Zobrazeno 1 - 10
of 30
pro vyhledávání: '"Kim Lian Tan"'
Publikováno v:
Journal of the Dermatology Nurses' Association. 8:59-63
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::aa201e2e3c53c8f23d4b118ac06b69c8
https://doi.org/10.1097/jdn.0000000000000187
https://doi.org/10.1097/jdn.0000000000000187
Autor:
Yong-Chui WEE1, Kim-Lian TAN1, Kek-Heng CHUA1, Elizabeth GEORGE2, Jin-Ai Mary Anne TAN1 maryanne@um.edu.my
Publikováno v:
Malaysian Journal of Medical Sciences. Jul-Sep2009, Vol. 16 Issue 3, p23-30. 8p. 1 Diagram, 1 Chart.
Autor:
Yong-Chui Wee, Noor Fadzlin Mahali, Kek Heng Chua, Kim-Lian Tan, Elizabeth George, Ping Chin Lee, Jin-Ai Mary Anne Tan
Publikováno v:
Journal of Biomedicine and Biotechnology
Journal of Biomedicine and Biotechnology, Vol 2010 (2010)
Journal of Biomedicine and Biotechnology, Vol 2010 (2010)
Thalassemia can lead to severe transfusion-dependent anemia, and it is the most common genetic disorder in Malaysia. This paper aims to determine the prevalence of thalassemia in the Kadazandusuns, the largest indigenous group in Sabah, East Malaysia
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c389bd98ef008a411daf057379506d02
https://doi.org/10.1155/2010/706872
https://doi.org/10.1155/2010/706872
Publikováno v:
Journal of Obstetrics and Gynaecology Research. 31:540-546
AIM Interactions between different determinants of alpha-thalassemia raises considerable problems, particularly during pregnancies where antenatal diagnosis is necessary. This study aims to determine the different types of deletional alpha-thalassemi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::103879b3c7d4085a1c6292e82479c9ca
https://doi.org/10.1111/j.1447-0756.2005.00333.x
https://doi.org/10.1111/j.1447-0756.2005.00333.x
Autor:
Yong Chui Wee, Mary Anne Tan Jin Ai, Yean Ching Wong, Juan Loong Kok, Sook Fan Yap, Kim Lian Tan
Publikováno v:
Acta Haematologica. 109:169-175
Molecular characterization of the compound heterozygous condition – Gγ(Aγδβ)o/β-thalassemia – in four families showing mild β-thalassemia intermedia was carried out using DNA amplification techniques. Using the Amplification Refractory Muta
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f0ebd2dc587b488f641af3c2c3c21bef
https://doi.org/10.1159/000070965
https://doi.org/10.1159/000070965
Publikováno v:
Genetic Testing. 5:17-22
Beta-thalassemia major patients have chronic anemia and are dependent on blood transfusions to sustain life. Molecular characterization and prenatal diagnosis of beta3-thalassemia is essential in Malaysia because about 4.5% of the population are hete
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d87b03779a10dc5d1eea5736480a7d60
https://doi.org/10.1089/109065701750168626
https://doi.org/10.1089/109065701750168626
Autor:
Eugene Sern Ting Tan, Irene Siew Heok Lim, Felicia Geok Ching Tan, Andy S.L. Tan, Kim Lian Tan, Hong Liang Tey
Publikováno v:
Archives of Dermatology. 148
To determine if watching a children's program on a portable video player reduces anxiety levels in preschool children before cryotherapy for cutaneous viral warts.Nonblinded before-after trial.General dermatology clinic.Consecutive patients aged 2 to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cdcf26ea9e765ef2125c0f1498be4c3b
https://doi.org/10.1001/archdermatol.2012.1656
https://doi.org/10.1001/archdermatol.2012.1656
Publikováno v:
Genesgenetic systems. 84(1)
Co-inheritance of alpha-thalassemia with homozygosity or compound heterozygosity for beta-thalassemia may ameliorate beta-thalassemia major. A wide range of clinical phenotypes is produced depending on the number of alpha-thalassemia alleles (-alpha/
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4673faa086baef85470de64a4db87a0d
https://pubmed.ncbi.nlm.nih.gov/19420802
https://pubmed.ncbi.nlm.nih.gov/19420802
Autor:
Jin-Ai Mary Anne Tan, Lee-Lee Chan, Kim-Lian Tan, Yong-Chui Wee, Elizabeth George, Khairul Zaman Omar
Publikováno v:
European journal of pediatrics. 168(9)
Interactions of different hemoglobin variants with thalassemia alleles can result in various clinical phenotypes. HbE-beta-thalassemia generally manifests with severe anemia where individuals exhibit beta-thalassemia major with regular blood transfus
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0f6539793788624584693028908451ce
https://pubmed.ncbi.nlm.nih.gov/19034506
https://pubmed.ncbi.nlm.nih.gov/19034506
Autor:
Yean Ching, Wong, Elizabeth, George, Kim Lian, Tan, Sook Fan, Yap, Lee Lee, Chan, Jin Ai Mary Anne, Tan
Publikováno v:
The Malaysian journal of pathology. 28(1)
The molecular basis of variable phenotypes in P-thalassaemia patients with identical genotypes has been associated with co-inheritance of alpha-thalassaemia and persistence of HbF production in adult life. The Xmn I restriction site at -158 position
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::086116768886663940e5a2e7a3001c06
https://pubmed.ncbi.nlm.nih.gov/17694955
https://pubmed.ncbi.nlm.nih.gov/17694955