Found: 6
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Incidence of Childhood Epilepsy in Estonia.
- Published in:
- Journal of Child Neurology, 2018, v. 33, n. 9, p. 587, doi. 10.1177/0883073818776760
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- Article
Biallelic CACNA1A mutations cause early onset epileptic encephalopathy with progressive cerebral, cerebellar, and optic nerve atrophy.
- Published in:
- American Journal of Medical Genetics. Part A, 2016, v. 170A, n. 8, p. 2173, doi. 10.1002/ajmg.a.37678
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- Article
A patient with the classic features of Phelan-McDermid syndrome and a high immunoglobulin E level caused by a cryptic interstitial 0.72-Mb deletion in the 22q13.2 region.
- Published in:
- American Journal of Medical Genetics. Part A, 2014, v. 164A, n. 3, p. 806, doi. 10.1002/ajmg.a.36358
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- Article
Coffin-Siris Syndrome with obesity, macrocephaly, hepatomegaly and hyperinsulinism caused by a mutation in the ARID1B gene.
- Published in:
- European Journal of Human Genetics, 2014, v. 22, n. 11, p. 1327, doi. 10.1038/ejhg.2014.25
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- Article
Epilepsy after perinatal stroke with different vascular subtypes.
- Published in:
- Epilepsia Open, 2018, v. 3, n. 2, p. 193, doi. 10.1002/epi4.12104
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- Article
The Birth Prevalence of Spinal Muscular Atrophy: A Population Specific Approach in Estonia.
- Published in:
- Frontiers in Genetics, 2021, v. 12, p. 1, doi. 10.3389/fgene.2021.796862
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- Article