The grainyhead like 2 gene (GRHL2), alias TFCP2L3, is associated with age-related hearing impairment (2008)
VAN LAER, L,
VAN EYKEN, E,
FRANSEN, E,
HUYGHE, JOKE,
TOPSAKAL, V,
HENDRICKX, JJ,
...
Contribution of the N-acetyltransferase 2 polymorphism NAT2*6A to age-related hearing impairment (2007)
VAN EYKEN, E,
VAN CAMP, G,
FRANSEN, E,
TOPSAKAL, V,
HENDRICKX, JJ,
DEMEESTER, K,
...
The contribution of GJB2 (Connexin 26) 35delG to age-related hearing impairment and noise-induced hearing loss (2007)
VAN EYKEN, E,
VAN LAER, L,
FRANSEN, E,
TOPSAKAL, V,
HENDRICKX, JJ,
DEMEESTER, K,
...
Familial aggregation of tinnitus: a European multicentre study (2007)
Huyghe, J. R.,
Demeester, K.,
Topsakal, V.,
Van Eyken, E.,
Fransen, E.,
...
Introduction and aim: Tinnitus is a common condition affecting approximately 20% of the older population. There is increasing evidence that changes in the central auditory system following cochlear...
Parents' views on the quality of life of their children 2 to 3 years after cochlear implantation (2005)
Huttunen, K.,
Riammanen, S.,
Vikman, S.,
Virokannas, N.,
Sorri, M.,
Archbold, S.M.,
...
Epidemiology of A3243G, the mutation for mitochondrial encephalomyopathy, lactic acidosis, and strokelike episodes: prevalence of the mutation in an adult population.
Majamaa, K,
Moilanen, J S,
Uimonen, S,
Remes, A M,
Salmela, P I,
Kärppä, M,
...
Mitochondrial diseases are characterized by considerable clinical variability and are most often caused by mutations in mtDNA. Because of the phenotypic variability, epidemiological studies of the...
Epidemiology of A3243G, the mutation for mitochondrial encephalomyopathy, lactic acidosis, and strokelike episodes: prevalence of the mutation in an adult population.
Majamaa, K,
Moilanen, J S,
Uimonen, S,
Remes, A M,
Salmela, P I,
Kärppä, M,
...
Mitochondrial diseases are characterized by considerable clinical variability and are most often caused by mutations in mtDNA. Because of the phenotypic variability, epidemiological studies of the...
Epidemiology of the mitochondrial DNA 8344A>G mutation for the myoclonus epilepsy and ragged red fibres (MERRF) syndrome
Remes, A,
Karppa, M,
Rusanen, H,
Majamaa, K,
Hassinen, I,
Moilanen, J,
...
Symptoms and diagnostic delay in patients with carcinoma of oesophagus and gastric cardia: a retrospective study of 225 patients
Ojala, K.,
Sorri, M.,
Jokinen, K.,
Kairaluoma, M. I.
A retrospective review of 225 patients was made with regard to the symptoms of carcinoma of the oesophagus and gastric cardia, and the duration of the symptoms before medical attention was sought and...