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Kyproula Christodoulou

This is a preview profile on BiomedExperts - the first literature-based scientific social network. It brings the right researchers together and allows them to collaborate online. Collexis and Dell provide the BiomedExperts network of +1.5 Million pre-calculated profiles free of charge to researchers worldwide.

Research Profile (preview)

Concepts & Ideas

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Cyprus

Disorders

Procedures

Physiology

Anatomy

Chromosomes, Human, Pair 9

Chemicals & Drugs

Genes & Molecular Sequences

Dominant Genes

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Publications

TOP 3
Dardiotis Efthimios; Koutsou Pantelitsa; Zamba-Papanicolaou Eleni; Vonta Ilia; Hadjivassiliou Marilena; Hadjigeorgiou Georgios; Cariolou Marios; Christodoulou Kyproula; Kyriakides Theodoros
Complement C1Q polymorphisms modulate onset in familial amyloidotic polyneuropathy TTR Val30Met.
Zamba-Papanicolaou E; Koutsou P; Daiou C; Gaglia E; Georghiou A; Christodoulou K
High frequency of Friedreich's ataxia carriers in the Paphos district of Cyprus.
Andreadou Elisabeth; Christodoulou Kyproula; Manta Panagiota; Karandreas Nicos; Loukaidis Panagiotis; Sfagos Constantinos; Vassilopoulos Demetrios
Familial asymmetric distal upper limb amyotrophy (Hirayama disease): report of a Greek family.

