Publications
250 results found
Middleton L, Ohno K, Christodoulou K, et al., 1999, Chromosome 17p-linked myasthenias stem from defects in the acetylcholine receptor ε-subunit gene, NEUROLOGY, Vol: 53, Pages: 1076-1082, ISSN: 0028-3878
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- Citations: 25
Christodoulou K, Papadopoulou E, Tsingis M, et al., 1999, Autosomal recessive form of hereditary inclusion body myopathy (AR HIBM): Genetic studies, ISSN: 1128-2460
Pattichis CS, Schofield I, Merletti R, et al., 1999, Introduction to this Special Issue - Intelligent data analysis in electromyography and electroneurography, MEDICAL ENGINEERING & PHYSICS, Vol: 21, Pages: 379-388, ISSN: 1350-4533
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- Citations: 6
Georgiou DM, Christodoulou K, Zamba E, et al., 1999, Molecular genetic studies in autosomal recessive CMT, ISSN: 1128-2460
Kyriakides T, Kassianides B, Papadopoulou E, et al., 1999, A Cypriot family with a novel γ-sarcoglycan mutation presenting clinically and immunocytochemically as Becker muscular dystrophy (BMD), ISSN: 1128-2460
Middleton LT, Christodoulou K, Mubaidin A, et al., 1999, Distal hereditary motor neuronopathy of the Jerash type, CHARCOT-MARIE-TOOTH DISORDERS, Vol: 883, Pages: 439-442, ISSN: 0077-8923
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- Citations: 8
Middleton LT, Christodoulou K, Mubaidin A, et al., 1999, Distal hereditary motor neuronopathy of the Jerash type, CHARCOT-MARIE-TOOTH DISORDERS, Vol: 883, Pages: 65-68, ISSN: 0077-8923
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- Citations: 5
Middleton LT, Pantzaris M, Zamba E, et al., 1998, Inherited myasthenic syndromes, Pages: 47-53, ISSN: 1128-2460
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- Citations: 1
Kyriakides T, Christodoulou K, Zamba E, et al., 1998, Hereditary motor neuronopathies, clinical, neurophysiological and genetic aspects, Pages: 55-58, ISSN: 1128-2460
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- Citations: 2
Christodoulou K, Papadopoulou E, Tsingis M, et al., 1998, Narrowing of the gene locus for autosomal-recessive quadriceps sparing inclusion-body myopathy (ARQS-IBM) to chromosome 9p1, Acta Myologica, Vol: 2, Pages: 7-9, ISSN: 1128-2460
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- Citations: 4
Kalaydjieva L, Nikolova A, Turnev I, et al., 1998, Hereditary motor and sensory neuropathy - Lom, a novel demyelinating neuropathy associated with deafness in gypsies - Clinical, electrophysiological and nerve biopsy findings, BRAIN, Vol: 121, Pages: 399-408, ISSN: 0006-8950
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- Citations: 106
Drousiotou A, Ioannou P, Georgiou T, et al., 1998, Neonatal screening for Duchenne muscular dystrophy: A novel semiquantitative application of the bioluminescence test for creatine kinase in a pilot national program in cyprus, GENETIC TESTING, Vol: 2, Pages: 55-60, ISSN: 1090-6576
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- Citations: 51
Middleton LT, Christodoulou K, Deymeer F, et al., 1998, Congenital myasthenic syndrome (CMS) Type Ia - Clinical and genetic diversity, MYASTHENIA GRAVIS AND RELATED DISEASES, Vol: 841, Pages: 157-166, ISSN: 0077-8923
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- Citations: 1
Christodoulou K, Deymeer F, Serdaroglu P, et al., 1997, Genetic heterogeneity in Friedreich's ataxia: indication for a second locus on chromosome 9., AMERICAN JOURNAL OF HUMAN GENETICS, Vol: 61, Pages: A271-A271, ISSN: 0002-9297
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- Citations: 1
Lennon F, Pericak-Vance MA, Speer MC, et al., 1997, CMT2 mapping progress: Confirmation of a second locus and evidence for additional genetic heterogeneity., AMERICAN JOURNAL OF HUMAN GENETICS, Vol: 61, Pages: A282-A282, ISSN: 0002-9297
