Find and Order Laboratory Tests

Voltage-Gated Calcium Channel Anti- body:

73,600 THB

Detects antibodies against voltage-gated calcium channels, used in diagnosing Lambert-Eaton myasthenic syndrome (LEMS).
1 mL serum Minimum Volume 0.2 mL
10513
Fatigue Muscle Weakness Neurological Disorders None VGCC Antibody Test

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
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.
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
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
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
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
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)
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
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
10488
Blood Cancers Easy Bruising Fatigue MRD Immunophenotyping for AML None

Description:

Alias:

Specimen:

Related Tests:

Filter By Categories

All Categories filter

Diseases Category

Symptoms Category

Lifestyle Category

Age Groups Category

Category by Diagnostic Methods

Category by Specimen

Sorry, no results match your search criteria.

购物车
滚动至顶部