Search Results - "BOTEVA, K. K"

  • Showing 1 - 13 results of 13
Refine Results
  1. 1

    Endoglin gene polymorphism as a risk factor for sporadic intracerebral hemorrhage by Alberts, M J, Davis, J P, Graffagnino, C, McClenny, C, Delong, D, Granger, C, Herbstreith, M H, Boteva, K, Marchuk, D A, Roses, A D

    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…”
    Get more information
    Journal Article
  2. 2

    Relationship Between Duration of Untreated Psychosis and Outcome in First-Episode Schizophrenia: A Critical Review and Meta-Analysis by Perkins, Diana O., Gu, Hongbin, Boteva, Kalina, Lieberman, Jeffrey A.

    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…”
    Get full text
    Journal Article
  3. 3

    Polymorphism and chromosomal localization of the GI-form of human glutathione peroxidase (GPX2) on 14q24.1 by in situ hybridization by FONG-FONG CHU, ROHAN DE SILVA, H. A, ESWORTHY, R. S, BOTEVA, K. K, WALTERS, C. E, ROSES, A, NAGESH RAO, P, PETTENATI, M. J

    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…”
    Get full text
    Journal Article
  4. 4

    The early stages of schizophrenia: speculations on pathogenesis, pathophysiology, and therapeutic approaches by Lieberman, Jeffrey A., Perkins, Diana, Belger, Aysenil, Chakos, Miranda, Jarskog, Fred, Boteva, Kalina, Gilmore, John

    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…”
    Get full text
    Journal Article Conference Proceeding
  5. 5

    Cystic fibrosis patients from the Black Sea region: the 1677delTA mutation by Angelicheva, D, Boteva, K, Jordanova, A, Savov, A, Kufardjieva, A, Tolun, A, Telatar, M, Akarsubaşi, A, Köprübaşi, F, Aydoğdu, S

    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…”
    Get more information
    Journal Article
  6. 6
  7. 7

    Reconsidering the classification of schizophrenia and manic depressive illness--a critical analysis and new conceptual model by Boteva, Kalina, Lieberman, Jeffrey

    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)…”
    Get full text
    Journal Article
  8. 8

    Polymorphism and Chromosomal Localization of the GI-Form of Human Glutathione Peroxidase (GPX2) on 14q24.1 byin SituHybridization by Chu, Fong-Fong, Rohan de Silva, H.A., Esworthy, R.Steven, Boteva, Kalina K., Walters, Claire E., Roses, Allen, Rao, P.Nagesh, Pettenati, Mark J.

    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…”
    Get full text
    Journal Article
  9. 9
  10. 10
  11. 11

    Genetic heterogeneity in adult dominant polycystic kidney disease in Cypriot families by CONSTANTINOU-DELTAS, C. D, PAPAGEORGIOU, E, BOTEVA, K, CHRISTODOULOU, K, BREUNING, M. H, PETERS, D. J. M, PIERIDES, A

    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…”
    Get full text
    Journal Article
  12. 12

    Description of a symptomless cystic fibrosis L346P/M348K compound heterozygous Cypriot individual by Deltas, Constantinou C., Boteva, Kalina, Georgiou, Andreas, Papageorgiou, Elena, Georgiou, Christina

    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…”
    Get full text
    Journal Article
  13. 13

    Novel cystic fibrosis mutation associated with mild disease in Cypriot patients by BOTEVA, K, PAPAGEORGIOU, E, GEORGIOU, C, ANGASTINIOTIS, M, MIDDLETON, L. T, CONSTANTINOU-DELTAS, C. D

    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…”
    Get full text
    Journal Article