Haataja L - Search Results

1

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

2

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

3

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

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

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.

7

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.

8

Mutation in type II procollagen (COL2A1) that substitutes aspartate for glycine alpha 1-67 and that causes cataracts and retinal detachment: evidence for molecular heterogeneity in the Wagner syndrome and the Stickler syndrome (arthro-ophthalmopathy).

Körkkö J, Ritvaniemi P, Haataja L, Kääriäinen H, Kivirikko KI, Prockop DJ, Ala-Kokko L. Körkkö J, et al. Among authors: haataja l. Am J Hum Genet. 1993 Jul;53(1):55-61. Am J Hum Genet. 1993. PMID: 8317498 Free PMC article.

9

Acoustic quality of cry in very-low-birth-weight infants at the age of 1 1/2 years.

Rautava L, Lempinen A, Ojala S, Parkkola R, Rikalainen H, Lapinleimu H, Haataja L, Lehtonen L; PIPARI Study Group. Rautava L, et al. Among authors: haataja l. Early Hum Dev. 2007 Jan;83(1):5-12. doi: 10.1016/j.earlhumdev.2006.03.004. Epub 2006 May 2. Early Hum Dev. 2007. PMID: 16650947

10

Mother-infant interaction is influenced by the amount of holding in preterm infants.

Korja R, Maunu J, Kirjavainen J, Savonlahti E, Haataja L, Lapinleimu H, Manninen H, Piha J, Lehtonen L; PIPARI Study Group. Korja R, et al. Among authors: haataja l. Early Hum Dev. 2008 Apr;84(4):257-67. doi: 10.1016/j.earlhumdev.2007.06.006. Epub 2007 Aug 16. Early Hum Dev. 2008. PMID: 17707118

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