Zobrazeno 1 - 10
of 33
pro vyhledávání: '"N. H. Hamidah"'
Autor:
E, Yap, N R, Tumian, R Z, Azma, N A, Sharifah, S, Salwati, N H, Hamidah, M H, Elias, C L, Wong
Publikováno v:
The Malaysian journal of pathology. 39(2)
Clinical resistance to imatinib (IM) in chronic myeloid leukemia (CML) carries adverse consequences. We investigated 22 CML patients who developed IM-resistance for BCR-ABL kinase domain (KD) mutations. The median follow-up for this study was 101.9 m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::65deb615c663adbd134bc2ca5aaea4bc
https://pubmed.ncbi.nlm.nih.gov/28866691
https://pubmed.ncbi.nlm.nih.gov/28866691
Publikováno v:
Hematology (Amsterdam, Netherlands). 1(3)
A previously healthy eleven month old male Malay infant presented with fever, upper respiratory tract infection and right knee swelling. Pallor, bilateral proptosis, hepatosplenomegaly, multiple scalp swellings and a right cheek swelling were observe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ea2f2b8adb0a55eb3ac4f0616cbb52f5
https://pubmed.ncbi.nlm.nih.gov/27406616
https://pubmed.ncbi.nlm.nih.gov/27406616
Autor:
Hamidah Alias, Mee Lee Looi, N. H. Hamidah, Hishamshah Ibrahim, Zarina Abdul Latiff, Rahman Jamal, Syed Zulkifli Syed Zakaria, Mageswary Sivalingam
Publikováno v:
International Journal of Laboratory Hematology. 34:377-382
Summary Introduction: To study the s-gene mutations spectrum, the genotype/phenotype correlation, the modulatory effect of co-inherited factors such as α-gene mutations and of Xmn1 polymorphism in a large cohort of Malaysian patients. Methods: A tot
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::02e167948379b9a808a432114dc6819e
https://doi.org/10.1111/j.1751-553x.2012.01405.x
https://doi.org/10.1111/j.1751-553x.2012.01405.x
Autor:
N H, Hamidah, A R, Munirah, A, Hafiza, A R, Farisah, A, Shuhaila, M N, Norzilawati, M Y, Jamil, O, Ainoon
Publikováno v:
The Malaysian journal of pathology. 36(3)
Prenatal diagnosis is essential in the new era of diagnosis and management of genetic diseases in obstetrics. Multiple ligation-dependent probe amplification (MLPA) is a recent technique for prenatal diagnosis for the relative quantification of 40 di
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::11cb052e3441a7ff9391ef83f03a0e86
https://pubmed.ncbi.nlm.nih.gov/25500514
https://pubmed.ncbi.nlm.nih.gov/25500514
Publikováno v:
La Clinica terapeutica. 165(3)
Primary nasal lymphomas are rare. One of the most common cellular subtypes in the Asian population is natural killer (NK)/T-cell lymphoma (NKTL) with a high association of EBV. We report a case of a 42-year-old female, who presented with a worsening
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::3fd5ebe781cf20ddc72824b01abf7987
https://pubmed.ncbi.nlm.nih.gov/24999566
https://pubmed.ncbi.nlm.nih.gov/24999566
Autor:
R Z, Azma, O, Ainoon, I, Azlin, H, Hamenuddin, N A, Hadi, W K, Tatt, I N, Syazana, A M, Asmaliza, S, Das, N H, Hamidah
Publikováno v:
La Clinica terapeutica. 163(4)
Anaemia is a global health problem including Malaysia. In adults, anaemia may affect work productivity. Iron deficiency anaemia and thalassaemia are common causes of anaemia in Malaysia. However, there is scarcity of data on national prevalence of ir
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::c5a4980b6cb07ea700bb4502ea137f73
https://pubmed.ncbi.nlm.nih.gov/23007811
https://pubmed.ncbi.nlm.nih.gov/23007811
Publikováno v:
La Clinica terapeutica. 163(2)
Chronic myeloproliferative diseases (MPDs) are heterogenous group of haematological malignant disorders. It is now a well recognized fact that the JAK2 (V617F) mutation occurs in majority of the patients with polycythaemia vera (PV) and half of those
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::d36b7ec8815f439307f16336e0e24872
https://pubmed.ncbi.nlm.nih.gov/22555824
https://pubmed.ncbi.nlm.nih.gov/22555824
Autor:
M, Sivalingam, M L, Looi, S Z S, Zakaria, N H, Hamidah, H, Alias, Z A, Latiff, H, Ibrahim, R, Jamal
Publikováno v:
International journal of laboratory hematology. 34(4)
To study the ß-gene mutations spectrum, the genotype/phenotype correlation, the modulatory effect of co-inherited factors such as α-gene mutations and of Xmn1 polymorphism in a large cohort of Malaysian patients.A total of 264 cases clinically diag
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::e1a4dd7be91cd122ce65aded5dd7e3fe
https://pubmed.ncbi.nlm.nih.gov/22335963
https://pubmed.ncbi.nlm.nih.gov/22335963
Publikováno v:
The Malaysian journal of pathology. 33(2)
Molecular pathogenesis of chronic myeloid leukemia (CML) is well established and molecular monitoring for patients with CML has become an important practice in the management of patients on imatinib therapy. In the present study, we report the use of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::fc4e8a5167ebf2c23878e5385c62784b
https://pubmed.ncbi.nlm.nih.gov/22299211
https://pubmed.ncbi.nlm.nih.gov/22299211
Publikováno v:
The Southeast Asian journal of tropical medicine and public health. 41(4)
Glucose-6-phosphate dehydrogenase (G6PD) deficiency is one of the commonest causes of neonatal jaundice in Malaysia. Screening of cord blood for G6PD deficiency by the semiquantitative fluorescent spot test (FST) is performed in Malaysia but this tes
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::f5fa57d2ae8b531ad85b4125c6ba927a
https://pubmed.ncbi.nlm.nih.gov/21073074
https://pubmed.ncbi.nlm.nih.gov/21073074