Munhoz RP - Search Results

1

SPATACSIN mutations cause autosomal recessive juvenile amyotrophic lateral sclerosis.

Orlacchio A, Babalini C, Borreca A, Patrono C, Massa R, Basaran S, Munhoz RP, Rogaeva EA, St George-Hyslop PH, Bernardi G, Kawarai T. Orlacchio A, et al. Among authors: munhoz rp. Brain. 2010 Feb;133(Pt 2):591-8. doi: 10.1093/brain/awp325. Epub 2010 Jan 28. Brain. 2010. PMID: 20110243 Free PMC article.

2

Clinical and genetic study of a Brazilian family with spastic paraplegia (SPG6 locus).

Munhoz RP, Kawarai T, Teive HA, Raskin S, Sato C, Liang Y, St George-Hyslop PH, Rogaeva E. Munhoz RP, et al. Mov Disord. 2006 Feb;21(2):279-81. doi: 10.1002/mds.20775. Mov Disord. 2006. PMID: 16267846

3

Clinical findings in a large family with a parkin ex3delta40 mutation.

Munhoz RP, Sa DS, Rogaeva E, Salehi-Rad S, Sato C, Medeiros H, Farrer M, Lang AE. Munhoz RP, et al. Arch Neurol. 2004 May;61(5):701-4. doi: 10.1001/archneur.61.5.701. Arch Neurol. 2004. PMID: 15148147

4

Global investigation and meta-analysis of the C9orf72 (G4C2)n repeat in Parkinson disease.

Theuns J, Verstraeten A, Sleegers K, Wauters E, Gijselinck I, Smolders S, Crosiers D, Corsmit E, Elinck E, Sharma M, Krüger R, Lesage S, Brice A, Chung SJ, Kim MJ, Kim YJ, Ross OA, Wszolek ZK, Rogaeva E, Xi Z, Lang AE, Klein C, Weissbach A, Mellick GD, Silburn PA, Hadjigeorgiou GM, Dardiotis E, Hattori N, Ogaki K, Tan EK, Zhao Y, Aasly J, Valente EM, Petrucci S, Annesi G, Quattrone A, Ferrarese C, Brighina L, Deutschländer A, Puschmann A, Nilsson C, Garraux G, LeDoux MS, Pfeiffer RF, Boczarska-Jedynak M, Opala G, Maraganore DM, Engelborghs S, De Deyn PP, Cras P, Cruts M, Van Broeckhoven C; GEO-PD Consortium. Theuns J, et al. Neurology. 2014 Nov 18;83(21):1906-13. doi: 10.1212/WNL.0000000000001012. Epub 2014 Oct 17. Neurology. 2014. PMID: 25326098 Free PMC article.

5

Unilateral pallidotomy in a patient with parkinsonism and G2019S LRRK2 mutation.

Munhoz RP, Teive HA, Francisco AN, Raskin S, Rogaeva E. Munhoz RP, et al. Mov Disord. 2009 Apr 15;24(5):791-2; author reply 792. doi: 10.1002/mds.21818. Mov Disord. 2009. PMID: 19012346 No abstract available.

6

Parkinsonism due to A53E α-synuclein gene mutation: Clinical, genetic, epigenetic, and biochemical features.

Picillo M, Lizarraga KJ, Friesen EL, Chau H, Zhang M, Sato C, Rooke G, Munhoz RP, Rogaeva E, Fraser PE, Kalia SK, Kalia LV. Picillo M, et al. Among authors: munhoz rp. Mov Disord. 2018 Dec;33(12):1950-1955. doi: 10.1002/mds.27506. Epub 2018 Nov 13. Mov Disord. 2018. PMID: 30423204

7

Diagnostic delay in Parkinson's disease caused by PRKN mutations.

Ruiz-Lopez M, Freitas ME, Oliveira LM, Munhoz RP, Fox SH, Rohani M, Rogaeva E, Lang AE, Fasano A. Ruiz-Lopez M, et al. Among authors: munhoz rp. Parkinsonism Relat Disord. 2019 Jun;63:217-220. doi: 10.1016/j.parkreldis.2019.01.010. Epub 2019 Jan 10. Parkinsonism Relat Disord. 2019. PMID: 30692050

8

The G2019S LRRK2 mutation in Brazilian patients with Parkinson's disease: phenotype in monozygotic twins.

Munhoz RP, Wakutani Y, Marras C, Teive HA, Raskin S, Werneck LC, Moreno D, Sato C, Lang AE, Rogaeva E. Munhoz RP, et al. Mov Disord. 2008 Jan 30;23(2):290-4. doi: 10.1002/mds.21832. Mov Disord. 2008. PMID: 17999435

9

LRRK2 and Parkin mutations in a family with parkinsonism-Lack of genotype-phenotype correlation.

Marras C, Klein C, Lang AE, Wakutani Y, Moreno D, Sato C, Yip E, Munhoz RP, Lohmann K, Djarmati A, Bi A, Rogaeva E. Marras C, et al. Among authors: munhoz rp. Neurobiol Aging. 2010 Apr;31(4):721-2. doi: 10.1016/j.neurobiolaging.2008.05.030. Epub 2008 Jul 21. Neurobiol Aging. 2010. PMID: 18644660

10

Using global team science to identify genetic parkinson's disease worldwide.

Vollstedt EJ, Kasten M, Klein C; MJFF Global Genetic Parkinson's Disease Study Group. Vollstedt EJ, et al. Ann Neurol. 2019 Aug;86(2):153-157. doi: 10.1002/ana.25514. Epub 2019 Jun 26. Ann Neurol. 2019. PMID: 31155756 Free PMC article. No abstract available.

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