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8 results for author:"Gomez Tortosa E." in Literature citations

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Population stratification may bias analysis of PGC-1alpha as a modifier of age at Huntington disease motor onset.

Ramos E.M., Latourelle J.C., Lee J.H., Gillis T., Mysore J.S., Squitieri F., Di Pardo A., Di Donato S., Hayden M.R., Morrison P.J. et al.

Hum. Genet. 131:1833-1840(2012) · Mapped (10)

TAA repeat variation in the GRIK2 gene does not influence age at onset in Huntington's disease.

Lee J.H., Lee J.M., Ramos E.M., Gillis T., Mysore J.S., Kishikawa S., Hadzi T., Hendricks A.E., Hayden M.R., Morrison P.J. et al.

Biochem. Biophys. Res. Commun. 424:404-408(2012) · Mapped (8)

Visual hallucinations and HLA class II antigens in cortical dementia.

Gomez-Tortosa E., Aguerri M., Sainz M.J., Losada M., Garcia-Ruiz P.J., Cardaba B.

Dement Geriatr Cogn Disord 30:8-11(2010) · Mapped (729)

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

Gomez-Tortosa E., Barquero M.S., Baron M., Sainz M.J., Manzano S., Payno M., Ros R., Almaraz C., Gomez-Garre P., Jimenez-Escrig A.

Arch. Neurol. 64:1743-1748(2007) · Mapped (5)

Evidence for a modifier of onset age in Huntington disease linked to the HD gene in 4p16.

Djousse L., Knowlton B., Hayden M.R., Almqvist E.W., Brinkman R.R., Ross C.A., Margolis R.L., Rosenblatt A., Durr A., Dode C. et al.

Neurogenetics 5:109-114(2004) · Mapped (2)

The new mutation, E46K, of alpha-synuclein causes Parkinson and Lewy body dementia.

Zarranz J.J., Alegre J., Gomez-Esteban J.C., Lezcano E., Ros R., Ampuero I., Vidal L., Hoenicka J., Rodriguez O., Atares B. et al.

Ann. Neurol. 55:164-173(2004) · UniProtKB (1)

Interaction of normal and expanded CAG repeat sizes influences age at onset of Huntington disease.

Djousse L., Knowlton B., Hayden M., Almqvist E.W., Brinkman R., Ross C., Margolis R., Rosenblatt A., Durr A., Dode C. et al.

Am. J. Med. Genet. A 119A:279-282(2003) · Mapped (4)

Senile dementia associated with amyloid beta protein angiopathy and tau perivascular pathology but not neuritic plaques in patients homozygous for the APOE-epsilon4 allele.

Vidal R., Calero M., Piccardo P., Farlow M.R., Unverzagt F.W., Mendez E., Jimenez-Huete A., Beavis R., Gallo G., Gomez-Tortosa E. et al.

Acta Neuropathol. 100:1-12(2000) · Mapped (5)

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