Found: 30
Select item for more details and to access through your institution.
Incidence of epilepsy in children born prematurely and small for gestational age at term gestation: A population-based cohort study.
- Published in:
- 2020
- By:
- Publication type:
- journal article
Association of poly(ADP-ribose) polymerase-1 polymorphism with Tourette syndrome.
- Published in:
- Neurological Sciences, 2013, v. 34, n. 11, p. 1911, doi. 10.1007/s10072-013-1405-x
- By:
- Publication type:
- Article
Clinical spectrum and the comorbidities of Dravet syndrome in Taiwan and the possible molecular mechanisms.
- Published in:
- Scientific Reports, 2021, v. 11, n. 1, p. 1, doi. 10.1038/s41598-021-98517-4
- By:
- Publication type:
- Article
Epilepsy and Neurodevelopmental Outcomes in Children With Etiologically Diagnosed Central Nervous System Infections: A Retrospective Cohort Study.
- Published in:
- Frontiers in Neurology, 2019, p. N.PAG, doi. 10.3389/fneur.2019.00528
- By:
- Publication type:
- Article
Bidirectional relation between schizophrenia and epilepsy: A population-based retrospective cohort study.
- Published in:
- Epilepsia (Series 4), 2011, v. 52, n. 11, p. 2036, doi. 10.1111/j.1528-1167.2011.03268.x
- By:
- Publication type:
- Article
Association of the Neuronal Nicotinic Acetylcholine Receptor Subunit α4 Polymorphisms with Febrile Convulsions.
- Published in:
- Epilepsia (Series 4), 2003, v. 44, n. 8, p. 1089, doi. 10.1046/j.1528-1157.2003.t01-1-44702.x
- By:
- Publication type:
- Article
Clinical Features and Vaccination Effects among Children with Post-Acute Sequelae of COVID-19 in Taiwan.
- Published in:
- Vaccines, 2024, v. 12, n. 8, p. 910, doi. 10.3390/vaccines12080910
- By:
- Publication type:
- Article
Is Preterm Birth a Risk Factor for Subsequent Autism Spectrum Disorder and Attention Deficit Hyperactivity Disorder in Children with Febrile Seizure?—A Retrospective Study.
- Published in:
- Life (2075-1729), 2021, v. 11, n. 8, p. 854, doi. 10.3390/life11080854
- By:
- Publication type:
- Article
FOXL2 mutations in Taiwanese patients with blepharophimosis, ptosis, epicanthus inversus syndrome.
- Published in:
- Clinical Chemistry & Laboratory Medicine, 2010, v. 48, n. 4, p. 485, doi. 10.1515/CCLM.2010.100
- By:
- Publication type:
- Article
Acupuncture Treatment is Associated with Reduced Dementia Risk in Patients with Migraine: A Propensity-Score–Matched Cohort Study of Real-World Data.
- Published in:
- Neuropsychiatric Disease & Treatment, 2022, v. 18, p. 1895, doi. 10.2147/NDT.S372076
- By:
- Publication type:
- Article
Genetic and clinical profiles of spondylocostal dysostosis patients in Taiwan.
- Published in:
- American Journal of Medical Genetics. Part A, 2011, v. 155A, n. 12, p. 3132, doi. 10.1002/ajmg.a.34301
- By:
- Publication type:
- Article
The intriguing relationship between epilepsy and type 1 diabetes mellitus. Reply to Sander JW, Novy J, Keezer MR [letter].
- Published in:
- 2016
- By:
- Publication type:
- Letter
Risk of epilepsy in type 1 diabetes mellitus: a population-based cohort study.
- Published in:
- Diabetologia, 2016, v. 59, n. 6, p. 1196, doi. 10.1007/s00125-016-3929-0
- By:
- Publication type:
- Article
Correlation between Epilepsy and Attention Deficit Hyperactivity Disorder: A Population-Based Cohort Study.
- Published in:
- PLoS ONE, 2013, v. 8, n. 3, p. 1, doi. 10.1371/journal.pone.0057926
- By:
- Publication type:
- Article
Attention-deficit-hyperactivity disorder increases risk of bone fracture: a population-based cohort study.
