J. Zarranz

发表

Sanfilippo disease: Buhot cells in the cerebrospinal fluid.

A. García-Riego, J. Prats, J. Zarranz, 1978, Acta cytologica.

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

J. Hoenicka, T. del Ser, D. Munoz, 2004, Annals of neurology.

Use of Ziprasidone in Parkinsonian Patients With Psychosis

J. Zarranz, J. Gómez-Esteban, E. Lezcano, 2005, Clinical neuropharmacology.

Autoantibodies to glutamic acid decarboxylase in three patients with cerebellar ataxia, late-onset insulin-dependent diabetes mellitus, and polyendocrine autoimmunity

E. Tolosa, R. Casamitjana, A. Saiz, 1997, Neurology.

[Neuropsychological changes and bilateral subthalamic deep brain stimulation in Parkinson's disease].

J. Zarranz, J. Garibi, P. Madoz, 2003, Neurologia.

Femoral neuropathy due to compression by retroperitoneal haemorrhage A modern evaluation

J. Zarranz, P. Salisachs, 1979, Journal of the Neurological Sciences.

Autonomic dysfunction in parkinsonian LRRK2 mutation carriers.

J. Zarranz, J. Sømme, T. Rodríguez, 2013, Parkinsonism & related disorders.

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

M. Farrer, I. Mata, M. D. de Pancorbo, 2007, Parkinsonism & related disorders.

Cardiac sympathetic denervation precedes nigrostriatal loss in the E46K mutation of the α-synuclein gene (SNCA)

J. Ruiz‐Martinez, J. Zarranz, J. Gómez-Esteban, 2010, Clinical Autonomic Research.

Multiple cervical artery dissections

P. Pástor, B. Puig, I. Ferrer, 2005, Neurology.

Autonomic involvement in Parkinsonian carriers of PARK2 gene mutations.

M. Luquin, J. Ruiz‐Martinez, M. Carmona, 2015, Parkinsonism & related disorders.

Fatal Familial Insomnia: Clinical Aspects and Molecular Alterations

I. Ferrer, I. Zerr, F. Llorens, 2017, Current Neurology and Neuroscience Reports.

A Novel Form of Human Disease

M. Pancorbo, J. Zarranz, R. Juste, 2013 .

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

I. Ferrer, M. D. de Pancorbo, J. Zarranz, 2010, BMC neurology.

Phenotypic variability in familial prion diseases due to the D178N mutation

M. Pancorbo, M. D. de Pancorbo, A. López de Munain, 2005, Journal of Neurology, Neurosurgery & Psychiatry.

Familial Prion Diseases in the Basque Country (Spain)

J. Zarranz, M. Fernández-Martínez, J. Martí-Massó, 2004, Neuroepidemiology.

LRRK2 mutations in Basque patients with Parkinson's disease

J. Zarranz, J. Gómez-Esteban, 2008, The Lancet Neurology.

Prevalence of neuropsychiatric symptoms in Alzheimer's disease and vascular dementia.

J. Zarranz, M. Fernández-Martínez, R. Ortega, 2008, Current Alzheimer research.

Pearls & Oy-sters: Challenges and Controversies in Wilson Disease

J. Zarranz, J. Gómez-Esteban, I. Gabilondo, 2022, Neurology.

REVERSIBLE CUTIS LAXA DUE TO MATERNAL D-PENICILLAMINE TREATMENT

J. Zarranz, J. Díaz-Pérez, J. Rodriguez-Alarcon, 1979, The Lancet.

Diaphragmatic flutter : A case report and literature review

J. Zarranz, P. Hurtado, L. Castaño, 2015 .

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

J. Zarranz, J. Gómez-Esteban, M. Agundez, 2011, Clinical Autonomic Research.

Sporadic adult‐onset leucodystrophy with axonal spheroids and pigmented glia with no mutations in the known targeted genes

I. Ferrer, L. Zaldumbide, J. Zarranz, 2016, Histopathology.

Dementia, amyotrophy, and periodic complexes on the electroencephalogram: a diagnostic challenge.

J. Zarranz, B. Atarés, F. Velasco, 2001, Archives of neurology.

Prevalence of neuropsychiatric symptoms in mild cognitive impairment and Alzheimer's disease, and its relationship with cognitive impairment.

J. Zarranz, M. Fernández-Martínez, A. Molano, 2010, Current Alzheimer research.

Coexistence of mixed phenotype Creutzfeldt‐Jakob disease, Lewy body disease and argyrophilic grain disease plus histological features of possible Alzheimer's disease: A multi‐protein disorder in an autopsy case

J. Zarranz, R. Juste, M. Geijo, 2015, Neuropathology : official journal of the Japanese Society of Neuropathology.

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

I. Ferrer, A. L. de Munain, J. Zarranz, 2012, Journal of Medical Case Reports.

Iowa APP mutation-related hereditary cerebral amyloid angiopathy (CAA): A new family from Spain

J. Zarranz, M. Fernández-Martínez, J. Baron, 2016, Journal of the Neurological Sciences.

Decreased Density of Presynaptic α2‐Adrenoceptors in Postmortem Brains of Patients with Alzheimer's Disease

J. Zarranz, F. Barturen, J. Javier Meana, 1992, Journal of neurochemistry.

Hirayama disease: Is surgery an option?

