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Results 1 - 10 of 55 for AM 114
  1. Doctor of osteopathic medicine 
    ... of osteopathy": expanding the scope of practice. J Am Osteopath Assoc . 2014;114(3):200-212. PMID: 24567273 pubmed.ncbi.nlm. ... the first use of the "DO" designation. J Am Osteopath Assoc . 2014;114(8):615-617. PMID: 25082967 pubmed.ncbi.nlm. ...
    https://medlineplus.gov/ency/article/002020.htm - Medical Encyclopedia
  2. Ulcerative colitis 
    ... MD. ACG clinical guidelines: ulcerative colitis in adults. Am J Gastroenterol . 2019:114(3):384-413. PMID: 30840605 pubmed.ncbi.nlm. ...
    https://medlineplus.gov/ency/article/000250.htm - Medical Encyclopedia
  3. Excessive Alcohol Use is a Risk to Women's Health (Centers for Disease Control and Prevention)  
    Alcohol Use Disorder (AUD)/Women ... Alcohol Use Disorder (AUD) ... Alcohol/Women ... Alcohol ... Centers for Disease Control and Prevention ... Excessive alcohol use can lead to ...
    https://www.cdc.gov/alcohol/fact-sheets/womens-health.htm - External Health Links
  4. Hidradenitis Suppurativa: Overview (American Academy of Dermatology)  
    Hidradenitis suppurativa causes deep, painful lumps that often begin where skin touches skin like the armpit or groin. ... Hidradenitis Suppurativa/Start Here
    https://www.aad.org/.../a-z/hidradenitis-suppurativa-overview?NoAds - External Health Links
  5. 22q13.3 deletion syndrome 
    ... PubMed Manning MA, Cassidy SB, Clericuzio C, Cherry AM, Schwartz S, Hudgins L, Enns GM, Hoyme HE. Terminal 22q deletion syndrome: a newly recognized cause of speech and language disability in the autism spectrum. Pediatrics. 2004 Aug;114(2):451-7. doi: 10.1542/peds.114. ...
    https://medlineplus.gov/genetics/condition/22q133-deletion-syndrome - Genetics
  6. Chromosome 22 
    ... PubMed Manning MA, Cassidy SB, Clericuzio C, Cherry AM, Schwartz S, Hudgins L, Enns GM, Hoyme HE. Terminal 22q deletion syndrome: a newly recognized cause of speech and language disability in the autism spectrum. Pediatrics. 2004 Aug;114(2):451-7. doi: 10.1542/peds.114. ...
    https://medlineplus.gov/genetics/chromosome/22 - Genetics
  7. FECH gene 
    ... Citation on PubMed Gouya L, Puy H, Robreau AM, Lyoumi S, Lamoril J, Da Silva V, Grandchamp B, Deybach JC. Modulation of penetrance by the wild-type allele in dominantly inherited erythropoietic protoporphyria and acute hepatic porphyrias. Hum Genet. 2004 Feb;114(3):256-62. doi: 10.1007/s00439-003- ...
    https://medlineplus.gov/genetics/gene/fech - Genetics
  8. CPOX gene 
    ... Citation on PubMed Gouya L, Puy H, Robreau AM, Lyoumi S, Lamoril J, Da Silva V, Grandchamp B, Deybach JC. Modulation of penetrance by the wild-type allele in dominantly inherited erythropoietic protoporphyria and acute hepatic porphyrias. Hum Genet. 2004 Feb;114(3):256-62. doi: 10.1007/s00439-003- ...
    https://medlineplus.gov/genetics/gene/cpox - Genetics
  9. CLN2 disease 
    ... Pearce DA, Dodelson de Kremer R, Oller-Ramirez AM, Noher de Halac I. Neuronal ceroid lipofuscinosis type CLN2: a new rationale for the construction of phenotypic subgroups based on a survey of 25 cases in South America. Gene. 2013 Mar 1;516(1):114-21. doi: 10.1016/j.gene.2012.12. ...
    https://medlineplus.gov/genetics/condition/cln2-disease - Genetics
  10. TPP1 gene 
    ... Pearce DA, Dodelson de Kremer R, Oller-Ramirez AM, Noher de Halac I. Neuronal ceroid lipofuscinosis type CLN2: a new rationale for the construction of phenotypic subgroups based on a survey of 25 cases in South America. Gene. 2013 Mar 1;516(1):114-21. doi: 10.1016/j.gene.2012.12. ...
    https://medlineplus.gov/genetics/gene/tpp1 - Genetics
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