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All Publications

2009: Dardiotis Efthimios; Koutsou Pantelitsa; Zamba-Papanicolaou Eleni; Vonta Ilia; Hadjivassiliou Marilena; Hadjigeorgiou Georgios; Cariolou Marios; Christodoulou Kyproula; Kyriakides Theodoros
Complement C1Q polymorphisms modulate onset in familial amyloidotic polyneuropathy TTR Val30Met.
Journal of the neurological sciences 2009;284(1-2):158-62.
2009: Zamba-Papanicolaou E; Koutsou P; Daiou C; Gaglia E; Georghiou A; Christodoulou K
High frequency of Friedreich's ataxia carriers in the Paphos district of Cyprus.
Acta myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology / edited by the Gaetano Conte Academy for the study of striated muscle diseases 2009;28(1):24-6.
2009: Andreadou Elisabeth; Christodoulou Kyproula; Manta Panagiota; Karandreas Nicos; Loukaidis Panagiotis; Sfagos Constantinos; Vassilopoulos Demetrios
Familial asymmetric distal upper limb amyotrophy (Hirayama disease): report of a Greek family.
The neurologist 2009;15(3):156-60.
2009: Mintchev Nikolay; Zamba-Papanicolaou Eleni; Kleopa Kleopas A; Christodoulou Kyproula
A novel ALS2 splice-site mutation in a Cypriot juvenile-onset primary lateral sclerosis family.
Neurology 2009;72(1):28-32.
2008: Yoon G; Westmacott R; MacMillan L; Quercia N; Koutsou P; Georghiou A; Christodoulou K; Banwell B
Complete deletion of the aprataxin gene: ataxia with oculomotor apraxia type 1 with severe phenotype and cognitive deficit.
Journal of neurology, neurosurgery, and psychiatry 2008;79(2):234-6.
2008: Butinar Dusan; Starr Arnold; Zidar Janez; Koutsou Pantelitsa; Christodoulou Kyproula
Auditory nerve is affected in one of two different point mutations of the neurofilament light gene.
Clinical neurophysiology : official journal of the International Federation of Clinical Neurophysiology 2008;119(2):367-75.
2008: Nicolaou Paschalis; Georghiou Anthi; Votsi Christina; Middleton Lefkos T; Zamba-Papanicolaou Eleni; Christodoulou Kyproula
A novel c.5308_5311delGAGA mutation in Senataxin in a Cypriot family with an autosomal recessive cerebellar ataxia.
BMC medical genetics 2008;9():28.
2007: Antoniades Loizos; Eftychiou Christos; Kyriakides Theodoros; Christodoulou Kyproula; Katritsis Demosthenes G
Malignant mutation in the lamin A/C gene causing progressive conduction system disease and early sudden death in a family with mild form of limb-girdle muscular dystrophy.
Journal of interventional cardiac electrophysiology : an international journal of arrhythmias and pacing 2007;19(1):1-7.
2006: Tsezou Aspasia; Karachalios Theophilos; Fytili Pelagia; Giannatou Eirini; Christodoulou Kyproula; Hadjigeorgiou Georgios M; Malizos Konstantinos N
Absence of linkage to chromosomes 6q and 16p in a Greek population with knee osteoarthritis.
Journal of orthopaedic research : official publication of the Orthopaedic Research Society 2006;24(9):1900-5.
2006: Georgiou Domna-Maria; Nicolaou Paschalis; Chitayat David; Koutsou Pantelitsa; Babul-Hirji Riyana; Vajsar Jiri; Murphy Jillian; Christodoulou Kyproula
A novel GDAP1 mutation 439delA is associated with autosomal recessive CMT disease.
The Canadian journal of neurological sciences. Le journal canadien des sciences neurologiques 2006;33(3):311-6.
2006: Kleanthous Marina; Patsalis Philippos C; Drousiotou Anthi; Motazacker Mehdi; Christodoulou Kyproula; Cariolou Marios; Baysal Erol; Khrizi Kimia; Moghimi Babak; Pourfarzad Farzin; van Baal Sjozef; Deltas Constantinos; Najmabadi Hossein; Patrinos George P
The cypriot and Iranian National Mutation Frequency Databases.
Human mutation 2006;27(6):598-9.
2006: Kleopa K A; Zamba-Papanicolaou E; Alevra X; Nicolaou P; Georgiou D-M; Hadjisavvas A; Kyriakides T; Christodoulou K
Phenotypic and cellular expression of two novel connexin32 mutations causing CMT1X.
Neurology 2006;66(3):396-402.
2005: Sivakumar Kumaraswamy; Kyriakides Theodoros; Puls Imke; Nicholson Garth A; Funalot Benoît; Antonellis Anthony; Sambuughin Nyamkhishig; Christodoulou Kyproula; Beggs John L; Zamba-Papanicolaou Eleni; Ionasescu Victor; Dalakas Marinos C; Green Eric D; Fischbeck Kenneth H; Goldfarb Lev G
Phenotypic spectrum of disorders associated with glycyl-tRNA synthetase mutations.
Brain : a journal of neurology 2005;128(Pt 10):2304-14.
2004: Kleopa Kleopas A; Georgiou Domna-Maria; Nicolaou Paschalis; Koutsou Pantelitsa; Papathanasiou Eleftherios; Kyriakides Theodoros; Christodoulou Kyproula
A novel PMP22 mutation Ser22Phe in a family with hereditary neuropathy with liability to pressure palsies and CMT1A phenotypes.
Neurogenetics 2004;5(3):171-5.
2003: Sismani Carolina; Syrrou Maria; Christodoulou Kyproula; Hamel Ben; Chelly Jamel; Yntema Helger G; van Bokhoven Hans; Tzoufi Meropi; Georgiou Ioannis; Patsalis Philippos C
A gene for nonsyndromic X-linked mental retardation (MRX77) maps to Xq12-Xq21.33.
American journal of medical genetics. Part A 2003;122A(1):46-50.
2003: Antonellis Anthony; Ellsworth Rachel E; Sambuughin Nyamkhishig; Puls Imke; Abel Annette; Lee-Lin Shih-Queen; Jordanova Albena; Kremensky Ivo; Christodoulou Kyproula; Middleton Lefkos T; Sivakumar Kumaraswamy; Ionasescu Victor; Funalot Benoit; Vance Jeffery M; Goldfarb Lev G; Fischbeck Kenneth H; Green Eric D
Glycyl tRNA synthetase mutations in Charcot-Marie-Tooth disease type 2D and distal spinal muscular atrophy type V.
