María Cruz Rodríguez-Oroz

María Cruz Rodríguez-Oroz


Research Focus & Metrics

Academic Career Length

29Years (1998-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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24 January 2012 in Movement Disorders
Verified
Journal Article
Closed access
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ILIrene Litvan
Irene Litvan
JGJennifer G. Goldman
Jennifer G. Goldman
ATAlexander I. Tröster
Alexander I. Tröster
BSBen A. Schmand
Ben A. Schmand
DWDaniel Weintraub
Daniel Weintraub
MEMurat Emre
Murat Emre

14 October 2010 in Nature Reviews Neuroscience
Verified
Journal Article
Closed access
PDF file
PRPeter Redgrave
Peter Redgrave
MRManuel Rodriguez
Manuel Rodriguez
YSYoland Smith
Yoland Smith
MRMaría Cruz Rodríguez-Oroz
María Cruz Rodríguez-Oroz
SLStephane Lehericy
Stephane Lehericy
JOJose A. Obeso
Jose A. Obeso

23 June 2005 in Brain
Verified
Journal Article
Open access
PDF file
MRMaría Cruz Rodríguez-Oroz
María Cruz Rodríguez-Oroz
JOJ. A. Obeso
J. A. Obeso
ALA. E. Lang
A. E. Lang
JHJ.-L. Houeto
J.-L. Houeto
PPP. Pollak
P. Pollak
NBN. Van Blercom
N. Van Blercom
Deep brain stimulation (DBS) is associated with significant improvement of motor complications in patients with severe Parkinson's disease after some 6–12 months of treatment. Long-term results in a large number of patients have been reported only from a single study centre. We report 69 Parkinson's disease patients treated with bilateral DBS of the subthalamic nucleus (STN, n = 49) or globus pallidus internus (GPi, n = 20) included in a multicentre study. Patients were assessed preoperatively and at 1 year and 3–4 years after surgery. The primary outcome measure was the change in the ‘off’ medication score of the Unified Parkinson's Disease Rating Scale motor part (UPDRS-III) at 3–4 years. Stimulation of the STN or GPi induced a significant improvement (50 and 39%; P < 0.0001) of the ‘off’ medication UPDRS-III score at 3–4 years with respect to baseline. Stimulation improved cardinal features and activities of daily living (ADL) (P < 0.0001 and P < 0.02 for STN and GPi, respectively) and prolonged the ‘on’ time spent with good mobility without dyskinesias (P < 0.00001). Daily dosage of levodopa was significantly reduced (35%) in the STN-treated group only (P < 0.001). Comparison of the improvement induced by stimulation at 1 year with 3–4 years showed a significant worsening in the ‘on’ medication motor states of the UPDRS-III, ADL and gait in both STN and GPi groups, and speech and postural stability in the STN-treated group. Adverse events (AEs) included cognitive decline, speech difficulty, instability, gait disorders and depression. These were more common in patients treated with DBS of the STN. No patient abandoned treatment as a result of these side effects. This experience, which represents the first multicentre study assessing the long-term efficacy of either STN or GPi stimulation, shows a significant and substantial clinically important therapeutic benefit for at least 3–4 years in a large cohort of patients with severe Parkinson's disease.

1 December 2009 in The Lancet Neurology
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Journal Article
Closed access
MRMaría Cruz Rodríguez-Oroz
María Cruz Rodríguez-Oroz
MJMarjan Jahanshahi
Marjan Jahanshahi
PKPaul Krack
Paul Krack
ILIrene Litvan
Irene Litvan
RMRaúl Macias
Raúl Macias
JOJosé A Obeso
José A Obeso

9 June 2011 in Movement Disorders
Verified
Journal Article
Closed access
PDF file
ILIrene Litvan
Irene Litvan
DADag Aarsland
Dag Aarsland
CACharles H. Adler
Charles H. Adler
JGJennifer G. Goldman
Jennifer G. Goldman
JKJaime Kulisevsky
Jaime Kulisevsky
DWDaniel Weintraub
Daniel Weintraub

1 October 2000 in Trends in Neurosciences
Verified
Journal Article
Closed access
JOJosé A. Obeso
José A. Obeso
MRMaría Cruz Rodríguez-Oroz
María Cruz Rodríguez-Oroz
MRManuel Rodriguez
Manuel Rodriguez
Jose L. LanciegoJose L. Lanciego
Jose L. Lanciego
JAJulio Artieda
Julio Artieda
COC. Warren Olanow
C. Warren Olanow