J. Zarranz, J. Barredo, M. Agundez, 2015, Neurologia.

[Spontaneous internal carotid artery dissection as a cause of unilateral lower cranial nerve palsies].

J. Zarranz, J. I. Martín-Gómez, J. Ruiz, 1995, Neurologia.

MR Imaging of Presumed Olivary Hypertrophy in Palatal Myoclonus

J. Zarranz, A. Fontán, I. Forcadas, 2022 .

Kuru plaques in the brain of two cases with Creutzfeldt-Jakob disease A common origin for the two diseases?

J. Zarranz, P. Salisachs, J. M. RiveraPomar, 1979, Journal of the Neurological Sciences.

Molecular evidence of founder effects of fatal familial insomnia through SNP haplotypes around the D178N mutation

M. Pancorbo, I. Zerr, R. Sánchez-Valle, 2008, Neurogenetics.

The anatomical basis of symptomatic hemidystonia.

C. Marsden, J. Obeso, J. Obeso, 1985, Brain : a journal of neurology.

Monozygotic Twins Suffering from Huntington’s Disease Show Different Cognitive and Behavioural Symptoms

J. Zarranz, J. Gómez-Esteban, Í. Garamendi, 2006, European Neurology.

Ancestral origins of the prion protein gene D178N mutation in the Basque Country

J. Yagüe, M. Pancorbo, R. Sánchez-Valle, 2005, Human Genetics.

Human T lymphotropic virus type I (HTLV-1) associated myelopathy acquired through a liver transplant

J. Zarranz, J. Gómez-Esteban, I. Rouco, 2001, Journal of neurology, neurosurgery, and psychiatry.

Clinical and molecular aspects of progressive degenerative aphasias

J. Zarranz, 2018, ANALES RANM.

5-Hydroxytryptamine 6 receptor (5-HT6) receptor and apolipoprotein E (ApoE) polymorphisms in patients with Alzheimer's disease in the Basque Country

M. Pancorbo, J. Zarranz, M. Fernández-Martínez, 2003, Neuroscience Letters.

Application of depression criteria (DSM-IV) in patients with Parkinson's disease

J. Zarranz, J. Gómez-Esteban, J. Sømme, 2009, Clinical Neurology and Neurosurgery.

High-affinity choline uptake carrier in Alzheimer's disease: implications for the cholinergic hypothesis of dementia

Á. Pazos, J. Zarranz, J. Berciano, 1991, Brain Research.

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

J. Zarranz, J. Gómez-Esteban, P. Madoz, 2005, Movement Disorders.

Cranial neuropathies and liver failure due to hepatitis A

J. Zarranz, A. Sagasta, J. Ruiz, 1996, Neurology.

OUTCOME OF BILATERAL DEEP BRAIN SUBTHALAMIC STIMULATION IN PATIENTS CARRYING THE R1441G MUTATION IN THE LRRK2 DARDARIN GENE

J. Zarranz, J. Gómez-Esteban, J. Garibi, 2008, Neurosurgery.

Relationship between sleep and dysautonomic symptoms assessed by self‐report scales

J. Zarranz, J. Gómez-Esteban, J. Sømme, 2011, Movement disorders : official journal of the Movement Disorder Society.

Long-term impact on quality of life of subthalamic nucleus stimulation in Parkinson’s disease

J. Zarranz, J. Gómez-Esteban, I. Gabilondo, 2016, Journal of Neurology.

Orthostatic hypotension associated with an epidermoid tumor of the IV ventricle

J. Zarranz, J. Gómez-Esteban, J. Bárcena, 2009, Journal of Neurology.

Necrotising haemorrhagic encephalomyelopathy in an adult: Leigh's disease.

J. Zarranz, T. Tuñón, J. Gállego, 1987, Journal of neurology, neurosurgery, and psychiatry.

J. Jankovic, M. Pancorbo, V. Álvarez, 2009, neurogenetics.

Cardiocirculatory manifestations in Parkinson's disease patients without orthostatic hypotension

Á. Sánchez-Ferro, J. Zarranz, M. Acera, 2015, Journal of Human Hypertension.

Cognitive and behavioral symptoms in Parkinson's disease patients with the G2019S and R1441G mutations of the LRRK2 gene.

J. Zarranz, J. Gómez-Esteban, J. Sømme, 2015, Parkinsonism & related disorders.

Neurogenetic Disorders in the Basque Population

A. López de Munain, J. Zarranz, D. Otaegui, 2015, Annals of human genetics.

Cardiac sympathetic denervation in symptomatic and asymptomatic carriers of the E46K mutation in the α synuclein gene.

