Nishimura PY - Search Results

Save citations to file

Email citations

Your saved search

Your RSS Feed

Page 1

Exome Sequencing Identifies a Novel Nonsense Mutation of MYO6 as the Cause of Deafness in a Brazilian Family.

Sampaio-Silva J, Batissoco AC, Jesus-Santos R, Abath-Neto O, Scarpelli LC, Nishimura PY, Galindo LT, Bento RF, Oiticica J, Lezirovitz K. Sampaio-Silva J, et al. Among authors: nishimura py. Ann Hum Genet. 2018 Jan;82(1):23-34. doi: 10.1111/ahg.12213. Epub 2017 Oct 17. Ann Hum Genet. 2018. PMID: 29044474

Muscle biopsy with dystrophic pattern and rimmed vacuoles: GNE myopathy in a Brazilian patient.

Estephan EP, Moreno CAM, Silva AMS, Mendonça RH, Abath Neto O, Nishimura PY, Galindo LT, Zanoteli E. Estephan EP, et al. Among authors: nishimura py. Arq Neuropsiquiatr. 2017 Jan;75(1):72-73. doi: 10.1590/0004-282X20160171. Arq Neuropsiquiatr. 2017. PMID: 28099567 Free article. No abstract available.

Laser application effects on the bite strength of the masseter muscle, as an orofacial pain treatment.

de Medeiros JS, Vieira GF, Nishimura PY. de Medeiros JS, et al. Among authors: nishimura py. Photomed Laser Surg. 2005 Aug;23(4):373-6. doi: 10.1089/pho.2005.23.373. Photomed Laser Surg. 2005. PMID: 16144479

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

3 results

Search Page

Filters