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Items: 1 to 50 of 55

1.

Correspondence regarding "Are thyroid function tests in neonates born to mothers with hypothyroidism clinically useful?"

Balomenou F, Siomou E, Kolios G, Bairaktari E, Tzoufi M, Giapros V.

Early Hum Dev. 2019 Oct 25:104905. doi: 10.1016/j.earlhumdev.2019.104905. [Epub ahead of print] No abstract available.

PMID:
31668677
2.

An update on renal scarring after urinary tract infection in children: what are the risk factors?

Kosmeri C, Kalaitzidis R, Siomou E.

J Pediatr Urol. 2019 Sep 16. pii: S1477-5131(19)30296-7. doi: 10.1016/j.jpurol.2019.09.010. [Epub ahead of print] Review.

PMID:
31591046
3.

Investigation of Autoimmune Disease in Children with Chronic Spontaneous Urticaria.

Kosmeri C, Siomou E, Challa A, Tsabouri S.

Int Arch Allergy Immunol. 2019 Sep 13:1-5. doi: 10.1159/000502521. [Epub ahead of print]

PMID:
31522183
4.

Are thyroid function tests in neonates born to mothers with hypothyroidism clinically useful?

Balomenou F, Siomou E, Kolios G, Bairaktari E, Tzoufi M, Giapros V.

Early Hum Dev. 2019 Sep 7;139:104877. doi: 10.1016/j.earlhumdev.2019.104877. [Epub ahead of print]

PMID:
31505311
5.

Autism spectrum disorder, anxiety and severe depression in a male patient with deletion and duplication in the 21q22.3 region: A case report.

Orru S, Papoulidis I, Siomou E, Papadimitriou DT, Sotiriou S, Nikolaidis P, Eleftheriades M, Papanikolaou E, Thomaidis L, Manolakos E.

Biomed Rep. 2019 Jun;1(1):1-5. doi: 10.3892/br.2019.1210. Epub 2019 May 13.

6.

Vitamin D supplementation and bone markers in ambulatory children on long-term valproic acid therapy. A prospective interventional study.

Papassava M, Nakou I, Siomou E, Cholevas V, Challa A, Tzoufi M.

Epilepsy Behav. 2019 Aug;97:192-196. doi: 10.1016/j.yebeh.2019.05.029. Epub 2019 Jun 26.

PMID:
31252278
7.

Elevated 1-hour post-load plasma glucose identifies obese youth with abnormal glucose metabolism and an unfavourable inflammatory profile.

Serbis A, Giapros V, Challa A, Chaliasos N, Siomou E.

Clin Endocrinol (Oxf). 2018 Dec;89(6):757-764. doi: 10.1111/cen.13859. Epub 2018 Oct 11.

PMID:
30229983
8.

Review shows that lipid disorders are associated with endothelial but not renal dysfunction in children.

Kosmeri C, Siomou E, Vlahos AP, Milionis H.

Acta Paediatr. 2019 Jan;108(1):19-27. doi: 10.1111/apa.14529. Epub 2018 Aug 22. Review.

PMID:
30066344
9.

Does idiopathic hypercalciuria affect bone metabolism during childhood? A prospective case-control study.

Pavlou M, Giapros V, Challa A, Chaliasos N, Siomou E.

Pediatr Nephrol. 2018 Dec;33(12):2321-2328. doi: 10.1007/s00467-018-4027-y. Epub 2018 Jul 25.

PMID:
30043116
10.

Copy-number variation analysis in familial nonsyndromic congenital anomalies of the kidney and urinary tract: Evidence for the causative role of a transposable element-associated genomic rearrangement.

Siomou E, Mitsioni AG, Giapros V, Bouba I, Noutsopoulos D, Georgiou I.

Mol Med Rep. 2017 Jun;15(6):3631-3636. doi: 10.3892/mmr.2017.6462. Epub 2017 Apr 12.

11.

Non-invasive prenatal screening versus prenatal diagnosis by array comparative genomic hybridization: a comparative retrospective study.

