Zatz M - Search Results

1

Dystrophin Is Required for Proper Functioning of Luminance and Red-Green Cone Opponent Mechanisms in the Human Retina.

Barboni MT, Martins CM, Nagy BV, Tsai T, Damico FM, da Costa MF, de Cassia R, Pavanello M, Lourenço NC, de Cerqueira AM, Zatz M, Kremers J, Ventura DF. Barboni MT, et al. Among authors: zatz m. Invest Ophthalmol Vis Sci. 2016 Jul 1;57(8):3581-7. doi: 10.1167/iovs.16-19287. Invest Ophthalmol Vis Sci. 2016. PMID: 27388051

2

Red-green color vision impairment in Duchenne muscular dystrophy.

Costa MF, Oliveira AG, Feitosa-Santana C, Zatz M, Ventura DF. Costa MF, et al. Among authors: zatz m. Am J Hum Genet. 2007 Jun;80(6):1064-75. doi: 10.1086/518127. Epub 2007 Apr 13. Am J Hum Genet. 2007. PMID: 17503325 Free PMC article.

3

Repression of phosphatidylinositol transfer protein α ameliorates the pathology of Duchenne muscular dystrophy.

Vieira NM, Spinazzola JM, Alexander MS, Moreira YB, Kawahara G, Gibbs DE, Mead LC, Verjovski-Almeida S, Zatz M, Kunkel LM. Vieira NM, et al. Among authors: zatz m. Proc Natl Acad Sci U S A. 2017 Jun 6;114(23):6080-6085. doi: 10.1073/pnas.1703556114. Epub 2017 May 22. Proc Natl Acad Sci U S A. 2017. PMID: 28533404 Free PMC article.

4

Longitudinal visual acuity development in ZIKV-exposed children.

Lima DDS, Baran LCP, Hamer RD, Costa MFD, Vidal KS, Damico FM, Barboni MTS, França VCRM, Martins CMG, Tabares HS, Dias SL, Silva LA, Decleva D, Zatz M, Bertozzi APAP, Gazeta RE, Passos SD, Ventura DF. Lima DDS, et al. Among authors: zatz m. J AAPOS. 2020 Feb;24(1):23.e1-23.e6. doi: 10.1016/j.jaapos.2019.11.005. Epub 2020 Jan 8. J AAPOS. 2020. PMID: 31926367

5

A Novel Saliva RT-LAMP Workflow for Rapid Identification of COVID-19 Cases and Restraining Viral Spread.

Kobayashi GS, Brito LA, Moreira DP, Suzuki AM, Hsia GSP, Pimentel LF, de Paiva APB, Dias CR, Lourenço NCV, Oliveira BA, Manuli ER, Corral MA, Cavaçana N, Mitne-Neto M, Sales MM, Dell' Aquila LP, Filho AR, Parrillo EF, Mendes-Corrêa MC, Sabino EC, Costa SF, Leal FE, Sgro GG, Farah CS, Zatz M, Passos-Bueno MR. Kobayashi GS, et al. Among authors: zatz m. Diagnostics (Basel). 2021 Aug 3;11(8):1400. doi: 10.3390/diagnostics11081400. Diagnostics (Basel). 2021. PMID: 34441334 Free PMC article.

6

A deletion including the brain promoter of the Duchenne muscular dystrophy gene is not associated with mental retardation.

Rapaport D, Passos-Bueno MR, Takata RI, Campiotto S, Eggers S, Vainzof M, Makover A, Nudel U, Yaffe D, Zatz M. Rapaport D, et al. Among authors: zatz m. Neuromuscul Disord. 1992;2(2):117-20. doi: 10.1016/0960-8966(92)90043-6. Neuromuscul Disord. 1992. PMID: 1422198

7

Dystrophin immunostaining in muscles from patients with different types of muscular dystrophy: a Brazilian study.

Vainzof M, Pavanello RC, Pavanello Filho I, Passos-Bueno MR, Rapaport D, Hsi CT, Zatz M. Vainzof M, et al. Among authors: zatz m. J Neurol Sci. 1990 Sep;98(2-3):221-33. doi: 10.1016/0022-510x(90)90263-m. J Neurol Sci. 1990. PMID: 1700808

8

Is dystrophin always altered in Becker muscular dystrophy patients?

Vainzof M, Passos-Bueno MR, Pavanello RC, Zatz M. Vainzof M, et al. Among authors: zatz m. J Neurol Sci. 1995 Jul;131(1):99-104. doi: 10.1016/0022-510x(95)00104-a. J Neurol Sci. 1995. PMID: 7561956

9

Is the maintainance of the C-terminus domain of dystrophin enough to ensure a milder Becker muscular dystrophy phenotype?

Vainzof M, Takata RI, Passos-Bueno MR, Pavanello RC, Zatz M. Vainzof M, et al. Among authors: zatz m. Hum Mol Genet. 1993 Jan;2(1):39-42. doi: 10.1093/hmg/2.1.39. Hum Mol Genet. 1993. PMID: 8490621

10

Novel point mutations in the dystrophin gene.

Sitnik R, Campiotto S, Vainzof M, Pavanello RC, Takata RI, Zatz M, Passos-Bueno MR. Sitnik R, et al. Among authors: zatz m. Hum Mutat. 1997;10(3):217-22. doi: 10.1002/(SICI)1098-1004(1997)10:3<217::AID-HUMU7>3.0.CO;2-F. Hum Mutat. 1997. PMID: 9298822

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