Publicaciones
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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
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Hoenicka J, Pérez M, Pérez-Tur J, Barabash A, Godoy M, Vidal L, Astarloa R, Avila J, Nygaard T and de Yébenes JG.
Th tau gene A0 allele and progressive supranuclear palsy
NEUROLOGY . 53(6): 1219-1225. Nº de citas: 50
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Rodríguez-Pombo P, Hoenicka J, Muro S, Pérez B, Pérez-Cerdá C, Richard E, Desviat LR and Ugarte M.
Human propionyl-CoA carboxylase ß subunit gene:: Exon-intron definition and mutation spectrum in Spanish and Latin American propionic acidemia patients
AMERICAN JOURNAL OF HUMAN GENETICS . 63(2): 360-369. Nº de citas: 44
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Pérez-Cerdá C, Merinero B, Martí M, Cabrera JC, Peña L, García MJ, Gangoiti J, Sanz P, Rodríguez-Pombo P, Hoenicka J, Richard E, Muro S and Ugarte M.
An unusual late-onset case of propionic acidaemia:: biochemical investigations, neuroradiological findings and mutation analysis
EUROPEAN JOURNAL OF PEDIATRICS . 157(1): 50-52. Nº de citas: 33
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Hoenicka J, Rodríguez-Pombo P, Pérez-Cerdá C, Muro S, Richard E and Ugarte M.
New frequent mutation in the PCCB gene in Spanish propionic acidemia patients
HUMAN MUTATION . : 234-236. Nº de citas: 9
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Del Pozo L, Abarca D, Hoenicka J and Lmenez A.
2 DIFFERENT GENES FROM SCHWANNIOMYCES-OCCIDENTALIS DETERMINE RIBOSOMAL RESISTANCE TO CYCLOHEXIMIDE
EUROPEAN JOURNAL OF BIOCHEMISTRY . 213(2): 849-857. Nº de citas: 18
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OLIVER, SG, VANDERAART, QJM, AGOSTONI-CARBONE, ML, AIGLE, M, ALBERGHINA, L, ALEXANDRAKI, D, ANTOINE, G, ANWAR, R, BALLESTA, JPG, BENIT, P, BERBEN, G, BERGANTINO, E, BITEAU, N, BOLLE, PA, BOLOTINFUKUHARA, M, BROWN, A, BROWN, AJP, BUHLER, JM, CARCANO, C, CARIGNANI, G, CEDERBERG, H, CHANET, R, CONTRERAS, R, CROUZET, M, DAIGNANFORNIER, B, DEFOOR, E, DELGADO, M, DEMOLDER, J, DOIRA, C, DUBOIS, E, DUJON, B, DUSTERHOFT, A, ERDMANN, D, ESTEBAN, M, FABRE, F, FAIRHEAD, C, FAYE, G, FELDMANN, H, FIERS, W, FRANCINGUESGAILLARD, MC, FRANCO, L, FRONTALI, L, FUKUHARA, H, FULLER, LJ, GALLAND, P, GENT, ME, GIGOT, D, GILLIQUET, V, GLANSDORFF, N, GOFFEAU, A, GRENSON, M, GRISANTI, P, GRIVELL, LA, DEHAAN, M, HAASEMANN, M, HATAT, D, Hoenicka J, HEGEMANN, J, HERBERT, CJ, HILGER, F, HOHMANN, S, HOLLENBERG, CP, HUSE, K, IBORRA, F, INDGE, KJ, ISONO, K, JACQ, C, JACQUET, M, JAMES, CM, JAUNIAUX, JC, JIA, Y, JIMENEZ, A, KELLY, A, KLEINHANS, U, KREISL, P, LANFRANCHI, G, LEWIS, C, VANDERLINDEN, CG, LUCCHINI, G, LUTZENKIRCHEN, K, MAAT, MJ, MALLET, L, MANNHAUPT, G, MARTEGANI, E, MATHIEU, A, MAURER, CTC, MCCONNELL, D, MCKEE, RA, MESSENGUY, F, MEWES, HW, MOLEMANS, F, MONTAGUE, MA, FALCONI, MM, NAVAS, L, NEWLON, CS, NOONE, D, PALLIER, C, PANZERI, L, PEARSON, BM, PEREA, J, PHILIPPSEN, P, PIERARD, A, PLANTA, RJ, PLEVANI, P, POETSCH, B, POHL, F, PURNELLE, B, RAD, MR, RASMUSSEN, SW, RAYNAL, A, REMACHA, M, RICHTERICH, P, ROBERTS, AB, RODRIGUEZ, F, SANZ, E, SCHAAFFGERSTENSCHLAGER, I, SCHERENS, B, SCHWEITZER, B, SHU, Y, SKALA, J, SLONIMSKI, PP, SOR, F, SOUSTELLE, C, SPIEGELBERG, R, STATEVA, LI, STEENSMA, HY, STEINER, S, THIERRY, A, THIREOS, G, TZERMIA, M, URRESTARAZU, LA, VALLE, G, VETTER, I, VANVLIETREEDIJK, JC, VOET, M, VOLCKAERT, G, VREKEN, P, WANG, H, WARMINGTON, JR, VON WETTSTEIN, D, WICKSTEED, BL, WILSON, C, WURST, H, XU, G, YOSHIKAWA, A, ZIMMERMANN, FK and SGOUROS, JG.
THE COMPLETE DNA-SEQUENCE OF YEAST CHROMOSOME-III
NATURE . 357(6373): 38-46. Nº de citas: 980
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Maingon R, Gerke R, Rodriguez M, Urbina J, Hoenicka J, Negri S, Aguirre T, Nehlin J, Knapp T and Crampton J.
THE TUBULIN GENES OF TRYPANOSOMA-CRUZI
EUROPEAN JOURNAL OF BIOCHEMISTRY . 171(1-2): 285-291. Nº de citas: 27
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Lim KS, Periñan MT, Chew EGY, Lee PS, Akçimen F, Lim JL, Koretsky MJ, Funayama M, Yoshino H, Hattori N, Kaiyrzhanov R, Houlden H, Isayan M, Tay YW, Toh TS, Lit LC, Khairul Anuar AN, Ding HX, Screven L, Ibrahim NM, Lin CH, Kim HJ, Lee JY, Chung SJ, Foo JN, Tan EK, Lim SY, Tan AH, Bandres-Ciga S and Ahmad-Annuar A.
Association of LRRK2 p.A419V with Parkinson's Disease in East Asians and analysis of age at onset.
npj Parkinsons Disease . : .