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Anna Duat-Rodríguez

Showing results (1-10 of 37) with videos related to

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Journal Der Deutschen Dermatologischen Gesellschaft = Journal of the German Society of Dermatology : JDDG|January 15, 2021
Congenital cutaneous neurofibromas in neurofibromatosis type 1: Clinicopathological features in early infancyFrancisco Javier García-Martínez, Daniel Azorín, Anna Duat-Rodríguez, et al.
Journal Der Deutschen Dermatologischen Gesellschaft = Journal of the German Society of Dermatology : JDDG|January 25, 2021
Francisco Javier García-Martínez, Daniel Azorín, Anna Duat-Rodríguez, et al.
Pediatric Neurology|August 10, 2010
Facial capillary malformation and Dyke-Davidoff-Masson syndromeLorea Bagazgoitia, Juan José García-Peñas, Anna Duat-Rodríguez, et al.
Revista De Neurologia|February 11, 2010
[Contiguous gene deletion syndrome in Xp21]Anna Duat-Rodríguez, Luis G Gutiérrez-Solana, Juan José García-Peñas, et al.
Pediatric Neurology|April 16, 2013
Clinical case of anti-N-methyl-D-aspartate receptor encephalitis in an 8-month-old patient with hyperkinetic movement disorderVerónica Cantarín-Extremera, Anna Duat-Rodríguez, Luis González-Gutiérrez-Solana, et al.
Ultraschall in Der Medizin (Stuttgart, Germany : 1980)|November 25, 2021
Clinical and Sonographic Classification of Neurofibromas in Children with Neurofibromatosis Type 1 - A Cluster AnalysisFrancisco Javier García-Martínez, Fernando Alfageme, Anna Duat-Rodríguez, et al.
Pediatric Neurology|November 26, 2013
Neurofibromatosis type 1 associated with moyamoya syndrome in childrenAnna Duat-Rodríguez, Fernando Carceller Lechón, Miguel Ángel López Pino, et al.
Anales De Pediatria|February 25, 2019
[Induced atypical absence seizures during treatment with perampanel]Anna Duat Rodríguez, Verónica Cantarín Extremera, Marta García Fernández, et al.
Anales De Pediatria|March 19, 2026
Non-epileptic paroxismal episodes in pediatrics: experience in a pediatric emergency departmentSonia Clavero Sánchez, Juan Manuel Guijarro Núñez, Caridad Jun García García, et al.
Revista De Neurologia|June 8, 2013
[MCT8-specific thyroid hormone cell transporter deficiency: a case report and review of the literature]Laura López-Marín, Mónica Martín-Belinchón, Luis G Gutiérrez-Solana, et al.
Pageof 4

Showing results (1-10 of 37) with videos related to

Sort By:
Pageof 4
Journal Der Deutschen Dermatologischen Gesellschaft = Journal of the German Society of Dermatology : JDDG|January 15, 2021
Congenital cutaneous neurofibromas in neurofibromatosis type 1: Clinicopathological features in early infancyFrancisco Javier García-Martínez, Daniel Azorín, Anna Duat-Rodríguez, et al.
Journal Der Deutschen Dermatologischen Gesellschaft = Journal of the German Society of Dermatology : JDDG|January 25, 2021
Francisco Javier García-Martínez, Daniel Azorín, Anna Duat-Rodríguez, et al.
Pediatric Neurology|August 10, 2010
Facial capillary malformation and Dyke-Davidoff-Masson syndromeLorea Bagazgoitia, Juan José García-Peñas, Anna Duat-Rodríguez, et al.
Revista De Neurologia|February 11, 2010
[Contiguous gene deletion syndrome in Xp21]Anna Duat-Rodríguez, Luis G Gutiérrez-Solana, Juan José García-Peñas, et al.
Pediatric Neurology|April 16, 2013
Clinical case of anti-N-methyl-D-aspartate receptor encephalitis in an 8-month-old patient with hyperkinetic movement disorderVerónica Cantarín-Extremera, Anna Duat-Rodríguez, Luis González-Gutiérrez-Solana, et al.
Ultraschall in Der Medizin (Stuttgart, Germany : 1980)|November 25, 2021
Clinical and Sonographic Classification of Neurofibromas in Children with Neurofibromatosis Type 1 - A Cluster AnalysisFrancisco Javier García-Martínez, Fernando Alfageme, Anna Duat-Rodríguez, et al.
Pediatric Neurology|November 26, 2013
Neurofibromatosis type 1 associated with moyamoya syndrome in childrenAnna Duat-Rodríguez, Fernando Carceller Lechón, Miguel Ángel López Pino, et al.
Anales De Pediatria|February 25, 2019
[Induced atypical absence seizures during treatment with perampanel]Anna Duat Rodríguez, Verónica Cantarín Extremera, Marta García Fernández, et al.
Anales De Pediatria|March 19, 2026
Non-epileptic paroxismal episodes in pediatrics: experience in a pediatric emergency departmentSonia Clavero Sánchez, Juan Manuel Guijarro Núñez, Caridad Jun García García, et al.
Revista De Neurologia|June 8, 2013
[MCT8-specific thyroid hormone cell transporter deficiency: a case report and review of the literature]Laura López-Marín, Mónica Martín-Belinchón, Luis G Gutiérrez-Solana, et al.
Pageof 4