Järvelä I - Search Results

1

Molecular genetics of neuronal ceroid lipofuscinoses.

Järvelä I, Vesa J, Santavuori P, Hellsten E, Peltonen L. Järvelä I, et al. Pediatr Res. 1992 Dec;32(6):645-8. doi: 10.1203/00006450-199212000-00003. Pediatr Res. 1992. PMID: 1287553 Review.

2

[Gene localization will explain the basic causes of neuronal ceroid lipofuscinoses].

Järvelä I, Palotie L, Santavuori P, Rapola J. Järvelä I, et al. Duodecim. 1991;107(8):632-5. Duodecim. 1991. PMID: 1364917 Review. Finnish. No abstract available.

3

Linkage map of the chromosomal region surrounding the infantile neuronal ceroid lipofuscinosis on 1p.

Järvelä I, Santavuori P, Puhakka L, Haltia M, Peltonen L. Järvelä I, et al. Am J Med Genet. 1992 Feb 15;42(4):546-8. doi: 10.1002/ajmg.1320420425. Am J Med Genet. 1992. PMID: 1609836

4

The neuronal ceroid lipofuscinoses: unfolding the genetic defect.

Rapola J, Järvelä I, Peltonen L. Rapola J, et al. Among authors: jarvela i. Pediatr Pathol. 1991 Nov-Dec;11(6):799-806. doi: 10.3109/15513819109065477. Pediatr Pathol. 1991. PMID: 1663617 Review. No abstract available.

5

Infantile form of neuronal ceroid lipofuscinosis (CLN1) maps to the short arm of chromosome 1.

Järvelä I, Schleutker J, Haataja L, Santavuori P, Puhakka L, Manninen T, Palotie A, Sandkuijl LA, Renlund M, White R, et al. Järvelä I, et al. Genomics. 1991 Jan;9(1):170-3. doi: 10.1016/0888-7543(91)90235-7. Genomics. 1991. PMID: 1672288

6

DNA-based prenatal diagnosis of the infantile form of neuronal ceroid lipofuscinosis (INCL, CLN1).

Järvelä I, Rapola J, Peltonen L, Puhakka L, Vesa J, Ammälä P, Salonen R, Ryynänen M, Haring P, Mustonen A, et al. Järvelä I, et al. Prenat Diagn. 1991 May;11(5):323-8. doi: 10.1002/pd.1970110508. Prenat Diagn. 1991. PMID: 1680233

7

Infantile neuronal ceroid lipofuscinosis (CLN1): linkage disequilibrium in the Finnish population and evidence that variant late infantile form (variant CLN2) represents a nonallelic locus.

Järvelä I. Järvelä I. Genomics. 1991 Jun;10(2):333-7. doi: 10.1016/0888-7543(91)90316-7. Genomics. 1991. PMID: 2071142

8

Linkage analysis of late-infantile neuronal ceroid-lipofuscinosis.

Sharp J, Savukoski M, Wheeler RB, Harris J, Järvelä I, Peltonen L, Gardiner M, Williams R. Sharp J, et al. Among authors: jarvela i. Am J Med Genet. 1995 Jun 5;57(2):348-9. doi: 10.1002/ajmg.1320570249. Am J Med Genet. 1995. PMID: 7668361

9

Identification of YAC clones for human chromosome 1p32 and physical mapping of the infantile neuronal ceroid lipofuscinosis (INCL) locus.

Hellsten E, Vesa J, Heiskanen M, Mäkelä TP, Järvelä I, Cowell JK, Mead S, Alitalo K, Palotie A, Peltonen L. Hellsten E, et al. Among authors: jarvela i. Genomics. 1995 Jan 20;25(2):404-12. doi: 10.1016/0888-7543(95)80040-s. Genomics. 1995. PMID: 7789974

10

Batten disease gene, CLN3: linkage disequilibrium mapping in the Finnish population, and analysis of European haplotypes.

Mitchison HM, O'Rawe AM, Taschner PE, Sandkuijl LA, Santavuori P, de Vos N, Breuning MH, Mole SE, Gardiner RM, Järvelä IE. Mitchison HM, et al. Among authors: jarvela ie. Am J Hum Genet. 1995 Mar;56(3):654-62. Am J Hum Genet. 1995. PMID: 7887419 Free PMC article.

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