Zobrazeno 1 - 10
of 27
pro vyhledávání: '"Kitonyi GW"'
Autor:
Amal Gedleh, Siwon Lee, Jessica A. Hill, Philip Odiyo, Kitonyi Gw, Helen Dimaras, Yvonne Umukunda, Seemi Qaiser
Publikováno v:
Journal of Global Oncology, Vol 4, Pp 1-9 (2017)
Journal of Global Oncology
Journal of Global Oncology
IntroductionBreast cancer ranks among the most common adult cancers in Kenya. Individuals with a family history of the disease are at increased risk. Mutations most commonly associated with breast cancer affect BRCA1 and BRCA2; mutations in several o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5a220b8ade18ae9234e4ef3536b66bd5
http://ascopubs.org/doi/10.1200/JGO.17.00061
http://ascopubs.org/doi/10.1200/JGO.17.00061
Autor:
Njambi L, Kahaki Kimani, Helen Dimaras, Amal Gedleh, Kitonyi Gw, Jessica A. Hill, Joy Kabiru, Siwon Lee, Seemi Qaiser, Yvonne Umukunda
Publikováno v:
Journal of genetic counseling. 27(3)
Genetic testing and counseling have become integral to the timely control of heritable cancers, like the childhood eye cancer retinoblastoma. This study aimed to determine attitudes, knowledge and experiences related to retinoblastoma genetics, among
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::761eb20285d72dbfa473997851955f62
https://pubmed.ncbi.nlm.nih.gov/29170903
https://pubmed.ncbi.nlm.nih.gov/29170903
Publikováno v:
African Journal of Rheumatology; Vol 3, No 1 (2015); 27-33
Background: Anaemia is the commonest extra articular manifestation of Rheumatoid Arthritis (RA). Anaemia is an independent predictor of morbidity and mortality in the population. When RA is complicated by anaemia it is associated with a more severe d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=78975075580c::4da079ef7d4b4fdbb36282280ae9dc83
https://www.ajol.info/index.php/ajr/article/view/117384
https://www.ajol.info/index.php/ajr/article/view/117384
Publikováno v:
African Journal of Rheumatology; Vol 1, No 1 (2013); 28-32
Background: Rheumatoid arthritis (RA) is a disease associated with significant morbidity and mortality. Thrombocytosis is one of the haematological manifestations of rheumatoid arthritis that occurs in active disease. Platelet counts may vary dependi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=78975075580c::490f433b9a843ef363b69bfacecb4688
https://www.ajol.info/index.php/ajr/article/view/97385
https://www.ajol.info/index.php/ajr/article/view/97385
Publikováno v:
East African Medical Journal; Vol 87, No 2 (2010); 82-84
CCongenital afibrinogenaemia (CA), is a rare inherited bleeding disorder characterised by complete deficiency of fibrinogen in the plasma. Blood clotting tests are indefinitely prolonged in patients. The mode of inheritance is autosomal recessive. Ty
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a6820553bde8cfdfcc08af557a45765d
https://pubmed.ncbi.nlm.nih.gov/23057260
https://pubmed.ncbi.nlm.nih.gov/23057260
Autor:
Kitonyi Gw, JM Kitonyi
Publikováno v:
East African Medical Journal; Vol 86, No 12 (2009): Supplement; 71-75
Background: Ablation of the synovium with radiopharmaceuticals, referred to as radiation synovectomy, (RS), has emerged as a simple affordable and safe procedure that is highly effective in preventing chronic disabling end stage arthritis in haemophi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::03e9290e9bbfa28aa3a9aeebace265c3
https://doi.org/10.4314/eamj.v86i12.62907
https://doi.org/10.4314/eamj.v86i12.62907
Publikováno v:
East African Medical Journal; Vol 86, No 12 (2009): Supplement; 58-61
Europe PubMed Central
Europe PubMed Central
Background: Cytomegalovirus (CMV) infection in susceptible patients is associated with serious morbidity and a high mortality. Transmission of cytomegalovirus infection through blood transfusion is markedly reduced by transfusion of CMV seronegative
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::18a3cb9be591776cad0ba86d9b4e5b29
https://doi.org/10.4314/eamj.v86i12.62903
https://doi.org/10.4314/eamj.v86i12.62903
Publikováno v:
East African Medical Journal; Vol 85, No 8 (2008); 412-416
Hereditary haemorrhagic telangiectasia, (HHT) or Rendu-Osler-Weber disease is a genetic autosomal dominant disorder that is characterised by telangiectasias, (small vascular malformations), in mucocutaneous tissues and arterial venous malformations,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b86e3c81377638557a3a9680f8d0192e
https://www.ajol.info/index.php/eamj/article/view/9659
https://www.ajol.info/index.php/eamj/article/view/9659
Publikováno v:
Haemophilia. 17:e244-e244
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5f439bd37c6061f8a795c34a6fba326a
https://doi.org/10.1111/j.1365-2516.2010.02353.x
https://doi.org/10.1111/j.1365-2516.2010.02353.x
Publikováno v:
Scopus-Elsevier
East African Medical Journal; Vol 86, No 12 (2009): Supplement; 39-45
East African Medical Journal; Vol 86, No 12 (2009): Supplement; 39-45
To determine clinical-pathologic characteristics, treatment modalities and treatment outcomes of children diagnosed with neuroblastoma.Cross-sectional descriptive study based on secondary data from patient records.Records department of Kenyatta Natio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7c2bccc0244c6b7971b407985b8b9491
http://www.scopus.com/inward/record.url?eid=2-s2.0-79960665396&partnerID=MN8TOARS
http://www.scopus.com/inward/record.url?eid=2-s2.0-79960665396&partnerID=MN8TOARS