H. Kaufmann, J. Ruiz‐Martinez, J. Zarranz, 2013, Parkinsonism & related disorders.

Gait Ataxia during Omeprazole Therapy

J. Zarranz, J. Ruiz, L. Varona, 1996, The Annals of pharmacotherapy.

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

J. Zarranz, J. Gómez-Esteban, J. Sømme, 2013, Journal of Neurology.

Restless legs syndrome in Parkinson's disease

J. Zarranz, J. Gómez-Esteban, E. Lezcano, 2007, Movement disorders : official journal of the Movement Disorder Society.

Improvement in quality of life in patients with advanced Parkinson's disease following bilateral deep‐brain stimulation in subthalamic nucleus

J. Zarranz, J. Gómez-Esteban, I. Pomposo, 2004, European journal of neurology.

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

D. Low, C. Mathias, J. Zarranz, 2012, Parkinsonism & related disorders.

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

J. Zarranz, J. Gómez-Esteban, J. Sømme, 2011, Journal of the Neurological Sciences.

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

J. Zarranz, J. Gómez-Esteban, J. Sømme, 2011, Journal of Neurology.

Influence of Motor Symptoms upon the Quality of Life of Patients with Parkinson’s Disease

J. Zarranz, J. Gómez-Esteban, Í. Garamendi, 2007, European Neurology.

Loss of high-affinity α 2-adrenoceptors in Alzheimer's disease: An autoradiographic study in frontal cortex and hippocampus

Á. Pazos, J. Zarranz, J. García-Sevilla, 1992, Neuroscience Letters.

Central hypoventilation as the presenting symptom in Hu associated paraneoplastic encephalomyelitis

A. Saiz, J. Zarranz, F. Graus, 2007, Journal of Neurology Neurosurgery & Psychiatry.

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

J. Zarranz, J. Gómez-Esteban, E. Lezcano, 2006, Movement disorders : official journal of the Movement Disorder Society.

Motor and non-motor symptoms of Parkinson's disease and their impact on quality of life and on different clinical subgroups.

J. Zarranz, J. Gómez-Esteban, I. Gabilondo, 2016, Neurologia.

Prevalence of Neuropsychiatric Symptoms in Mild Cognitive Impairment and Alzheimers Disease, and its Relationship with Cognitive Impairment

J. Zarranz, M. Fernández-Martínez, Manuel Fernández-Martínez, 2010 .

Motor and non-motor symptoms of Parkinson's disease and their impact on quality of life and on different clinical subgroups

Iñigo Gabilondo, J. Zarranz, J. Gómez-Esteban, 2016 .

[Dementia caused by miliary cerebral metastasis of a hepatocarcinoma].

J. Zarranz, I. Forcadas, A. Fontán, 1989, Medicina clinica.

[Posterior cortical atrophy with progressive visual agnosia].

X. Beristain, J. Zarranz, E. Lezcano, 1995, Neurología.

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

J. Zarranz, J. Gómez-Esteban, Elena Lezcano, 2004, Movement disorders : official journal of the Movement Disorder Society.

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

A. Saiz, J. Zarranz, J. Gómez-Esteban, 2010, Journal of Neurology.

Ergotism: an infrequent aetiology of intermittent claudication.

J. Zarranz, M. Egurbide, J. Ruiz, 1996, Postgraduate medical journal.

Postural orthostatic tachycardia syndrome, neurally-mediated syncope, and joint hypermobility: a case report.

J. Zarranz, J. Gómez-Esteban, B. Tijero, 2014, Neurologia.

[Prevalence of dementia in the elderly aged above 65 in a district in the Basque Country].

J. Zarranz, M. Fernandez, J. Castro-Flores, 2008, Revista de neurologia.

Charcot-Marie-Tooth disease associated with 'essential tremor' and normal and/or slightly diminished motor conduction velocity. Report of 7 cases.

J. Zarranz, A. Codina, P. Salisachs, 1979, European neurology.

The applause sign and neuropsychological profile in progressive supranuclear palsy and Parkinson's disease

J. Zarranz, J. Gómez-Esteban, J. Sømme, 2013, Clinical Neurology and Neurosurgery.

Preserved cortical somatosensory evoked potentials in apnoeic coma with loss of brain-stem reflexes

J. Zarranz, 2004, Journal of Neurology.

Neurological manifestations in Erdheim-Chester disease: Two case reports.

J. Zarranz, J. Aróstegui, A. Cánovas, 2016, Neurologia.

MR imaging of presumed olivary hypertrophy in

J. Zarranz, A. Fontan, 2013 .

Selective cortical decrease of high-affinity choline uptake carrier in Alzheimer's disease: An autoradiographic study using3H-hemicholinium-3

Á. Pazos, J. Zarranz, J. Pascual, 1994, Journal of neural transmission. Parkinson's disease and dementia section.

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

J. Zarranz, J. Gómez-Esteban, J. Sømme, 2009, Clinical neuropharmacology.

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

D. Low, C. Mathias, J. Zarranz, 2012, Parkinsonism & related disorders.

Sleep complaints and their relation with drug treatment in patients suffering from Parkinson's disease

J. Zarranz, J. Gómez-Esteban, E. Lezcano, 2006, Movement disorders : official journal of the Movement Disorder Society.