Haataja L - Search Results

1

The genetic locus for free sialic acid storage disease maps to the long arm of chromosome 6.

Haataja L, Schleutker J, Laine AP, Renlund M, Savontaus ML, Dib C, Weissenbach J, Peltonen L, Aula P. Haataja L, et al. Am J Hum Genet. 1994 Jun;54(6):1042-9. Am J Hum Genet. 1994. PMID: 8198127 Free PMC article.

2

Exclusion map of Salla disease: attempts to localize the disease gene using a computer program.

Haataja L, Schleutker J, Renlund M, Palotie A, Peltonen L, Aula P. Haataja L, et al. Hum Genet. 1992 Jan;88(3):298-300. doi: 10.1007/BF00197263. Hum Genet. 1992. PMID: 1733832

3

Confirmation of the chromosomal localization of human lamp genes and their exclusion as candidate genes for Salla disease.

Schleutker J, Haataja L, Renlund M, Puhakka L, Viitala J, Peltonen L, Aula P. Schleutker J, et al. Among authors: haataja l. Hum Genet. 1991 Nov;88(1):95-7. doi: 10.1007/BF00204936. Hum Genet. 1991. PMID: 1959930

4

Linkage disequilibrium utilized to establish a refined genetic position of the Salla disease locus on 6q14-q15.

Schleutker J, Laine AP, Haataja L, Renlund M, Weissenbach J, Aula P, Peltonen L. Schleutker J, et al. Among authors: haataja l. Genomics. 1995 May 20;27(2):286-92. doi: 10.1006/geno.1995.1044. Genomics. 1995. PMID: 7557994

5

Phenotypic variation and magnetic resonance imaging (MRI) in Salla disease, a free sialic acid storage disorder.

Haataja L, Parkkola R, Sonninen P, Vanhanen SL, Schleutker J, Aärimaa T, Turpeinen U, Renlund M, Aula P. Haataja L, et al. Neuropediatrics. 1994 Oct;25(5):238-44. doi: 10.1055/s-2008-1073028. Neuropediatrics. 1994. PMID: 7885532

6

Increased brain glucose utilization in Salla disease (free sialic acid storage disorder).

Suhonen-Polvi H, Varho T, Metsähonkala L, Haataja L, Ruotsalainen U, Haaparanta M, Bergman J, Solin O, Aärimaa T, Holopainen I, Vainionpää L, Manner T, Jääskeläinen S, Renlund M, Sillanpää M, Aula P. Suhonen-Polvi H, et al. Among authors: haataja l. J Nucl Med. 1999 Jan;40(1):12-8. J Nucl Med. 1999. PMID: 9935050 Free article.

7

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. Among authors: haataja l. Genomics. 1991 Jan;9(1):170-3. doi: 10.1016/0888-7543(91)90235-7. Genomics. 1991. PMID: 1672288

8

The motor profile of preterm infants at 11 y of age.

Setänen S, Lehtonen L, Parkkola R, Matomäki J, Haataja L. Setänen S, et al. Among authors: haataja l. Pediatr Res. 2016 Sep;80(3):389-94. doi: 10.1038/pr.2016.90. Epub 2016 Apr 13. Pediatr Res. 2016. PMID: 27074125

9

Prediction of neuromotor outcome in infants born preterm at 11 years of age using volumetric neonatal magnetic resonance imaging and neurological examinations.

Setänen S, Lehtonen L, Parkkola R, Aho K, Haataja L; PIPARI Study Group. Setänen S, et al. Among authors: haataja l. Dev Med Child Neurol. 2016 Jul;58(7):721-7. doi: 10.1111/dmcn.13030. Epub 2016 Jan 27. Dev Med Child Neurol. 2016. PMID: 27307195 Free article.

10

Predictive value of neonatal brain MRI on the neurodevelopmental outcome of preterm infants by 5 years of age.

Setänen S, Haataja L, Parkkola R, Lind A, Lehtonen L. Setänen S, et al. Among authors: haataja l. Acta Paediatr. 2013 May;102(5):492-7. doi: 10.1111/apa.12191. Epub 2013 Mar 4. Acta Paediatr. 2013. PMID: 23398524

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