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Juhani Rapola

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Juha Sinisalo; Juhani Rapola; Juhani Rossinen; Markku Kupari
Simplifying the estimation of jugular venous pressure.
Arvi-Matti Kuusniemi; Jussi Merenmies; Anne-Tiina Lahdenkari; Christer Holmberg; K Salmela; Riitta Karikoski; Juhani Rapola; Hannu Jalanko
Glomerular sclerosis in kidneys with congenital nephrotic syndrome (NPHS1).
Salli Virta; Juhani Rapola; Anu Jalanko; Minna Laine
Use of nonviral promoters in adenovirus-mediated gene therapy: reduction of lysosomal storage in the aspartylglucosaminuria mouse.

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All Publications

2007: Juha Sinisalo; Juhani Rapola; Juhani Rossinen; Markku Kupari
Simplifying the estimation of jugular venous pressure.
The American journal of cardiology 2007;100(12):1779-81.
2006: Arvi-Matti Kuusniemi; Jussi Merenmies; Anne-Tiina Lahdenkari; Christer Holmberg; K Salmela; Riitta Karikoski; Juhani Rapola; Hannu Jalanko
Glomerular sclerosis in kidneys with congenital nephrotic syndrome (NPHS1).
Kidney international 2006;70(8):1423-31.
2006: Salli Virta; Juhani Rapola; Anu Jalanko; Minna Laine
Use of nonviral promoters in adenovirus-mediated gene therapy: reduction of lysosomal storage in the aspartylglucosaminuria mouse.
The journal of gene medicine 2006;8(6):699-706.
2005: Arvi-Matti Kuusniemi; Risto Lapatto; Christer Holmberg; Riitta Karikoski; Juhani Rapola; Hannu Jalanko
Kidneys with heavy proteinuria show fibrosis, inflammation, and oxidative stress, but no tubular phenotypic change.
Kidney international 2005;68(1):121-32.
2005: Anu Jalanko; Jouni Vesa; Tuula Manninen; Carina von Schantz; Helena Minye; Anna-Liisa Fabritius; Tarja Salonen; Juhani Rapola; Massimiliano Gentile; Outi Kopra; Leena Peltonen
Mice with Ppt1Deltaex4 mutation replicate the INCL phenotype and show an inflammation-associated loss of interneurons.
Neurobiology of disease 2005;18(1):226-41.
2004: M Laine; Laura Ahtiainen; Juhani Rapola; J Richter; Anu Jalanko
Bone marrow transplantation in young aspartylglucosaminuria mice: improved clearance of lysosomal storage in brain by using wild type as compared to heterozygote donors.
Bone marrow transplantation 2004;34(11):1001-3.
2004: Outi Kopra; Jouni Vesa; Carina von Schantz; Tuula Manninen; Helena Minye; Anna-Liisa Fabritius; Juhani Rapola; Otto P van Diggelen; Janna Saarela; Anu Jalanko; Leena Peltonen
A mouse model for Finnish variant late infantile neuronal ceroid lipofuscinosis, CLN5, reveals neuropathology associated with early aging.
Human molecular genetics 2004;13(23):2893-906.
2003: Marita Lipsanen-Nyman; Jaakko Perheentupa; Juhani Rapola; Anssi Sovijärvi; Markku Kupari
Mulibrey heart disease: clinical manifestations, long-term course, and results of pericardiectomy in a series of 49 patients born before 1985.
Circulation 2003;107(22):2810-5.
2002: Pekka Lahdenne; Juhani Rapola; Heikki Ylijoki; Jarkko Haapasaari
Hepatotoxicity in patients with juvenile idiopathic arthritis receiving longterm methotrexate therapy.
The Journal of rheumatology 2002;29(11):2442-5.
2002: Jaakko Patrakka; Paula Martin; Riitta Salonen; Marjo Kestilä; Vesa Ruotsalainen; Minna Männikkö; Markku Ryynänen; Juhani Rapola; Christer Holmberg; Karl Tryggvason; Hannu Jalanko
Proteinuria and prenatal diagnosis of congenital nephrosis in fetal carriers of nephrin gene mutations.
