, Hiroyuki Sato, J. Nakajima, 2019 .

Efficacy of macrolides on gastric motility in extremely low birth weight infants.

H. Kawashima, J. Nakajima, D. Sunohara, 2019, Journal of neonatal-perinatal medicine.

Novel compound heterozygous DPH1 mutations in a patient with the unique clinical features of airway obstruction and external genital abnormalities

N. Matsumoto, N. Miyake, M. Nakashima, 2018, Journal of Human Genetics.