Sotiriadis A, Papoulidis I, Siomou E, Papageorgiou E, Eleftheriades M, Papadopoulos V, Alexiou M, Manolakos E, Athanasiadis A.

Prenat Diagn. 2017 Jun;37(6):583-592. doi: 10.1002/pd.5051. Epub 2017 May 23.

PMID:
28406537
12.

Repetitive reddish discoloration of the urine in an adolescent female following short-distance walking on a smooth road: Answers.

Siomou E, Baziou M, Premetis E, Vercellati C, Chaliasos N, Makis A.

Pediatr Nephrol. 2017 Dec;32(12):2255-2257. doi: 10.1007/s00467-017-3611-x. Epub 2017 Feb 13. No abstract available.

PMID:
28194572
13.

Repetitive reddish discoloration of urine in a female adolescent following short-distance walking on a smooth road: Questions.

Siomou E, Baziou M, Premetis E, Vercellati C, Chaliasos N, Makis A.

Pediatr Nephrol. 2017 Dec;32(12):2253-2254. doi: 10.1007/s00467-017-3596-5. Epub 2017 Feb 13.

PMID:
28194571
14.

Prenatal diagnosis of 1p34.3 interstitial microdeletion by aCGH in a fetus with jaw bone abnormalities.

Dagklis T, Papageorgiou E, Siomou E, Paspaliaris V, Zerva C, Chatzis P, Thomaidis L, Manolakos E, Papoulidis I.

Mol Cytogenet. 2016 Oct 6;9:77. eCollection 2016.

15.

Low-birth-weight, but not catch-up growth, correlates with insulin resistance and resistin level in SGA infants at 12 months.

Giapros V, Vavva E, Siomou E, Kolios G, Tsabouri S, Cholevas V, Bairaktari E, Tzoufi M, Challa A.

J Matern Fetal Neonatal Med. 2017 Aug;30(15):1771-1776. doi: 10.1080/14767058.2016.1224838. Epub 2016 Sep 9.

PMID:
27609490
16.

ROBO2 gene variants in children with primary nonsyndromic vesicoureteral reflux with or without renal hypoplasia/dysplasia.

Mitsioni AG, Siomou E, Bouba I, Petridi S, Siamopoulou A, Georgiou I.

Pediatr Res. 2016 Jul;80(1):72-6. doi: 10.1038/pr.2016.51. Epub 2016 Mar 22.

PMID:
27002985
17.

aHUS associated with C3 gene mutation: a case with numerous relapses and favorable 20-year outcome.

Siomou E, Gkoutsias A, Serbis A, Kollios K, Chaliasos N, Frémeaux-Bacchi V.

Pediatr Nephrol. 2016 Mar;31(3):513-7. doi: 10.1007/s00467-015-3267-3. Epub 2015 Nov 16.

PMID:
26572892
18.

Interstitial deletion at 11q14.2-11q22.1 may cause severe learning difficulties, mental retardation and mild heart defects in 13-year old male.

Papoulidis I, Paspaliaris V, Siomou E, Orru S, Murru R, Sifakis S, Nikolaidis P, Garas A, Sotiriou S, Thomaidis L, Manolakos E.

Mol Cytogenet. 2015 Sep 17;8:71. doi: 10.1186/s13039-015-0175-y. eCollection 2015.

19.

Routine use of array comparative genomic hybridization (aCGH) as standard approach for prenatal diagnosis of chromosomal abnormalities. Clinical experience of 1763 prenatal cases.

Papoulidis I, Sotiriadis A, Siomou E, Papageorgiou E, Eleftheriades M, Papadopoulos V, Oikonomidou E, Orru S, Manolakos E, Athanasiadis A.

Prenat Diagn. 2015 Dec;35(13):1269-77. doi: 10.1002/pd.4685. Epub 2015 Oct 26.

PMID:
26289927
20.

The relation of vitamin D status with metabolic syndrome in childhood and adolescence: an update.

Challa AS, Makariou SE, Siomou EC.

J Pediatr Endocrinol Metab. 2015 Nov 1;28(11-12):1235-45. doi: 10.1515/jpem-2014-0485. Review.

PMID:
26053006
21.

