Results 1 - 10 of 14,586 for 1S -"Hydroxy-(2S)-glutathionyl-1,2-dihydronaphthalene"
Did you mean 1S -"Hydroxy-(2S)-glutathione-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 ...
    https://medlineplus.gov/alpha1antitrypsindeficiency.html - Health Topics
  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 ...
    https://medlineplus.gov/diabetestype1.html - Health Topics
  3. Alpha-1 Antitrypsin Test: MedlinePlus Medical Test 
    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 ...
    https://medlineplus.gov/lab-tests/alpha-1-antitrypsin-test - Medical Tests
  4. Complete plasminogen activator inhibitor 1 deficiency 
    Complete plasminogen activator inhibitor 1 deficiency (complete PAI-1 deficiency) is a disorder that causes abnormal bleeding. In people with this disorder, bleeding ...
    https://medlineplus.gov/...sminogen-activator-inhibitor-1-deficiency - Genetics
  5. 1q21.1 microdeletion 
    1q21.1 microdeletion is a chromosomal change in which a small piece of chromosome 1 is deleted in each ...
    https://medlineplus.gov/genetics/condition/1q211-microdeletion - Genetics
  6. 1q21.1 microduplication 
    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 ...
    https://medlineplus.gov/genetics/condition/1q211-microduplication - Genetics
  7. Type 1 diabetes 
    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 ...
    https://medlineplus.gov/genetics/condition/type-1-diabetes - Genetics
  8. Combined oxidative phosphorylation deficiency 1 
    Combined oxidative phosphorylation deficiency 1 is a severe condition that primarily impairs neurological and liver function.Most people with combined oxidative ...
    https://medlineplus.gov/...ed-oxidative-phosphorylation-deficiency-1 - Genetics
  9. Leukocyte adhesion deficiency type 1 
    Leukocyte adhesion deficiency type 1 is a disorder that causes the immune system to malfunction, resulting in a form of immunodeficiency. Immunodeficiencies are ...
    https://medlineplus.gov/.../leukocyte-adhesion-deficiency-type-1 - Genetics
  10. X-linked chondrodysplasia punctata 1 
    X-linked chondrodysplasia punctata 1 is a disorder of cartilage and bone development that occurs almost exclusively in males. Chondrodysplasia punctata ...
    https://medlineplus.gov/.../x-linked-chondrodysplasia-punctata-1 - Genetics
previous · 1 · 2 · 3 · 4 · 5 · 6 · 7 · 8 · 9 · 10 · next