Dietary Intake, Mediterranean Diet Adherence and Caloric Intake in Huntington’s Disease: A Review

por Christodoulou, Christiana C., Demetriou, Christiana A., Zamba-Papanicolaou, Eleni
Publicado 2020

A novel c.5308_5311delGAGA mutation in Senataxin in a Cypriot family with an autosomal recessive cerebellar ataxia

por Nicolaou, Paschalis, Georghiou, Anthi, Votsi, Christina, Middleton, Lefkos T, Zamba-Papanicolaou, Eleni, Christodoulou, Kyproula
Publicado 2008

Quality of Life of Cypriot Patients Suffering with Huntington’s Disease

por Varda, Eleni, Demetriou, Christiana A., Heraclides, Alexandros, Christou, Yiolanda P., Zamba-Papanicolaou, Eleni
Publicado 2016

A Novel SPG7 Gene Pathogenic Variant in a Cypriot Family With Autosomal Recessive Spastic Ataxia

por Votsi, Christina, Ververis, Antonis, Nicolaou, Paschalis, Christou, Yiolanda-Panayiota, Christodoulou, Kyproula, Zamba-Papanicolaou, Eleni
Publicado 2022

A Novel CLN6 Variant Associated With Juvenile Neuronal Ceroid Lipofuscinosis in Patients With Absence of Visual Loss as a Presenting Feature

por Nicolaou, Paschalis, Tanteles, George A., Votsi, Christina, Zamba-Papanicolaou, Eleni, Papacostas, Savvas S., Christodoulou, Kyproula, Christou, Yiolanda-Panayiota
Publicado 2021

Investigating the Transition of Pre-Symptomatic to Symptomatic Huntington’s Disease Status Based on Omics Data

por Christodoulou, Christiana C., Zachariou, Margarita, Tomazou, Marios, Karatzas, Evangelos, Demetriou, Christiana A., Zamba-Papanicolaou, Eleni, Spyrou, George M.
Publicado 2020

Retrospective longitudinal study of ALS in Cyprus: Clinical characteristics, management and survival

por Demetriou, Christiana A., Hadjivasiliou, Petros M., Kleopa, Kleopas A., Christou, Yiolanda P., Leonidou, Eleni, Kyriakides, Theodoros, Zamba-Papanicolaou, Eleni
Publicado 2019

Biochemical Characterization of the GBA2 c.1780G>C Missense Mutation in Lymphoblastoid Cells from Patients with Spastic Ataxia

por Malekkou, Anna, Samarani, Maura, Drousiotou, Anthi, Votsi, Christina, Sonnino, Sandro, Pantzaris, Marios, Chiricozzi, Elena, Zamba-Papanicolaou, Eleni, Aureli, Massimo, Loberto, Nicoletta, Christodoulou, Kyproula
Publicado 2018

Risk factors for breast cancer brain metastases: a systematic review

por Koniali, Lola, Hadjisavvas, Andreas, Constantinidou, Anastasia, Christodoulou, Kyproula, Christou, Yiolanda, Demetriou, Christiana, Panayides, Andreas S., Pitris, Constantinos, Pattichis, Constantinos S., Zamba-Papanicolaou, Eleni, Kyriacou, Kyriacos
Publicado 2020

Genetic Study of Early Onset Parkinson’s Disease in Cyprus

por Abu Manneh, Rana, Chairta, Paraskevi P., Mitsi, Ellie, Loizidou, Maria A., Georgiou, Andrea N., Christou, Yiolanda P., Pantzaris, Marios, Zamba-Papanicolaou, Eleni, Hadjisavvas, Andreas
Publicado 2022

Prediction of Parkinson’s Disease Risk Based on Genetic Profile and Established Risk Factors

por Chairta, Paraskevi P., Hadjisavvas, Andreas, Georgiou, Andrea N., Loizidou, Maria A., Yiangou, Kristia, Demetriou, Christiana A., Christou, Yiolanda P., Pantziaris, Marios, Michailidou, Kyriaki, Zamba-Papanicolaou, Eleni
Publicado 2021

Mitochondrial superclusters influence age of onset of Parkinson’s disease in a gender specific manner in the Cypriot population: A case-control study

por Georgiou, Andrea, Demetriou, Christiana A., Heraclides, Alexandros, Christou, Yiolanda P., Leonidou, Eleni, Loukaides, Panayiotis, Yiasoumi, Elena, Panagiotou, Dimitris, Manoli, Panayiotis, Thomson, Pippa, Loizidou, Maria A., Hadjisavvas, Andreas, Zamba-Papanicolaou, Eleni
Publicado 2017

Genetic and Environmental Factors Contributing to Parkinson's Disease: A Case-Control Study in the Cypriot Population

por Georgiou, Andrea, Demetriou, Christiana A., Christou, Yiolanda P., Heraclides, Alexandros, Leonidou, Eleni, Loukaides, Panayiotis, Yiasoumi, Elena, Pantziaris, Marios, Kleopa, Kleopas A., Papacostas, Savvas S., Loizidou, Maria A., Hadjisavvas, Andreas, Zamba-Papanicolaou, Eleni
Publicado 2019

