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Results 1 - 10 of 745 for Sm
  1. SMS gene 
    The SMS gene provides instructions for making an enzyme called spermine synthase. This enzyme is involved in the production of spermine, which is a type ...
    https://medlineplus.gov/genetics/gene/sms - Genetics
  2. Loteprednol Ophthalmic 
    Lotemax® SM ... treat different eye conditions: Loteprednol (Inveltys, Lotemax, Lotemax SM) is used to treat swelling and pain after ... for 2 weeks. Loteprednol 0.38% gel (Lotemax SM) is usually instilled 3 times a day beginning ...
    https://medlineplus.gov/druginfo/meds/a619025.html - Drugs and Supplements
  3. Smith-Magenis syndrome 
    ... deletion syndrome Deletion 17p syndrome Partial monosomy 17p SMS Genetic Testing Registry: Smith-Magenis syndrome Smith-Magenis ... Rare Disorders (NORD) ClinicalTrials.gov SMITH-MAGENIS SYNDROME; SMS PubMed Carmona-Mora P, Encina CA, Canales CP, ...
    https://medlineplus.gov/genetics/condition/smith-magenis-syndrome - Genetics
  4. RAI1 gene 
    ... About This Health Condition KIAA1820 RAI1_HUMAN SMCR SMS Tests of RAI1 PubMed RETINOIC ACID-INDUCED GENE ...
    https://medlineplus.gov/genetics/gene/rai1 - Genetics
  5. Nearsightedness 
    ... Yonova-Doing E, Klein R, Klein BE, Hosseini SM, Paterson AD; Diabetes Control and Complications Trial/Epidemiology ... D, Mackey DA, Klaver CC, Wong TY, Saw SM, Baird PN. Nine loci for ocular axial length ...
    https://medlineplus.gov/genetics/condition/nearsightedness - Genetics
  6. Tasimelteon 
    ... of age and older with Smith-Magenis Syndrome (SMS; a developmental disorder). Tasimelteon is in a class ...
    https://medlineplus.gov/druginfo/meds/a615004.html - Drugs and Supplements
  7. Snyder-Robinson syndrome 
    ... Snyder-Robinson syndrome results from mutations in the SMS gene. This gene provides instructions for making an ... other parts of the body.Mutations in the SMS gene greatly reduce or eliminate the activity of ...
    https://medlineplus.gov/genetics/condition/snyder-robinson-syndrome - Genetics
  8. Autosomal dominant hyper-IgE syndrome 
    ... P, Matta JR, Hadigan C, Pettigrew RI, Holland SM, Gharib AM. Coronary artery abnormalities in Hyper-IgE ... LS, Darnell D, Davis J, Puck JM, Holland SM. Brain abnormalities in patients with hyperimmunoglobulin E syndrome. ...
    https://medlineplus.gov/.../autosomal-dominant-hyper-ige-syndrome - Genetics
  9. Facioscapulohumeral muscular dystrophy 
    ... M, Venance SL, Frants RR, van der Maarel SM, Tawil R. Clinical features of facioscapulohumeral muscular dystrophy ... S, Padberg GW, Lunt PW, van der Maarel SM. Best practice guidelines on genetic diagnostics of Facioscapulohumeral ...
    https://medlineplus.gov/.../facioscapulohumeral-muscular-dystrophy - Genetics
  10. Chromosome 1 
    ... PI, Grange DK, Naqvi S, Garnica AD, Bernes SM, Fong CT, Summers A, Walters WD, Lupski JR, ... R, Bryant SP, Burford DC, Burrill WD, Clegg SM, Dhami P, Dovey O, Faulkner LM, Gribble SM, ...
    https://medlineplus.gov/genetics/chromosome/1 - Genetics
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