Results 1 - 10 of 14,605 for 1S -"Hydroxy-(2S)-glutathionyl-1,2-dihydronaphthalene"
  1. Alpha-1 Antitrypsin Deficiency (National Library of Medicine)  
    Alpha-1 antitrypsin deficiency (AAT deficiency) is an inherited condition that raises your risk for lung and liver disease. Alpha-1 antitrypsin (AAT) is a protein that protects the ...
  2. Diabetes Type 1 (National Library of Medicine)  
    ... blood sugar, levels are too high. With type 1 diabetes, your pancreas does not make insulin. Insulin ... eyes, kidneys, nerves, and gums and teeth. Type 1 diabetes happens most often in children and young ...
  3. Alpha-1 Antitrypsin Test What is an alpha-1 antitrypsin (AAT) test? This test measures the amount of alpha-1 antitrypsin (AAT) in the blood. AAT is a ... risk for disease. Other names: A1AT, AAT, alpha-1-antiprotease deficiency, α1-antitrypsin What is it used ...
  4. Complete plasminogen activator inhibitor 1 deficiency (complete PAI-1 deficiency) is a disorder that causes abnormal bleeding. In people with this disorder, bleeding ...
  5. 1q21.1 microdeletion is a chromosomal change in which a small piece of chromosome 1 is deleted in each ...
  6. 1q21.1 microduplication is a chromosomal change in which a small amount of genetic material on chromosome 1 is abnormally copied (duplicated). The duplication occurs on ...
  7. Type 1 diabetes is a disorder characterized by abnormally high blood sugar levels. In this form of diabetes, specialized cells in the pancreas called beta ...
  8. Combined oxidative phosphorylation deficiency 1 is a severe condition that primarily impairs neurological and liver function.Most people with combined oxidative ...
  9. Leukocyte adhesion deficiency type 1 is a disorder that causes the immune system to malfunction, resulting in a form of immunodeficiency. Immunodeficiencies are ...
  10. X-linked chondrodysplasia punctata 1 is a disorder of cartilage and bone development that occurs almost exclusively in males. Chondrodysplasia punctata ...
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