J. Miyahara

发表

Survival of an infant with massive fetomaternal hemorrhage with a neonatal hemoglobin concentration of 1.2 g/dL without evident neurodevelopmental sequelae

H. Sugiura, S. Ohki, J. Miyahara, 2020, SAGE open medical case reports.

Clinical and mutational spectrum of Japanese patients with Charcot‐Marie‐Tooth disease caused by GDAP1 variants

S. Tsuji, T. Nakamura, K. Haginoya, 2017, Clinical genetics.

Mannosyl‐oligosaccharide glucosidase – congenital disorder of glycosylation: A patient with novel variants

H. Sugiura, S. Ohki, J. Miyahara, 2020, Pediatrics International.

Successful management of acquired left bronchial stenosis caused by massive atelectasis

H. Sugiura, S. Ohki, Takuya Ohhashi, 2019, SAGE open medical case reports.

A novel PLP mutation in a Japanese patient with mild Pelizaeus-Merzbacher disease

K. Yokochi, T. Kibe, A. Iwaki, 2009, Brain and Development.

Case report A novel PLP mutation in a Japanese patient with mild Pelizaeus-Merzbacher disease

K. Yokochi, T. Kibe, A. Iwaki, 2009 .

Adult-onset Repeat Rhabdomyolysis with a Very Long-chain Acyl-CoA Dehydrogenase Deficiency Due to Compound Heterozygous ACADVL Mutations

Yoshihiko Saito, I. Nishino, T. Fukuda, 2020, Internal medicine.

Dietary chloride deficiency due to new liquid nutritional products

K. Yokochi, J. Miyahara, S. Aramaki, 2009, Pediatrics International.

The evaluation of the efficacy and safety of non-invasive neurally adjusted ventilatory assist in combination with INtubation-SURfactant-Extubation technique for infants at 28 to 33 weeks of gestation with respiratory distress syndrome

H. Sugiura, S. Ohki, J. Miyahara, 2019, SAGE open medicine.