Directori

DOLORS CASELLAS VIDAL

Trastorns del neurodesenvolupament

Firma

DOLORS CASELLAS-VIDAL

Posició

Investigador/a Post-doctoral – R2

Investigadors/es Post-doctorals – R2

Projectes

Neurodegeneració i Neuroinflamació

EM-Line!Kids: rehabilitació cognitiva des de casa per a pacients en edat pediàtrica.

Codi oficial: 2024 PROD 00183 Data inici: 02/12/2024 Data fi: 01/06/2026 Investigador/a principal: JORDI GICH FULLÀ Organisme finançador: AGÈNCIA DE GESTIÓ UNIVERSITARIS I RECERCA

Publicacions

Endocrinologia pediàtrica , Trastorns del neurodesenvolupament

Casellas-Vidal, D, Font-Lladó, R, Osiniri, I, Camos-Carreras, M, Ruiz-Eizmendi, A, Serrano-Ferrer, J, Casellas, J, López-Bermejo, A, Prats-Puig, A

Upper and lower limb muscle stiffness in children with cerebral palsy compared to typically developing children: Insights from shear wave elastography

JOURNAL OF BIOMECHANICS, 2025, 184, 112667-112667 dx.doi.org/10.1016/j.jbiomech.2025.112667

Trastorns del neurodesenvolupament

Turón-Viñas E, Boronat S, Gich I, González Álvarez V, García-Puig M, Camós Carreras M, Rodriguez-Palmero A, Felipe-Rucián A, Aznar-Laín G, Jiménez-Fàbrega X, Pérez de la Ossa N

Design and Interrater Reliability of the Pediatric Version of the Race Scale: PedRACE.

Stroke, 2024, 55, 2240-2246 dx.doi.org/10.1161/STROKEAHA.124.046846

Trastorns del neurodesenvolupament

Mademont-Soler, I, Camós-Carreras, M, Palacín, A, Casellas-Vidal, D, Hernández-Gallego, G, Garrido, C, Queralt, X, Esteba-Castillo, S, Obón, M

Additional Evidence of ERBB4 as a Haploinsufficient Gene Associated with Neurodevelopmental Disorders

EUROPEAN JOURNAL OF HUMAN GENETICS, 2024, 32, 1496-1497

Oncologia de Precisió de Girona , Trastorns del neurodesenvolupament , Investigació en Salut Vascular

Casellas-Vidal D, Mademont-Soler I, Sánchez J, Plaja A, Castells N, Camós M, Nieto-Moragas J, Del Mar García M, Rodriguez-Solera C, Rivera H, Brunet J, Álvarez S, Perapoch J, Queralt X, Obón M

ZDHHC15 as a candidate gene for autism spectrum disorder.

AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2023, 191, 941-947 dx.doi.org/10.1002/ajmg.a.63099

Imatge Mèdica , Trastorns del neurodesenvolupament , Recerca Metabòlica Materno-Fetal

Mademont-Soler I, Casellas-Vidal D, Trujillo A, Espuña-Capote N, MAROTO, A., García-González MDM, Ruiz MD, Diego-Álvarez D, Queralt X, Perapoch J, Obón M

GLYT1 encephalopathy: Further delineation of disease phenotype and discussion of pathophysiological mechanisms

AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2021, 185, 476-485 dx.doi.org/10.1002/ajmg.a.61996

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Patronat

Centre de

Directori

DOLORS CASELLAS VIDAL

Projectes

Publicacions

Upper and lower limb muscle stiffness in children with cerebral palsy compared to typically developing children: Insights from shear wave elastography

Design and Interrater Reliability of the Pediatric Version of the Race Scale: PedRACE.

Additional Evidence of ERBB4 as a Haploinsufficient Gene Associated with Neurodevelopmental Disorders

ZDHHC15 as a candidate gene for autism spectrum disorder.

GLYT1 encephalopathy: Further delineation of disease phenotype and discussion of pathophysiological mechanisms

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