Skip navigation

Official websites use .gov
A .gov website belongs to an official government organization in the United States.

Secure .gov websites use HTTPS
A lock ( ) or https:// means you’ve safely connected to the .gov website. Share sensitive information only on official, secure websites.

Results 21 - 30 of 14,310 for 1S -"1-(1H-INDOL-3-YLMETHYL)-2-(2-PYRIDIN-4-YL-[1,7]NAPHTYRIDIN-5-YLOXY)-EHYLAMINE"
Did you mean 1S -"1-(1H-INDOL-3-methyl)-2-(2-PYRIDIN-4-YL-[1,7]NAPHTYRIDIN-5-YLOXY)-hyaline"?
  1. Choking - adult or child over 1 year 
    ... resuscitation and emergency cardiovascular care. Pediatrics . 2020;145(1):e20191358. PMID: 31727861 pubmed.ncbi.nlm.nih.gov/ ... resuscitation and emergency cardiovascular care. Circulation . 2018;137(1):e7-e13. PMID: 29114008 pubmed.ncbi.nlm.nih. ...
    https://medlineplus.gov/ency/article/000049.htm - Medical Encyclopedia
  2. Alpha-1 antitrypsin deficiency 
    Alpha-1 antitrypsin (AAT) deficiency is a condition in which the body does not make enough of AAT, a ... The spectrum of clinical sequelae associated with alpha-1 antitrypsin deficiency. Ther Adv Chronic Dis . 2021;12_ ...
    https://medlineplus.gov/ency/article/000120.htm - Medical Encyclopedia
  3. Optic atrophy type 1 
    Optic atrophy type 1 is a condition that often causes slowly worsening vision, usually beginning in childhood. People with optic atrophy type 1 typically experience a narrowing of their field of ...
    https://medlineplus.gov/genetics/condition/optic-atrophy-type-1 - Genetics
  4. Neurofibromatosis type 1 
    Neurofibromatosis type 1 is a condition characterized by changes in skin coloring (pigmentation) and the growth of tumors along nerves in ... early childhood, almost all people with neurofibromatosis type 1 have multiple café-au-lait spots, which are ...
    https://medlineplus.gov/genetics/condition/neurofibromatosis-type-1 - Genetics
  5. Atelosteogenesis type 1 
    Atelosteogenesis type 1 is a disorder that affects the development of bones throughout the body. Affected individuals are born with inward- ...
    https://medlineplus.gov/genetics/condition/atelosteogenesis-type-1 - Genetics
  6. Congenital bile acid synthesis defect type 1 
    Congenital bile acid synthesis defect type 1 is a disorder characterized by cholestasis, a condition that impairs the production and release of a digestive fluid ...
    https://medlineplus.gov/...genital-bile-acid-synthesis-defect-type-1 - Genetics
  7. Medullary cystic kidney disease type 1 
    Medullary cystic kidney disease type 1 (MCKD1) is an inherited condition that affects the kidneys. It leads to scarring (fibrosis) and impaired function of the kidneys, usually ...
    https://medlineplus.gov/.../medullary-cystic-kidney-disease-type-1 - Genetics
  8. Pseudohypoaldosteronism type 1 
    Pseudohypoaldosteronism type 1 (PHA1) is a condition characterized by problems regulating the amount of sodium in the body. Sodium regulation, which ... as the sweat glands and colon. Pseudohypoaldosteronism type 1 is named for its characteristic signs and symptoms, ...
    https://medlineplus.gov/.../condition/pseudohypoaldosteronism-type-1 - Genetics
  9. Pelizaeus-Merzbacher-like disease type 1 
    Pelizaeus-Merzbacher-like disease type 1 is an inherited condition involving the brain and spinal cord (central nervous system). This disease is one of a group ...
    https://medlineplus.gov/.../pelizaeus-merzbacher-like-disease-type-1 - Genetics
  10. Autosomal recessive cerebellar ataxia type 1 
    Autosomal recessive cerebellar ataxia type 1 (ARCA1) is a condition characterized by progressive problems with movement due to a loss (atrophy) of nerve cells in the part ...
    https://medlineplus.gov/...osomal-recessive-cerebellar-ataxia-type-1 - Genetics
previous · 1 · 2 · 3 · 4 · 5 · 6 · 7 · 8 · 9 · 10 · next