AAAAAA
Results:
1-12
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Results: 12
Authors:
Perez, JM
Cerrillo, V
Matesanz, AI
Millan, JM
Navarro, P
Alonso, C
Souza, P
Citation: Jm. Perez et al., DNA interstrand cross-linking efficiency and cytotoxic activity of novel cadmium(II) - Thiocarbodiazone complexes, CHEMBIOCHEM, 2(2), 2001, pp. 119-123
Authors:
Porta-Etessam, J
Ruiz-Morales, J
Millan, JM
Ramos, A
Martinez-Salio, A
Berbel-Garcia, A
Citation: J. Porta-etessam et al., Epilepsia partialis continua and frontal features as a debut of anti-Hu paraneoplastic encephalomyelitis with focal frontal encephalitis, EUR J NEUR, 8(4), 2001, pp. 359-360
Authors:
Miano, MG
Testa, F
Filippini, F
Trujillo, M
Conte, I
Lanzara, C
Millan, JM
De Bernardo, C
Grammatico, B
Mangino, M
Torrente, I
Carrozzo, R
Simonelli, F
Rinaldi, E
Ventruto, V
D'Urso, M
Ayuso, C
Ciccodicola, A
Citation: Mg. Miano et al., Identification of novel RP2 mutations in a subset of X-linked Retinitis Pigmentosa families and prediction of new domains, HUM MUTAT, 18(2), 2001, pp. 109-119
Authors:
Martinez, F
Martinez-Garay, I
Millan, JM
Perez-Aytes, A
Molto, MD
Orellana, C
Prieto, F
Citation: F. Martinez et al., Localization of non-specific X-linked mental retardation gene (MRX73) to Xp22.2, AM J MED G, 102(2), 2001, pp. 200-204
Authors:
Orellana, C
Martinez, F
Badia, L
Millan, JM
Montero, MR
Andres, J
Prieto, F
Citation: C. Orellana et al., Trisomy rescue by postzygotic unbalanced (X;14) translocation in a girl with dysmorphic features, CLIN GENET, 60(3), 2001, pp. 206-211
Authors:
Lopez-Pelaez, MF
Millan, JM
de Vergas, J
Citation: Mf. Lopez-pelaez et al., Fatal cerebral venous sinus thrombosis as major complication of metastaticcervical mass: computed tomography and magnetic resonance findings, J LARYNG OT, 114(10), 2000, pp. 798-801
Authors:
Revilla, TY
Ramos, A
Gonzalez, P
Alday, R
Millan, JM
Citation: Ty. Revilla et al., Arachnoiditis ossificans diagnosis with helical computed tomography, CLIN IMAG, 23(1), 1999, pp. 1-4
Authors:
Martinez, F
Millan, JM
Orellana, C
Prieto, F
Citation: F. Martinez et al., X-linked anhidrotic (hypohidrotic) ectodermal dysplasia caused by a novel mutation in EDA1 gene: 406T > G (Leu55Arg), J INVES DER, 113(2), 1999, pp. 285-286
Authors:
Millan, JM
Martinez, F
Cadroy, A
Gandia, J
Casquero, M
Beneyto, M
Badin, L
Prieto, F
Citation: Jm. Millan et al., Screening for FMR1 mutations among the mentally retarded: prevalence of the fragile X syndrome in Spain, CLIN GENET, 56(1), 1999, pp. 98-99
Authors:
Lossi, AM
Millan, JM
Villard, L
Orellana, C
Cardoso, C
Prieto, F
Fontes, M
Martinez, F
Citation: Am. Lossi et al., Mutation of the XNP/ATR-X gene in a family with severe mental retardation,spastic paraplegia and skewed pattern of X inactivation: Demonstration that the mutation is involved in the inactivation bias, AM J HU GEN, 65(2), 1999, pp. 558-562
Phase II trial of cisplatin and Gemcitabine in advanced squamous-cell carcinoma of the head and neck
Authors:
Hitt, R
Castellano, D
Hidalgo, M
Garcia-Carbonero, R
Pena, M
Brandariz, A
Millan, JM
Vincent, JJA
Cortes-Funes, H
Citation: R. Hitt et al., Phase II trial of cisplatin and Gemcitabine in advanced squamous-cell carcinoma of the head and neck, ANN ONCOL, 9(12), 1998, pp. 1347-1349
Authors:
Cuevas, JM
Espinos, C
Millan, JM
Sanchez, F
Trujillo, MJ
Garcia-Sandoval, B
Ayuso, C
Najera, C
Beneyto, M
Citation: Jm. Cuevas et al., Detection of a novel Cys628STOP mutation of the myosin VIIA gene in Usher syndrome type Ib, MOL CELL PR, 12(6), 1998, pp. 417-420
Risultati:
1-12
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