H. Terasawa

发表

Sequential Bilateral Medial Medullary Infarction due to Vertebral Artery Dissection

S. Kataoka, H. Terasawa, H. Tohji, 2007, Cerebrovascular Diseases.

Dinucleotide repeat polymorphisms in the Neprilysin gene are not associated with sporadic Alzheimer's disease

M. Oda, H. Kawakami, H. Morino, 2002, Neuroscience Letters.

Increased serum alkaline phosphatase and early neurological deterioration in patients with atherothrombotic brain infarction attributable to intracranial atherosclerosis

H. Terasawa, T. Uehara, Koji Yoshida, 2020, eNeurologicalSci.

A novel haplotype of spinocerebellar ataxia type 6 contributes to the highest prevalence in Western Japan

M. Oda, H. Kawakami, H. Morino, 2004, Neuroscience Letters.

A homozygous mutation of VWA3B causes cerebellar ataxia with intellectual disability

I. Imoto, T. Kawarai, A. Orlacchio, 2015, Journal of Neurology, Neurosurgery & Psychiatry.

Possible reduced penetrance of expansion of 44 to 47 CAG/CAA repeats in the TATA-binding protein gene in spinocerebellar ataxia type 17.

M. Oda, H. Kawakami, H. Morino, 2004, Archives of neurology.

An NEFH founder mutation causes broad phenotypic spectrum in multiple Japanese families

H. Ishiura, J. Mitsui, E. Matsuura, 2022, Journal of Human Genetics.

[A case of Wegener's granulomatosis presenting with tonic-clonic status epilepticus].

S. Kataoka, H. Terasawa, H. Tohji, 2010, Rinsho shinkeigaku = Clinical neurology.

Lack of an association between cystatin C gene polymorphisms in Japanese patients with Alzheimer’s disease

M. Oda, H. Kawakami, H. Morino, 2001, Neurology.

Robot-assisted total gastrectomy for gastric cancer in a patient with amyotrophic lateral sclerosis receiving long-term tracheostomy invasive ventilation

Katsuya Tanaka, M. Shimada, Y. Izumi, 2021, International Cancer Conference Journal.