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Items: 47

1.

Neonatal outcome of 58 infants exposed to maternal buprenorphine in utero.

Hytinantti T, Kahila H, Renlund M, Järvenpää AL, Halmesmäki E, Kivitie-Kallio S.

Acta Paediatr. 2008 Aug;97(8):1040-4. doi: 10.1111/j.1651-2227.2008.00838.x. Epub 2008 May 16.

PMID:
18474065
2.

No improvement in outcome of nationwide extremely low birth weight infant populations between 1996-1997 and 1999-2000.

Tommiska V, Heinonen K, Lehtonen L, Renlund M, Saarela T, Tammela O, Virtanen M, Fellman V.

Pediatrics. 2007 Jan;119(1):29-36.

PMID:
17200268
3.

Expanding screening for rare metabolic disease in the newborn: an analysis of costs, effect and ethical consequences for decision-making in Finland.

Autti-Rämö I, Mäkelä M, Sintonen H, Koskinen H, Laajalahti L, Halila R, Kääriäinen H, Lapatto R, Näntö-Salonen K, Pulkki K, Renlund M, Salo M, Tyni T.

Acta Paediatr. 2005 Aug;94(8):1126-36.

PMID:
16188860
4.

Geographical and ethnic variation of the 677C>T allele of 5,10 methylenetetrahydrofolate reductase (MTHFR): findings from over 7000 newborns from 16 areas world wide.

Wilcken B, Bamforth F, Li Z, Zhu H, Ritvanen A, Renlund M, Stoll C, Alembik Y, Dott B, Czeizel AE, Gelman-Kohan Z, Scarano G, Bianca S, Ettore G, Tenconi R, Bellato S, Scala I, Mutchinick OM, López MA, de Walle H, Hofstra R, Joutchenko L, Kavteladze L, Bermejo E, Martínez-Frías ML, Gallagher M, Erickson JD, Vollset SE, Mastroiacovo P, Andria G, Botto LD.

J Med Genet. 2003 Aug;40(8):619-25. No abstract available. Erratum in: J Med Genet. 2004 May;41(5):400. Redlund, M [corrected to Renlund, M].

5.

Natal and neonatal teeth in relation to environmental toxicants.

Alaluusua S, Kiviranta H, Leppäniemi A, Hölttä P, Lukinmaa PL, Lope L, Järvenpää AL, Renlund M, Toppari J, Virtanen H, Kaleva M, Vartiainen T.

Pediatr Res. 2002 Nov;52(5):652-5.

PMID:
12409509
6.

Phenotypic spectrum of Salla disease, a free sialic acid storage disorder.

Varho TT, Alajoki LE, Posti KM, Korhonen TT, Renlund MG, Nyman SR, Sillanpää ML, Aula PP.

Pediatr Neurol. 2002 Apr;26(4):267-73.

PMID:
11992753
7.

The auditory sensory memory trace decays rapidly in newborns.

Cheour M, Ceponiené R, Leppänen P, Alho K, Kujala T, Renlund M, Fellman V, Näätänen R.

Scand J Psychol. 2002 Feb;43(1):33-9.

PMID:
11885758
8.

Event-related potential features indexing central auditory discrimination by newborns.

Ceponiene R, Kushnerenko E, Fellman V, Renlund M, Suominen K, Näätänen R.

Brain Res Cogn Brain Res. 2002 Feb;13(1):101-13.

PMID:
11867255
9.

Central auditory processing of durational changes in complex speech patterns by newborns: an event-related brain potential study.

Kushnerenko E, Cheour M, Ceponiene R, Fellman V, Renlund M, Soininen K, Alku P, Koskinen M, Sainio K, Näätänen R.

Dev Neuropsychol. 2001;19(1):83-97.

PMID:
11411423
10.

Prenatal detection of free sialic acid storage disease: genetic and biochemical studies in nine families.

Salomäki P, Aula N, Juvonen V, Renlund M, Aula P.

Prenat Diagn. 2001 May;21(5):354-8.

PMID:
11360275
11.

A national short-term follow-Up study of extremely low birth weight infants born in Finland in 1996-1997.

Tommiska V, Heinonen K, Ikonen S, Kero P, Pokela ML, Renlund M, Virtanen M, Fellman V.