Lancet 2002;359(9317):1575-7.
2002: Juhani Rapola; Päivi Heikkilä; Vineta Fellman
Pathology of lethal fetal growth retardation syndrome with aminoaciduria, iron overload, and lactic acidosis (GRACILE).
Pediatric pathology & molecular medicine 2002;21(2):183-93.
2002: Hannu Sariola; Jussi Huttunen; Markku Kaste; Marjatta Leirisalo-Repo; Pekka Lähteenmäki; Juhani Rapola; Kari Teramo
[Time is our most important capital].
Duodecim; lääketieteellinen aikakauskirja 2002;118(23):2357-9.
2001: Tuula Lönnqvist; Sanna-Leena Vanhanen; Kim Vettenranta; Taina Autti; Juhani Rapola; Pirkko Santavuori; Ulla M Saarinen-Pihkala
Hematopoietic stem cell transplantation in infantile neuronal ceroid lipofuscinosis.
Neurology 2001;57(8):1411-6.
2000: Jaakko Patrakka; Marjo Kestilä; Jorma Wartiovaara; Vesa Ruotsalainen; P Tissari; U Lenkkeri; Minna Männikkö; Ilona Visapää; Christer Holmberg; Juhani Rapola; Karl Tryggvason; Hannu Jalanko
Congenital nephrotic syndrome (NPHS1): features resulting from different mutations in Finnish patients.
Kidney international 2000;58(3):972-80.
2000: Mari Auranen; Juhani Rapola; Helena Pihko; Matti Haltia; Ilmo V V Leivo; Seppo Soinila; Ismo Virtanen; Hannu Kalimo; Louise V B Anderson; Pirkko Santavuori; Hannu Somer
Muscle membrane-skeleton protein changes and histopathological characterization of muscle-eye-brain disease.
Neuromuscular disorders : NMD 2000;10(1):16-23.
1999: Taina Autti; Juhani Rapola; Pirkko Santavuori; Raili Raininko; Martin Renlund; Elina Liukkonen; Leena Lauronen; Kari O Wirtavuori; M Hietala; Ulla M Saarinen-Pihkala
Bone marrow transplantation in aspartylglucosaminuria--histopathological and MRI study.
Neuropediatrics 1999;30(6):283-8.
1999: M Laine; J Richter; C Fahlman; Juhani Rapola; Martin Renlund; Leena Peltonen; S Karlsson; Anu Jalanko
Correction of peripheral lysosomal accumulation in mice with aspartylglucosaminuria by bone marrow transplantation.
Experimental hematology 1999;27(9):1467-74.
1999: Nina Linder; Juhani Rapola; Kari O Raivio
Cellular expression of xanthine oxidoreductase protein in normal human tissues.
Laboratory investigation; a journal of technical methods and pathology 1999;79(8):967-74.
1999: Juhani Rapola; Jaana Lähdetie; Juha Isosomppi; P Helminen; Maila Penttinen; Irma Järvelä
Prenatal diagnosis of variant late infantile neuronal ceroid lipofuscinosis (vLINCL[Finnish]; CLN5).
Prenatal diagnosis 1999;19(7):685-8.
1999: Sirpa Ala-Mello; Olli Koskimies; Juhani Rapola; Helena Kääriäinen
Nephronophthisis in Finland: epidemiology and comparison of genetically classified subgroups.
European journal of human genetics : EJHG 1999;7(2):205-11.
1998: M Peltola; Aija Kyttälä; Outi Kopra; Juhani Rapola; Tiina Paunio; F Revah; Leena Peltonen; Anu Jalanko
Adenovirus-mediated gene transfer results in decreased lysosomal storage in brain and total correction in liver of aspartylglucosaminuria (AGU) mouse.
Gene therapy 1998;5(10):1314-21.
1998: Juhani Rapola; Jarmo Virtamo; Samuli Ripatti; Jari Haukka; Juha Huttunen; Demetrius Albanes; Philip R Taylor; OP Heinonen
Effects of alpha tocopherol and beta carotene supplements on symptoms, progression, and prognosis of angina pectoris.
