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September 20, 2018
Characteristics of auditory evaluation in Williams syndrome: a systematic review
Liliane 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 disorders
Kette D Valente, Alessandra Freitas, Lia A Fiore, et al.
Neurology
|
April 16, 2014
Remote spinal cord injury in mucopolysaccharidosis type IVA after cervical decompression
Felippe 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 mutation
Marcelo Valente, Kette D Valente, Sofia S M Sugayama, et al.
International Journal of Pediatric Otorhinolaryngology
|
May 9, 2021
Auditory hypersensitivity in Williams syndrome
Liliane Aparecida Fagundes Silva, Rachel Sayuri Honjo Kawahira, Chong Ae Kim, et al.
Codas
|
January 19, 2022
Audiological profile and cochlear functionality in Williams syndrome
Liliane 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 syndrome
Liliane 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 patients
José 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.
Arquivos Brasileiros De Cardiologia
|
November 13, 2014
Investigation of copy number variation in children with conotruncal heart defects
Carla Marques Rondon Campos, Evelin Aline Zanardo, Roberta Lelis Dutra, et al.
Page
of 15
Search research articles
Search
Showing results (1-10 of 150) with videos related to
Sort By:
Page
of 15
Codas
|
September 20, 2018
Characteristics of auditory evaluation in Williams syndrome: a systematic review
Liliane 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 disorders
Kette D Valente, Alessandra Freitas, Lia A Fiore, et al.
Neurology
|
April 16, 2014
Remote spinal cord injury in mucopolysaccharidosis type IVA after cervical decompression
Felippe 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 mutation
Marcelo Valente, Kette D Valente, Sofia S M Sugayama, et al.
International Journal of Pediatric Otorhinolaryngology
|
May 9, 2021
Auditory hypersensitivity in Williams syndrome
Liliane Aparecida Fagundes Silva, Rachel Sayuri Honjo Kawahira, Chong Ae Kim, et al.
Codas
|
January 19, 2022
Audiological profile and cochlear functionality in Williams syndrome
Liliane 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 syndrome
Liliane 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 patients
José 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.
Arquivos Brasileiros De Cardiologia
|
November 13, 2014
Investigation of copy number variation in children with conotruncal heart defects
Carla Marques Rondon Campos, Evelin Aline Zanardo, Roberta Lelis Dutra, et al.
Page
of 15