Velez-Pardo C - Search Results

1

New mutation (T1232P) of the ATP-7B gene associated with neurologic and neuropsychiatric dominance onset of Wilson's disease in three unrelated Colombian kindred.

Velez-Pardo C, Rio MJ, Moreno S, Ramírez-Gomez L, Correa G, Lopera F. Velez-Pardo C, et al. Neurosci Lett. 2004 Sep 9;367(3):360-4. doi: 10.1016/j.neulet.2004.06.032. Neurosci Lett. 2004. PMID: 15337266

2

Familial Alzheimer's disease: oxidative stress, beta-amyloid, presenilins, and cell death.

Velez-Pardo C, Jimenez Del Rio M, Lopera F. Velez-Pardo C, et al. Gen Pharmacol. 1998 Nov;31(5):675-81. doi: 10.1016/s0306-3623(98)00189-x. Gen Pharmacol. 1998. PMID: 9809462 Review.

3

Ultrastructure evidence of necrotic neural cell death in familial Alzheimer's disease brains bearing presenilin-1 E280A mutation.

Velez-Pardo C, Arroyave ST, Lopera F, Castaño AD, Jimenez Del Rio M. Velez-Pardo C, et al. J Alzheimers Dis. 2001 Aug;3(4):409-415. doi: 10.3233/jad-2001-3408. J Alzheimers Dis. 2001. PMID: 12214045

4

DNA Damage does not Correlate with Amyloid-beta-Plaques and Neurofibrillary Tangles in Familial Alzheimer's Disease Presenilin-1 [E280A] Mutation.

Velez-Pardo C, Lopera F, Jimenez Del Rio M. Velez-Pardo C, et al. J Alzheimers Dis. 2000 Mar;2(1):47-57. doi: 10.3233/jad-2000-2106. J Alzheimers Dis. 2000. PMID: 12214110

5

[Neuronal DNA damage correlates with a positive detection of c-Jun, nuclear factor kB, p53 and Par-4 transcription factors in Alzheimer's disease].

García-Ospina GP, Jímenez-Del Río M, Lopera F, Vélez-Pardo C. García-Ospina GP, et al. Rev Neurol. 2003 Jun 1-15;36(11):1004-10. Rev Neurol. 2003. PMID: 12808492 Free article. Spanish.

6

Autosomal recessive juvenile parkinsonism Cys212Tyr mutation in parkin renders lymphocytes susceptible to dopamine- and iron-mediated apoptosis.

Jimenez Del Rio M, Moreno S, Garcia-Ospina G, Buritica O, Uribe CS, Lopera F, Velez-Pardo C. Jimenez Del Rio M, et al. Mov Disord. 2004 Mar;19(3):324-30. doi: 10.1002/mds.10670. Mov Disord. 2004. PMID: 15022188

7

CA1 hippocampal neuronal loss in familial Alzheimer's disease presenilin-1 E280A mutation is related to epilepsy.

Velez-Pardo C, Arellano JI, Cardona-Gomez P, Jimenez Del Rio M, Lopera F, De Felipe J. Velez-Pardo C, et al. Epilepsia. 2004 Jul;45(7):751-6. doi: 10.1111/j.0013-9580.2004.55403.x. Epilepsia. 2004. PMID: 15230697 Free article.

8

Paraquat induces apoptosis in human lymphocytes: protective and rescue effects of glucose, cannabinoids and insulin-like growth factor-1.

Rio MJ, Velez-Pardo C. Rio MJ, et al. Growth Factors. 2008 Feb;26(1):49-60. doi: 10.1080/08977190801984205. Growth Factors. 2008. PMID: 18365879

9

Variable frequency of LRRK2 variants in the Latin American research consortium on the genetics of Parkinson's disease (LARGE-PD), a case of ancestry.

Cornejo-Olivas M, Torres L, Velit-Salazar MR, Inca-Martinez M, Mazzetti P, Cosentino C, Micheli F, Perandones C, Dieguez E, Raggio V, Tumas V, Borges V, Ferraz HB, Rieder CRM, Shumacher-Schuh A, Velez-Pardo C, Jimenez-Del-Rio M, Lopera F, Chang-Castello J, Andreé-Munoz B, Waldherr S, Yearout D, Zabetian CP, Mata IF. Cornejo-Olivas M, et al. NPJ Parkinsons Dis. 2017 Jun 2;3:19. doi: 10.1038/s41531-017-0020-6. eCollection 2017. NPJ Parkinsons Dis. 2017. PMID: 28649619 Free PMC article.

10

The distribution and risk effect of GBA variants in a large cohort of PD patients from Colombia and Peru.

Velez-Pardo C, Lorenzo-Betancor O, Jimenez-Del-Rio M, Moreno S, Lopera F, Cornejo-Olivas M, Torres L, Inca-Martinez M, Mazzetti P, Cosentino C, Yearout D, Waldherr SM, Zabetian CP, Mata IF. Velez-Pardo C, et al. Parkinsonism Relat Disord. 2019 Jun;63:204-208. doi: 10.1016/j.parkreldis.2019.01.030. Epub 2019 Feb 4. Parkinsonism Relat Disord. 2019. PMID: 30765263 Free PMC article.

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