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Developmental Neuroscience|January 1, 1991
Sialic acid storage disorders: observations on clinical and biochemical variationG M Mancini, F W Verheijen, C E Beerens, et al.Human Genetics|October 1, 1993
The spectrum of mitochondrial DNA mutations in families with Leber hereditary optic neuroretinopathyK Huoponen, T Lamminen, V Juvonen, et al.Human Mutation|January 1, 1997
Tissue distribution of the ND4/11778 mutation in heteroplasmic lineages with Leber hereditary optic neuropathyV Juvonen, E Nikoskelainen, T Lamminen, et al.Clinical Genetics|October 1, 1985
Norrie disease caused by a gene deletion allowing carrier detection and prenatal diagnosisA de la Chapelle, E M Sankila, M Lindlöf, et al.The Journal of Pediatrics|November 1, 1979
Microscopic hematuria in school children: epidemiology and clinicopathologic evaluationV M Vehaskari, J Rapola, O Koskimies, et al.Acta Chirurgica Scandinavica|January 1, 1986
C-reactive protein compared with white blood cell count and erythrocyte sedimentation rate in the diagnosis of acute appendicitis in childrenH Peltola, J Ahlqvist, J Rapola, et al.Life Sciences|January 1, 1990
Elevated levels of serum dolichol in aspartylglucosaminuriaM Salaspuro, K Salmela, K Humaloja, et al.APMIS : Acta Pathologica, Microbiologica, Et Immunologica Scandinavica|February 1, 1994
Pathology of renal arteries of dyslipidemic children with congenital nephrosisM Antikainen, H Sariola, J Rapola, et al.Ophthalmologica. Journal International D'Ophtalmologie. International Journal of Ophthalmology. Zeitschrift Fur Augenheilkunde|January 1, 1984
Orbital granulocytic sarcoma as a presenting sign in acute myelogenous leukemiaJ Rajantie, A Tarkkanen, J Rapola, et al.Journal of Medical Genetics|August 1, 1990
Genetics of congenital nemaline myopathy: a study of 10 familiesC Wallgren-Pettersson, H Kääriäinen, J Rapola, et al.Pageof 27