Pediatrics. 2001 Jan;107(1):E2.

PMID:
11134466
12.

Breast-feeding and the development of cows' milk protein allergy.

Saarinen KM, Juntunen-Backman K, Järvenpää AL, Klemetti P, Kuitunen P, Lope L, Renlund M, Siivola M, Vaarala O, Savilahti E.

Adv Exp Med Biol. 2000;478:121-30.

PMID:
11065065
13.

Thrombocytopenia in term infants: a population-based study.

Sainio S, Järvenpää AL, Renlund M, Riikonen S, Teramo K, Kekomäki R.

Obstet Gynecol. 2000 Mar;95(3):441-6.

PMID:
10711560
14.

Bone marrow transplantation in aspartylglucosaminuria--histopathological and MRI study.

Autti T, Rapola J, Santavuori P, Raininko R, Renlund M, Liukkonen E, Lauronen L, Wirtavuori K, Hietala M, Saarinen-Pihkala U.

Neuropediatrics. 1999 Dec;30(6):283-8.

PMID:
10706021
15.

Correction of peripheral lysosomal accumulation in mice with aspartylglucosaminuria by bone marrow transplantation.

Laine M, Richter J, Fahlman C, Rapola J, Renlund M, Peltonen L, Karlsson S, Jalanko A.

Exp Hematol. 1999 Sep;27(9):1467-74.

PMID:
10480438
16.

Supplementary feeding in maternity hospitals and the risk of cow's milk allergy: A prospective study of 6209 infants.

Saarinen KM, Juntunen-Backman K, Järvenpää AL, Kuitunen P, Lope L, Renlund M, Siivola M, Savilahti E.

J Allergy Clin Immunol. 1999 Aug;104(2 Pt 1):457-61.

PMID:
10452771
17.

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.

J Nucl Med. 1999 Jan;40(1):12-8.

18.

Bone-marrow transplantation in aspartylglucosaminuria.

Autti T, Santavuori P, Raininko R, Renlund M, Rapola J, Saarinen-Pihkala U.

Lancet. 1997 May 10;349(9062):1366-7. No abstract available.

PMID:
9149703
19.

The ontogenetically earliest discriminative response of the human brain.

Cheour-Luhtanen M, Alho K, Sainio K, Rinne T, Reinikainen K, Pohjavuori M, Renlund M, Aaltonen O, Eerola O, Näätänen R.

Psychophysiology. 1996 Jul;33(4):478-81.

PMID:
8753948
20.

Impairment of ganglioside metabolism in cultured fibroblasts from Salla patients.

Pitto M, Chigorno V, Renlund M, Tettamanti G.

Clin Chim Acta. 1996 Mar 29;247(1-2):143-57.

PMID:
8920233
21.

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.

Genomics. 1995 May 20;27(2):286-92.

PMID:
7557994
22.

Mismatch negativity indicates vowel discrimination in newborns.

Cheour-Luhtanen M, Alho K, Kujala T, Sainio K, Reinikainen K, Renlund M, Aaltonen O, Eerola O, Näätänen R.

Hear Res. 1995 Jan;82(1):53-8.

PMID:
7744713
23.

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.

Neuropediatrics. 1994 Oct;25(5):238-44.

PMID:
7885532
24.

Linkage disequilibrium patterns vary with chromosomal location: a case study from the von Willebrand factor region.

Watkins WS, Zenger R, O'Brien E, Nyman D, Eriksson AW, Renlund M, Jorde LB.

Am J Hum Genet. 1994 Aug;55(2):348-55.

25.

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.

Am J Hum Genet. 1994 Jun;54(6):1042-9.

26.

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.

Hum Genet. 1992 Jan;88(3):298-300.

PMID:
1733832
27.

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.

Hum Genet. 1991 Nov;88(1):95-7.

PMID:
1959930
28.

Sialic acid storage disorders: observations on clinical and biochemical variation.

Mancini GM, Verheijen FW, Beerens CE, Renlund M, Aula P.

Dev Neurosci. 1991;13(4-5):327-30. Review.

PMID:
1817039
29.

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.

Genomics. 1991 Jan;9(1):170-3.

