M. J. Sainz

发表

Variability of age at onset in siblings with familial Alzheimer disease.

M. Barquero, P. Gómez-Garre, A. Jiménez-Escrig, 2007, Archives of neurology.

Visual Hallucinations and HLA Class II Antigens in Cortical Dementia

E. Gómez-Tortosa, M. J. Sainz, M. Aguerri, 2010, Dementia and Geriatric Cognitive Disorders.

Clinical-genetic correlations in familial Alzheimer's disease caused by presenilin 1 mutations.

D. Munoz, R. Guerrero, A. Jiménez-Escrig, 2010, Journal of Alzheimer's disease : JAD.

Deep brain stimulation in chorea acanthocytosis

A. Danek, M. J. Sainz, P. G. Garcia Ruiz, 2009, Movement disorders : official journal of the Movement Disorder Society.

Diversity of Cognitive Phenotypes Associated with C9ORF72 Hexanucleotide Expansion.

E. Gómez-Tortosa, C. Ayuso, M. J. Sainz, 2016, Journal of Alzheimer's disease : JAD.

Familial primary lateral sclerosis or dementia associated with Arg573Gly TBK1 mutation

C. van Broeckhoven, M. Cruts, J. van der Zee, 2017, Journal of Neurology, Neurosurgery, and Psychiatry.

C9ORF72 hexanucleotide expansions of 20–22 repeats are associated with frontotemporal deterioration

A. Marcos, E. Gómez-Tortosa, C. Ayuso, 2013, Neurology.

Alcoholic cognitive deterioration and nutritional deficiencies

F. Jiménez-Jiménez, J. Molina, F. Bermejo, 1994, Acta neurologica Scandinavica.

SORL1 Variants in Familial Alzheimer's Disease.

E. Gómez-Tortosa, M. J. Sainz, C. Ordás, 2018, Journal of Alzheimer's disease : JAD.

α-Secretase nonsense mutation (ADAM10 Tyr167*) in familial Alzheimer’s disease

A. Jiménez-Escrig, E. Gómez-Tortosa, M. García‐Ayllón, 2020, Alzheimer's research & therapy.

Familial benign frontotemporal deterioration with C9ORF72 hexanucleotide expansion

E. Gómez-Tortosa, M. J. Sainz, Soledad Serrano, 2014, Alzheimer's & Dementia.

Outcome of mild cognitive impairment comparing early memory profiles.

R. Guerrero, E. Gómez-Tortosa, I. Mahíllo-Fernández, 2012, The American journal of geriatric psychiatry : official journal of the American Association for Geriatric Psychiatry.

Cerebrospinal fluid markers in dementia with lewy bodies compared with Alzheimer disease.

T. del Ser, E. Gómez-Tortosa, M. J. Sainz, 2003, Archives of neurology.

Presence of tau astrogliopathy in frontotemporal dementia caused by a novel Grn nonsense (Trp2*) mutation

C. van Broeckhoven, J. van der Zee, E. Gómez-Tortosa, 2019, Neurobiology of Aging.

Behavioral Evolution of Progressive Semantic Aphasia in Comparison with Nonfluent Aphasia

E. Gómez-Tortosa, I. Mahíllo-Fernández, R. Rigual, 2015, Dementia and Geriatric Cognitive Disorders.

Plasma progranulin levels in cortical dementia phenotypes with asymmetric perisylvian atrophy

T. del Ser, E. Gómez-Tortosa, E. Gil-Neciga, 2013, European journal of neurology.

TRIM25 mutation (p.C168*), coding for an E3 ubiquitin ligase, is a cause of early‐onset autosomal dominant dementia with amyloid load and parkinsonism

C. van Broeckhoven, J. van der Zee, E. Gómez-Tortosa, 2022, Alzheimer's & dementia : the journal of the Alzheimer's Association.

P3-224: Clinical phenotype of familial Alzheimer's disease caused by the H163R presenilin 1 mutation

D. Munoz, M. Barquero, A. Jiménez-Escrig, 2008, Alzheimer's & Dementia.

ADAM10 Gene Variants in AD Patients and Their Relationship to CSF Protein Levels

E. Gómez-Tortosa, I. Mahíllo-Fernández, M. García‐Ayllón, 2023, International journal of molecular sciences.

REM sleep behavior disorder in patients with DJ‐1 mutations and parkinsonism‐dementia‐ALS complex

M. J. Sainz, P. G. Garcia Ruiz, Fernando Alonso Frech, 2009, Movement disorders : official journal of the Movement Disorder Society.

De Novo PS1 Mutation (Pro436Gln) in a Very Early-Onset Posterior Variant of Alzheimer's Disease Associated with Spasticity: A Case Report.

E. Gómez-Tortosa, M. J. Sainz, I. Lorda, 2021, Journal of Alzheimer's disease : JAD.

REM sleep behavior disorder in patients with DJ‐1 mutations and parkinsonism‐dementia‐ALS complex

M. J. Sainz, P. G. Garcia Ruiz, B. Bader, 2009, Movement disorders : official journal of the Movement Disorder Society.