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 no Nutrients (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 em 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 no PLoS Curr (2016)

A novel LRSAM1 mutation is associated with autosomal dominant axonal Charcot-Marie-Tooth disease

Por Nicolaou, Paschalis, Cianchetti, Carlo, Minaidou, Anna, Marrosu, Giovanni, Zamba-Papanicolaou, Eleni, Middleton, Lefkos, Christodoulou, Kyproula
Publicado em 2013

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 no Int J Mol Sci (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 no PLoS One (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 no Int J Mol Sci (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 no Oncotarget (2020)

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 no PLoS One (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 no Front Neurol (2019)

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 no J Med Genet (2020)

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 no Hum Mutat (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 no Ann Neurol (2019)