Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Additional filters

Article Language

Species

Sex

Age

Other

Search Results

16 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Publication Date timeline is not available.
Page 1
CHCHD2 mutational screening in Brazilian patients with familial Parkinson's disease.
Voigt DD, Nascimento CM, de Souza RB, Cabello Acero PH, Campos Júnior M, da Silva CP, Pereira JS, Rosso AL, Araujo Leite MA, Vasconcellos LFR, Della Coletta MV, da Silva DJ, Nicaretta DH, Gonçalves AP, Dos Santos JM, Calassara V, Santos-Rebouças CB, Pimentel MMG. Voigt DD, et al. Among authors: della coletta mv. Neurobiol Aging. 2019 Feb;74:236.e7-236.e8. doi: 10.1016/j.neurobiolaging.2018.09.026. Epub 2018 Sep 27. Neurobiol Aging. 2019. PMID: 30342766
Parkinson disease: α-synuclein mutational screening and new clinical insight into the p.E46K mutation.
Pimentel MM, Rodrigues FC, Leite MA, Campos Júnior M, Rosso AL, Nicaretta DH, Pereira JS, Silva DJ, Della Coletta MV, Vasconcellos LF, Abreu GM, Dos Santos JM, Santos-Rebouças CB. Pimentel MM, et al. Among authors: della coletta mv. Parkinsonism Relat Disord. 2015 Jun;21(6):586-9. doi: 10.1016/j.parkreldis.2015.03.011. Epub 2015 Mar 14. Parkinsonism Relat Disord. 2015. PMID: 25817515
Autosomal dominant Parkinson's disease: Incidence of mutations in LRRK2, SNCA, VPS35 and GBA genes in Brazil.
Abreu GM, Valença DC, Campos M Júnior, da Silva CP, Pereira JS, Araujo Leite MA, Rosso AL, Nicaretta DH, Vasconcellos LF, da Silva DJ, Della Coletta MV, Dos Santos JM, Gonçalves AP, Santos-Rebouças CB, Pimentel MM. Abreu GM, et al. Among authors: della coletta mv. Neurosci Lett. 2016 Dec 2;635:67-70. doi: 10.1016/j.neulet.2016.10.040. Epub 2016 Oct 21. Neurosci Lett. 2016. PMID: 27777137
Clinical profiles associated with LRRK2 and GBA mutations in Brazilians with Parkinson's disease.
da Silva CP, de M Abreu G, Cabello Acero PH, Campos M Júnior, Pereira JS, de A Ramos SR, Nascimento CM, Voigt DD, Rosso AL, Araujo Leite MA, Vasconcellos LFR, Nicaretta DH, Della Coletta MV, da Silva DJ, Gonçalves AP, Dos Santos JM, Calassara V, Valença DCT, de M Martins CJ, Santos-Rebouças CB, Pimentel MMG. da Silva CP, et al. Among authors: della coletta mv. J Neurol Sci. 2017 Oct 15;381:160-164. doi: 10.1016/j.jns.2017.08.3249. Epub 2017 Aug 24. J Neurol Sci. 2017. PMID: 28991672
Glucocerebrosidase N370S and L444P mutations as risk factors for Parkinson's disease in Brazilian patients.
Guimarães Bde C, Pereira AC, Rodrigues Fda C, dos Santos AV, Campos M Jr, dos Santos JM, dos Santos FL, de Rosso AL, Nicaretta DH, Pereira JS, da Silva DJ, Della Coletta MV, Santos-Rebouças CB, Pimentel MM. Guimarães Bde C, et al. Among authors: della coletta mv. Parkinsonism Relat Disord. 2012 Jun;18(5):688-9. doi: 10.1016/j.parkreldis.2011.11.028. Epub 2011 Dec 21. Parkinsonism Relat Disord. 2012. PMID: 22192918 No abstract available.
Worldwide barriers to genetic testing for movement disorders.
Gatto EM, Walker RH, Gonzalez C, Cesarini M, Cossu G, Stephen CD, Balint B, Rodríguez-Violante M, Jankovic J, Morgante F, Jinnah HA; Rare Movement Disorders Study Group of the International Parkinson Disease, Movement Disorders Society. Gatto EM, et al. Eur J Neurol. 2021 Jun;28(6):1901-1909. doi: 10.1111/ene.14826. Epub 2021 Apr 9. Eur J Neurol. 2021. PMID: 33730413
Tics and Tourette syndrome: clinical evaluation of 44 cases.
Teive HA, Germiniani FM, Della Coletta MV, Werneck LC. Teive HA, et al. Among authors: della coletta mv. Arq Neuropsiquiatr. 2001 Sep;59(3-B):725-8. doi: 10.1590/s0004-282x2001000500014. Arq Neuropsiquiatr. 2001. PMID: 11593273 Free article.
Hereditary spastic paraplegia associated with thin corpus callosum.
Teive HA, Iwamoto FM, Della Coletta MV, Camargo CH, Bezerra RD, Minguetti G, Werneck LC. Teive HA, et al. Among authors: della coletta mv. Arq Neuropsiquiatr. 2001 Sep;59(3-B):790-2. doi: 10.1590/s0004-282x2001000500025. Arq Neuropsiquiatr. 2001. PMID: 11593284 Free article.
16 results