Tao YY, Blomeier H, Richards C, et al., 1997, Refinement of the Charcot-Marie-Tooth type 2 (CMT2A) region on chromosome 1p36.2 and formation of a YAC/PAC contig., AMERICAN JOURNAL OF HUMAN GENETICS, Vol: 61, Pages: A245-A245, ISSN: 0002-9297
Neocleous V, Middleton LT, Christodoulou K, 1997, Mutation screening in the synaptobrevin-2 gene in patients with familial infantile myasthenia., AMERICAN JOURNAL OF HUMAN GENETICS, Vol: 61, Pages: A341-A341, ISSN: 0002-9297
Pericak-Vance MA, Speer MC, Lennon F, et al., 1997, Confirmation of a second locus for CMT2 and evidence for additional genetic heterogeneity, NEUROGENETICS, Vol: 1, Pages: 89-93, ISSN: 1364-6745
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- Citations: 21
Christodoulou K, Tsingis M, Deymeer F, et al., 1997, Mapping of the familial infantile myasthenia (congenital myasthenic syndrome type Ia) gene to chromosome 17p with evidence of genetic homogeneity, HUMAN MOLECULAR GENETICS, Vol: 6, Pages: 635-640, ISSN: 0964-6906
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- Citations: 20
Dean G, Aksoy H, Akalin T, et al., 1997, Multiple sclerosis in the Turkish- and Greek-speaking communities of Cyprus - A United Nations (UNHCR) Bicommunal Project, JOURNAL OF THE NEUROLOGICAL SCIENCES, Vol: 145, Pages: 163-168, ISSN: 0022-510X
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- Citations: 23
Patsalis PC, Sismani C, Hadjimarcou MI, et al., 1997, Cytogenetic and fragile X molecular testing of individuals with mental retardation of unknown etiology, GENETIC COUNSELING, Vol: 8, Pages: 1-6, ISSN: 1015-8146
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- Citations: 3
Angastiniotis M, Middleton L, 1997, Genetic services in cyprus, EUROPEAN JOURNAL OF HUMAN GENETICS, Vol: 5, Pages: 51-57, ISSN: 1018-4813
Kyriakides T, Christodoulou K, Socdiono O, et al., 1996, Severe childhood autosomal recessive muscular dystrophy (SCARMD) in jordan exhibits heterogeneity at protein and DNA level, ISSN: 1124-8874
Kalaydjieva L, Hallmayer J, Chandler D, et al., 1996, Gene mapping in Gypsies identifies a novel demyelinating neuropathy on chromosome 8q24, NATURE GENETICS, Vol: 14, Pages: 214-217, ISSN: 1061-4036
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- Citations: 165
Middleton LT, 1996, Congenital myasthenic syndromes - 34th ENMC international workshop, 10-11 June 1995, NEUROMUSCULAR DISORDERS, Vol: 6, Pages: 133-136, ISSN: 0960-8966
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- Citations: 27
NOGUCHI S, MCNALLY EM, BENOTHMANE K, et al., 1995, MUTATIONS IN THE DYSTROPHIN-ASSOCIATED PROTEIN GAMMA-SARCOGLYCAN IN CHROMOSOME-13 MUSCULAR-DYSTROPHY, SCIENCE, Vol: 270, Pages: 819-822, ISSN: 0036-8075
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- Citations: 468
CHRISTODOULOU K, KYRIAKIDES T, HRISTOVA AH, et al., 1995, MAPPING OF AN AUTOSOMAL-DOMINANT DISTAL FORM OF SPINAL MUSCULAR-ATROPHY TO CHROMOSOME 7P, AMERICAN JOURNAL OF HUMAN GENETICS, Vol: 57, Pages: 1082-1082, ISSN: 0002-9297
BENOTHMANE K, SPEER MC, STAUFFER J, et al., 1995, EVIDENCE FOR LINKAGE DISEQUILIBRIUM IN CHROMOSOME 13-LINKED DUCHENNE-LIKE MUSCULAR-DYSTROPHY (LGMD2C), AMERICAN JOURNAL OF HUMAN GENETICS, Vol: 57, Pages: 732-734, ISSN: 0002-9297
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- Citations: 33
CHRISTODOULOU K, KYRIAKIDES T, HRISTOVA AH, et al., 1995, MAPPING OF A DISTAL FORM OF SPINAL MUSCULAR-ATROPHY WITH UPPER-LIMB PREDOMINANCE TO CHROMOSOME 7P, HUMAN MOLECULAR GENETICS, Vol: 4, Pages: 1629-1632, ISSN: 0964-6906
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- Citations: 96
PATTICHIS CS, CHARALAMBOUS C, MIDDLETON LT, 1995, EFFICIENT TRAINING OF NEURAL-NETWORK MODELS IN CLASSIFICATION OF ELECTROMYOGRAPHIC DATA, MEDICAL & BIOLOGICAL ENGINEERING & COMPUTING, Vol: 33, Pages: 499-503, ISSN: 0140-0118
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- Citations: 5
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