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The new mutation, E46K, of α-synuclein causes parkinson and Lewy body dementia

Annals of neurology, 2004-02, Vol.55 (2), p.164-173

2004

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Impact of psychiatric symptoms and sleep disorders on the quality of life of patients with Parkinson’s disease

Journal of neurology, 2011-03, Vol.258 (3), p.494-499

2011

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A novel form of human disease with a protease-sensitive prion protein and heterozygosity methionine/valine at codon 129: Case report

BMC neurology, 2010-10, Vol.10 (1), p.99-99, Article 99

2010

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Outcome of bilateral deep brain subthalamic stimulation in patients carrying the R1441G mutation in the LRRK2 dardarin gene

Neurosurgery, 2008-04, Vol.62 (4), p.857-863

2008

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Lrrk2-associated parkinsonism is a major cause of disease in Northern Spain

Parkinsonism & related disorders, 2007-12, Vol.13 (8), p.509-515

2007

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Coexistence of protease sensitive and resistant prion protein in 129VV homozygous sporadic Creutzfeldt-Jakob disease: a case report

Journal of medical case reports, 2012-10, Vol.6 (1), p.348-348, Article 348

2012

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Lrrk2 R1441G-related Parkinson's disease: evidence of a common founding event in the seventh century in Northern Spain

Neurogenetics, 2009-10, Vol.10 (4), p.347-353

2009

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Nocturnal hypertension and dysautonomia in patients with Parkinson’s disease: are they related?

Journal of neurology, 2013-07, Vol.260 (7), p.1752-1756

2013

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Restless legs syndrome in Parkinson's disease

Movement disorders, 2007-10, Vol.22 (13), p.1912-1916

2007

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Initial neuropsychological impairments in patients with the E46K mutation of the α-synuclein gene (PARK 1)

Journal of the neurological sciences, 2011-11, Vol.310 (1), p.86-89

2011

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SCOPA-AUT scale in different parkinsonisms and its correlation with (123) I-MIBG cardiac scintigraphy

Parkinsonism & related disorders, 2012-01, Vol.18 (1), p.45-48

2012

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Abnormal multifocal cerebral blood flow on Tc-99m HMPAO SPECT in a patient with anti-NMDA-receptor encephalitis

Journal of neurology, 2010-09, Vol.257 (9), p.1568-1569

2010

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Tako-tsubo cardiomyopathy in a patient with bilateral lesions in the dorsal medulla

Clinical autonomic research, 2011-02, Vol.21 (1), p.65-67

2011

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LRRK2 mutations in Basque patients with Parkinson's disease

Lancet neurology, 2008-10, Vol.7 (10), p.866-867

2008

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Factors influencing the symmetry of Parkinson's disease symptoms

Clinical neurology and neurosurgery, 2010-05, Vol.112 (4), p.302-305

2010

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Orthostatic hypotension associated with an epidermoid tumor of the IV ventricle

Journal of neurology, 2009-08, Vol.256 (8), p.1357-1359

2009

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Parkinson's disease-like presentation of multiple system atrophy with poor response to STN stimulation: A clinicopathological case report

Movement disorders, 2004-08, Vol.19 (8), p.973-977

2004

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Clinical and molecular aspects of progressive degenerative aphasias

Anales de la Real Academia Nacional de Medicina, Madrid, 2018-12, Vol.135 (135(02)), p.52-58

Zarranz, Juan J.

2018

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Central hypoventilation as the presenting symptom in Hu associated paraneoplastic encephalomyelitis

Journal of neurology, neurosurgery and psychiatry, 2007-10, Vol.78 (10), p.1143-1145

2007

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Abnormal sleep architecture is an early feature in the E46K familial synucleinopathy

Movement disorders, 2005-10, Vol.20 (10), p.1310-1315

2005

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Neuroleptic malignant syndrome and serotonin syndrome in a female patient: a clinicopathologic case

Clinical neuropharmacology, 2009-09, Vol.32 (5), p.299-300

2009

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Lrrk2 R1441G-related Parkinson’s disease: evidence of a common founding event in the seventh century in Northern Spain

Neurogenetics, 2009-10, Vol.10 (4), p.347-353

2009

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Teratoma in a case of encephalitis due to antibodies against the NMDA receptor

Revista de neurologiá, 2011-11, Vol.53 (9), p.574

2011

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Tau-predominant-associated pathology in a sporadic late-onset Hallervorden-Spatz syndrome

Movement disorders, 2006-01, Vol.21 (1), p.107-111

2006

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Fatal familial insomnia: mitochondrial and protein synthesis machinery decline in the mediodorsal thalamus

Brain pathology (Zurich, Switzerland), 2017-01, Vol.27 (1), p.95-106

2017

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The new mutation, E46K, of α-synuclein causes parkinson and Lewy body dementia

Impact of psychiatric symptoms and sleep disorders on the quality of life of patients with Parkinson’s disease

A novel form of human disease with a protease-sensitive prion protein and heterozygosity methionine/valine at codon 129: Case report

Outcome of bilateral deep brain subthalamic stimulation in patients carrying the R1441G mutation in the LRRK2 dardarin gene

Lrrk2-associated parkinsonism is a major cause of disease in Northern Spain

Coexistence of protease sensitive and resistant prion protein in 129VV homozygous sporadic Creutzfeldt-Jakob disease: a case report

Lrrk2 R1441G-related Parkinson's disease: evidence of a common founding event in the seventh century in Northern Spain

Nocturnal hypertension and dysautonomia in patients with Parkinson’s disease: are they related?

Restless legs syndrome in Parkinson's disease

Initial neuropsychological impairments in patients with the E46K mutation of the α-synuclein gene (PARK 1)

SCOPA-AUT scale in different parkinsonisms and its correlation with (123) I-MIBG cardiac scintigraphy

Abnormal multifocal cerebral blood flow on Tc-99m HMPAO SPECT in a patient with anti-NMDA-receptor encephalitis

Tako-tsubo cardiomyopathy in a patient with bilateral lesions in the dorsal medulla

LRRK2 mutations in Basque patients with Parkinson's disease

Factors influencing the symmetry of Parkinson's disease symptoms

Orthostatic hypotension associated with an epidermoid tumor of the IV ventricle

Parkinson's disease-like presentation of multiple system atrophy with poor response to STN stimulation: A clinicopathological case report

Clinical and molecular aspects of progressive degenerative aphasias

Central hypoventilation as the presenting symptom in Hu associated paraneoplastic encephalomyelitis

Abnormal sleep architecture is an early feature in the E46K familial synucleinopathy

Neuroleptic malignant syndrome and serotonin syndrome in a female patient: a clinicopathologic case

Lrrk2 R1441G-related Parkinson’s disease: evidence of a common founding event in the seventh century in Northern Spain

Teratoma in a case of encephalitis due to antibodies against the NMDA receptor

Tau-predominant-associated pathology in a sporadic late-onset Hallervorden-Spatz syndrome

Fatal familial insomnia: mitochondrial and protein synthesis machinery decline in the mediodorsal thalamus

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