American journal of human genetics 2003;72(5):1293-9.
2002: Zamba-Papanicolaou E; Christodoulou K; Christodoulou C; Kyriakidesl T; Middleton L T
Hereditary motor neuronopathies.
Revue neurologique 2002;158(12 Pt 1):1220-4.
2002: Georgiou Donna-Maria; Zidar Janez; Korosec Marko; Middleton Lefkos T; Kyriakides Theodoros; Christodoulou Kyproula
A novel NF-L mutation Pro22Ser is associated with CMT2 in a large Slovenian family.
Neurogenetics 2002;4(2):93-6.
2001: Christodoulou K; Deymeer F; Serdaroglu P; Ozdemir C; Poda M; Georgiou D M; Ioannou P; Tsingis M; Zamba E; Middleton L T
Mapping of the second Friedreich's ataxia (FRDA2) locus to chromosome 9p23-p11: evidence for further locus heterogeneity.
Neurogenetics 2001;3(3):127-32.
2000: Christodoulou K; Zamba E; Tsingis M; Mubaidin A; Horani K; Abu-Sheik S; El-Khateeb M; Kyriacou K; Kyriakides T; Al-Qudah A K; Middleton L
A novel form of distal hereditary motor neuronopathy maps to chromosome 9p21.1-p12.
Annals of neurology 2000;48(6):877-84.
2000: Wang H L; Ohno K; Milone M; Brengman J M; Evoli A; Batocchi A P; Middleton L T; Christodoulou K; Engel A G; Sine S M
Fundamental gating mechanism of nicotinic receptor channel revealed by mutation causing a congenital myasthenic syndrome.
The Journal of general physiology 2000;116(3):449-62.
2000: Bolino A; Muglia M; Conforti F L; LeGuern E; Salih M A; Georgiou D M; Christodoulou K; Hausmanowa-Petrusewicz I; Mandich P; Schenone A; Gambardella A; Bono F; Quattrone A; Devoto M; Monaco A P
Charcot-Marie-Tooth type 4B is caused by mutations in the gene encoding myotubularin-related protein-2.
Nature genetics 2000;25(1):17-9.
1999: Middleton L T; Christodoulou K; Mubaidin A; Zamba E; Tsingis M; Kyriacou K; Abu-Sheikh S; Kyriakides T; Neocleous V; Georgiou D M; el-Khateeb M; al-Qudah A; Horany K
Distal hereditary motor neuronopathy of the Jerash type.
Annals of the New York Academy of Sciences 1999;883():439-42.
1999: Middleton L T; Christodoulou K; Mubaidin A; Zamba E; Tsingis M; Kyriacou K; Abu-Sheikh S; Kyriakides T; Neocleous V; Georgiou D M; el-Khateeb M; al-Qudah A; Horany K
Distal hereditary motor neuronopathy of the Jerash type.
Annals of the New York Academy of Sciences 1999;883():65-8.
1999: Middleton L; Ohno K; Christodoulou K; Brengman J; Milone M; Neocleous V; Serdaroglu P; Deymeer F; Ozdemir C; Mubaidin A; Horany K; Al-Shehab A; Mavromatis I; Mylonas I; Tsingis M; Zamba E; Pantzaris M; Kyriallis K; Engel A G
Chromosome 17p-linked myasthenias stem from defects in the acetylcholine receptor epsilon-subunit gene.
Neurology 1999;53(5):1076-82.
1998: Middleton L T; Christodoulou K; Deymeer F; Serdaroglu P; Ozdemir C; al-Qudah A K; al-Shehab A; Mavromatis I; Mylonas I; Evoli A; Tsingis M; Zamba E; Kyriallis K
Congenital myasthenic syndrome. (CMS) type Ia. Clinical and genetic diversity.
Annals of the New York Academy of Sciences 1998;841():157-66.
1998: Stavrou C; Pierides A; Zouvani I; Kyriacou K; Antignac C; Neophytou P; Christodoulou K; Deltas C C
Medullary cystic kidney disease with hyperuricemia and gout in a large Cypriot family: no allelism with nephronophthisis type 1.
American journal of medical genetics 1998;77(2):149-54.
1998: Christodoulou K; Tsingis M; Stavrou C; Eleftheriou A; Papapavlou P; Patsalis P C; Ioannou P; Pierides A; Constantinou Deltas C
Chromosome 1 localization of a gene for autosomal dominant medullary cystic kidney disease.
Human molecular genetics 1998;7(5):905-11.
1997: Christodoulou K; Tsingis M; Deymeer F; Serdaroglu P; Ozdemir C; Al-Shehab A; Bairactaris C; Mavromatis I; Mylonas I; Evoli A; Kyriallis K; Middleton L T
Mapping of the familial infantile myasthenia (congenital myasthenic syndrome type Ia) gene to chromosome 17p with evidence of genetic homogeneity.
Human molecular genetics 1997;6(4):635-40.
1996: Deltas C C; Christodoulou K; Tjakouri C; Pierides A
Presymptomatic molecular diagnosis of autosomal dominant polycystic kidney disease using PKD1- and PKD2-linked markers in Cypriot families.
Clinical genetics 1996;50(1):10-8.
1995: Christodoulou K; Kyriakides T; Hristova A H; Georgiou D M; Kalaydjieva L; Yshpekova B; Ivanova T; Weber J L; Middleton L T
Mapping of a distal form of spinal muscular atrophy with upper limb predominance to chromosome 7p.
Human molecular genetics 1995;4(9):1629-32.
1995: Constantinou-Deltas C D; Papageorgiou E; Boteva K; Christodoulou K; Breuning M H; Peter D J; Pierides A
Genetic heterogeneity in adult dominant polycystic kidney disease in Cypriot families.
Human genetics 1995;95(4):416-23.
1995: Constantinou-Deltas C D; Papageorgiou E; Boteva K; Christodoulou K; Pierides A
Weak evidence for allelic association in the cypriot PKD1 population.
Contributions to nephrology 1995;115():93-6.
1994: Christodoulou K; Ioannou P; Middleton L
Molecular genetic detection of Xp21 muscular dystrophy carriers in Cyprus.
Biomedicine & pharmacotherapy = Biomédecine & pharmacothérapie 1994;48(8-9):355-8.

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Kyproula Christodoulou

Research Profile (preview)

Concepts & Ideas

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Disorders

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Physiology

Anatomy

Chemicals & Drugs

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