Is the common LRRK2 G2019S mutation related to dyskinesias in North African Parkinson disease?

Neurology ◽  
2008 ◽  
Vol 71 (19) ◽  
pp. 1550-1552 ◽  
Author(s):  
S. Lesage ◽  
S. Belarbi ◽  
A. Troiano ◽  
C. Condroyer ◽  
N. Hecham ◽  
...  
Keyword(s):  
Parkinson Disease ◽  
North African ◽  
G2019s Mutation ◽  
Lrrk2 G2019s ◽  
The Common

scholarly journals Neurite Collapse and Altered ER Ca2+ Control in Human Parkinson Disease Patient iPSC-Derived Neurons with LRRK2 G2019S Mutation

2019 ◽  
Vol 12 (1) ◽  
pp. 29-41 ◽  
Author(s):  
Joanna A. Korecka ◽  
Sebastien Talbot ◽  
Teresia M. Osborn ◽  
Sherida M. de Leeuw ◽  
Simon A. Levy ◽  
...  
Keyword(s):  
Parkinson Disease ◽  
Disease Patient ◽  
Parkinson Disease Patient ◽  
G2019s Mutation ◽  
Lrrk2 G2019s

The LRRK2 G2019S mutation is associated with Parkinson disease and concomitant non-skin cancers

Neurology ◽  
2012 ◽  
Vol 78 (11) ◽  
pp. 781-786 ◽  
Author(s):  
R. Inzelberg ◽  
O. S. Cohen ◽  
J. Aharon-Peretz ◽  
I. Schlesinger ◽  
R. Gershoni-Baruch ◽  
...  
Keyword(s):  
Parkinson Disease ◽  
G2019s Mutation ◽  
Skin Cancers ◽  
Lrrk2 G2019s

scholarly journals LRRK2 Haplotype Analyses in European and North African Families with Parkinson Disease: A Common Founder for the G2019S Mutation Dating from the 13th Century

2005 ◽  
Vol 77 (2) ◽  
pp. 330-332 ◽  
Author(s):  
Suzanne Lesage ◽  
Anne-Louise Leutenegger ◽  
Pablo Ibanez ◽  
Sabine Janin ◽  
Ebba Lohmann ◽  
...  
Keyword(s):  
Parkinson Disease ◽  
North African ◽  
13Th Century ◽  
G2019s Mutation ◽  
Common Founder ◽  
African Families

The LRRK2 G2019S mutation in Ashkenazi Jews with Parkinson disease: Is there a gender effect?

Neurology ◽  
2007 ◽  
Vol 69 (16) ◽  
pp. 1595-1602 ◽  
Author(s):  
A. Orr-Urtreger ◽  
C. Shifrin ◽  
U. Rozovski ◽  
S. Rosner ◽  
D. Bercovich ◽  
...  
Keyword(s):  
Parkinson Disease ◽  
Gender Effect ◽  
Ashkenazi Jews ◽  
G2019s Mutation ◽  
Lrrk2 G2019s

First North African record of a melanistic common genet (Genetta genetta Linnaeus, 1758)

Mammalia ◽  
2021 ◽  
Vol 0 (0) ◽  
Author(s):  
Mourad Ahmim ◽  
Hafid Aroudj ◽  
Farouk Aroudj ◽  
Saaid Saidi ◽  
Samir Aroudj
Keyword(s):  
North Africa ◽  
Evolutionary History ◽  
North African ◽  
Mammal Species ◽  
Genetta Genetta ◽  
History Of ◽  
The Common ◽  
True Occurrence

Abstract The common genet (Genetta genetta Linnaeus, 1758) is a rare and protected mammal species in Algeria. We report the first melanistic individual of this species ever recorded in North Africa. Such animals have only been recorded in Spain and Portugal so far. It is unclear why melanistic common genets seem to be so rare in its African range. More research is needed to determine the true occurrence of melanistic individuals, and what the evolutionary history of melanism is in common genets.

scholarly journals Evidence for prehistoric origins of the G2019S mutation in the North African Berber population

PLoS ONE ◽  
2017 ◽  
Vol 12 (7) ◽  
pp. e0181335 ◽  
Author(s):  
Rafiqua Ben El Haj ◽  
Ayyoub Salmi ◽  
Wafa Regragui ◽  
Ahmed Moussa ◽  
Naima Bouslam ◽  
...  
Keyword(s):  
North African ◽  
The North ◽  
G2019s Mutation

scholarly journals Motor Phenotype of LRRK2 G2019S Carriers in Early-Onset Parkinson Disease

2009 ◽  
Vol 66 (12) ◽  
Author(s):  
Roy N. Alcalay ◽  
Helen Mejia-Santana ◽  
Ming Xin Tang ◽  
Llency Rosado ◽  
Miguel Verbitsky ◽  
...  
Keyword(s):  
Parkinson Disease ◽  
Early Onset ◽  
Lrrk2 G2019s ◽  
Motor Phenotype

Mitochondrial impairment in patients with Parkinson disease with the G2019S mutation in LRRK2

Neurology ◽  
2010 ◽  
Vol 75 (22) ◽  
pp. 2017-2020 ◽  
Author(s):  
H. Mortiboys ◽  
K. K. Johansen ◽  
J. O. Aasly ◽  
O. Bandmann
Keyword(s):  
Parkinson Disease ◽  
G2019s Mutation ◽  
Mitochondrial Impairment
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