A Case of Class I 17p13.3 Microduplication Syndrome with Unilateral Hearing Loss

por Vittas, Spiros, Bisba, Maria, Christopoulou, Georgia, Apostolakopoulou, Loukia, Pons, Roser, Constantoulakis, Pantelis
Publicado 2023

Assessment of Donor Derived Cell Free DNA (dd-cfDNA) at Surveillance and at Clinical Suspicion of Acute Rejection in Renal Transplantation

por Mantios, Evangelos, Filiopoulos, Vassilis, Constantoulakis, Pantelis, Liapis, George, Vittoraki, Angeliki, Casas, Silvia, Marinaki, Smaragdi, Boletis, John N
Publicado 2023

In vivo expression of innate immunity markers in patients with mycobacterium tuberculosis infection

por Constantoulakis, Pantelis, Filiou, Eftihia, Rovina, Nikoletta, Chras, George, Hamhougia, Aggeliki, Karabela, Simona, Sotiriou, Adamandia, Roussos, Charis, Poulakis, Nikolaos
Publicado 2010

A case report of recessive restrictive cardiomyopathy caused by a novel mutation in cardiac troponin I (TNNI3)

por Pantou, Malena P., Gourzi, Polyxeni, Gkouziouta, Aggeliki, Armenis, Iakovos, Kaklamanis, Loukas, Zygouri, Christianna, Constantoulakis, Pantelis, Adamopoulos, Stamatis, Degiannis, Dimitrios
Publicado 2019

Association of lysyl oxidase-like 1 gene common sequence variants in Greek patients with pseudoexfoliation syndrome and pseudoexfoliation glaucoma

por Metaxaki, Ioanna, Constantoulakis, Pantelis, Papadimitropoulos, Miltiadis, Filiou, Eftihia, Georgopoulos, Gerasimos, Chamchougia, Aggeliki, Papakonstantinou, Dimitrios, Markomichelakis, Nikos, Koutsandrea, Chrysanthi, Halkiadakis, Ioannis
Publicado 2013

Progressive Multifocal Leukoencephalopathy in Systemic Lupus Erythematosus: A Consequence of Patient-Intrinsic or -Extrinsic Factors?

por Emmanouilidou, Evgenia, Kosmara, Despoina, Papadaki, Efrosini, Mastorodemos, Vasileios, Constantoulakis, Pantelis, Repa, Argyro, Christopoulou, Georgia, Kalpadakis, Christina, Avgoustidis, Nestor, Thomas, Konstantinos, Boumpas, Dimitrios, Sidiropoulos, Prodromos, Bertsias, George
Publicado 2023

Targeted capture enrichment followed by NGS: development and validation of a single comprehensive NIPT for chromosomal aneuploidies, microdeletion syndromes and monogenic diseases

por Koumbaris, George, Achilleos, Achilleas, Nicolaou, Michalis, Loizides, Charalambos, Tsangaras, Kyriakos, Kypri, Elena, Mina, Petros, Sismani, Carolina, Velissariou, Voula, Christopoulou, Georgia, Constantoulakis, Pantelis, Manolakos, Emmanouil, Papoulidis, Ioannis, Stambouli, Danai, Ioannides, Marios, Patsalis, Philippos
Publicado 2019

Recommendations for accurate genotyping of SARS-CoV-2 using amplicon-based sequencing of clinical samples

por Kubik, Slawomir, Marques, Ana Claudia, Xing, Xiaobin, Silvery, Janine, Bertelli, Claire, De Maio, Flavio, Pournaras, Spyros, Burr, Tom, Duffourd, Yannis, Siemens, Helena, Alloui, Chakib, Song, Lin, Wenger, Yvan, Saitta, Alexandra, Macheret, Morgane, Smith, Ewan W., Menu, Philippe, Brayer, Marion, Steinmetz, Lars M., Si-Mohammed, Ali, Chuisseu, Josiane, Stevens, Richard, Constantoulakis, Pantelis, Sali, Michela, Greub, Gilbert, Tiemann, Carsten, Pelechano, Vicent, Willig, Adrian, Xu, Zhenyu
Publicado 2021