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I-Ching Chou

Showing results (21-30 of 106) with videos related to

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Pediatrics and Neonatology|November 23, 2017
Novel mutations in the cartilage oligomeric matrix protein gene identified in two Taiwanese patients with pseudoachondroplasia and multiple epiphyseal dysplasiaWei-De Lin, I-Ching Chou, Chung-Hsing Wang, et al.
Children (Basel, Switzerland)|November 27, 2021
Cytomegalovirus Infection in Infancy May Increase the Risk of Subsequent Epilepsy and Autism Spectrum Disorder in ChildhoodChien-Heng Lin, I-Ching Chou, Inn-Chi Lee, et al.
Acta Ophthalmologica|February 1, 2014
A novel one-base insertion mutation in the retinitis pigmentosa 2 gene in a large X-linked Taiwanese familyWei- De Lin, Chung-Hsing Wang, I-Ching Chou, et al.
Frontiers in Pediatrics|October 10, 2022
The impact of parenting stress on parents of school-age children with drug-resistant epilepsyHsin-Hui Lu, Chun-Yu Tsai, I-Ching Chou, et al.
Pediatric Neurology|November 21, 2007
Association of the Slit and Trk-like 1 gene in Taiwanese patients with Tourette syndromeI-Ching Chou, Lei Wan, Su-Ching Liu, et al.
Psychiatric Genetics|December 14, 2007
Association study between Tourette's syndrome and polymorphisms of noradrenergic genes (ADRA2A, ADRA2C)I-Ching Chou, Chang-Hai Tsai, Lei Wan, et al.
Life (Basel, Switzerland)|August 27, 2021
Is Preterm Birth a Risk Factor for Subsequent Autism Spectrum Disorder and Attention Deficit Hyperactivity Disorder in Children with Febrile Seizure?-A Retrospective StudyChien-Heng Lin, Wei-De Lin, I-Ching Chou, et al.
Children (Basel, Switzerland)|November 27, 2021
Lamotrigine Induced DRESS Syndrome in a Child: A Case Report and Literature ReviewChien-Heng Lin, Sheng-Shing Lin, Syuan-Yu Hong, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|May 3, 2011
Association study in Taiwanese girls with precocious pubertyI-Ching Chou, Chung-Hsing Wang, Wei-De Lin, et al.
Pediatrics and Neonatology|September 15, 2015
Identification and Characterization of Mutations in the CLCN7 Gene in a Taiwanese Patient with Infantile Malignant OsteopetrosisWei-De Lin, Chung-Hsing Wang, Kang-His Wu, et al.
Pageof 11

Showing results (21-30 of 106) with videos related to

Sort By:
Pageof 11
Pediatrics and Neonatology|November 23, 2017
Novel mutations in the cartilage oligomeric matrix protein gene identified in two Taiwanese patients with pseudoachondroplasia and multiple epiphyseal dysplasiaWei-De Lin, I-Ching Chou, Chung-Hsing Wang, et al.
Children (Basel, Switzerland)|November 27, 2021
Cytomegalovirus Infection in Infancy May Increase the Risk of Subsequent Epilepsy and Autism Spectrum Disorder in ChildhoodChien-Heng Lin, I-Ching Chou, Inn-Chi Lee, et al.
Acta Ophthalmologica|February 1, 2014
A novel one-base insertion mutation in the retinitis pigmentosa 2 gene in a large X-linked Taiwanese familyWei- De Lin, Chung-Hsing Wang, I-Ching Chou, et al.
Frontiers in Pediatrics|October 10, 2022
The impact of parenting stress on parents of school-age children with drug-resistant epilepsyHsin-Hui Lu, Chun-Yu Tsai, I-Ching Chou, et al.
Pediatric Neurology|November 21, 2007
Association of the Slit and Trk-like 1 gene in Taiwanese patients with Tourette syndromeI-Ching Chou, Lei Wan, Su-Ching Liu, et al.
Psychiatric Genetics|December 14, 2007
Association study between Tourette's syndrome and polymorphisms of noradrenergic genes (ADRA2A, ADRA2C)I-Ching Chou, Chang-Hai Tsai, Lei Wan, et al.
Life (Basel, Switzerland)|August 27, 2021
Is Preterm Birth a Risk Factor for Subsequent Autism Spectrum Disorder and Attention Deficit Hyperactivity Disorder in Children with Febrile Seizure?-A Retrospective StudyChien-Heng Lin, Wei-De Lin, I-Ching Chou, et al.
Children (Basel, Switzerland)|November 27, 2021
Lamotrigine Induced DRESS Syndrome in a Child: A Case Report and Literature ReviewChien-Heng Lin, Sheng-Shing Lin, Syuan-Yu Hong, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|May 3, 2011
Association study in Taiwanese girls with precocious pubertyI-Ching Chou, Chung-Hsing Wang, Wei-De Lin, et al.
Pediatrics and Neonatology|September 15, 2015
Identification and Characterization of Mutations in the CLCN7 Gene in a Taiwanese Patient with Infantile Malignant OsteopetrosisWei-De Lin, Chung-Hsing Wang, Kang-His Wu, et al.
Pageof 11