Publicaciones
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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
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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.
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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
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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
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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
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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