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Lipoprotein Electropheresis:
2,349 THB
Separates and measures different lipoproteins (LDL, HDL, VLDL) in the blood.
8-12 hour-fasting serum 1 ml
Lipid Panel
10497
Cardiovascular Disorders Heart Disease High Cholesterol Lipoprotein Profile None
Adenovirus antibody IgG:
1,620 THB
Detects IgG antibodies to adenovirus, used in diagnosing past or current infections.
serum 1 ml or Clotted blood 5 ml
Viral Panel
10498
Adenovirus IgG Test Cough None Sore Throat Viral Infections
Immunophenotyping for Lymphocyte all subset:
6,900 THB
Evaluates lymphocyte subpopulations (T cells, B cells, NK cells), used to assess immune function.
EDTA blood 3 ml.
Immune Panel
10499
Immunodeficiencies Lymphocyte Immunophenotyping None Recurrent Infections
Bile:
1,148 THB
Detects bile in urine or body fluids, used to diagnose liver or biliary diseases.
urine or body fluid 2 ml
Liver Function Panel
10500
Bile Test in Urine or Body Fluid Dark Urine Jaundice Liver Disorders None
Mandelic acid plus Phenylglyoxylic acid:
1,404 THB
Measures mandelic acid and phenylglyoxylic acid to assess exposure to styrene and ethylbenzene.
Urine end of shift 15 mL
Toxicology Panel
10501
Dizziness Fatigue Occupational Exposure Styrene Exposure Test Toxicology
Non Hodgkin Lymphoma panel:
16,625 THB
Detects and classifies non-Hodgkin lymphoma cells based on surface markers.
Turnaround Time9 days
Lymphoma Panel
10486
Fatigue Lymphoma Lymphoma Panel NHL Panel None Swollen Lymph Nodes
Mercury:
1,877 THB
Measures mercury levels in the urine, used to assess exposure to mercury.
Urine 24 hrs 50 ml.(no preservative) Pease note total volume every case
Heavy Metal Panel
10502
Fatigue Neurological Symptoms Occupational Exposure Toxicology Urine Mercury Test
SCA type 7:
5,865 THB
Detects mutations in the ATXN7 gene, responsible for spinocerebellar ataxia type 7.
EDTA whole blood 6 ml (minimum 3 ml)
Genetic Testing Panel
10487
Coordination Problems Family History Neurological Disorders Spinocerebellar Ataxia Type 7 Test Vision Loss
Prenatal chromosomal microarray:
34,020 THB
Detects chromosomal abnormalities in fetuses, used in prenatal genetic diagnosis.
Amniotic Fluid 15-20 ml ,EDTA cord blood 2 ml, Fetal autopsy in sterile Normal saline
Chromosome Analysis Panel
10503
Birth Defects Developmental Delays Fetal Microarray Analysis Genetic Disorders Maternity
Immunophenotyping for Minimal Residual Disease for Acute Myeloid Leukemia:
14,250 THB
Detects minimal residual disease in acute myeloid leukemia (AML) after treatment.
1. Heparinized or EDTA bone marrow 5 ml+ 2 slidesof bone marrow smear (Unstain) or 2. Heparinized or EDTA Peripheral blood 5 mL
Leukemia Panel
10488
Blood Cancers Easy Bruising Fatigue MRD Immunophenotyping for AML None
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