Eila Airaksinen - Concepedia

Author

Eila Airaksinen

Kuopio University Hospital

Also Known As

EILA M. AIRAKSINEN, Eila Airaksinen, Eila M. Airaksinen

Publications

793

Citations

H-Index

Concepts

All Affiliations

Kuopio University Hospital University of Eastern Finland University of Helsinki Antwerp University Hospital University of Antwerp

About

Eila Airaksinen is an author at Kuopio University Hospital specializing in medicine, social sciences, and pediatrics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	7	7	420
2	Social Sciences	5	5	364
3	Public Health	3	3	75
4	Behavioral Sciences	1	1	15
5	Child Development	1	1	15

Eila Airaksinen

Publications

766

Citations

H-Index

Page 1

	Year	Citations
Mutations in SEPT9 cause hereditary neuralgic amyotrophy Gregor Kuhlenbäumer, Mark Hannibal, Eva Nelis, Nature Genetics Neurodegenerative DiseasesAmyotrophic Lateral SclerosisMolecular NeuroscienceGenetic DisorderGenetics	2005	259
Dual cerebral processing of elementary auditory input in children Jari Karhu, Eila Herrgård, Ari Pääkkönen, Neuroreport	1997	79
A Population‐Based Study on Epilepsy in Mentally Retarded Children Eila Airaksinen, Riitta Matilainen, Tarja Mononen, Epilepsia	2000	65
Histamine in Cerebrospinal Fluid of Children with Febrile Convulsions Tuula Kiviranta, Leena Tuomisto, Eila Airaksinen Epilepsia	1995	51
Clinical Spectrum and Diagnostic Difficulties of Infantile Ponto-Cerebellar Hypoplasia Type 1 F. Muntoni, Fiona Goodwin, Caroline A. Sewry, Neuropediatrics	1999	37
Uptake of Taurine, GAB A, 5‐HT, and Dopamine by Blood Platelets in Progressive Myoclonus Epilepsy Eila Airaksinen Epilepsia Progressive Myoclonus EpilepsyClinical NeurosciencePharmacotherapySocial SciencesNeurobiology Of Disease	1979	36
High prevalence of aspartylglycosaminuria among school-age children in eastern Finland Tarja Mononen, Ilkka Mononen, Riitta Matilainen, Human Genetics Population ChildrenClinical EpidemiologyPediatricsHigh PrevalencePediatric Gastroenterology	1991	35
West syndrome: individualized ACTH therapy Hannu Heiskala, Raili Riikonen, Pirkko Santavuori, Brain and Development Down SyndromeWest SyndromePediatric EndocrinologyStereotypic Movement DisorderMedicine	1996	35
Genetic refinement of the hereditary neuralgic amyotrophy (HNA) locus at chromosome 17q25 Jan Meuleman, Gregor Kuhlenbäumer, Anja Schirmacher, European Journal of Human Genetics Neurodegenerative DiseasesMolecular NeuroscienceHereditary Neuralgic AmyotrophyChromosome 17Q25Genetic Disorder	1999	30
Osmolality and electrolytes in cerebrospinal fluid and serum of febrile children with and without seizures T Kiviranta, Leena Tuomisto, Eila Airaksinen European Journal of Pediatrics Electrolyte DisorderPediatric HydrocephalusCerebrospinal FluidPhysiologyFebrile Children	1996	26

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