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Genetic Epilepsy with Febrile Seizures Plus Latest Advances
Find the Latest Research About Genetic Epilepsy with Febrile Seizures Plus
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Last Updated : 05/19/2022
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Found 34 publications
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Sodium voltage-gated channel alpha subunit 9 mutation in epilepsy.
Journal:
European review for medical and pharmacological sciences
Published:
January 04, 2022
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Summary:
Sodium voltage-gated channel alpha subunit 9 mutation in epilepsy.
Evaluation of risk factors associated with first episode febrile seizure.
Journal:
European review for medical and pharmacological sciences
Published:
December 03, 2021
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Summary:
Evaluation of risk factors associated with first episode febrile seizure.
A novel de novo hemizygous ARHGEF9 mutation associated with severe intellectual disability and epilepsy: a case report.
Journal:
The Journal of international medical research
Published:
December 01, 2021
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Summary:
A novel de novo hemizygous ARHGEF9 mutation associated with severe intellectual disability and epilepsy: a case report.
A case of 16p13.11 microdeletion syndrome with febrile convulsion as the main manifestation.
Journal:
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published:
October 09, 2021
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Summary:
A case of 16p13.11 microdeletion syndrome with febrile convulsion as the main manifestation.
No association between children's febrile seizures and S100B protein levels: A meta-analysis.
Journal:
Seizure
Published:
September 15, 2021
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Summary:
No association between children's febrile seizures and S100B protein levels: A meta-analysis.
Inpatient medical cost of status epilepticus in children: A national-wide, multicenter study from China.
Journal:
Epilepsy & behavior : E&B
Published:
August 29, 2021
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Summary:
Inpatient medical cost of status epilepticus in children: A national-wide, multicenter study from China.
Breastmilk Feeding during the First 4 to 6 Months of Age and Childhood Disease Burden until 10 Years of Age.
Journal:
Nutrients
Published:
August 27, 2021
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Summary:
Breastmilk Feeding during the First 4 to 6 Months of Age and Childhood Disease Burden until 10 Years of Age.
Genetic analysis of a case with MEF2C deletion in association with 5q14.3 microdeletion syndrome.
Journal:
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published:
August 08, 2021
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Summary:
Genetic analysis of a case with MEF2C deletion in association with 5q14.3 microdeletion syndrome.
Analysis of clinical phenotype and SCN1A gene variant in a pedigree affected with genetic epilepsy with febrile seizures.
Journal:
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published:
August 08, 2021
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Summary:
Analysis of clinical phenotype and SCN1A gene variant in a pedigree affected with genetic epilepsy with febrile seizures.
Zinc Supplementation for Prevention of Febrile Seizures Recurrences in Children: A Systematic Review and Meta-Analysis.
Condition:
Prevention of Febrile Seizures Recurrences in Children
Journal:
Indian pediatrics
Treatment Used:
Zinc Supplementation
Number of Patients:
350
Published:
August 02, 2021
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Summary:
Zinc Supplementation for Prevention of Febrile Seizures Recurrences in Children: A Systematic Review and Meta-Analysis.
Therapeutic plasma exchange in clinical pediatric neurology practice: Experience from a tertiary referral hospital.
Condition:
Children with Neuroimmunological Disorders
Journal:
Clinical neurology and neurosurgery
Treatment Used:
Therapeutic Plasma Exchange (TPE)
Number of Patients:
23
Published:
July 25, 2021
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Summary:
Therapeutic plasma exchange in clinical pediatric neurology practice: Experience from a tertiary referral hospital.
Improving early diagnosis of rare diseases using Natural Language Processing in unstructured medical records: an illustration from Dravet syndrome.
Journal:
Orphanet journal of rare diseases
Published:
July 14, 2021
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Summary:
Improving early diagnosis of rare diseases using Natural Language Processing in unstructured medical records: an illustration from Dravet syndrome.
Showing 1-12 of 34
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Last Updated : 05/19/2022