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Randomised trial of α-tocopherol and β-carotene supplements on incidence of major coronary events in men with previous myocardial infarction

The Lancet (British edition), 1997-06, Vol.349 (9067), p.1715-1720

1997

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Severe heart failure and rhabdomyolysis associated with propofol infusion in a burn patient

Journal of burn care & research, 2014-09, Vol.35 (5), p.e364-e367

2014

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Transaortic Transcatheter Aortic Valve Implantation as a second choice over the Transapical access

Scandinavian journal of surgery, 2016-03, Vol.105 (1), p.35-41

2016

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Glomerular sclerosis in kidneys with congenital nephrotic syndrome (NPHS1)

Kidney international, 2006-10, Vol.70 (8), p.1423-1431

2006

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Effects of α tocopherol and β carotene supplements on symptoms, progression, and prognosis of angina pectoris

Heart (British Cardiac Society), 1998-05, Vol.79 (5), p.454-458

1998

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Validity of Diagnoses of Major Coronary Events in National Registers of Hospital Diagnoses and Deaths in Finland

European journal of epidemiology, 1997-02, Vol.13 (2), p.133-138

1997

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Hematopoietic stem cell transplantation in infantile neuronal ceroid lipofuscinosis

Neurology, 2001-10, Vol.57 (8), p.1411-1416

2001

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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 (Basingstoke), 2004-12, Vol.34 (11), p.1001-1003

2004

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Immunohistochemical spectrum of rhabdomyosarcoma and rhabdomyosarcoma-like tumors. Expression of cytokeratin and the 68-kD neurofilament protein

The American journal of surgical pathology, 1989-02, Vol.13 (2), p.120-132

1989

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Lysosomal Storage Diseases in Adults

Pathology, research and practice, 1994-09, Vol.190 (8), p.759-766

Rapola, J.

1994

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Effect of vitamin E and beta carotene on the incidence of primary nonfatal myocardial infarction and fatal coronary heart disease

Archives of internal medicine (1960), 1998-03, Vol.158 (6), p.668

1998

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Osteitis caused by bacille Calmette-Guérin vaccination: a retrospective analysis of 222 cases

The Journal of infectious diseases, 1995-08, Vol.172 (2), p.574-576

1995

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Should we prescribe antioxidants to patients with coronary heart disease?

European heart journal, 1998-04, Vol.19 (4), p.530-532

Rapola, J M

1998

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In vivo purging of bone marrow in children with poor-risk neuroblastoma for marrow collection and autologous bone marrow transplantation

Journal of clinical oncology, 1996-10, Vol.14 (10), p.2791-2802

1996

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Postmarathon paradox: insulin resistance in the face of glycogen depletion

American journal of physiology: endocrinology and metabolism, 1996-02, Vol.270 (2), p.E336-E343

1996

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Congenital nephrotic syndrome (NPHS1): Features resulting from different mutations in Finnish patients

Kidney international, 2000-09, Vol.58 (3), p.972-980

2000

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Kidneys with heavy proteinuria show fibrosis, inflammation, and oxidative stress, but no tubular phenotypic change

Kidney international, 2005-07, Vol.68 (1), p.121-132

2005

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Hypoparathyroidism in a patient with long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency caused by the G1528C mutation

The Journal of pediatrics, 1997-11, Vol.131 (5), p.766-768

1997

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Mutations in the palmitoyl protein thioesterase gene causing infantile neuronal ceroid lipofuscinosis

Nature (London), 1995-08, Vol.376 (6541), p.584-587

1995

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A mouse model for Finnish variant late infantile neuronal ceroid lipofuscinosis, CLN5, reveals neuropathology associated with early aging

Human molecular genetics, 2004-12, Vol.13 (23), p.2893-2906

2004

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Chronic arthritis in patients with aspartylglucosaminuria

Journal of rheumatology, 1998-06, Vol.25 (6), p.1131

1998

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Mice with Ppt1 mutation replicate the INCL phenotype and show an inflammation-associated loss of interneurons

Neurobiology of disease, 2005-02, Vol.18 (1), p.226-241

2005

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Nonspecific diskitis in children. A nonmicrobial disease?

Clinical orthopaedics and related research, 1993-12, Vol.297 (297), p.95-99

1993

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Post-transplantation nephrosis in congenital nephrotic syndrome of the Finnish type

Kidney international, 1993-10, Vol.44 (4), p.867-874

1993

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Why is congenital nephrotic syndrome associated with a rise in the concentration of alpha-fetoprotein in the amniotic fluid?

Pediatric nephrology (Berlin, West), 1990-03, Vol.4 (2), p.206-206

Rapola, J

1990

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Randomised trial of α-tocopherol and β-carotene supplements on incidence of major coronary events in men with previous myocardial infarction

Severe heart failure and rhabdomyolysis associated with propofol infusion in a burn patient

Transaortic Transcatheter Aortic Valve Implantation as a second choice over the Transapical access

Glomerular sclerosis in kidneys with congenital nephrotic syndrome (NPHS1)

Effects of α tocopherol and β carotene supplements on symptoms, progression, and prognosis of angina pectoris

Validity of Diagnoses of Major Coronary Events in National Registers of Hospital Diagnoses and Deaths in Finland

Hematopoietic stem cell transplantation in infantile neuronal ceroid lipofuscinosis

Bone marrow transplantation in young aspartylglucosaminuria mice: improved clearance of lysosomal storage in brain by using wild type as compared to heterozygote donors

Immunohistochemical spectrum of rhabdomyosarcoma and rhabdomyosarcoma-like tumors. Expression of cytokeratin and the 68-kD neurofilament protein

Lysosomal Storage Diseases in Adults

Effect of vitamin E and beta carotene on the incidence of primary nonfatal myocardial infarction and fatal coronary heart disease

Osteitis caused by bacille Calmette-Guérin vaccination: a retrospective analysis of 222 cases

Should we prescribe antioxidants to patients with coronary heart disease?

In vivo purging of bone marrow in children with poor-risk neuroblastoma for marrow collection and autologous bone marrow transplantation

Postmarathon paradox: insulin resistance in the face of glycogen depletion

Congenital nephrotic syndrome (NPHS1): Features resulting from different mutations in Finnish patients

Kidneys with heavy proteinuria show fibrosis, inflammation, and oxidative stress, but no tubular phenotypic change

Hypoparathyroidism in a patient with long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency caused by the G1528C mutation

Mutations in the palmitoyl protein thioesterase gene causing infantile neuronal ceroid lipofuscinosis

A mouse model for Finnish variant late infantile neuronal ceroid lipofuscinosis, CLN5, reveals neuropathology associated with early aging

Chronic arthritis in patients with aspartylglucosaminuria

Mice with Ppt1 mutation replicate the INCL phenotype and show an inflammation-associated loss of interneurons

Nonspecific diskitis in children. A nonmicrobial disease?

Post-transplantation nephrosis in congenital nephrotic syndrome of the Finnish type

Why is congenital nephrotic syndrome associated with a rise in the concentration of alpha-fetoprotein in the amniotic fluid?

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