- Published in:
- Developmental Medicine & Child Neurology, 2014, v. 56, n. 11, p. 1111, doi. 10.1111/dmcn.12501
- By:
- Publication type:
- Article
Regression of Neonatal Cardiac Rhabdomyoma in Two Months Through Low-Dose Everolimus Therapy: A Report of Three Cases.
- Published in:
- Pediatric Cardiology, 2017, v. 38, n. 7, p. 1478, doi. 10.1007/s00246-017-1688-4
- By:
- Publication type:
- Article
Menarche—a journey into womanhood: age at menarche and health-related outcomes in East Asians.
- Published in:
- Human Reproduction, 2024, v. 39, n. 6, p. 1336, doi. 10.1093/humrep/deae060
- By:
- Publication type:
- Article
Epileptic spasms in PPP1CB-associated Noonan-like syndrome: a case report with clinical and therapeutic implications.
- Published in:
- 2018
- By:
- Publication type:
- journal article
Genetic Testing in Children with Developmental and Epileptic Encephalopathies: A Review of Advances in Epilepsy Genomics.
- Published in:
- Children, 2023, v. 10, n. 3, p. 556, doi. 10.3390/children10030556
- By:
- Publication type:
- Article
Association of Tyrosyl-DNA Phosphodiesterase 1 Polymorphism With Tourette Syndrome in Taiwanese Patients.
- Published in:
- Journal of Clinical Laboratory Analysis, 2013, v. 27, n. 4, p. 323, doi. 10.1002/jcla.21606
- By:
- Publication type:
- Article
Association of Genetic Variations in X-Ray Repair Cross-Complementing Group 1 and Tourette Syndrome.
- Published in:
- Journal of Clinical Laboratory Analysis, 2012, v. 26, n. 5, p. 321, doi. 10.1002/jcla.21525
- By:
- Publication type:
- Article
Interleukin (IL)-1beta, IL-1 receptor antagonist, IL-6, IL-8, IL-10, and tumor necrosis factor alpha gene polymorphisms in patients with febrile seizures.
- Published in:
- 2010
- By:
- Publication type:
- journal article
Interleukin (IL)-1β, IL-1 receptor antagonist, IL-6, IL-8, IL-10, and tumor necrosis factor α gene polymorphisms in patients with febrile seizures.
- Published in:
- Journal of Clinical Laboratory Analysis, 2010, v. 24, n. 3, p. 154, doi. 10.1002/jcla.20374
- By:
- Publication type:
- Article
Association of idiopathic generalized epilepsy with polymorphisms in the neuronal nicotinic acetylcholine receptor subunits.
- Published in:
- Journal of Clinical Laboratory Analysis, 2007, v. 21, n. 2, p. 67, doi. 10.1002/jcla.20155
- By:
- Publication type:
- Article
Association Between Kawasaki Disease and Childhood Epilepsy: A Nationwide Cohort Study in Taiwan.
- Published in:
- Frontiers in Neurology, 2021, v. 11, p. N.PAG, doi. 10.3389/fneur.2021.627712
- By:
- Publication type:
- Article
A novel one-base insertion mutation in the retinitis pigmentosa 2 gene in a large X-linked Taiwanese family.
- Published in:
- Acta Ophthalmologica (1755375X), 2014, v. 92, n. 2, p. e161, doi. 10.1111/aos.12226
- By:
- Publication type:
- Article
Heterogeneous neurodevelopmental disorders in children with Kawasaki disease: what is new today?
- Published in:
- 2019
- By:
- Publication type:
- journal article
Genetic predisposition to bone mineral density and their health conditions in East Asians.
- Published in:
- Journal of Bone & Mineral Research, 2024, v. 39, n. 7, p. 929, doi. 10.1093/jbmr/zjae078
- By:
- Publication type:
- Article
Whole exome sequencing in Dandy-Walker variant with intellectual disability reveals an activating CIP2A mutation as novel genetic cause.
- Published in:
- Neurogenetics, 2018, v. 19, n. 3, p. 157, doi. 10.1007/s10048-018-0548-6
- By:
- Publication type:
- Article
Early versus late diagnosis of LAMA2 congenital muscular dystrophy: a distinct consequence.
- Published in:
- Egyptian Journal of Neurology, Psychiatry & Neurosurgery, 2024, v. 60, n. 1, p. 1, doi. 10.1186/s41983-023-00777-6
- By:
- Publication type:
- Article