PMID:
1672288
30.

Renal handling of free sialic acid in normal humans and patients with Salla disease or renal disease.

Seppala R, Renlund M, Bernardini I, Tietze F, Gahl WA.

Lab Invest. 1990 Aug;63(2):197-203.

PMID:
2381164
31.

Defective lysosomal egress of free sialic acid (N-acetylneuraminic acid) in fibroblasts of patients with infantile free sialic acid storage disease.

Tietze F, Seppala R, Renlund M, Hopwood JJ, Harper GS, Thomas GH, Gahl WA.

J Biol Chem. 1989 Sep 15;264(26):15316-22.

32.

Neonatal septicaemia in Finland 1981-85. Predominance of group B streptococcal infections with very early onset.

Vesikari T, Isolauri E, Tuppurainen N, Renlund M, Koivisto M, Janas M, Ikonen RS, Kero P, Heinonen K, Nyman R, et al.

Acta Paediatr Scand. 1989 Jan;78(1):44-50.

PMID:
2645740
33.

Neuropathology of Salla disease.

Autio-Harmainen H, Oldfors A, Sourander P, Renlund M, Dammert K, Similä S.

Acta Neuropathol. 1988;75(5):481-90. Review.

PMID:
3287834
34.

Prenatal detection of Salla disease based upon increased free sialic acid in amniocytes.

Renlund M, Aula P.

Am J Med Genet. 1987 Oct;28(2):377-84.

PMID:
3425617
35.

Studies on the elevated amniotic fluid SP1 in Meckel's syndrome: modified glycosylation of SP1.

Heikinheimo M, Jalanko H, Renlund M, Rapola J, Wahlström T.

Placenta. 1987 Jul-Aug;8(4):427-32.

PMID:
3317390
36.

Screening of inherited oligosaccharidurias among mentally retarded patients in northern Finland.

Aula P, Renlund M, Raivio KO, Koskela SL.

J Ment Defic Res. 1986 Dec;30 ( Pt 4):365-8.

PMID:
3806663
37.

Defective sialic acid egress from isolated fibroblast lysosomes of patients with Salla disease.

Renlund M, Tietze F, Gahl WA.

Science. 1986 May 9;232(4751):759-62.

PMID:
3961501
39.

Neonatal septicaemia.

Vesikari T, Janas M, Grönroos P, Tuppurainen N, Renlund M, Kero P, Koivisto M, Kunnas M, Heinonen K, Nyman R, et al.

Arch Dis Child. 1985 Jun;60(6):542-6.

40.
41.

Free N-acetylneuraminic acid in tissues in Salla disease and the enzymes involved in its metabolism.

Renlund M, Chester MA, Lundblad A, Parkkinen J, Krusius T.

Eur J Biochem. 1983 Jan 17;130(1):39-45.

42.

Salla disease: a new lysosomal storage disorder with disturbed sialic acid metabolism.

Renlund M, Aula P, Raivio KO, Autio S, Sainio K, Rapola J, Koskela SL.

Neurology. 1983 Jan;33(1):57-66.

PMID:
6681560
43.

[Salla disease - a new inherited Finnish disease].

Aula P, Renlund M, Raivio K, Autio S, Koskela SL, Rapola J.

Duodecim. 1981;97(2):59-69. Finnish. No abstract available.

PMID:
7249964
44.

Increased urinary excretion of free N-acetylneuraminic acid in thirteen patients with Salla disease.

Renlund M, Chester MA, Lundblad A, Aula P, Raivio KO, Autio S, Koskela SL.

Eur J Biochem. 1979 Nov 1;101(1):245-50.

45.

[Neonatal septicemia].

Renlund M, Pettay O.

Duodecim. 1979;95(23):1586-93. Finnish. No abstract available.

PMID:
544232
46.

Pharmacokinetics and clinical efficacy of cefuroxime in the newborn period.

Renlund M, Pettay O.

Proc R Soc Med. 1977;70(Suppl 9):179-82. No abstract available.

47.

Erythropoietin and renin after renal transplantation.

Fyhrquist F, Renlund M, Kuhlbäck B.

Scand J Urol Nephrol. 1975 Mar 6-7;(29 Suppl):143-5.

PMID:
781810

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