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316 results on '"Kälviäinen, R."'

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1. New insights into the genetic etiology of Alzheimer's disease and related dementias

2. Providing Quality Care for People with CDKL5 Deficiency Disorder (CDD): An Expert Panel Opinion on the European Patient Journey.

3. Preoperative Clinical Evaluation, Outline of Surgical Technique and Outcome in Temporal Lobe Epilepsy

4. Topographic divergence of atypical cortical asymmetry and atrophy patterns in temporal lobe epilepsy

6. Exome sequencing reveals predominantly de novo variants in disorders with intellectual disability (ID) in the founder population of Finland

17. Analysis of shared heritability in common disorders of the brain

18. Structural brain abnormalities in the common epilepsies assessed in a worldwide ENIGMA study

21. Long-Term TGB Monotherapy.

24. Analysis of shared heritability in common disorders of the brain

25. Tuberoosiskleroosi - suomalainen diagnoosi- ja seurantasuositus

28. Brain hub - digital healthcare services to patients with brain diseases, citizens and professionals

31. Common genetic variation and susceptibility to partial epilepsies: a genome-wide association study

32. PP6.7 – 1623 Acute liver failure in patients with POLG1 mutations after valproate exposure and their prognosis after liver transplantation

33. Visual field defects with vigabatrin: epidemiology and therapeutic implications.

40. Comparison of [18F]FDG-PET, [99mTc]-HMPAO-SPECT, and [123I]-iomazenil-SPECT in localising the epileptogenic cortex.

47. Auditory P300 in untreated epilepsy

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