Heart (British Cardiac Society) 1998;79(5):454-8.
1998: Jarmo Virtamo; Juhani Rapola; Samuli Ripatti; OP Heinonen; Philip R Taylor; Demetrius Albanes; Juha Huttunen
Effect of vitamin E and beta carotene on the incidence of primary nonfatal myocardial infarction and fatal coronary heart disease.
Archives of internal medicine 1998;158(6):668-75.
1998: Laura E Aberg; Irma Järvelä; Juhani Rapola; Taina Autti; Erika Kirveskari; Marjatta Lappi; L Sipilä; Pirkko Santavuori
Atypical juvenile neuronal ceroid lipofuscinosis with granular osmiophilic deposit-like inclusions in the autonomic nerve cells of the gut wall.
Acta neuropathologica 1998;95(3):306-12.
1998: Vineta Fellman; Juhani Rapola; Helena Pihko; Teppo Varilo; Kari O Raivio
Iron-overload disease in infants involving fetal growth retardation, lactic acidosis, liver haemosiderosis, and aminoaciduria.
Lancet 1998;351(9101):490-3.
1998: JM Teikari; Leila Laatikainen; Juhani Rapola; Jarmo Virtamo; Jari Haukka; K Liesto; P Taylor; OP Heinonen
Retinal vascular changes following supplementation with alpha-tocopherol or beta-carotene.
Acta ophthalmologica Scandinavica 1998;76(1):68-73.
1998: Anu Jalanko; K Tenhunen; CE McKinney; Mary E LaMarca; Juhani Rapola; Taina Autti; Raimo Joensuu; Tuula Manninen; I Sipilä; S Ikonen; P Riekkinen; Edward I Ginns; Leena Peltonen
Mice with an aspartylglucosaminuria mutation similar to humans replicate the pathophysiology in patients.
Human molecular genetics 1998;7(2):265-72.
1997: Tiina Tyni; Juhani Rapola; A Palotie; Helena Pihko
Hypoparathyroidism in a patient with long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency caused by the G1528C mutation.
The Journal of pediatrics 1997;131(5):766-8.
1997: Juhani Rapola; Jarmo Virtamo; Samuli Ripatti; Juha Huttunen; Demetrius Albanes; Philip R Taylor; OP Heinonen
Randomised trial of alpha-tocopherol and beta-carotene supplements on incidence of major coronary events in men with previous myocardial infarction.
Lancet 1997;349(9067):1715-20.
1997: Taina Autti; Pirkko Santavuori; Raili Raininko; Martin Renlund; Juhani Rapola; Ulla M Saarinen-Pihkala
Bone-marrow transplantation in aspartylglucosaminuria.
Lancet 1997;349(9062):1366-7.
1997: Tiina Tyni; Juhani Rapola; Anders Paetau; A Palotie; Helena Pihko
Pathology of long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency caused by the G1528C mutation.
Pediatric pathology & laboratory medicine : journal of the Society for Pediatric Pathology, affiliated with the International Paediatric Pathology Association 1997;17(3):427-47.
1997: Juhani Rapola; Jarmo Virtamo; Pasi Korhonen; J Haapakoski; Anne M Hartman; Brenda K Edwards; OP Heinonen
Validity of diagnoses of major coronary events in national registers of hospital diagnoses and deaths in Finland.
European journal of epidemiology 1997;13(2):133-8.
1996: Tiina Tyni; A Majander; Hannu Kalimo; Juhani Rapola; Helena Pihko
Pathology of skeletal muscle and impaired respiratory chain function in long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency with the G1528C mutation.
Neuromuscular disorders : NMD 1996;6(5):327-37.
1996: Juhani Rapola; Jarmo Virtamo; Jari Haukka; OP Heinonen; Demetrius Albanes; P R Taylor; J K Huttunen
Effect of vitamin E and beta carotene on the incidence of angina pectoris. A randomized, double-blind, controlled trial.
JAMA : the journal of the American Medical Association 1996;275(9):693-8.
