Papadimitriou A - Search Results

1

Genetic assessment of familial and early-onset Parkinson's disease in a Greek population.

Bozi M, Papadimitriou D, Antonellou R, Moraitou M, Maniati M, Vassilatis DK, Papageorgiou SG, Leonardos A, Tagaris G, Malamis G, Theofilopoulos D, Kamakari S, Stamboulis E, Hadjigeorgiou GM, Athanassiadou A, Michelakakis H, Papadimitriou A, Gasser T, Stefanis L. Bozi M, et al. Among authors: papadimitriou d, papadimitriou a. Eur J Neurol. 2014 Jul;21(7):963-8. doi: 10.1111/ene.12315. Epub 2013 Dec 7. Eur J Neurol. 2014. PMID: 24313877

2

Mutated alpha-synuclein gene in two Greek kindreds with familial PD: incomplete penetrance?

Papadimitriou A, Veletza V, Hadjigeorgiou GM, Patrikiou A, Hirano M, Anastasopoulos I. Papadimitriou A, et al. Neurology. 1999 Feb;52(3):651-4. doi: 10.1212/wnl.52.3.651. Neurology. 1999. PMID: 10025809

3

Clinical characteristics of the alpha-synuclein mutation (G209A)-associated Parkinson's disease in comparison with other forms of familial Parkinson's disease in Greece.

Papapetropoulos S, Ellul J, Paschalis C, Athanassiadou A, Papadimitriou A, Papapetropoulos T. Papapetropoulos S, et al. Among authors: papadimitriou a. Eur J Neurol. 2003 May;10(3):281-6. doi: 10.1046/j.1468-1331.2003.00576.x. Eur J Neurol. 2003. PMID: 12752402

4

Screening for SNCA and LRRK2 mutations in Greek sporadic and autosomal dominant Parkinson's disease: identification of two novel LRRK2 variants.

Xiromerisiou G, Hadjigeorgiou GM, Gourbali V, Johnson J, Papakonstantinou I, Papadimitriou A, Singleton AB. Xiromerisiou G, et al. Among authors: papadimitriou a. Eur J Neurol. 2007 Jan;14(1):7-11. doi: 10.1111/j.1468-1331.2006.01551.x. Eur J Neurol. 2007. PMID: 17222106

5

Clinical phenotype in patients with alpha-synuclein Parkinson's disease living in Greece in comparison with patients with sporadic Parkinson's disease.

Papapetropoulos S, Paschalis C, Athanassiadou A, Papadimitriou A, Ellul J, Polymeropoulos MH, Papapetropoulos T. Papapetropoulos S, et al. Among authors: papadimitriou a. J Neurol Neurosurg Psychiatry. 2001 May;70(5):662-5. doi: 10.1136/jnnp.70.5.662. J Neurol Neurosurg Psychiatry. 2001. PMID: 11309462 Free PMC article.

6

Alpha-1 antichymotrypsin gene signal peptide a/t polymorphism and primary intracerebral hemorrhage.

Dardiotis E, Hadjigeorgiou GM, Dardioti M, Scarmeas N, Paterakis K, Aggelakis K, Komnos A, Tasiou A, Xiromerisiou G, Gabranis I, Zintzaras E, Papadimitriou A, Karantanas A. Dardiotis E, et al. Among authors: papadimitriou a. Eur Neurol. 2008;59(6):307-14. doi: 10.1159/000121420. Epub 2008 Apr 11. Eur Neurol. 2008. PMID: 18408372

7

A novel missense adenine nucleotide translocator-1 gene mutation in a Greek adPEO family.

Napoli L, Bordoni A, Zeviani M, Hadjigeorgiou GM, Sciacco M, Tiranti V, Terentiou A, Moggio M, Papadimitriou A, Scarlato G, Comi GP. Napoli L, et al. Among authors: papadimitriou a. Neurology. 2001 Dec 26;57(12):2295-8. doi: 10.1212/wnl.57.12.2295. Neurology. 2001. PMID: 11756613

8

Myoglobinuria due to quail poisoning.

Papadimitriou A, Hadjigeorgiou GM, Tsairis P, Papadimitriou E, Ouzounelli C, Ouzounellis T. Papadimitriou A, et al. Among authors: papadimitriou e. Eur Neurol. 1996;36(3):142-5. doi: 10.1159/000117231. Eur Neurol. 1996. PMID: 8738943

9

Partial depletion and multiple deletions of muscle mtDNA in familial MNGIE syndrome.

Papadimitriou A, Comi GP, Hadjigeorgiou GM, Bordoni A, Sciacco M, Napoli L, Prelle A, Moggio M, Fagiolari G, Bresolin N, Salani S, Anastasopoulos I, Giassakis G, Divari R, Scarlato G. Papadimitriou A, et al. Neurology. 1998 Oct;51(4):1086-92. doi: 10.1212/wnl.51.4.1086. Neurology. 1998. PMID: 9781534

10

Continuous muscle fiber activity associated with morphea (localized scleroderma).

Papadimitriou A, Chroni E, Anastasopoulos I, Avramidis T, Hadjigeorgiou G, Koutroumanidis M. Papadimitriou A, et al. Neurology. 1998 Dec;51(6):1763-4. doi: 10.1212/wnl.51.6.1763. Neurology. 1998. PMID: 9855545 No abstract available.

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