E-LIB Suche - Ergebnisse für: Lorenzo‐Betancor, Oswaldo

1

Homozygous CADPS2 Mutations Cause Neurodegenerative Disease..:

Lorenzo‐Betancor, Oswaldo ; Galosi, Livio ; Bonfili, Laura...
Movement Disorders. 37 (2022) 12 - p. 2345-2354 , 2022

Link: https://doi.org/10.1002/..

2

PNPLA6‐Related Disorder with Levodopa‐Responsive Parkinsoni..:

Kazanci, Serdar ; Witt, Jennifer ; Su, Kimmy...
Movement Disorders Clinical Practice. 10 (2022) 2 - p. 338-340 , 2022

Link: https://doi.org/10.1002/..

3

Multiple system atrophy and apolipoprotein E:

Ogaki, Kotaro ; Martens, Yuka A. ; Heckman, Michael G....
Movement Disorders. 33 (2018) 4 - p. 647-650 , 2018

Link: https://doi.org/10.1002/..

4

Rare variants in MC1R/TUBB3 exon 1 are not associated with ..:

Lorenzo‐Betancor, Oswaldo ; Wszolek, Zbigniew K. ; Ross, Owen A.
Annals of Neurology. 79 (2016) 2 - p. 331-331 , 2016

Link: https://doi.org/10.1002/..

5

MAPT haplotype H1G is associated with increased risk of dem..:

Labbé, Catherine ; Heckman, Michael G. ; Lorenzo‐Betancor, Oswaldo...
Alzheimer's & Dementia. 12 (2016) 12 - p. 1297-1304 , 2016

Link: https://doi.org/10.1016/..

6

Automated Neuromelanin Imaging as a Diagnostic Biomarker fo..:

Castellanos, Gabriel ; Fernández‐Seara, María A. ; Lorenzo‐Betancor, Oswaldo...
Movement Disorders. 30 (2015) 7 - p. 945-952 , 2015

Link: https://doi.org/10.1002/..

7

(Patho‐)physiological relevance ofPINK1‐dependent ubiquitin..:

Fiesel, Fabienne C ; Ando, Maya ; Hudec, Roman...
EMBO reports. 16 (2015) 9 - p. 1114-1130 , 2015

Link: https://doi.org/10.15252..

8

Common variation in the LRRK2 gene is a risk factor for Par..:

Mata, Ignacio F. ; Checkoway, Harvey ; Hutter, Carolyn M....
Movement Disorders. 27 (2012) 14 - p. 1823-1826 , 2012

Link: https://doi.org/10.1002/..

9

LINGO1 gene analysis in Parkinson's disease phenotypes:

Lorenzo‐Betancor, Oswaldo ; Samaranch, Lluís ; García‐Martín, Elena...
Movement Disorders. 26 (2011) 4 - p. 722-727 , 2011

Link: https://doi.org/10.1002/..

10

Replication of MAPT and SNCA, but not PARK16‐18, as suscept..:

Mata, Ignacio F. ; Yearout, Dora ; Alvarez, Victoria...
Movement Disorders. 26 (2011) 5 - p. 819-823 , 2011

Link: https://doi.org/10.1002/..

11

Homozygous CADPS2 mutations cause neurodegenerative disease..:

Lorenzo-Betancor, Oswaldo ; Galosi, Livio ; Bonfili, Laura...
Neurology. 98 (2022) 18_supplement - p. , 2022

Link: https://doi.org/10.1212/..

12

Novel compound heterozygous FBXO7 mutations in a family wit..:

Lorenzo-Betancor, Oswaldo ; Lin, Yi-Han ; Samii, Ali...
Parkinsonism & Related Disorders. 80 (2020) - p. 142-147 , 2020

Link: https://doi.org/10.1016/..

13

The distribution and risk effect of GBA variants in a large..:

Velez-Pardo, Carlos ; Lorenzo-Betancor, Oswaldo ; Jimenez-Del-Rio, Marlene...
Parkinsonism & Related Disorders. 63 (2019) - p. 204-208 , 2019

Link: https://doi.org/10.1016/..

14

X-Linked Lymphoproliferative Syndrome Presenting as Adult-O..:

Blackburn, Patrick R ; Lin, Wen-Lang ; Miller, David A...
Journal of Neuropathology & Experimental Neurology. 78 (2019) 5 - p. 460-466 , 2019

Link: https://doi.org/10.1093/..

15

Age- and disease-dependent increase of the mitophagy marker..:

Hou, Xu ; Fiesel, Fabienne C. ; Truban, Dominika...
Autophagy. 14 (2018) 8 - p. 1404-1418 , 2018

Link: https://doi.org/10.1080/..