Renal manifestations of Henoch–Schönlein purpura in a 6-month prospective study of 223 children von Jauhola, Outi, Ronkainen, Jaana, Koskimies, Olli, Ala-Houhala, Marja, Arikoski, Pekka, Hölttä, Tuula, Jahnukainen, Timo, Rajantie, Jukka, Örmälä, Timo, Turtinen, Juha, Nuutinen, Matti

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The adult kidney 24 years after childhood Henoch-Schönlein purpura: a retrospective cohort study von Ronkainen, Jaana, Nuutinen, Matti, Koskimies, Olli

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Clinical course of extrarenal symptoms in Henoch–Schönlein purpura: a 6-month prospective study von Jauhola, Outi, Ronkainen, Jaana, Koskimies, Olli, Ala-Houhala, Marja, Arikoski, Pekka, Hölttä, Tuula, Jahnukainen, Timo, Rajantie, Jukka, Örmälä, Timo, Nuutinen, Matti

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Predominance of Class II papG Allele of Escherichia coli in Pyelonephritis in Infants with Normal Urinary Tract Anatomy von Jantunen, M. E., Siitonen, A., Koskimies, O., Wikström, S., Kärkkäinen, UM, Salo, E., Saxén, H.

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Podocytes are firmly attached to glomerular basement membrane in kidneys with heavy proteinuria von LAHDENKARI, Anne-Tiina, LOUNATMAA, Kari, PATRAKKA, Jaakko, HOLMBERG, Christer, WARTIOVAARA, Jorma, KESTILÄ, Marjo, KOSKIMIES, Olli, JALANKO, Hannu

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Nephrin gene (NPHS1) in patients with minimal change nephrotic syndrome (MCNS) von Lahdenkari, Anne-Tiina, Kestilä, Marjo, Holmberg, Christer, Koskimies, Olli, Jalanko, Hannu

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Spectrum of COL4A5 mutations in Finnish Alport syndrome patients von Martin, Paula, Heiskari, Niina, Pajari, Heli, Grönhagen-Riska, Carola, Kääriäinen, Helena, Koskimies, Olli, Tryggvason, Karl

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Using Data Item Relationships to Adaptively Select Data for Synchronization von Koskimies, Oskari

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Molecular studies in Finnish patients with familial juvenile nephronophthisis exclude a founder effect and support a common mutation causing mechanism von Ala-Mello, S, Sankila, E M, Koskimies, O, de la Chapelle, A, Kääriäinen, H

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Familial juvenile nephronophthisis: An ultrasonographic follow-up of seven patients von Ala-Mello, S., Jääskeläinen, J., Koskimies, O.

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Long-term outcome of primary nephrotic syndrome von Koskimies, O, Vilska, J, Rapola, J, Hallman, N

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Diagnostic sonographic changes in the kidneys of 20 infants with congenital nephrotic syndrome of the Finnish type von Saraga, M., J skel inen, J., Koskimies, O.

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Evidence for pre‐hepatic metabolism of oral cyclosporine in children von Hoppu, K, Koskimies, O, Holmberg, C, Hirvisalo, EL

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Dominant and recessive polycystic kidney disease in children: evaluation of clinical features and laboratory data von KAARIAINEN, H, KOSKIMIES, O, NORIO, R

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Wireless Java RMI von Campadello, S., Koskimies, O., Raatikainen, K., Helin, H.

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Clinical features and outcome of childhood minimal change nephrotic syndrome: is genetics involved? von Lahdenkari, Anne-Tiina, Suvanto, Maija, Kajantie, Eero, Koskimies, Olli, Kestilä, Marjo, Jalanko, Hannu

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Percutaneous needle biopsy preceding preoperative chemotherapy in the management of massive renal tumors in children von SAARINEN, U. M, WIKSTRÖM, S, KOSKIMIES, O, SARIOLA, H

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Diagnostic accuracy of urinary tract infection and subsequent development of renal scars von Koskimies, O

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Henoch-Schönlein nephritis: long-term prognosis of unselected patients von Koskimies, O, Mir, S, Rapola, J, Vilska, J

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Arterial Hypertension Developing 10 Years After Radiotherapy For Wilms's Tumour von Koskimies, Olli

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