Campdelacreu J - Search Results

1

Relative high frequency of the c.255delA parkin gene mutation in Spanish patients with autosomal recessive parkinsonism.

Muñoz E, Tolosa E, Pastor P, Martí MJ, Valldeoriola F, Campdelacreu J, Oliva R. Muñoz E, et al. Among authors: campdelacreu j. J Neurol Neurosurg Psychiatry. 2002 Nov;73(5):582-4. doi: 10.1136/jnnp.73.5.582. J Neurol Neurosurg Psychiatry. 2002. PMID: 12397156 Free PMC article.

2

A novel intronic mutation in the DDP1 gene in a family with X-linked dystonia-deafness syndrome.

Ezquerra M, Campdelacreu J, Muñoz E, Tolosa E, Martí MJ. Ezquerra M, et al. Among authors: campdelacreu j. Arch Neurol. 2005 Feb;62(2):306-8. doi: 10.1001/archneur.62.2.306. Arch Neurol. 2005. PMID: 15710860

3

Sequence analysis of tau 3'untranslated region and saitohin gene in sporadic progressive supranuclear palsy.

Ezquerra M, Campdelacreu J, Muñoz E, Oliva R, Tolosa E. Ezquerra M, et al. Among authors: campdelacreu j. J Neurol Neurosurg Psychiatry. 2004 Jan;75(1):155-7. J Neurol Neurosurg Psychiatry. 2004. PMID: 14707330 Free PMC article.

4

Mutational study of the nuclear factor kappa B inducing kinase gene in patients with progressive supranuclear palsy.

Campdelacreu J, Ezquerra M, Muñoz E, Oliva R, Tolosa E. Campdelacreu J, et al. Neurosci Lett. 2003 Apr 10;340(2):158-60. doi: 10.1016/s0304-3940(03)00105-8. Neurosci Lett. 2003. PMID: 12668260

5

Clinical overview of the synucleinopathies.

Martí MJ, Tolosa E, Campdelacreu J. Martí MJ, et al. Among authors: campdelacreu j. Mov Disord. 2003 Sep;18 Suppl 6:S21-7. doi: 10.1002/mds.10559. Mov Disord. 2003. PMID: 14502652 Review.

6

Association study of the G258S transferrin gene polymorphism and Parkinson's disease in the Spanish population.

Ezquerra M, Campdelacreu J, Muñoz E, Tolosa E. Ezquerra M, et al. Among authors: campdelacreu j. J Neurol. 2005 Oct;252(10):1269-70. doi: 10.1007/s00415-005-0695-1. Epub 2005 Aug 1. J Neurol. 2005. PMID: 16047113 No abstract available.

7

Lack of association of APOE and tau polymorphisms with dementia in Parkinson's disease.

Ezquerra M, Campdelacreu J, Gaig C, Compta Y, Muñoz E, Martí MJ, Valldeoriola F, Tolosa E. Ezquerra M, et al. Among authors: campdelacreu j. Neurosci Lett. 2008 Dec 19;448(1):20-3. doi: 10.1016/j.neulet.2008.10.018. Epub 2008 Oct 10. Neurosci Lett. 2008. PMID: 18930114

8

Generalised dystonia with an abnormal magnetic resonance imaging signal in the basal ganglia: a case of adult-onset GM1 gangliosidosis.

Campdelacreu J, Muñoz E, Gómez B, Pujol T, Chabás A, Tolosa E. Campdelacreu J, et al. Mov Disord. 2002 Sep;17(5):1095-7. doi: 10.1002/mds.10247. Mov Disord. 2002. PMID: 12360569

9

Severe cerebral white matter involvement in a case of dentatorubropallidoluysian atrophy studied at autopsy.

Muñoz E, Campdelacreu J, Ferrer I, Rey MJ, Cardozo A, Gómez B, Tolosa E. Muñoz E, et al. Among authors: campdelacreu j. Arch Neurol. 2004 Jun;61(6):946-9. doi: 10.1001/archneur.61.6.946. Arch Neurol. 2004. PMID: 15210537

10

No evidence of CRHR1 gene involvement in progressive supranuclear palsy.

Campdelacreu J, Gaig C, Ezquerra M, Muñoz E, Martí MJ, Valldeoriola F, Tolosa E. Campdelacreu J, et al. Neurosci Lett. 2006 Nov 27;409(1):61-4. doi: 10.1016/j.neulet.2006.09.017. Epub 2006 Sep 28. Neurosci Lett. 2006. PMID: 17010515

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