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1S -"1-CYCLOPROPYL-2-[(2S)-4-(2,5-DIFLUOROPHENYL)-2-PHENYL-2,5-DIHYDRO-1H-patrol-1-YL]-2-OXOETHANAMINE"
- 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 ...
- 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 provider may order an IGF-1 ...
- 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 ...
- 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- ...
- Complete plasminogen activator inhibitor 1 deficiency (complete PAI-1 deficiency) is a disorder that causes abnormal bleeding. In people with this disorder, bleeding ...
- 1q21.1 microdeletion is a chromosomal change in which a small piece of chromosome 1 is deleted in each ...
- 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 ...
- 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 ...
- Leukocyte adhesion deficiency type 1 is a disorder that causes the immune system to malfunction, resulting in a form of immunodeficiency. Immunodeficiencies are ...
- Spinal muscular atrophy with respiratory distress type 1 (SMARD1) is an inherited condition that causes muscle weakness and respiratory failure typically beginning ...