Deletion of 4.4 Mb at 2q33.2q33.3 May Cause Growth Deficiency in a Patient with Mental Retardation, Facial Dysmorphic Features and Speech Delay.

Papoulidis I, Paspaliaris V, Papageorgiou E, Siomou E, Dagklis T, Sotiriou S, Thomaidis L, Manolakos E.

Cytogenet Genome Res. 2015;145(1):19-24. doi: 10.1159/000381568. Epub 2015 Apr 24.

PMID:
25925190
22.
23.

An audit analysis of a guideline for the investigation and initial therapy of diarrhea negative (atypical) hemolytic uremic syndrome.

Johnson S, Stojanovic J, Ariceta G, Bitzan M, Besbas N, Frieling M, Karpman D, Landau D, Langman C, Licht C, Pecoraro C, Riedl M, Siomou E, van de Kar N, Walle JV, Loirat C, Taylor CM.

Pediatr Nephrol. 2014 Oct;29(10):1967-78. doi: 10.1007/s00467-014-2817-4. Epub 2014 May 11.

PMID:
24817340
24.

Arterial hypertension during treatment with triptorelin in a child with Williams-Beuren syndrome.

Siomou E, Kosmeri C, Pavlou M, Vlahos AP, Argyropoulou MI, Siamopoulou A.

Pediatr Nephrol. 2014 Sep;29(9):1633-6. doi: 10.1007/s00467-014-2795-6. Epub 2014 Mar 7.

PMID:
24604705
25.
26.

A patient with partial trisomy 21 and 7q deletion expresses mild Down syndrome phenotype.

Papoulidis I, Papageorgiou E, Siomou E, Oikonomidou E, Thomaidis L, Vetro A, Zuffardi O, Liehr T, Manolakos E, Vassilis P.

Gene. 2014 Feb 25;536(2):441-3. doi: 10.1016/j.gene.2013.11.078. Epub 2013 Dec 13.

PMID:
24334122
27.

Prenatal detection of TAR syndrome in a fetus with compound inheritance of an RBM8A SNP and a 334‑kb deletion: a case report.

Papoulidis I, Oikonomidou E, Orru S, Siomou E, Kontodiou M, Eleftheriades M, Bacoulas V, Cigudosa JC, Suela J, Thomaidis L, Manolakos E.

Mol Med Rep. 2014 Jan;9(1):163-5. doi: 10.3892/mmr.2013.1788. Epub 2013 Nov 11.

PMID:
24220582
28.

Prenatal diagnosis of two de novo 4q35-qter deletions characterized by array-CGH.

Manolakos E, Kefalas K, Vetro A, Oikonomidou E, Daskalakis G, Psara N, Siomou E, Papageorgiou E, Sevastopoulou E, Konstantinidou A, Vrachnis N, Thomaidis L, Zuffardi O, Papoulidis I.

Mol Cytogenet. 2013 Oct 31;6(1):47. doi: 10.1186/1755-8166-6-47.

29.

Growth and function in childhood of a normal solitary kidney from birth or from early infancy.

Siomou E, Giapros V, Papadopoulou F, Pavlou M, Fotopoulos A, Siamopoulou A.

Pediatr Nephrol. 2014 Feb;29(2):249-56. doi: 10.1007/s00467-013-2623-4. Epub 2013 Sep 17.

PMID:
24043649
30.

A rare case report of simultaneous presentation of myopathy, Addison's disease, primary hypoparathyroidism, and Fanconi syndrome in a child diagnosed with Kearns-Sayre syndrome.

Tzoufi M, Makis A, Chaliasos N, Nakou I, Siomou E, Tsatsoulis A, Zikou A, Argyropoulou M, Bonnefont JP, Siamopoulou A.

Eur J Pediatr. 2013 Apr;172(4):557-61. doi: 10.1007/s00431-012-1798-1. Epub 2012 Aug 9.

PMID:
22875312
31.

FGF-23 in children with CKD: a new player in the development of CKD-mineral and bone disorder.

Siomou E, Stefanidis CJ.

