Tzoufi M - Search Results

1

A gene for nonsyndromic X-linked mental retardation (MRX77) maps to Xq12-Xq21.33.

Sismani C, Syrrou M, Christodoulou K, Hamel B, Chelly J, Yntema HG, van Bokhoven H, Tzoufi M, Georgiou I, Patsalis PC. Sismani C, et al. Among authors: tzoufi m. Am J Med Genet A. 2003 Sep 15;122A(1):46-50. doi: 10.1002/ajmg.a.20284. Am J Med Genet A. 2003. PMID: 12949971

2

Mosaic trisomy r(14) associated with epilepsy and mental retardation.

Tzoufi M, Kanioglou C, Dasoula A, Asproudis I, Tsatsoulis A, Sismani C, Patsalis PC, Georgiou I, Syrrou M. Tzoufi M, et al. J Child Neurol. 2007 Jul;22(7):869-73. doi: 10.1177/0883073807304196. J Child Neurol. 2007. PMID: 17715281

3

Refining the locus of branchio-otic syndrome 2 (BOS2) to a 5.25 Mb locus on chromosome 1q31.3q32.1.

Thienpont B, Dimitriadou E, Theodoropoulos K, Breckpot J, Fryssira H, Kitsiou-Tzeli S, Tzoufi M, Vermeesch JR, Syrrou M, Devriendt K. Thienpont B, et al. Among authors: tzoufi m. Eur J Med Genet. 2009 Nov-Dec;52(6):393-7. doi: 10.1016/j.ejmg.2009.09.005. Epub 2009 Sep 17. Eur J Med Genet. 2009. PMID: 19772953

4

UGT1A6- and UGT2B7-related valproic acid pharmacogenomics according to age groups and total drug concentration levels.

Chatzistefanidis D, Lazaros L, Giaka K, Nakou I, Tzoufi M, Georgiou I, Kyritsis A, Markoula S. Chatzistefanidis D, et al. Among authors: tzoufi m. Pharmacogenomics. 2016 Jun;17(8):827-35. doi: 10.2217/pgs-2016-0014. Epub 2016 May 27. Pharmacogenomics. 2016. PMID: 27232006

5

Idiopathic intracranial hypertension and facial palsy: case report and review of the literature.

Tzoufi M, Makis A, Grammeniatis V, Nakou I, Exarchakos G, Asproudis I, Zikou A, Argyropoulou M, Siamopoulou-Mavridou A. Tzoufi M, et al. J Child Neurol. 2010 Dec;25(12):1529-34. doi: 10.1177/0883073810375849. Epub 2010 Oct 4. J Child Neurol. 2010. PMID: 20921567 Review.

6

Isolated abducens nerve palsy after closed head injury in a child.

Asproudis I, Vourda E, Zafeiropoulos P, Katsanos A, Tzoufi M. Asproudis I, et al. Among authors: tzoufi m. Oman J Ophthalmol. 2015 Sep-Dec;8(3):179-80. doi: 10.4103/0974-620X.169905. Oman J Ophthalmol. 2015. PMID: 26903725 Free PMC article.

7

Valproate-induced eosinophilia in children with epilepsy: role of interleukin-5.

Makis AC, Tzoufi M, Kateri MD, Bourantas KL, Papadopoulou ZL. Makis AC, et al. Among authors: tzoufi m. J Child Neurol. 2005 Feb;20(2):150-2. doi: 10.1177/08830738050200022201. J Child Neurol. 2005. PMID: 15794184

8

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. Tzoufi M, et al. Eur J Pediatr. 2013 Apr;172(4):557-61. doi: 10.1007/s00431-012-1798-1. Epub 2012 Aug 9. Eur J Pediatr. 2013. PMID: 22875312

9

Genetic risk factors associated with thrombosis in children with congenital neurologic disorders.

Tzoufi M, Giotopoulou S, Papadimitriou P, Dokou E, Kolaitis NI, Siamopoulou A, Vartholomatos G. Tzoufi M, et al. J Child Neurol. 2005 Jun;20(6):509-12. doi: 10.1177/08830738050200060701. J Child Neurol. 2005. PMID: 15996400

10

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. Papassava M, et al. Among authors: tzoufi m. Epilepsy Behav. 2019 Aug;97:192-196. doi: 10.1016/j.yebeh.2019.05.029. Epub 2019 Jun 26. Epilepsy Behav. 2019. PMID: 31252278

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