Search Results - "BOTEVA, K. K"
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1
Endoglin gene polymorphism as a risk factor for sporadic intracerebral hemorrhage
Published in Annals of neurology (01-05-1997)“…Intracerebral hemorrhage (ICH) is a common and serious type of stroke. Recent studies have shown that inherited factors that affect the development of the…”
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2
Relationship Between Duration of Untreated Psychosis and Outcome in First-Episode Schizophrenia: A Critical Review and Meta-Analysis
Published in The American journal of psychiatry (01-10-2005)“…OBJECTIVE: The duration of untreated psychosis may influence response to treatment, reflecting a potentially malleable progressive pathological process. The…”
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3
Polymorphism and chromosomal localization of the GI-form of human glutathione peroxidase (GPX2) on 14q24.1 by in situ hybridization
Published in Genomics (San Diego, Calif.) (01-03-1996)“…We have isolated a 3.3-kb DNA containing the two exons and a 2.6-kb intron of the human CPX2 gene. This gene encodes the intestinal isoenzyme of glutathione…”
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4
The early stages of schizophrenia: speculations on pathogenesis, pathophysiology, and therapeutic approaches
Published in Biological psychiatry (1969) (01-12-2001)“…Schizophrenia is commonly considered a neurodevelopmental disorder that is associated with significant morbidity; however, unlike other neurodevelopmental…”
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5
Cystic fibrosis patients from the Black Sea region: the 1677delTA mutation
Published in Human mutation (1994)“…A 2 bp deletion in exon 10 of the CFTR gene, 1677delTA, which is very rare among CF chromosomes worldwide, was found to be a relatively common cause of cystic…”
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Weak evidence for allelic association in the cypriot PKD1 population
Published in Contributions to nephrology (1995)Get more information
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7
Reconsidering the classification of schizophrenia and manic depressive illness--a critical analysis and new conceptual model
Published in The world journal of biological psychiatry (01-04-2003)“…The idea of 'disease entity' in psychiatry and the nosologic map of insanity with the distinction between dementia praecox (schizophrenia since Bleuler 1911)…”
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8
Polymorphism and Chromosomal Localization of the GI-Form of Human Glutathione Peroxidase (GPX2) on 14q24.1 byin SituHybridization
Published in Genomics (San Diego, Calif.) (01-03-1996)“…We have isolated a 3.3-kb DNA containing the two exons and a 2.6-kb intron of the humanGPX2gene. This gene encodes the intestinal isoenzyme of glutathione…”
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9
Mutation analysis of presenillin 1 gene in Alzheimer's disease
Published in The Lancet (British edition) (13-01-1996)Get more information
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10
67 In-situ localization of S182 mRNA in sporadic Alzheimer's disease (AD)
Published in Neurobiology of aging (1996)Get full text
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11
Genetic heterogeneity in adult dominant polycystic kidney disease in Cypriot families
Published in Human genetics (01-04-1995)“…Polycystic kidney disease is an inherited heterogeneous disorder that affects approximately 1:1000 Europeans. It is characterized mainly by the formation of…”
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12
Description of a symptomless cystic fibrosis L346P/M348K compound heterozygous Cypriot individual
Published in Molecular and cellular probes (01-08-1996)“…During the past few years we have been testing the hypothesis that Cyprus may have been spared many severe cystic fibrosis (CF) cases but not cystic fibrosis…”
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13
Novel cystic fibrosis mutation associated with mild disease in Cypriot patients
Published in Human genetics (01-05-1994)“…Cyprus is an island in the eastern Mediterranean basin inhabited by people of Caucasian extraction, mostly Greek-Cypriots. The most common inherited disease…”
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