Adolfo Lopez de Munain
Adolfo Lopez de Munain
Jefe del Servicio de Neurología - Hospital Universitario Donostia / Director Área de Neurociencias
Verified email at osakidetza.eus
Title
Cited by
Cited by
Year
Cloning of the gene containing mutations that cause PARK8-linked Parkinson's disease
C Paisán-Ruı́z, S Jain, EW Evans, WP Gilks, J Simón, M Van Der Brug, ...
Neuron 44 (4), 595-600, 2004
22292004
Global surveillance of trends in cancer survival 2000–14 (CONCORD-3): analysis of individual records for 37 513 025 patients diagnosed with one of 18 cancers from 322 …
C Allemani, T Matsuda, V Di Carlo, R Harewood, M Matz, M Nikšić, ...
The Lancet 391 (10125), 1023-1075, 2018
11202018
Common variants at 7p21 are associated with frontotemporal lobar degeneration with TDP-43 inclusions
VM Van Deerlin, PMA Sleiman, M Martinez-Lage, A Chen-Plotkin, ...
Nature genetics 42 (3), 234-239, 2010
3972010
Mutations in the LGI1/Epitempin gene on 10q24 cause autosomal dominant lateral temporal epilepsy
JM Morante-Redolat, A Gorostidi-Pagola, S Piquer-Sirerol, A Sáenz, ...
Human molecular genetics 11 (9), 1119-1128, 2002
3342002
Calpain 3 deficiency is associated with myonuclear apoptosis and profound perturbation of the IκBα/NF-κB pathway in limb-girdle muscular dystrophy type 2A
S Baghdiguian, M Martin, I Richard, F Pons, C Astier, N Bourg, RT Hay, ...
Nature medicine 5 (5), 503-511, 1999
3241999
Calpain 3 deficiency is associated with myonuclear apoptosis and profound perturbation of the IκBα/NF-κB pathway in limb-girdle muscular dystrophy type 2A
S Baghdiguian, M Martin, I Richard, F Pons, C Astier, N Bourg, RT Hay, ...
Nature medicine 5 (5), 503-511, 1999
3231999
Calpain 3 deficiency is associated with myonuclear apoptosis and profound perturbation of the IκBα/NF-κB pathway in limb-girdle muscular dystrophy type 2A
S Baghdiguian, M Martin, I Richard, F Pons, C Astier, N Bourg, RT Hay, ...
Nature medicine 5 (5), 503-511, 1999
3231999
Association between total, processed, red and white meat consumption and all-cause, CVD and IHD mortality: a meta-analysis of cohort studies
I Abete, D Romaguera, AR Vieira, AL de Munain, T Norat
British Journal of Nutrition 112 (5), 762-775, 2014
2662014
Mapping of a second locus for familial hemiplegic migraine to 1q21–q23 and evidence of further heterogeneity
A Ducros, A Joutel, M Cecillon, E Tournier‐Lasserve, K Vahedi, ...
Annals of Neurology: Official Journal of the American Neurological …, 1997
2601997
Differential micro RNA expression in PBMC from multiple sclerosis patients
D Otaegui, SE Baranzini, R Armañanzas, B Calvo, M Muñoz-Culla, ...
PloS one 4 (7), e6309, 2009
2512009
Misregulated alternative splicing of BIN1 is associated with T tubule alterations and muscle weakness in myotonic dystrophy
C Fugier, AF Klein, C Hammer, S Vassilopoulos, Y Ivarsson, A Toussaint, ...
Nature medicine 17 (6), 720-725, 2011
2472011
A small noncoding RNA signature found in exosomes of GBM patient serum as a diagnostic tool
L Manterola, E Guruceaga, JG Pérez-Larraya, M González-Huarriz, ...
Neuro-oncology 16 (4), 520-527, 2014
2232014
Calpainopathy—a survey of mutations and polymorphisms
I Richard, C Roudaut, A Saenz, R Pogue, J Grimbergen, LVB Anderson, ...
The American Journal of Human Genetics 64 (6), 1524-1540, 1999
2031999
Genetic and epigenetic modifications of Sox2 contribute to the invasive phenotype of malignant gliomas
MM Alonso, R Diez-Valle, L Manterola, A Rubio, D Liu, N Cortes-Santiago, ...
PloS one 6 (11), e26740, 2011
1982011
Oncogenicity of the developmental transcription factor Sox9
A Matheu, M Collado, C Wise, L Manterola, L Cekaite, AJ Tye, ...
Cancer research 72 (5), 1301-1315, 2012
1852012
Limb-girdle muscular dystrophy in Guipúzcoa (Basque Country, Spain).
M Urtasun, A Saenz, C Roudaut, JJ Poza, JA Urtizberea, AM Cobo, ...
Brain: a journal of neurology 121 (9), 1735-1747, 1998
1791998
Genetics of Charcot-Marie-Tooth disease type 4A: mutations, inheritance, phenotypic variability, and founder effect
R Claramunt, L Pedrola, T Sevilla, AL de Munain, J Berciano, A Cuesta, ...
Journal of medical genetics 42 (4), 358-365, 2005
1732005
Burden and centralised treatment in Europe of rare tumours: results of RARECAREnet—a population-based study
G Gatta, R Capocaccia, L Botta, S Mallone, R De Angelis, E Ardanaz, ...
The Lancet Oncology 18 (8), 1022-1039, 2017
1682017
Clinical correlations with Lewy body pathology in LRRK2-related Parkinson disease
LV Kalia, AE Lang, LN Hazrati, S Fujioka, ZK Wszolek, DW Dickson, ...
JAMA neurology 72 (1), 100-105, 2015
1632015
Clinical correlations with Lewy body pathology in LRRK2-related Parkinson disease
LV Kalia, AE Lang, LN Hazrati, S Fujioka, ZK Wszolek, DW Dickson, ...
JAMA neurology 72 (1), 100-105, 2015
1632015
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