1995: A Majander; Juhani Rapola; Hannu Sariola; Anu Suomalainen; Maija Pohjavuori; Helena Pihko
Diagnosis of fatal infantile defects of the mitochondrial respiratory chain: age dependence and postmortem analysis of enzyme activities.
Journal of the neurological sciences 1995;134(1-2):95-102.
1993: Juhani Rapola; R Salonen; P Ammälä; Pirkko Santavuori
Prenatal diagnosis of infantile neuronal ceroid-lipofuscinosis, INCL: morphological aspects.
Journal of inherited metabolic disease 1993;16(2):349-52.
1993: Pirkko Santavuori; Juhani Rapola; Raili Raininko; Taina Autti; Marjatta Lappi; A Nuutila; Jyrki Launes; Kirsi Sainio
Early juvenile neuronal ceroid-lipofuscinosis or variant Jansky-Bielschowsky disease: diagnostic criteria and nomenclature.
Journal of inherited metabolic disease 1993;16(2):230-2.
1993: Juhani Rapola
Neuronal ceroid-lipofuscinoses in childhood.
Perspectives in pediatric pathology 1993;17():7-44.
1991: Juhani Rapola; Irma Järvelä; Leena Peltonen
The neuronal ceroid lipofuscinoses: unfolding the genetic defect.
Pediatric pathology / affiliated with the International Paediatric Pathology Association 1991;11(6):799-806.
1991: Pirkko Santavuori; Juhani Rapola; A Nuutila; Raili Raininko; Marjatta Lappi; Jyrki Launes; Riitta Herva; Kirsi Sainio
The spectrum of Jansky-Bielschowsky disease.
Neuropediatrics 1991;22(2):92-6.
1990: Carina Wallgren-Pettersson; Helena Kääriäinen; Juhani Rapola; T Salmi; Juha Jääskeläinen; M Donner
Genetics of congenital nemaline myopathy: a study of 10 families.
Journal of medical genetics 1990;27(8):480-7.
1990: Anna-Elina Lehesjoki; Eeva-Marja Sankila; J Miao; Mirja Somer; R Salonen; Juhani Rapola; Albert de La Chapelle
X linked neonatal myotubular myopathy: one recombination detected with four polymorphic DNA markers from Xq28.
Journal of medical genetics 1990;27(5):288-91.
1990: Harry Holthöfer; T Kumpulainen; Juhani Rapola
Polycystic disease of the kidney. Evaluation and classification based on nephron segment and cell-type specific markers.
Laboratory investigation; a journal of technical methods and pathology 1990;62(3):363-9.
1989: M Lindlöf; A Kiuru; Helena Kääriäinen; Hannu Kalimo; H Lang; Helena Pihko; Juhani Rapola; Hannu Somer; Mirja Somer; Marja-Liisa Savontaus
Gene deletions in X-linked muscular dystrophy.
American journal of human genetics 1989;44(4):496-503.
1989: Juhani Rapola
Kidneys in Meckel's syndrome as a model of abnormal renal differentiation.
The International journal of developmental biology 1989;33(1):177-82.
1989: Pirkko Santavuori; Hannu Somer; Kirsi Sainio; Juhani Rapola; S Kruus; T Nikitin; L Ketonen; J Leisti
Muscle-eye-brain disease (MEB)
Brain & development 1989;11(3):147-53.
1988: Carina Wallgren-Pettersson; Juhani Rapola; M Donner
Pathology of congenital nemaline myopathy. A follow-up study.
Journal of the neurological sciences 1988;83(2-3):243-57.
1988: Juhani Rapola; Pirkko Santavuori; Hannu Heiskala
Placental pathology and prenatal diagnosis of infantile type of neuronal ceroid-lipofuscinosis.
American journal of medical genetics. Supplement 1988;5():99-103.
1985: Pirkko Santavuori; Tuomas Westermarck; Juhani Rapola; P Pohja; R Moren; Marjatta Lappi; U Vuonnala
Antioxidant treatment in Spielmeyer-Sjögren's disease.
Acta neurologica Scandinavica 1985;71(2):136-45.