Hadjigeorgiou GM - Search Results

1

A new stop codon mutation (Y52X) in the myophosphorylase gene in a Greek patient with McArdle's disease.

Hadjigeorgiou GM, Papadimitriou A, Musumeci O, Paterakis K, Flabouriari K, Shanske S, DiMauro S. Hadjigeorgiou GM, et al. J Neurol Sci. 2002 Feb 15;194(1):83-6. doi: 10.1016/s0022-510x(01)00662-1. J Neurol Sci. 2002. PMID: 11809171

2

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.

3

Molecular genetic study of myophosphorylase deficiency (McArdle's disease) in two Yemenite-Jewish families.

Hadjigeorgiou GM, Sadeh M, Musumeci O, Dabby R, De Girolami L, Naini A, Papadimitriou A, Shanske S, DiMauro S. Hadjigeorgiou GM, et al. Neuromuscul Disord. 2002 Nov;12(9):824-7. doi: 10.1016/s0960-8966(02)00028-7. Neuromuscul Disord. 2002. PMID: 12398832 Clinical Trial.

4

Increased frequency of white matter lesions in patients with osteonecrosis (WMLeOn) of the femoral head.

Hadjigeorgiou GM, Karantanas AH, Zibis A, Dardiotis E, Aggelakis K, Papadimitriou A, Malizos K. Hadjigeorgiou GM, et al. Eur J Radiol. 2004 Jun;50(3):278-84. doi: 10.1016/j.ejrad.2004.01.025. Eur J Radiol. 2004. PMID: 15145488

5

Cervical spinal cord intramedullary teratoma.

Paterakis KN, Karantanas AH, Barbanis S, Hadjigeorgiou GM, Karavelis A. Paterakis KN, et al. Among authors: hadjigeorgiou gm. Clin Neurol Neurosurg. 2006 Jul;108(5):514-7. doi: 10.1016/j.clineuro.2005.02.006. Clin Neurol Neurosurg. 2006. PMID: 16099092 Review.

6

Association of alpha-synuclein Rep1 polymorphism and Parkinson's disease: influence of Rep1 on age at onset.

Hadjigeorgiou GM, Xiromerisiou G, Gourbali V, Aggelakis K, Scarmeas N, Papadimitriou A, Singleton A. Hadjigeorgiou GM, et al. Mov Disord. 2006 Apr;21(4):534-9. doi: 10.1002/mds.20752. Mov Disord. 2006. PMID: 16250025

7

The human prion gene M129V polymorphism is not associated with idiopathic Parkinson's disease in three distinct populations.

Scholz SW, Xiromerisiou G, Fung HC, Eerola J, Hellström O, Papadimitriou A, Hadjigeorgiou GM, Tienari PJ, Fernandez HH, Mandel R, Okun MS, Gwinn-Hardy K, Singleton AB. Scholz SW, et al. Among authors: hadjigeorgiou gm. Neurosci Lett. 2006 Mar 13;395(3):227-9. doi: 10.1016/j.neulet.2005.10.081. Epub 2005 Nov 18. Neurosci Lett. 2006. PMID: 16298483

8

Retroclival epidural hematoma secondary to a longitudinal clivus fracture.

Paterakis KN, Karantanas AH, Hadjigeorgiou GM, Anagnostopoulos V, Karavelis A. Paterakis KN, et al. Among authors: hadjigeorgiou gm. Clin Neurol Neurosurg. 2005 Dec;108(1):67-72. doi: 10.1016/j.clineuro.2004.11.010. Epub 2005 Jan 9. Clin Neurol Neurosurg. 2005. PMID: 16311151

9

Re: Lack of association between the IL1A gene (-889) polymorphism and outcome after head injury. Tanriverdi T et al. Surg Neurol 2006;65:7-10; discussion 10.

Dardiotis E, Dardioti M, Hadjigeorgiou GM, Paterakis K. Dardiotis E, et al. Among authors: hadjigeorgiou gm. Surg Neurol. 2006 Sep;66(3):334-5. doi: 10.1016/j.surneu.2006.05.042. Surg Neurol. 2006. PMID: 16935657 No abstract available.

10

Autoantibodies to alpha-synuclein in inherited Parkinson's disease.

Papachroni KK, Ninkina N, Papapanagiotou A, Hadjigeorgiou GM, Xiromerisiou G, Papadimitriou A, Kalofoutis A, Buchman VL. Papachroni KK, et al. Among authors: hadjigeorgiou gm. J Neurochem. 2007 May;101(3):749-56. doi: 10.1111/j.1471-4159.2006.04365.x. J Neurochem. 2007. PMID: 17448146 Free PMC article.

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