Nephrol Dial Transplant. 2012 Dec;27(12):4259-62. doi: 10.1093/ndt/gfs315. Epub 2012 Jul 29.

PMID:
22848110
32.

A 725 kb deletion at 22q13.1 chromosomal region including SOX10 gene in a boy with a neurologic variant of Waardenburg syndrome type 2.

Siomou E, Manolakos E, Petersen M, Thomaidis L, Gyftodimou Y, Orru S, Papoulidis I.

Eur J Med Genet. 2012 Nov;55(11):641-5. doi: 10.1016/j.ejmg.2012.07.002. Epub 2012 Jul 25.

PMID:
22842075
33.

ANCA-associated glomerulonephritis/systemic vasculitis in childhood: clinical features-outcome.

Siomou E, Tramma D, Bowen C, Milford DV.

Pediatr Nephrol. 2012 Oct;27(10):1911-20. doi: 10.1007/s00467-012-2198-5. Epub 2012 May 31.

PMID:
22648163
34.

Dual testing with QF-PCR and karyotype analysis for prenatal diagnosis of chromosomal abnormalities. Evaluation of 13,500 cases with consideration of using QF-PCR as a stand-alone test according to referral indications.

Papoulidis I, Siomou E, Sotiriadis A, Efstathiou G, Psara A, Sevastopoulou E, Anastasakis E, Sifakis S, Tsiligianni T, Kontodiou M, Malamaki C, Tzimina M, Petersen MB, Manolakos E, Athanasiadis A.

Prenat Diagn. 2012 Jul;32(7):680-5. doi: 10.1002/pd.3888. Epub 2012 Apr 18.

PMID:
22513450
35.

Tetrasomy 9p mosaicism associated with a normal phenotype in two cases.

Papoulidis I, Kontodiou M, Tzimina M, Saitis I, Hamid AB, Klein E, Kosyakova N, Kordass U, Kunz J, Siomou E, Nicolaides P, Orru S, Thomaidis L, Liehr T, Petersen MB, Manolakos E.

Cytogenet Genome Res. 2012;136(4):237-41. doi: 10.1159/000337520. Epub 2012 Apr 5. Review.

36.

Visfatin levels in prepubertal children born small or large for gestational age.

Giapros VI, Kiortsis DN, Evagelidou EN, Challa AS, Cholevas VK, Siomou EC, Bairaktari ET, Andronikou SK.

Horm Metab Res. 2012 Feb;44(2):135-9. doi: 10.1055/s-0031-1299729. Epub 2012 Jan 13.

PMID:
22314334
37.

Renal function and kidney length in preterm infants with nephrocalcinosis: a longitudinal study.

Giapros V, Tsoni C, Challa A, Cholevas V, Argyropoulou M, Papadopoulou F, Siomou E, Drougia A, Andronikou S.

Pediatr Nephrol. 2011 Oct;26(10):1873-80. doi: 10.1007/s00467-011-1895-9. Epub 2011 May 1.

PMID:
21533868
38.

Serum osteoprotegerin, RANKL and fibroblast growth factor-23 in children with chronic kidney disease.

Siomou E, Challa A, Printza N, Giapros V, Petropoulou F, Mitsioni A, Papachristou F, Stefanidis CJ.

Pediatr Nephrol. 2011 Jul;26(7):1105-14. doi: 10.1007/s00467-011-1870-5. Epub 2011 Apr 9.

PMID:
21479768
39.

Autosomal dominant polycystic kidney disease (ADPKD) associated with steroid-sensitive nephrotic syndrome in childhood.

Siomou E, Jarvis J, Hulton SA.

Pediatr Nephrol. 2011 Apr;26(4):643-4. doi: 10.1007/s00467-010-1710-z. Epub 2010 Nov 30. No abstract available.

PMID:
21116827
40.

Comparative study of quantitative ultrasonography and dual-energy X-ray absorptiometry for evaluating renal osteodystrophy in children with chronic kidney disease.

Christoforidis A, Printza N, Gkogka C, Siomou E, Challa A, Kazantzidou E, Kollios K, Papachristou F.

