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Chong Ae Kim

Showing results (1-10 of 150) with videos related to

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Codas|September 20, 2018
Characteristics of auditory evaluation in Williams syndrome: a systematic reviewLiliane Aparecida Fagundes Silva, Chong Ae Kim, Carla Gentile Matas
Brain & Development|May 28, 2003
A study of EEG and epilepsy profile in Wolf-Hirschhorn syndrome and considerations regarding its correlation with other chromosomal disordersKette D Valente, Alessandra Freitas, Lia A Fiore, et al.
Neurology|April 16, 2014
Remote spinal cord injury in mucopolysaccharidosis type IVA after cervical decompressionFelippe Borlot, Paula Ricci Arantes, Alberto Carlos Capel Cardoso, et al.
AJNR. American Journal of Neuroradiology|December 1, 2004
Malformation of cortical and vascular development in one family with parietal foramina determined by an ALX4 homeobox gene mutationMarcelo Valente, Kette D Valente, Sofia S M Sugayama, et al.
International Journal of Pediatric Otorhinolaryngology|May 9, 2021
Auditory hypersensitivity in Williams syndromeLiliane Aparecida Fagundes Silva, Rachel Sayuri Honjo Kawahira, Chong Ae Kim, et al.
Codas|January 19, 2022
Audiological profile and cochlear functionality in Williams syndromeLiliane Aparecida Fagundes Silva, Rachel Sayuri Honjo Kawahira, Chong Ae Kim, et al.
European Journal of Medical Genetics|February 11, 2021
Abnormal auditory event-related potentials in Williams syndromeLiliane Aparecida Fagundes Silva, Rachel Sayuri Honjo Kawahira, Chong Ae Kim, et al.
Arquivos De Neuro-Psiquiatria|January 22, 2015
Mowat-Wilson syndrome: neurological and molecular study in seven patientsJosé Albino da Paz, Chong Ae Kim, Michael Goossens, et al.
Revista Do Hospital Das Clinicas|November 16, 2004
Renal and urinary findings in 20 patients with Williams-Beuren syndrome diagnosed by fluorescence in situ hybridization (FISH)Sofia Mizuho Miura Sugayama, Vera Hermina Kalika Koch, Erica Arai Furusawa, et al.
Ophthalmic Genetics|August 19, 2017
Multimodal image analysis of the retina in Hunter syndrome (mucopolysaccharidosis type II): Case reportIsadora Darriba Macedo Salvucci, Simone Finzi, Maria Kiyoko Oyamada, et al.
Pageof 15

Showing results (1-10 of 150) with videos related to

Sort By:
Pageof 15
Codas|September 20, 2018
Characteristics of auditory evaluation in Williams syndrome: a systematic reviewLiliane Aparecida Fagundes Silva, Chong Ae Kim, Carla Gentile Matas
Brain & Development|May 28, 2003
A study of EEG and epilepsy profile in Wolf-Hirschhorn syndrome and considerations regarding its correlation with other chromosomal disordersKette D Valente, Alessandra Freitas, Lia A Fiore, et al.
Neurology|April 16, 2014
Remote spinal cord injury in mucopolysaccharidosis type IVA after cervical decompressionFelippe Borlot, Paula Ricci Arantes, Alberto Carlos Capel Cardoso, et al.
AJNR. American Journal of Neuroradiology|December 1, 2004
Malformation of cortical and vascular development in one family with parietal foramina determined by an ALX4 homeobox gene mutationMarcelo Valente, Kette D Valente, Sofia S M Sugayama, et al.
International Journal of Pediatric Otorhinolaryngology|May 9, 2021
Auditory hypersensitivity in Williams syndromeLiliane Aparecida Fagundes Silva, Rachel Sayuri Honjo Kawahira, Chong Ae Kim, et al.
Codas|January 19, 2022
Audiological profile and cochlear functionality in Williams syndromeLiliane Aparecida Fagundes Silva, Rachel Sayuri Honjo Kawahira, Chong Ae Kim, et al.
European Journal of Medical Genetics|February 11, 2021
Abnormal auditory event-related potentials in Williams syndromeLiliane Aparecida Fagundes Silva, Rachel Sayuri Honjo Kawahira, Chong Ae Kim, et al.
Arquivos De Neuro-Psiquiatria|January 22, 2015
Mowat-Wilson syndrome: neurological and molecular study in seven patientsJosé Albino da Paz, Chong Ae Kim, Michael Goossens, et al.
Revista Do Hospital Das Clinicas|November 16, 2004
Renal and urinary findings in 20 patients with Williams-Beuren syndrome diagnosed by fluorescence in situ hybridization (FISH)Sofia Mizuho Miura Sugayama, Vera Hermina Kalika Koch, Erica Arai Furusawa, et al.
Ophthalmic Genetics|August 19, 2017
Multimodal image analysis of the retina in Hunter syndrome (mucopolysaccharidosis type II): Case reportIsadora Darriba Macedo Salvucci, Simone Finzi, Maria Kiyoko Oyamada, et al.
Pageof 15