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You searched for: Author/Creator Nomura, Emi

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1. A case of a heterozygous ABCC6 mutation showing recurrent ischemic strokes and intracranial hemorrhages. Issue 2 (4th February 2022)

2. A case of successful renal transplantation of Charcot‐Marie‐Tooth disease associated with FSGS due to mutation of the INF2 gene. Issue 5 (5th July 2022)

3. A Japanese case of successful surgical resection of cerebral cavernous malformations with a CCM2 mutation. Issue 5 (29th June 2022)

4. A Japanese patient with a VCP mutation c.290G > A (p.G97E) presenting a rapid progressive respiratory failure. Issue 6 (3rd October 2019)

5. A migration case of Kii amyotrophic lateral sclerosis/parkinsonism dementia complex with the shortest stay in the endemic area and the longest incubation to develop the disease. (December 2017)

8. Case of congenital fibrosis of the extraocular muscles type 1 with progressive cerebellar ataxia. Issue 2 (28th December 2017)

10. Direct arterial damage and neurovascular unit disruption by mechanical thrombectomy in a rat stroke model. Issue 10 (18th June 2020)