PheWAS and cross-disorder analysis reveal genetic architecture, pleiotropic loci and phenotypic correlations across 11 autoimmune disorders

por Topaloudi, Apostolia, Jain, Pritesh, Martinez, Melanie B., Bryant, Josephine K., Reynolds, Grace, Zagoriti, Zoi, Lagoumintzis, George, Zamba-Papanicolaou, Eleni, Tzartos, John, Poulas, Konstantinos, Kleopa, Kleopas A., Tzartos, Socrates, Georgitsi, Marianthi, Drineas, Petros, Paschou, Peristera
Publicado 2023

Transcriptomic characterization of tissues from patients and subsequent pathway analyses reveal biological pathways that are implicated in spastic ataxia

por Kakouri, Andrea C., Votsi, Christina, Oulas, Anastasis, Nicolaou, Paschalis, Aureli, Massimo, Lunghi, Giulia, Samarani, Maura, Compagnoni, Giacomo M., Salani, Sabrina, Di Fonzo, Alessio, Christophides, Thalis, Tanteles, George A., Zamba-Papanicolaou, Eleni, Pantzaris, Marios, Spyrou, George M., Christodoulou, Kyproula
Publicado 2022

Distal hereditary motor neuronopathy of the Jerash type is caused by a novel SIGMAR1 c.500A>T missense mutation

por Ververis, Antonis, Dajani, Rana, Koutsou, Pantelitsa, Aloqaily, Ahmad, Nelson-Williams, Carol, Loring, Erin, Arafat, Ala, Mubaidin, Ammar Fayez, Horany, Khalid, Bader, Mai B, Al-Baho, Yaqoub, Ali, Bushra, Muhtaseb, Abdurrahman, DeSpenza Jr, Tyrone, Al-Qudah, Abdelkarim A, Middleton, Lefkos T, Zamba-Papanicolaou, Eleni, Lifton, Richard, Christodoulou, Kyproula
Publicado 2020

miR-223-3p and miR-24-3p as novel serum-based biomarkers for myotonic dystrophy type 1

por Koutalianos, Demetris, Koutsoulidou, Andrie, Mytidou, Chrystalla, Kakouri, Andrea C., Oulas, Anastasis, Tomazou, Marios, Kyriakides, Tassos C., Prokopi, Marianna, Kapnisis, Konstantinos, Nikolenko, Nikoletta, Turner, Chris, Lusakowska, Anna, Janiszewska, Katarzyna, Papadimas, George K., Papadopoulos, Constantinos, Kararizou, Evangelia, Spyrou, George M., Gourdon, Geneviève, Zamba Papanicolaou, Eleni, Gorman, Grainne, Anayiotos, Andreas, Lochmüller, Hanns, Phylactou, Leonidas A.
Publicado 2021

Goldberg–Shprintzen syndrome is determined by the absence, or reduced expression levels, of KIFBP

por MacKenzie, Katherine C., de Graaf, Bianca M., Syrimis, Andreas, Zhao, Yuying, Brosens, Erwin, Mancini, Grazia M. S., Schot, Rachel, Halley, Dicky, Wilke, Martina, Vøllo, Arve, Flinter, Frances, Green, Andrew, Mansour, Sahar, Pilch, Jacek, Stark, Zornitza, Zamba‐Papanicolaou, Eleni, Christophidou‐Anastasiadou, Violetta, Hofstra, Robert M. W., Jongbloed, Jan D. H., Nicolaou, Nayia, Tanteles, George A., Brooks, Alice S., Alves, Maria M.
Publicado 2020

PDXK mutations cause polyneuropathy responsive to pyridoxal 5′‐phosphate supplementation

por Chelban, Viorica, Wilson, Matthew P., Warman Chardon, Jodi, Vandrovcova, Jana, Zanetti, M. Natalia, Zamba‐Papanicolaou, Eleni, Efthymiou, Stephanie, Pope, Simon, Conte, Maria R., Abis, Giancarlo, Liu, Yo‐Tsen, Tribollet, Eloise, Haridy, Nourelhoda A., Botía, Juan A., Ryten, Mina, Nicolaou, Paschalis, Minaidou, Anna, Christodoulou, Kyproula, Kernohan, Kristin D., Eaton, Alison, Osmond, Matthew, Ito, Yoko, Bourque, Pierre, Jepson, James E. C., Bello, Oscar, Bremner, Fion, Cordivari, Carla, Reilly, Mary M., Foiani, Martha, Heslegrave, Amanda, Zetterberg, Henrik, Heales, Simon J. R., Wood, Nicholas W., Rothman, James E., Boycott, Kym M., Mills, Philippa B., Clayton, Peter T., Houlden, Henry
Publicado 2019