Santavuori P - Search Results

1

[18F]fluorodopa PET shows striatal dopaminergic dysfunction in juvenile neuronal ceroid lipofuscinosis.

Ruottinen HM, Rinne JO, Haaparanta M, Solin O, Bergman J, Oikonen VJ, Järvelä I, Santavuori P. Ruottinen HM, et al. Among authors: santavuori p. J Neurol Neurosurg Psychiatry. 1997 Jun;62(6):622-5. doi: 10.1136/jnnp.62.6.622. J Neurol Neurosurg Psychiatry. 1997. PMID: 9219750 Free PMC article.

2

Delayed classic and protracted phenotypes of compound heterozygous juvenile neuronal ceroid lipofuscinosis.

Lauronen L, Munroe PB, Järvelä I, Autti T, Mitchison HM, O'Rawe AM, Gardiner RM, Mole SE, Puranen J, Häkkinen AM, Kirveskari E, Santavuori P. Lauronen L, et al. Among authors: santavuori p. Neurology. 1999 Jan 15;52(2):360-5. doi: 10.1212/wnl.52.2.360. Neurology. 1999. PMID: 9932957

3

Decreased striatal dopamine transporter density in JNCL patients with parkinsonian symptoms.

Aberg L, Liewendahl K, Nikkinen P, Autti T, Rinne JO, Santavuori P. Aberg L, et al. Among authors: santavuori p. Neurology. 2000 Mar 14;54(5):1069-74. doi: 10.1212/wnl.54.5.1069. Neurology. 2000. PMID: 10720276

4

A favorable response to antiparkinsonian treatment in juvenile neuronal ceroid lipofuscinosis.

Aberg LE, Rinne JO, Rajantie I, Santavuori P. Aberg LE, et al. Among authors: santavuori p. Neurology. 2001 May 8;56(9):1236-9. doi: 10.1212/wnl.56.9.1236. Neurology. 2001. PMID: 11342698

5

Positron emission tomography shows reduced striatal dopamine D1 but not D2 receptors in juvenile neuronal ceroid lipofuscinosis.

Rinne JO, Ruottinen HM, Någren K, Aberg LE, Santavuori P. Rinne JO, et al. Among authors: santavuori p. Neuropediatrics. 2002 Jun;33(3):138-41. doi: 10.1055/s-2002-33677. Neuropediatrics. 2002. PMID: 12200743

6

Refined assignment of the infantile neuronal ceroid-lipofuscinosis (INCL) locus at 1p32 and the current status of prenatal and carrier diagnostics.

Hellsten E, Vesa J, Järvelä I, Mäkelä TP, Santavuori P, Peltonen L. Hellsten E, et al. Among authors: santavuori p. J Inherit Metab Dis. 1993;16(2):335-8. doi: 10.1007/BF00710277. J Inherit Metab Dis. 1993. PMID: 8411993 Review. No abstract available.

7

Clinical and magnetic resonance imaging findings in Batten disease: analysis of the major mutation (1.02-kb deletion).

Järvelä I, Autti T, Lamminranta S, Aberg L, Raininko R, Santavuori P. Järvelä I, et al. Among authors: santavuori p. Ann Neurol. 1997 Nov;42(5):799-802. doi: 10.1002/ana.410420517. Ann Neurol. 1997. PMID: 9392580

8

Atypical juvenile neuronal ceroid lipofuscinosis with granular osmiophilic deposit-like inclusions in the autonomic nerve cells of the gut wall.

Aberg L, Järvelä I, Rapola J, Autti T, Kirveskari E, Lappi M, Sipilä L, Santavuori P. Aberg L, et al. Among authors: santavuori p. Acta Neuropathol. 1998 Mar;95(3):306-12. doi: 10.1007/s004010050803. Acta Neuropathol. 1998. PMID: 9542598

9

Juvenile-onset neuronal ceroid lipofuscinosis with infantile CLN1 mutation and palmitoyl-protein thioesterase deficiency.

Kälviäinen R, Eriksson K, Losekoot M, Sorri I, Harvima I, Santavuori P, Järvelä I, Autti T, Vanninen R, Salmenperä T, van Diggelen OP. Kälviäinen R, et al. Among authors: santavuori p. Eur J Neurol. 2007 Apr;14(4):369-72. doi: 10.1111/j.1468-1331.2007.01668.x. Eur J Neurol. 2007. PMID: 17388982

10

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. Among authors: santavuori p. Am J Med Genet. 1992 Feb 15;42(4):546-8. doi: 10.1002/ajmg.1320420425. Am J Med Genet. 1992. PMID: 1609836

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

142 results

Search Page

Filters