Xaidara A - Search Results

1

Alternating hemiplegia of childhood: a syndrome inherited with an autosomal dominant trait.

Kanavakis E, Xaidara A, Papathanasiou-Klontza D, Papadimitriou A, Velentza S, Youroukos S. Kanavakis E, et al. Among authors: xaidara a. Dev Med Child Neurol. 2003 Dec;45(12):833-6. doi: 10.1017/s0012162203001543. Dev Med Child Neurol. 2003. PMID: 14667076 Free article.

2

Alternating hemiplegia of childhood or familial hemiplegic migraine? A novel ATP1A2 mutation.

Swoboda KJ, Kanavakis E, Xaidara A, Johnson JE, Leppert MF, Schlesinger-Massart MB, Ptacek LJ, Silver K, Youroukos S. Swoboda KJ, et al. Among authors: xaidara a. Ann Neurol. 2004 Jun;55(6):884-7. doi: 10.1002/ana.20134. Ann Neurol. 2004. PMID: 15174025

3

Paroxysmal non-kinesigenic dyskinesia due to a PNKD recurrent mutation: report of two Southern European families.

Pons R, Cuenca-León E, Miravet E, Pons M, Xaidara A, Youroukos S, Macaya A. Pons R, et al. Among authors: xaidara a. Eur J Paediatr Neurol. 2012 Jan;16(1):86-9. doi: 10.1016/j.ejpn.2011.09.008. Epub 2011 Oct 1. Eur J Paediatr Neurol. 2012. PMID: 21962874

4

Family pattern of idiopathic hypercalciuria and its subtypes.

Nicolaidou P, Themeli S, Karpathios T, Georgouli H, Athanassaki K, Xaidara A, Messaritakis J. Nicolaidou P, et al. Among authors: xaidara a. J Urol. 1996 Mar;155(3):1042-4. J Urol. 1996. PMID: 8583560

5

Insulin dependent diabetes mellitus (IDDM) and autoimmune thyroiditis in a boy with a ring chromosome 18: additional evidence of autoimmunity or IDDM gene(s) on chromosome 18.

Dacou-Voutetakis C, Sertedaki A, Maniatis-Christidis M, Sarri C, Karadima G, Petersen MB, Xaidara A, Kanariou M, Nicolaidou P. Dacou-Voutetakis C, et al. Among authors: xaidara a. J Med Genet. 1999 Feb;36(2):156-8. J Med Genet. 1999. PMID: 10051018 Free PMC article.

6

Neuroblastoma metastatic to brain.

Xaidara A, Andrioti M, Mikraki V, Prodromou N, Grafacos S, Arvanitis D, Hadjigeorgi C, Tzortzatou-Stathopoulou F. Xaidara A, et al. Med Pediatr Oncol. 1996 Mar;26(3):208-14. doi: 10.1002/(SICI)1096-911X(199603)26:3<208::AID-MPO11>3.0.CO;2-C. Med Pediatr Oncol. 1996. PMID: 8544805 No abstract available.

7

Chitotriosidase plasma activity in nephropathic cystinosis.

Xaidara A, Karavitakis EM, Kosma K, Emma F, Dimitriou E, Michelakakis H. Xaidara A, et al. J Inherit Metab Dis. 2009 Dec;32 Suppl 1:S157-9. doi: 10.1007/s10545-009-1118-8. Epub 2009 May 20. J Inherit Metab Dis. 2009. PMID: 19455402

8

Niemann-Pick type C disease: a novel NPC1 mutation segregating in a Greek island.

Mavridou I, Cozar M, Douzgou S, Xaidara A, Lianou D, Vanier MT, Dimitriou E, Grinberg D, Vilageliu L, Michelakakis H. Mavridou I, et al. Among authors: xaidara a. Clin Genet. 2014 Jun;85(6):543-7. doi: 10.1111/cge.12200. Epub 2013 Jun 12. Clin Genet. 2014. PMID: 23701245

9

Evolution of Fabry disease in male patients: the Greek experience.

Andrikos E, Iatrou C, Boletis JN, Diamandopoulos A, Katsinas C, Kalaitzidis K, Galinas A, Xaidara A, Pappas M, Siamopoulos KC. Andrikos E, et al. Among authors: xaidara a. Clin Nephrol. 2010 Jan;73(1):58-63. doi: 10.5414/cnp73058. Clin Nephrol. 2010. PMID: 20040353

10

Propranolol treatment for severe infantile hemangiomas: a single-centre 3-year experience.

Georgountzou A, Karavitakis E, Klimentopoulou A, Xaidara A, Kakourou T. Georgountzou A, et al. Among authors: xaidara a. Acta Paediatr. 2012 Oct;101(10):e469-74. doi: 10.1111/j.1651-2227.2012.02783.x. Epub 2012 Jul 24. Acta Paediatr. 2012. PMID: 22804809

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