Neou P - Search Results

1

Pseudodominant inheritance of DFNB1 deafness due to the common 35delG mutation.

Pampanos A, Neou P, Iliades T, Apostolopoulos N, Voyiatzis N, Grigoriadou M, Katsichti L, Skevas A, Petersen MB. Pampanos A, et al. Among authors: neou p. Clin Genet. 2000 Mar;57(3):232-4. doi: 10.1034/j.1399-0004.2000.570311.x. Clin Genet. 2000. PMID: 10782932 No abstract available.

2

Prelingual nonsyndromic hearing loss in Greece. Molecular and clinical findings.

Iliades T, Eleftheriades N, Iliadou V, Pampanos A, Voyiatzis N, Economides J, Leotsakos P, Neou P, Tsakanikos M, Antoniadi T, Konstantopoulou I, Yannoukakos D, Grigoriadou M, Skevas A, Petersen MB. Iliades T, et al. Among authors: neou p. ORL J Otorhinolaryngol Relat Spec. 2002 Sep-Oct;64(5):321-3. doi: 10.1159/000066088. ORL J Otorhinolaryngol Relat Spec. 2002. PMID: 12417772

3

The A1555G mitochondrial DNA mutation in Greek patients with non-syndromic, sensorineural hearing loss.

Kokotas H, Grigoriadou M, Korres GS, Ferekidou E, Papadopoulou E, Neou P, Giannoulia-Karantana A, Kandiloros D, Korres S, Petersen MB. Kokotas H, et al. Among authors: neou p. Biochem Biophys Res Commun. 2009 Dec 18;390(3):755-7. doi: 10.1016/j.bbrc.2009.10.044. Epub 2009 Oct 14. Biochem Biophys Res Commun. 2009. PMID: 19835846

4

Etiological diagnosis of bilateral, sensorineural hearing impairment in a pediatric Greek population.

Riga M, Psarommatis I, Lyra Ch, Douniadakis D, Tsakanikos M, Neou P, Apostolopoulos N. Riga M, et al. Among authors: neou p. Int J Pediatr Otorhinolaryngol. 2005 Apr;69(4):449-55. doi: 10.1016/j.ijporl.2004.11.007. Epub 2005 Jan 4. Int J Pediatr Otorhinolaryngol. 2005. PMID: 15763280

5

Button battery ingestion: the Greek experience and review of the literature.

Amanatidou V, Sofidiotou V, Fountas K, Kalostou A, Tsamadou A, Papathanassiou V, Neou P. Amanatidou V, et al. Among authors: neou p. Pediatr Emerg Care. 2011 Mar;27(3):186-8. doi: 10.1097/PEC.0b013e31820d6556. Pediatr Emerg Care. 2011. PMID: 21346675

6

Prevalence of GJB2 mutations in prelingual deafness in the Greek population.

Pampanos A, Economides J, Iliadou V, Neou P, Leotsakos P, Voyiatzis N, Eleftheriades N, Tsakanikos M, Antoniadi T, Hatzaki A, Konstantopoulou I, Yannoukakos D, Gronskov K, Brondum-Nielsen K, Grigoriadou M, Gyftodimou J, Iliades T, Skevas A, Petersen MB. Pampanos A, et al. Among authors: neou p. Int J Pediatr Otorhinolaryngol. 2002 Sep 2;65(2):101-8. doi: 10.1016/s0165-5876(02)00177-5. Int J Pediatr Otorhinolaryngol. 2002. PMID: 12176179

7

M-mode echocardiographic evaluation of systolic function, LV volume and mass in children on growth hormone therapy.

Stamoyannou L, Georgacopoulos D, Trapali C, Neou P, Bartsocas CS, Margetakis A. Stamoyannou L, et al. Among authors: neou p. J Pediatr Endocrinol Metab. 2000 Feb;13(2):157-61. doi: 10.1515/jpem.2000.13.2.157. J Pediatr Endocrinol Metab. 2000. PMID: 10711660

8

Growth and growth hormone therapy in children with achondroplasia: a two-year experience.

Stamoyannou L, Karachaliou F, Neou P, Papataxiarchou K, Pistevos G, Bartsocas CS. Stamoyannou L, et al. Among authors: neou p. Am J Med Genet. 1997 Oct 3;72(1):71-6. Am J Med Genet. 1997. PMID: 9295079

9

Melnick-Needles syndrome in a mother and her son.

Neou P, Kyrkanides S, Gioureli E, Bartsocas CS. Neou P, et al. Genet Couns. 1996;7(2):123-9. Genet Couns. 1996. PMID: 8831131

10

Familial bilateral blepharoptosis and subvalvular aortic stenosis.

Bazopoulou-Kyrkanidou E, Neou P, Bartsocas CS, Kyrkanides S, Fanourakis I. Bazopoulou-Kyrkanidou E, et al. Among authors: neou p. Genet Couns. 1995;6(3):227-32. Genet Couns. 1995. PMID: 8588851

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