J Bone Miner Metab. 2011 May;29(3):321-7. doi: 10.1007/s00774-010-0220-1. Epub 2010 Sep 16.

PMID:
20845051
41.

Prothrombotic state, cardiovascular, and metabolic syndrome risk factors in prepubertal children born large for gestational age.

Evagelidou EN, Giapros VI, Challa AS, Cholevas VK, Vartholomatos GA, Siomou EC, Kolaitis NI, Bairaktari ET, Andronikou SK.

Diabetes Care. 2010 Nov;33(11):2468-70. doi: 10.2337/dc10-1190. Epub 2010 Aug 19.

42.

A fetus with ring chromosome 21 characterized by aCGH shows no clinical findings after birth.

Papoulidis I, Manolakos E, Siomou E, Kefalas K, Thomaidis L, Liehr T, Vetro A, Athanasiadis A, Zuffardi O, Petersen MB.

Prenat Diagn. 2010 Jun;30(6):586-8. doi: 10.1002/pd.2524. No abstract available.

PMID:
20509162
43.

Implications of 99mTc-DMSA scintigraphy performed during urinary tract infection in neonates.

Siomou E, Giapros V, Fotopoulos A, Aasioti M, Papadopoulou F, Serbis A, Siamopoulou A, Andronikou S.

Pediatrics. 2009 Sep;124(3):881-7. doi: 10.1542/peds.2008-1963. Epub 2009 Aug 3.

PMID:
19661052
44.

Absence of mutations in the HOXA11 and HOXD11 genes in children with congenital renal malformations.

Bouba I, Siomou E, Stefanidis CJ, Emmanouilidou A, Galidi A, Hatzi E, Markoula S, Mitsioni A, Siamopoulou A, Georgiou I.

Pediatr Nephrol. 2009 Aug;24(8):1569-72. doi: 10.1007/s00467-009-1140-y. Epub 2009 Mar 3.

PMID:
19255789
45.

Harmonic voiding urosonography with a second-generation contrast agent for the diagnosis of vesicoureteral reflux.

Papadopoulou F, Anthopoulou A, Siomou E, Efremidis S, Tsamboulas C, Darge K.

Pediatr Radiol. 2009 Mar;39(3):239-44. doi: 10.1007/s00247-008-1080-x. Epub 2008 Dec 19.

PMID:
19096835
46.

Wnt regulates axon behavior through changes in microtubule growth directionality: a new role for adenomatous polyposis coli.

Purro SA, Ciani L, Hoyos-Flight M, Stamatakou E, Siomou E, Salinas PC.

J Neurosci. 2008 Aug 20;28(34):8644-54. doi: 10.1523/JNEUROSCI.2320-08.2008.

47.

Masked severe stenosing ureteritis: a rare complication of Henoch-Schönlein purpura.

Siomou E, Serbis A, Salakos C, Papadopoulou F, Stefanidis CJ, Siamopoulou A.

Pediatr Nephrol. 2008 May;23(5):821-5. doi: 10.1007/s00467-007-0698-5. Epub 2008 Jan 25.

PMID:
18219497
48.

Rare combination of unilateral renal agenesis, congenital obstructive posterior urethral membrane, and enlarged prostatic utricle, with absence of hydroureteronephrosis.

Siomou E, Papadopoulou F, Salakos C, Giapros V, Andonikou S, Siamopoulou A.

Urology. 2007 Nov;70(5):1008.e1-3. Erratum in: Urology. 2008 Jun;71(6):1234.

PMID:
18068471
49.

Angiotensin II type 2 receptor gene polymorphism in Caucasian children with a wide spectrum of congenital anomalies of the kidney and urinary tract.

Siomou E, Bouba I, Kollios KD, Papadopoulou F, Syrrou M, Georgiou I, Siamopoulou A.

Pediatr Res. 2007 Jul;62(1):83-7.

PMID:
17515833
50.

Imaging strategies for vesicoureteral reflux diagnosis.

Stefanidis CJ, Siomou E.

Pediatr Nephrol. 2007 Jul;22(7):937-47. Epub 2007 Jan 10.

PMID:
17216249

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