Light and electron micropscopical changes in congenital nephrotic syndrome

Por Rapola, J.
Publicado em 1973

Particulate fraction in amniotic fluid at second trimester.

Por Jalanko, H, Rapola, J, Lehtonen, E
Publicado em 1985

Henoch-Schönlein nephritis: long-term prognosis of unselected patients.

Por Koskimies, O, Mir, S, Rapola, J, Vilska, J
Publicado em 1981

Long-term outcome of primary nephrotic syndrome.

Por Koskimies, O, Vilska, J, Rapola, J, Hallman, N
Publicado em 1982

Chronic rejection of rat renal allograft. III. Ultrastructure of vascular and glomerular changes.

Por Yilmaz, A., Yilmaz, S., Paavonen, T., Rapola, J., Häyry, P.
Publicado em 1992

Characterization of high endothelial-like properties of peritubular capillary endothelium during acute renal allograft rejection.

Por Renkonen, R., Turunen, J. P., Rapola, J., Häyry, P.
Publicado em 1990

Cell kinetics in the jejunal crypt epithelium in malabsorption syndrome with cow's milk protein intolerance and in coeliac disease of childhood.

Por Kosnai, I, Kuitunen, P, Savilahti, E, Rapola, J, Köhegyi, J
Publicado em 1980

Disturbed calcium and phosphate homeostasis during treatment with ACTH of infantile spasms.

Por Riikonen, R, Simell, O, Jääskeläinen, J, Rapola, J, Perheentupa, J
Publicado em 1986

Extracellular matrix and epithelial differentiation of Wilms' tumor.

Por Sariola, H., Ekblom, P., Rapola, J., Vaheri, A., Timpl, R.
Publicado em 1985

Genetics of congenital nemaline myopathy: a study of 10 families.

Por Wallgren-Pettersson, C, Kääriäinen, H, Rapola, J, Salmi, T, Jääskeläinen, J, Donner, M
Publicado em 1990

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

Por Rapola, J, Virtamo, J, Ripatti, S, Haukka, J, Huttunen, J, Albanes, D, Taylor, P, Heinonen, O
Publicado em 1998

Reversible mitochondrial myopathy with cytochrome c oxidase deficiency.

Por Salo, M K, Rapola, J, Somer, H, Pihko, H, Koivikko, M, Tritschler, H J, DiMauro, S
Publicado em 1992

X linked neonatal myotubular myopathy: one recombination detected with four polymorphic DNA markers from Xq28.

Por Lehesjoki, A E, Sankila, E M, Miao, J, Somer, M, Salonen, R, Rapola, J, de la Chapelle, A
Publicado em 1990