Personas / Equipo Humano

Janet Hoenicka

Buscador de publicaciones

Publicaciones

  • 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]

  • Hoenicka J, Arrasate M, de Yebenes JG and Avila J.

    A two-hybrid screening of human Tau protein: interactions with Alu-derived domain

    Neuroreport . 13(3): 343-349. Nº de citas: 9

    [doi:10.1097/00001756-200203040-00019]

  • Jiménez-Jiménez F, Martínez-Castrillo JC, Barón-Rubio M, Zurdo JM, de Toledo-Heras M, Vidal L and Hoenicka J.

    Familial focal dystonia

    European Neurology . 48(4): 232-234. Nº de citas: 3

    [doi:10.1159/000066171]

  • Hoenicka J, Vidal L, Godoy M, Ochoa JJ and García de Yébenes J.

    New nonsense mutation in the GTP-cyclohydrolase I gene in L-DOPA responsive dystonia-parkinsonism

    MOVEMENT DISORDERS . 16(2): 364-366. Nº de citas: 3

    [doi:10.1002/mds.1044]