Palotie A - Search Results

1

Mitochondrial EFTs defects in juvenile-onset Leigh disease, ataxia, neuropathy, and optic atrophy.

Ahola S, Isohanni P, Euro L, Brilhante V, Palotie A, Pihko H, Lönnqvist T, Lehtonen T, Laine J, Tyynismaa H, Suomalainen A. Ahola S, et al. Among authors: palotie a. Neurology. 2014 Aug 19;83(8):743-51. doi: 10.1212/WNL.0000000000000716. Epub 2014 Jul 18. Neurology. 2014. PMID: 25037205 Free PMC article.

2

Hypoparathyroidism in a patient with long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency caused by the G1528C mutation.

Tyni T, Rapola J, Palotie A, Pihko H. Tyni T, et al. Among authors: palotie a. J Pediatr. 1997 Nov;131(5):766-8. doi: 10.1016/s0022-3476(97)70111-2. J Pediatr. 1997. PMID: 9403664

3

Pathology of long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency caused by the G1528C mutation.

Tyni T, Rapola J, Paetau A, Palotie A, Pihko H. Tyni T, et al. Among authors: palotie a. Pediatr Pathol Lab Med. 1997 May-Jun;17(3):427-47. Pediatr Pathol Lab Med. 1997. PMID: 9185222

4

Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency with the G1528C mutation: clinical presentation of thirteen patients.

Tyni T, Palotie A, Viinikka L, Valanne L, Salo MK, von Döbeln U, Jackson S, Wanders R, Venizelos N, Pihko H. Tyni T, et al. Among authors: palotie a. J Pediatr. 1997 Jan;130(1):67-76. doi: 10.1016/s0022-3476(97)70312-3. J Pediatr. 1997. PMID: 9003853

5

Assignment of the disease locus for lethal congenital contracture syndrome to a restricted region of chromosome 9q34, by genome scan using five affected individuals.

Mäkelä-Bengs P, Järvinen N, Vuopala K, Suomalainen A, Ignatius J, Sipilä M, Herva R, Palotie A, Peltonen L. Mäkelä-Bengs P, et al. Among authors: palotie a. Am J Hum Genet. 1998 Aug;63(2):506-16. doi: 10.1086/301968. Am J Hum Genet. 1998. PMID: 9683599 Free PMC article.

6

Shared loci for migraine and epilepsy on chromosomes 14q12-q23 and 12q24.2-q24.3.

Polvi A, Siren A, Kallela M, Rantala H, Artto V, Sobel EM, Palotie A, Lehesjoki AE, Wessman M. Polvi A, et al. Among authors: palotie a. Neurology. 2012 Jan 17;78(3):202-9. doi: 10.1212/WNL.0b013e31823fcd87. Epub 2012 Jan 4. Neurology. 2012. PMID: 22218271 Free PMC article.

7

LCCS: a lethal motoneuron disease of the fetus maps to chromosome 9q34.

Järvinen N, Mäkelä-Bengs P, Suomalainen A, Vuopala K, Herva R, Palotie A, Peltonen L. Järvinen N, et al. Among authors: palotie a. Ann N Y Acad Sci. 1998 Oct 23;857:260-2. doi: 10.1111/j.1749-6632.1998.tb10127.x. Ann N Y Acad Sci. 1998. PMID: 9917852 No abstract available.

8

A visual migraine aura locus maps to 9q21-q22.

Tikka-Kleemola P, Artto V, Vepsäläinen S, Sobel EM, Räty S, Kaunisto MA, Anttila V, Hämäläinen E, Sumelahti ML, Ilmavirta M, Färkkilä M, Kallela M, Palotie A, Wessman M. Tikka-Kleemola P, et al. Among authors: palotie a. Neurology. 2010 Apr 13;74(15):1171-7. doi: 10.1212/WNL.0b013e3181d8ffcb. Neurology. 2010. PMID: 20385888 Free PMC article.

9

Presymptomatic DNA and MRI diagnosis of neurofibromatosis 2 with mild clinical course in an extended pedigree.

Sainio M, Strachan T, Blomstedt G, Salonen O, Setälä K, Palotie A, Palo J, Pyykkö I, Peltonen L, Jääskeläinen J. Sainio M, et al. Among authors: palotie a. Neurology. 1995 Jul;45(7):1314-22. doi: 10.1212/wnl.45.7.1314. Neurology. 1995. PMID: 7617190

10

Novel splice site CACNA1A mutation causing episodic ataxia type 2.

Kaunisto MA, Harno H, Kallela M, Somer H, Sallinen R, Hämäläinen E, Miettinen PJ, Vesa J, Orpana A, Palotie A, Färkkilä M, Wessman M. Kaunisto MA, et al. Among authors: palotie a. Neurogenetics. 2004 Feb;5(1):69-73. doi: 10.1007/s10048-003-0161-0. Epub 2003 Oct 7. Neurogenetics. 2004. PMID: 14530926

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