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Publications by S. Finnila

Increased Risk of Sensorineural Hearing Loss and Migraine in Patients With a Rare Mitochondrial DNA Variant 4336A>G in tRNAGln

Journal of Medical Genetics
Genetics
2001English

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Lack of a Modulative Factor in Locus 8p23 in a Finnish Family With Nonsyndromic Sensorineural Hearing Loss Associated With the 1555A>G Mitochondrial DNA Mutation

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Mean Platelet Volume in Patients With Sensorineural Hearing Loss

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Frequency and Clinical Features of Patients With Sensorineural Hearing Loss Associated With the A3243G Mutation of the Mitochondrial DNA in Otorhinolaryngic Clinics

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Non Infectious Risk Factors in Pediatric Sensorineural Hearing Loss

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Sensorineural Hearing Loss

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