Ribeiro MH - Search Results

1

Variant Creutzfeldt-Jakob [corrected] disease: the second case in Portugal and in the same geographical region.

Machado A, Soares H, Antunes H, Magalhães Z, Ferreira C, Baldeiras I, Ribeiro MH, Santana I, Ramalheira J, Castro L, Carpenter S. Machado A, et al. Among authors: ribeiro mh. J Neurol Neurosurg Psychiatry. 2008 Feb;79(2):180-2. doi: 10.1136/jnnp.2007.128389. Epub 2007 Aug 31. J Neurol Neurosurg Psychiatry. 2008. PMID: 17766432

2

Sporadic Creutzfeldt-Jakob disease causing a 2-years slowly progressive isolated dementia.

Machado A, Ribeiro M, Rodrigues M, Ferreira C, Baldeiras I, Ribeiro MH, Santana I, Almeida R, Castro L, Carpenter S. Machado A, et al. Among authors: ribeiro m, ribeiro mh. Behav Neurol. 2009;21(3):175-9. doi: 10.3233/BEN-2009-0238. Behav Neurol. 2009. PMID: 19996514 Free PMC article.

3

CSF Tau proteins reduce misdiagnosis of sporadic Creutzfeldt-Jakob disease suspected cases with inconclusive 14-3-3 result.

Leitão MJ, Baldeiras I, Almeida MR, Ribeiro MH, Santos AC, Ribeiro M, Tomás J, Rocha S, Santana I, Oliveira CR. Leitão MJ, et al. Among authors: ribeiro m, ribeiro mh. J Neurol. 2016 Sep;263(9):1847-61. doi: 10.1007/s00415-016-8209-x. Epub 2016 Jun 29. J Neurol. 2016. PMID: 27357003

4

Sporadic Creutzfeldt-Jakob disease diagnostic accuracy is improved by a new CSF ELISA 14-3-3γ assay.

Leitão MJ, Baldeiras I, Almeida MR, Ribeiro MH, Santos AC, Ribeiro M, Tomás J, Rocha S, Santana I, Oliveira CR. Leitão MJ, et al. Among authors: ribeiro m, ribeiro mh. Neuroscience. 2016 May 13;322:398-407. doi: 10.1016/j.neuroscience.2016.02.057. Epub 2016 Mar 3. Neuroscience. 2016. PMID: 26940479

5

Diagnostic value of CSF protein profile in a Portuguese population of sCJD patients.

Baldeiras IE, Ribeiro MH, Pacheco P, Machado A, Santana I, Cunha L, Oliveira CR. Baldeiras IE, et al. Among authors: ribeiro mh. J Neurol. 2009 Sep;256(9):1540-50. doi: 10.1007/s00415-009-5160-0. Epub 2009 May 6. J Neurol. 2009. PMID: 19418113 Free article.

6

Portuguese family with the co-occurrence of frontotemporal lobar degeneration and neuronal ceroid lipofuscinosis phenotypes due to progranulin gene mutation.

Almeida MR, Macário MC, Ramos L, Baldeiras I, Ribeiro MH, Santana I. Almeida MR, et al. Among authors: ribeiro mh. Neurobiol Aging. 2016 May;41:200.e1-200.e5. doi: 10.1016/j.neurobiolaging.2016.02.019. Epub 2016 Mar 3. Neurobiol Aging. 2016. PMID: 27021778

7

Prognosis of Early-Onset vs. Late-Onset Mild Cognitive Impairment: Comparison of Conversion Rates and Its Predictors.

Tábuas-Pereira M, Baldeiras I, Duro D, Santiago B, Ribeiro MH, Leitão MJ, Oliveira C, Santana I. Tábuas-Pereira M, et al. Among authors: ribeiro mh. Geriatrics (Basel). 2016 Apr 25;1(2):11. doi: 10.3390/geriatrics1020011. Geriatrics (Basel). 2016. PMID: 31022805 Free PMC article.

8

Progranulin peripheral levels as a screening tool for the identification of subjects with progranulin mutations in a Portuguese cohort.

Almeida MR, Baldeiras I, Ribeiro MH, Santiago B, Machado C, Massano J, Guimarães J, Resende Oliveira C, Santana I. Almeida MR, et al. Among authors: ribeiro mh. Neurodegener Dis. 2014;13(4):214-23. doi: 10.1159/000352022. Epub 2013 Sep 6. Neurodegener Dis. 2014. PMID: 24022032

9

Association of HFE common mutations with Parkinson's disease, Alzheimer's disease and mild cognitive impairment in a Portuguese cohort.

Guerreiro RJ, Bras JM, Santana I, Januario C, Santiago B, Morgadinho AS, Ribeiro MH, Hardy J, Singleton A, Oliveira C. Guerreiro RJ, et al. Among authors: ribeiro mh. BMC Neurol. 2006 Jul 6;6:24. doi: 10.1186/1471-2377-6-24. BMC Neurol. 2006. PMID: 16824219 Free PMC article.

10

Association between butyrylcholinesterase and cerebrospinal fluid biomarkers in Alzheimer's disease patients.

Gabriel AJ, Almeida MR, Ribeiro MH, Durães J, Tábuas-Pereira M, Pinheiro AC, Pascoal R, Santana I, Baldeiras I. Gabriel AJ, et al. Among authors: ribeiro mh. Neurosci Lett. 2017 Feb 22;641:101-106. doi: 10.1016/j.neulet.2017.01.036. Epub 2017 Jan 17. Neurosci Lett. 2017. PMID: 28108398

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