Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Jalaluddin Bhuiyan"'
Autor:
Mathew P. Estey, Edward Randell, Donald Greenway, Tina Binesh Marvasti, Jocelyne Cousineau, Jalaluddin Bhuiyan, Benjamin Jung, Edgard Delvin, Ashley H. Cohen, David Colantonio, Vijaylaxmi Grey, Khosrow Adeli, David W. Seccombe, Qing H. Meng, Man Khun Chan
Publikováno v:
Clinical Biochemistry. 46:1197-1219
Objectives The CALIPER program recently established a comprehensive database of age- and sex-stratified pediatric reference intervals for 40 biochemical markers. However, this database was only directly applicable for Abbott ARCHITECT assays. We ther
Publikováno v:
Clinica Chimica Acta. 331:69-77
Background The optimal management of bladder cancer requires early detection of both primary tumor as well as recurrences. This study compared the methodologies of the following tumor markers and diagnostic tools: telomerase, bladder tumor-associated
Autor:
Dennis J. O'Kane, Jennifer A. Besse, Steven G. Roberts, Michael L. Blute, Jalaluddin Bhuiyan, Sanjay Ramakumar, Peter C. Wollan
Publikováno v:
Journal of Urology. 161:388-394
Purpose: We prospectively evaluate and compare the sensitivity and specificity of urine cytology, BTA stat, [dagger] NMP22, [double dagger] fibrin/fibrinogen degradation products (FDP), telomerase, chemiluminescent hemoglobin and hemoglobin dipstick
Autor:
SANJAY RAMAKUMAR, JALALUDDIN BHUIYAN, JENNIFER A. BESSE, STEVEN G. ROBERTS, PETER C. WOLLAN, MICHAEL L. BLUTE, DENNIS J. O'KANE
Publikováno v:
The Journal of Urology. :388-394
Publikováno v:
Metabolism. 44:1185-1189
Acyl-coenzyme A (CoA) binding protein (ACBP) is a 10-kd protein that binds acyl-CoA moieties and stimulates medium-chain fatty acid synthesis by goat mammary gland fatty acid synthetase. Its exact role in intermediary lipid metabolism has not been fu
Publikováno v:
Clinical Biochemistry. 28:451-458
This study examined the hypolipidemic effect of 4 weeks of L-carnitine treatment (170 mg/kg b.w./day) in New Zealand White rabbits fed a high fat diet (5% corn oil/0.5% cholesterol). Specifically, [3H] glycerol and [125I] very low density lipoprotein
Publikováno v:
Clinica chimica acta; international journal of clinical chemistry. 335(1-2)
Background : Type 3 glycogen storage disease is an inborn error of metabolism in young infants that often requires extensive workup. However, this disease manifests with few symptoms other than hepatosplenomegaly. At adolescence, this disease may cau
Autor:
Edgard Delvin, Ashley H. Cohen, David Colantonio, Vijaylaxmi Grey, Donald Greenway, Khosrow Adeli, Tina Binesh Marvasti, Man Khun Chan, Mathew P. Estey, Edward Randell, Jalaluddin Bhuiyan, Benjamin Jung, David W. Seccombe, Qing H. Meng, Jocelyne Cousineau
Publikováno v:
Clinical Biochemistry. 46:1916
Autor:
David W. Seccombe, Jalaluddin Bhuiyan
Publikováno v:
Lipids. 31(8)
Recently, a new class of lipid lowering agents [3-hydroxy-3-methylglutaryl (HMG)-CoA reductase inhibitors] was introduced into clinical practice. The use of these agents could lead to a secondary deficiency in carnitine, which may manifest clinically
Publikováno v:
Clinical Biochemistry. 45:1116