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NURIA RIBAS-VIDAL
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Publicacions

Viñas-Jornet M, Esteba-Castillo S, Baena N, Ribas-Vidal N, Ruiz A, Torrents-Rodas D, Gabau E, Vilella E, Martorell L, Armengol L, Novell R, Guitart M

High Incidence of Copy Number Variants in Adults with Intellectual Disability and Co-morbid Psychiatric Disorders.

BEHAVIOR GENETICS, 2018, 48, 323-336 dx.doi.org/10.1007/s10519-018-9902-6

Esteba-Castillo S, Torrents-Rodas D, García-Alba J, Ribas-Vidal N, Novell-Alsina R

Translation and validation of the Spanish version of the Health of the Nation Outcome Scales for People with Learning Disabilities (HoNOS-LD).

Revista De Psiquiatria Y Salud Mental, 2018, 11, 141-150 dx.doi.org/10.1016/j.rpsm.2016.11.002

Thygesen JH, Wolfe K, McQuillin A, Viñas-Jornet M, Baena N, Brison N, D'Haenens G, Esteba-Castillo S, Gabau E, Ribas-Vidal N, Ruiz A, Vermeesch J, Weyts E, Novell R, Buggenhout GV, Strydom A, Bass N, Guitart M, Vogels A

Neurodevelopmental risk copy number variants in adults with intellectual disabilities and comorbid psychiatric disorders.

BRITISH JOURNAL OF PSYCHIATRY, 2018, 212, 287-294 dx.doi.org/10.1192/bjp.2017.65

Pujol J, Fenoll R, Ribas-Vidal N, Martínez-Vilavella G, Blanco-Hinojo L, García-Alba J, Deus J, Novell R, Esteba-Castillo S

A longitudinal study of brain anatomy changes preceding dementia in Down syndrome.

NEUROIMAGE-CLINICAL, 2018, 18, 160-166 dx.doi.org/10.1016/j.nicl.2018.01.024

García-Alba J, Esteba-Castillo S, Castellanos López MÁ, Rodríguez Hidalgo E, Ribas Vidal N, Moldenhauer Díaz F, Novell-Alsina R

Validation and Normalization of the Tower of London-Drexel University Test 2nd Edition in an Adult Population with Intellectual Disability.

Spanish Journal Of Psychology, 2017, 20 dx.doi.org/10.1017/sjp.2017.30

Fenoll R, Pujol J, Esteba-Castillo S, de Sola S, Ribas-Vidal N, García-Alba J, Sánchez-Benavides G, Martínez-Vilavella G, Deus J, Dierssen M, Novell-Alsina R, de la Torre R

Anomalous White Matter Structure and the Effect of Age in Down Syndrome Patients.

JOURNAL OF ALZHEIMERS DISEASE, 2017, 57, 61-70 dx.doi.org/10.3233/JAD-161112

Viñas-Jornet M, Esteba-Castillo S, Gabau E, Ribas-Vidal N, Baena N, San J, Ruiz A, Coll MD, Novell R, Guitart M

A common cognitive, psychiatric, and dysmorphic phenotype in carriers of NRXN1 deletion.

Molecular genetics & genomic medicine, 2014, 2, 512-521 dx.doi.org/10.1002/mgg3.105

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