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American Journal of Hematology
|
October 1, 1991
Hb S/beta zero-thalassemia due to the approximately 1.4-kb deletion is associated with a relatively mild phenotype
J S Waye, D H Chui, B Eng, et al.
Blood
|
December 1, 1983
Adult hemoglobins are synthesized in murine fetal hepatic erythropoietic cells
P M Wong, S W Chung, J S White, et al.
The Journal of Clinical Investigation
|
June 8, 2000
Hla-DR2-restricted responses to proteolipid protein 95-116 peptide cause autoimmune encephalitis in transgenic mice
K Kawamura, T Yamamura, K Yokoyama, et al.
Singapore Medical Journal
|
December 5, 2009
Comparing histopathological classification with MYCN, 1p36 and 17q status detected by fluorescence in situ hybridisation from 14 untreated primary neuroblastomas in Singapore
M H Yong, W S Hwang, L A Knight, et al.
Addiction (Abingdon, England)
|
May 5, 2025
Associations of emotional experience with gaming duration and risk of gaming disorder among adolescent gamers: An ecological momentary assessment study
Camilla K M Lo, Edward W W Chan, Frederick K Ho, et al.
Archives of General Psychiatry
|
September 1, 1991
Temporal and hippocampal metabolic rate during an olfactory memory task assessed by positron emission tomography in patients with dementia of the Alzheimer type and controls. Preliminary studies
M S Buchsbaum, J P Kesslak, G Lynch, et al.
Clinical Nephrology
|
December 1, 1987
Studies of lymphocyte subpopulations and immunoglobulin production in IgA nephropathy
K N Lai, F M Lai, S H Chui, et al.
American Journal of Hematology
|
June 22, 2000
beta-thalassemia intermedia caused by compound heterozygosity for Hb Malay (beta codon 19 AAC-->AGC; asn-->Ser) and codons 41/42 (-CTTT) beta(0)-thalassemia mutation
S K Ma, E Y Chow, A Y Chan, et al.
Journal of Clinical Pathology
|
April 18, 2001
Should we screen for globin gene mutations in blood samples with mean corpuscular volume (MCV) greater than 80 fL in areas with a high prevalence of thalassaemia?
L C Chan, S K Ma, A Y Chan, et al.
Clinical and Laboratory Haematology
|
June 26, 2001
Haemoglobin Q-Thailand and hereditary spherocytosis in a Chinese family
K F Leung, W Y Au, A Y Chan, et al.
Page
of 30
Search research articles
Search
Showing results (191-200 of 293) with videos related to
Sort By:
Page
of 30
American Journal of Hematology
|
October 1, 1991
Hb S/beta zero-thalassemia due to the approximately 1.4-kb deletion is associated with a relatively mild phenotype
J S Waye, D H Chui, B Eng, et al.
Blood
|
December 1, 1983
Adult hemoglobins are synthesized in murine fetal hepatic erythropoietic cells
P M Wong, S W Chung, J S White, et al.
The Journal of Clinical Investigation
|
June 8, 2000
Hla-DR2-restricted responses to proteolipid protein 95-116 peptide cause autoimmune encephalitis in transgenic mice
K Kawamura, T Yamamura, K Yokoyama, et al.
Singapore Medical Journal
|
December 5, 2009
Comparing histopathological classification with MYCN, 1p36 and 17q status detected by fluorescence in situ hybridisation from 14 untreated primary neuroblastomas in Singapore
M H Yong, W S Hwang, L A Knight, et al.
Addiction (Abingdon, England)
|
May 5, 2025
Associations of emotional experience with gaming duration and risk of gaming disorder among adolescent gamers: An ecological momentary assessment study
Camilla K M Lo, Edward W W Chan, Frederick K Ho, et al.
Archives of General Psychiatry
|
September 1, 1991
Temporal and hippocampal metabolic rate during an olfactory memory task assessed by positron emission tomography in patients with dementia of the Alzheimer type and controls. Preliminary studies
M S Buchsbaum, J P Kesslak, G Lynch, et al.
Clinical Nephrology
|
December 1, 1987
Studies of lymphocyte subpopulations and immunoglobulin production in IgA nephropathy
K N Lai, F M Lai, S H Chui, et al.
American Journal of Hematology
|
June 22, 2000
beta-thalassemia intermedia caused by compound heterozygosity for Hb Malay (beta codon 19 AAC-->AGC; asn-->Ser) and codons 41/42 (-CTTT) beta(0)-thalassemia mutation
S K Ma, E Y Chow, A Y Chan, et al.
Journal of Clinical Pathology
|
April 18, 2001
Should we screen for globin gene mutations in blood samples with mean corpuscular volume (MCV) greater than 80 fL in areas with a high prevalence of thalassaemia?
L C Chan, S K Ma, A Y Chan, et al.
Clinical and Laboratory Haematology
|
June 26, 2001
Haemoglobin Q-Thailand and hereditary spherocytosis in a Chinese family
K F Leung, W Y Au, A Y Chan, et al.
Page
of 30