Koskimies O - Search Results

1

Nephronophthisis and ulcerative colitis in siblings: a new association.

Ala-Mello S, Kääriäinen H, Koskimies O. Ala-Mello S, et al. Among authors: koskimies o. Pediatr Nephrol. 2001 Jun;16(6):507-9. doi: 10.1007/s004670100597. Pediatr Nephrol. 2001. PMID: 11420917

2

Nephronophthisis in Finland: epidemiology and comparison of genetically classified subgroups.

Ala-Mello S, Koskimies O, Rapola J, Kääriäinen H. Ala-Mello S, et al. Among authors: koskimies o. Eur J Hum Genet. 1999 Feb-Mar;7(2):205-11. doi: 10.1038/sj.ejhg.5200268. Eur J Hum Genet. 1999. PMID: 10196704

3

The burden of genetic disease and attitudes towards gene testing in Alport syndrome.

Pajari H, Koskimies O, Muhonen T, Kääriäinen H. Pajari H, et al. Among authors: koskimies o. Pediatr Nephrol. 1999 Aug;13(6):471-6. doi: 10.1007/s004670050640. Pediatr Nephrol. 1999. PMID: 10452272

4

Mechanism underlying early anaemia in children with familial juvenile nephronophthisis.

Ala-Mello S, Kivivuori SM, Rönnholm KA, Koskimies O, Siimes MA. Ala-Mello S, et al. Among authors: koskimies o. Pediatr Nephrol. 1996 Oct;10(5):578-81. doi: 10.1007/s004670050164. Pediatr Nephrol. 1996. PMID: 8897559

5

Molecular studies in Finnish patients with familial juvenile nephronophthisis exclude a founder effect and support a common mutation causing mechanism.

Ala-Mello S, Sankila EM, Koskimies O, de la Chapelle A, Kääriäinen H. Ala-Mello S, et al. Among authors: koskimies o. J Med Genet. 1998 Apr;35(4):279-83. doi: 10.1136/jmg.35.4.279. J Med Genet. 1998. PMID: 9598719 Free PMC article.

6

Dominant and recessive polycystic kidney disease in children: evaluation of clinical features and laboratory data.

Kääriäinen H, Koskimies O, Norio R. Kääriäinen H, et al. Among authors: koskimies o. Pediatr Nephrol. 1988 Jul;2(3):296-302. doi: 10.1007/BF00858681. Pediatr Nephrol. 1988. PMID: 3153029

7

[Nephronophthisis--hereditary progressive renal disease].

Ala-Mello S, Koskimies O, Kääriäinen H. Ala-Mello S, et al. Among authors: koskimies o. Duodecim. 1995;111(13):1222-7. Duodecim. 1995. PMID: 9221230 Finnish. No abstract available.

8

Familial juvenile nephronophthisis. An ultrasonographic follow-up of seven patients.

Ala-Mello S, Jääskeläinen J, Koskimies O. Ala-Mello S, et al. Among authors: koskimies o. Acta Radiol. 1998 Jan;39(1):84-9. doi: 10.1080/02841859809172156. Acta Radiol. 1998. PMID: 9498877

9

Dominant and recessive polycystic kidney disease in children: classification by intravenous pyelography, ultrasound, and computed tomography.

Kääriäinen H, Jääskeläinen J, Kivisaari L, Koskimies O, Norio R. Kääriäinen H, et al. Among authors: koskimies o. Pediatr Radiol. 1988;18(1):45-50. doi: 10.1007/BF02395759. Pediatr Radiol. 1988. PMID: 3277138

10

Alport's syndrome in 78 patients: epidemiological and clinical study.

Pajari H, Kääriäinen H, Muhonen T, Koskimies O. Pajari H, et al. Among authors: koskimies o. Acta Paediatr. 1996 Nov;85(11):1300-6. doi: 10.1111/j.1651-2227.1996.tb13915.x. Acta Paediatr. 1996. PMID: 8955456

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