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Results 1 - 10 of 14,366 for 1S -"Hydroxy-(2S)-glutathionyl-1,2-dihydronaphthalene"
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  1. Alpha-1 Antitrypsin Deficiency (National Library of Medicine)  
    What is alpha-1 antitrypsin deficiency (AAT deficiency)? Alpha-1 antitrypsin deficiency (AAT deficiency, or AATD) is an inherited condition that raises your ...
    https://medlineplus.gov/alpha1antitrypsindeficiency.html - Health Topics
  2. IGF-1 (Insulin-like Growth Factor 1) Test: MedlinePlus Medical Test 
    IGF-1 (Insulin-like Growth Factor 1) Test What is an IGF-1 test? This test measures the amount of IGF-1 (insulin-like growth factor 1) in your ... facial features. Why do I need an IGF-1 test? Your health care provider may order an ... dysfunction in men What happens during an IGF-1 test? A health care professional will take a ...
    https://medlineplus.gov/.../igf-1-insulin-like-growth-factor-1-test - Medical Tests
  3. 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
  4. Alpha-1 Antitrypsin Testing: MedlinePlus Medical Test 
    Alpha-1 Antitrypsin Testing What is alpha-1 antitrypsin (AAT) testing? Alpha-1 antitrypsin (AAT) testing uses a sample of blood or a cheek swab to diagnose a condition called alpha-1 antitrypsin deficiency (AAT deficiency). This condition is sometimes ... would normally work. Other names: A1AT, AAT, alpha-1-antiprotease deficiency, α1-antitrypsin, serum AAT test, AAT ...
    https://medlineplus.gov/lab-tests/alpha-1-antitrypsin-testing - Medical Tests
  5. 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
  6. 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
  7. Developmental and epileptic encephalopathy 1 
    Developmental and epileptic encephalopathy 1 (DEE1) is a seizure disorder characterized by a type of seizure known as infantile spasms. The spasms usually appear before ...
    https://medlineplus.gov/...elopmental-and-epileptic-encephalopathy-1 - Genetics
  8. Type 1 diabetes 
    Type 1 diabetes is a disorder characterized by abnormally high levels of blood glucose, also called blood sugar. In this form of diabetes, specialized cells ...
    https://medlineplus.gov/genetics/condition/type-1-diabetes - Genetics
  9. 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
  10. Alpha-1 antitrypsin deficiency 
    Alpha-1 antitrypsin deficiency is an inherited disorder that may cause lung disease and liver disease. The signs and symptoms of the condition and the age ...
    https://medlineplus.gov/.../condition/alpha-1-antitrypsin-deficiency - Genetics
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