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George Kitsos

Showing results (21-30 of 35) with videos related to

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Clinical Ophthalmology (Auckland, N.Z.)|March 18, 2010
Periocular xanthogranuloma: A forgotten entity?Charalampos Papagoras, George Kitsos, Paraskevi V Voulgari, et al.
Journal of Ophthalmology|July 14, 2018
Psychological Aspects and Depression in Patients with Symptomatic KeratoconusMarilita M Moschos, Nikolaos S Gouliopoulos, Chris Kalogeropoulos, et al.
European Journal of Radiology|January 25, 2018
Pseudoexfoliation syndrome without glaucoma: White matter abnormalities detected by conventional MRI and diffusion tensor imagingAnastasia K Zikou, George Kitsos, Loukas G Astrakas, et al.
Clinical Ophthalmology (Auckland, N.Z.)|August 11, 2017
Investigation of associations of <i>ARMS2</i>, <i>CD14</i>, and <i>TLR4</i> gene polymorphisms with wet age-related macular degeneration in a Greek populationAntonia Sarli, Iosif Skalidakis, Aliki Velissari, et al.
Experimental and Therapeutic Medicine|March 27, 2014
Proximal 10q duplication in a child with severe central hypotonia characterized by array-comparative genomic hybridization: A case report and review of the literatureEmmanouil Manolakos, Annalisa Vetro, Antonios Garas, et al.
Molecular Cytogenetics|November 19, 2008
Complex chromosome rearrangement in a child with microcephaly, dysmorphic facial features and mosaicism for a terminal deletion del(18)(q21.32-qter) investigated by FISH and array-CGH: Case reportEmmanouil Manolakos, Nadezda Kosyakova, Loreta Thomaidis, et al.
Molecular Cytogenetics|December 16, 2014
A de novo 2.9 Mb interstitial deletion at 13q12.11 in a child with developmental delay accompanied by mild dysmorphic characteristicsMagdalini Lagou, Ioannis Papoulidis, Sandro Orru, et al.
Molecular Vision|May 21, 2013
Development of novel LOXL1 genotyping method and evaluation of LOXL1, APOE and MTHFR polymorphisms in exfoliation syndrome/glaucoma in a Greek populationDimitrios Chiras, Konstantina Tzika, Haris Kokotas, et al.
Molecular Cytogenetics|December 17, 2009
Detailed molecular and clinical investigation of a child with a partial deletion of chromosome 11 (Jacobsen syndrome)Emmanouil Manolakos, Sandro Orru, Rosita Neroutsou, et al.
Molecular Cytogenetics|February 25, 2011
Combined 22q11.1-q11.21 deletion with 15q11.2-q13.3 duplication identified by array-CGH in a 6 years old boyEmmanouil Manolakos, Catherine Sarri, Annalisa Vetro, et al.
Pageof 4

Showing results (21-30 of 35) with videos related to

Sort By:
Pageof 4
Clinical Ophthalmology (Auckland, N.Z.)|March 18, 2010
Periocular xanthogranuloma: A forgotten entity?Charalampos Papagoras, George Kitsos, Paraskevi V Voulgari, et al.
Journal of Ophthalmology|July 14, 2018
Psychological Aspects and Depression in Patients with Symptomatic KeratoconusMarilita M Moschos, Nikolaos S Gouliopoulos, Chris Kalogeropoulos, et al.
European Journal of Radiology|January 25, 2018
Pseudoexfoliation syndrome without glaucoma: White matter abnormalities detected by conventional MRI and diffusion tensor imagingAnastasia K Zikou, George Kitsos, Loukas G Astrakas, et al.
Clinical Ophthalmology (Auckland, N.Z.)|August 11, 2017
Investigation of associations of <i>ARMS2</i>, <i>CD14</i>, and <i>TLR4</i> gene polymorphisms with wet age-related macular degeneration in a Greek populationAntonia Sarli, Iosif Skalidakis, Aliki Velissari, et al.
Experimental and Therapeutic Medicine|March 27, 2014
Proximal 10q duplication in a child with severe central hypotonia characterized by array-comparative genomic hybridization: A case report and review of the literatureEmmanouil Manolakos, Annalisa Vetro, Antonios Garas, et al.
Molecular Cytogenetics|November 19, 2008
Complex chromosome rearrangement in a child with microcephaly, dysmorphic facial features and mosaicism for a terminal deletion del(18)(q21.32-qter) investigated by FISH and array-CGH: Case reportEmmanouil Manolakos, Nadezda Kosyakova, Loreta Thomaidis, et al.
Molecular Cytogenetics|December 16, 2014
A de novo 2.9 Mb interstitial deletion at 13q12.11 in a child with developmental delay accompanied by mild dysmorphic characteristicsMagdalini Lagou, Ioannis Papoulidis, Sandro Orru, et al.
Molecular Vision|May 21, 2013
Development of novel LOXL1 genotyping method and evaluation of LOXL1, APOE and MTHFR polymorphisms in exfoliation syndrome/glaucoma in a Greek populationDimitrios Chiras, Konstantina Tzika, Haris Kokotas, et al.
Molecular Cytogenetics|December 17, 2009
Detailed molecular and clinical investigation of a child with a partial deletion of chromosome 11 (Jacobsen syndrome)Emmanouil Manolakos, Sandro Orru, Rosita Neroutsou, et al.
Molecular Cytogenetics|February 25, 2011
Combined 22q11.1-q11.21 deletion with 15q11.2-q13.3 duplication identified by array-CGH in a 6 years old boyEmmanouil Manolakos, Catherine Sarri, Annalisa Vetro, et al.
Pageof 4