Personas / Equipo Humano

Janet Hoenicka

Buscador de publicaciones

Publicaciones

  • Ros R, Gómez Garre P, Hirano M, Tai YF, Ampuero I, Vidal L, Rojo A, Fontan A, Vazquez A, Fanjul S, Hernandez J, Cantarero S, Hoenicka J, Jones A, Ahsan RL, Pavese N, Piccini P, Brooks DJ, Perez-Tur J, Nyggard T and de Yébenes JG.

    Genetic linkage of autosomal dominant progressive supranuclear palsy to 1q31.1

    ANNALS OF NEUROLOGY . 57(5): 634-641. Nº de citas: 37

    [doi:10.1002/ana.20449]

  • Barrero FJ, Ampuero I, Morales B, Vives F, de Dios Luna Del Castillo J, Hoenicka J and García Yébenes J.

    Depression in Parkinson's disease is related to a genetic polymorphism of the cannabinoid receptor gene (CNR1)

    PHARMACOGENOMICS JOURNAL . 5(2): 135-141. Nº de citas: 108

    [doi:10.1038/sj.tpj.6500301]

  • Zarranz JJ, Alegre J, Gómez-Esteban JC, Lezcano E, Ros R, Ampuero I, Vidal L, Hoenicka J, Rodriguez O, Atarés B, Llorens V, Gomez Tortosa E, del Ser T, Muñoz DG and de Yebenes JG.

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

    ANNALS OF NEUROLOGY . 55(2): 164-173. Nº de citas: 2540

    [doi:10.1002/ana.10795]

  • Ponce G, Hoenicka J, Rodríguez-Jiménez R, Gozalo A, Jimenéz M, Monasor R, Aragüés M, Rubio G, Jiménez-Arriero MA, Ramos JA and Palomo T.

    DRD2 Taq IA polymorphism is associated with urinary homovanillic acid levels in a sample of Spanish male alcoholic patients

    NEUROTOXICITY RESEARCH . 6(5): 373-377. Nº de citas: 16

    [doi:10.1007/BF03033311]

  • Ponce G, Jimenez-Arriero MA, Rubio G, Hoenicka J, Ampuero I, Ramos JA and Palomo T.

    The A1 allele of the DRD2 gene (TaqI A polymorphisms) is associated with antisocial personality in a sample of alcohol-dependent patients

    EUROPEAN PSYCHIATRY . 18(7): 356-360. Nº de citas: 95

    [doi:10.1016/j.eurpsy.2003.06.006]

  • Carmona J, Burguera JA, Mollà B, Mulas F, Smeyers P, Carratalà F, De Yebenes JG, Hoenicka J and Palau F.

    Unique origin and low penetrance of the 946delGAG mutation in Valencian DYT1 families

    CLINICAL GENETICS . 64(2): 153-159. Nº de citas: 3

    [doi:10.1034/j.1399-0004.2003.00084.x]

  • Posada IJ, García-Morales I, Martínez MA, Hoenicka J and Bermejo F.

    CADASIL:: a case with clinical, radiological, histological and genetic diagnoses

    NEUROLOGIA . 18(4): 229-233. Nº de citas: 6

  • Morales B, Martínez A, Gonzalo I, Vidal L, Ros R, Gomez-Tortosa E, Rabano A, Ampuero I, Sánchez M, Hoenicka J and García De Yébenes J.

    Steele-Richardson-Olszewski syndrome in a patient with a single C212Y mutation in the parkin protein

    MOVEMENT DISORDERS . 17(6): 1374-1380. Nº de citas: 51

    [doi:10.1002/mds.10264]

  • Hoenicka J, Fernández Lobato M, Marín D and Jiménez A.

    The SCR1 gene from Schwanniomyces occidentalis encodes a highly hydrophobic polypeptide, which confers ribosomal resistance to cycloheximide

    Yeast . 19(9): 735-743.

    [doi:10.1002/yea.871]

  • Hoenicka J, Vidal L, Morales B, Ampuero I, Jiménez-Jiménez FJ, Berciano J, del Ser T, Jiménez A, Ruíz PG and de Yébenes JG.

    Molecular findings in familial Parkinson disease in Spain

    Archives of Neurology . 59(6): 966-970. Nº de citas: 52

    [doi:10.1001/archneur.59.6.966]