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Hypsarrhythmia paroxysm intensities that initiate and render physical and mental retardation irreversible in West syndrome

International journal of neuroscience, 2023-11, Vol.ahead-of-print (ahead-of-print), p.1-9

2023

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Das EEG bei Kindern mit Epilepsie

Das Neurophysiologie-Labor, 2015-09, Vol.37 (3), p.187-197

2015

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The severe epilepsy syndromes of infancy: A population‐based study

Epilepsia (Copenhagen), 2021-02, Vol.62 (2), p.358-370

2021

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Long‐term mortality of patients with West syndrome

Epilepsia open, 2016-09, Vol.1 (1-2), p.61-66

2016

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West syndrome and multiple sclerosis association

Romanian neurosurgery, 2023-06, Vol.37 (2)

2023

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Clinical phenotype and genotype of children with GABAA receptor α1 subunit gene-related epilepsy

Frontiers in neurology, 2022-07, Vol.13, p.941054-941054

2022

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The Utility of Genetic Testing in Infantile Epileptic Spasms Syndrome: A Step-Based Approach in the Next-Generation Sequencing Era

Pediatric neurology, 2024-08, Vol.157, p.100-107

2024

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Perceived efficacy of cannabidiol-enriched cannabis extracts for treatment of pediatric epilepsy: A potential role for infantile spasms and Lennox–Gastaut syndrome

Epilepsy & behavior, 2015-06, Vol.47, p.138-141

2015

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Hypoparathyroidism, sensorineural deafness, and renal dysplasia（HDR）syndrome accompanying severe developmental disorders with neurologic abnormalities during the neonatal period

Journal of Japan Society of Perinatal and Neonatal Medicine, 2023, Vol.59(2), pp.266-272

2023

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新生児期から神経学的異常を認めたHDR（hypoparathyroidism, sensorineural deafness, and renal dysplasia）症候群の1例

日本周産期・新生児医学会雑誌, 2023, Vol.59(2), pp.266-272

2023

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The underlying etiology of infantile spasms (West syndrome): Information from the International Collaborative Infantile Spasms Study (ICISS)

Epilepsia (Copenhagen), 2019-09, Vol.60 (9), p.1861-1869

2019

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Electroclinical Features of Infantile Epileptic Spasms Syndrome

Annals of the Indian Academy of Neurology, 2024-05, Vol.27 (3), p.227-235

2024

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Distribution of peripheral blood mononuclear cell subtypes in patients with West syndrome: Impact of synacthen treatment

Immunology letters, 2023-09, Vol.261, p.17-24

2023

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The Clinical Features and Long-Term Follow-Up of Vitamin B6-Responsive Infantile Spasms in a Chinese Cohort

Frontiers in neurology, 2022-05, Vol.13, p.895978-895978

2022

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Antiepileptogenic effects of rapamycin in a model of infantile spasms due to structural lesions

Epilepsia (Copenhagen), 2021-08, Vol.62 (8), p.1985-1999

2021

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Lennox‐Gastaut syndrome: A consensus approach to differential diagnosis

Epilepsia (Copenhagen), 2014-09, Vol.55 (s4), p.4-9

2014

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Computational EEG attributes predict response to therapy for epileptic spasms

Clinical neurophysiology, 2024-07, Vol.163, p.39-46

2024

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Neuronal Networks in West Syndrome as Revealed by Source Analysis and Renormalized Partial Directed Coherence

Brain topography, 2013-01, Vol.26 (1), p.157-170

2013

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Global and multi-partition local network analysis of scalp EEG in West syndrome before and after treatment

Neural networks, 2024-11, Vol.179, p.106540, Article 106540

2024

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Genetic heterogeneity in infantile spasms

Epilepsy research, 2019-10, Vol.156, p.106181-106181, Article 106181

2019

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A Novel PAFAH1B1 Splicing Variant Identified in a Patient with Classical Lissencephaly

Tokyo Women's Medical University Journal, 2020/12/25, Vol.4, pp.85-89

2020

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Electroclinical Landscape of Infantile Epileptic Spasms Syndrome

Indian journal of pediatrics, 2024-02

2024

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Electroencephalography complexity in infantile spasms and its association with treatment response

Clinical neurophysiology, 2021-02, Vol.132 (2), p.480-486

2021

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Quantitative pretreatment EEG predicts efficacy of ACTH therapy in infantile epileptic spasms syndrome

Clinical neurophysiology, 2022-12, Vol.144, p.83-90

2022

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The effectiveness and tolerability of clobazam in the pediatric population: Adjunctive therapy and monotherapy in a large-cohort multicenter study

Epilepsy research, 2022-08, Vol.184, p.106963-106963, Article 106963

2022

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Hypsarrhythmia paroxysm intensities that initiate and render physical and mental retardation irreversible in West syndrome

Das EEG bei Kindern mit Epilepsie

The severe epilepsy syndromes of infancy: A population‐based study

Long‐term mortality of patients with West syndrome

West syndrome and multiple sclerosis association

Clinical phenotype and genotype of children with GABAA receptor α1 subunit gene-related epilepsy

The Utility of Genetic Testing in Infantile Epileptic Spasms Syndrome: A Step-Based Approach in the Next-Generation Sequencing Era

Perceived efficacy of cannabidiol-enriched cannabis extracts for treatment of pediatric epilepsy: A potential role for infantile spasms and Lennox–Gastaut syndrome

Hypoparathyroidism, sensorineural deafness, and renal dysplasia（HDR）syndrome accompanying severe developmental disorders with neurologic abnormalities during the neonatal period

新生児期から神経学的異常を認めたHDR（hypoparathyroidism, sensorineural deafness, and renal dysplasia）症候群の1例

The underlying etiology of infantile spasms (West syndrome): Information from the International Collaborative Infantile Spasms Study (ICISS)

Electroclinical Features of Infantile Epileptic Spasms Syndrome

Distribution of peripheral blood mononuclear cell subtypes in patients with West syndrome: Impact of synacthen treatment

The Clinical Features and Long-Term Follow-Up of Vitamin B6-Responsive Infantile Spasms in a Chinese Cohort

Antiepileptogenic effects of rapamycin in a model of infantile spasms due to structural lesions

Lennox‐Gastaut syndrome: A consensus approach to differential diagnosis

Computational EEG attributes predict response to therapy for epileptic spasms

Neuronal Networks in West Syndrome as Revealed by Source Analysis and Renormalized Partial Directed Coherence

Global and multi-partition local network analysis of scalp EEG in West syndrome before and after treatment

Genetic heterogeneity in infantile spasms

A Novel PAFAH1B1 Splicing Variant Identified in a Patient with Classical Lissencephaly

Electroclinical Landscape of Infantile Epileptic Spasms Syndrome

Electroencephalography complexity in infantile spasms and its association with treatment response

Quantitative pretreatment EEG predicts efficacy of ACTH therapy in infantile epileptic spasms syndrome

The effectiveness and tolerability of clobazam in the pediatric population: Adjunctive therapy and monotherapy in a large-cohort multicenter study

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