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A simple blood test expedites the diagnosis of glucose transporter type 1 deficiency syndrome.
- Published in:
- 2017
- By:
- Publication type:
- journal article
A de novo 10p11.23-p12.1 deletion recapitulates the phenotype observed in WAC mutations and strengthens the role of WAC in intellectual disability and behavior disorders.
- Published in:
- American Journal of Medical Genetics. Part A, 2016, v. 170A, n. 7, p. 1912, doi. 10.1002/ajmg.a.37686
- By:
- Publication type:
- Article
Sleep architecture impairment in epileptic children and putative role of anti epileptic drugs.
- Published in:
- Neurological Sciences, 2013, v. 34, n. 1, p. 57, doi. 10.1007/s10072-012-0971-7
- By:
- Publication type:
- Article