Skip to main content
U.S. flag

An official website of the United States government

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.

Search help
17 results
  1. Detailed Methods - Screening for Elevated Blood Lead Levels in Pregnant Women: A Systematic Review for the U.S. ... 
    https://www.ncbi.nlm.nih.gov/books/NBK540428
    ... PMID: 9756679. Excluded: Wrong outcome. [ PubMed : 9756679 ] [ CrossRef ] 12. Awasthi S, Awasthi R, Srivastav RC. Maternal blood lead level and outcomes of pregnancy in Lucknow, North ...
  2. Handling Continuous Outcomes in Quantitative Synthesis - Methods Guide for Effectiveness and Comparative Effectiveness .... 
    https://www.ncbi.nlm.nih.gov/books/NBK154408
    ... patient characteristics. Stat Med. 2010 May 30; 29 (12):1312–24. [ PubMed : 20087842 ] 43. Higgins JP, White IR, Anzures-Cabrera J. Meta-analysis of skewed data: combining results ...
  3. Excluded Studies - Noninvasive Positive Pressure Ventilation in the Home - NCBI Bookshelf 
    https://www.ncbi.nlm.nih.gov/books/NBK554172
    ... in stable hypercapnic COPD: does high inspiratory pressure lead to respiratory muscle unloading? International Journal of Copd. 2017;12:243–57. PMID: 28138234. [Irrelevant intervention (or time ...
  4. Hereditary Folate Malabsorption - GeneReviews® - NCBI Bookshelf 
    https://www.ncbi.nlm.nih.gov/books/NBK1673
    ... 2007; 293 :C1669–C1678. [ PubMed : 17898134 ] Salojin KV, Cabrera RM, Sun W, Chang WC, Lin C, Duncan L, Platt KA, Read R, Vogel P, Liu Q, Finnell RH, Oravecz T. A mouse model of hereditary folate malabsorption: deletion of the PCFT gene leads to systemic folate deficiency. Blood. 2011; 117 :4895– ...
  5. CDH23 gene: MedlinePlus Genetics 
    https://medlineplus.gov/genetics/gene/cdh23
    ... K, Nothwang HG, Seeliger M, del C-Salcedo Cabrera M, Vila MC, Molina OP, Gal A, Kubisch C. Mutation of CDH23, encoding a new member of the cadherin gene family, causes Usher syndrome type 1D. Nat Genet. 2001 Jan;27(1):108-12. doi: 10.1038/83667. Citation on PubMed Bork ...
  6. List of Excluded Studies - Opioid Treatments for Chronic Pain - NCBI Bookshelf 
    https://www.ncbi.nlm.nih.gov/books/NBK556254
    ... PubMed : 26921493 ] [ CrossRef ] 766. LOJ ES, Scherber K, ... 29395284. Exclusion: E5 [ PubMed : 29395284 ] [ CrossRef ] ...
  7. Management - Non-Hodgkin's Lymphoma: Diagnosis and Management - NCBI Bookshelf 
    https://www.ncbi.nlm.nih.gov/books/NBK385280
    ... most cost-effective option with an ICER of £12,246 per QALY compared to ... would lead to increased autologous transplantation and may result in ...
  8. List of Excluded Studies - Use of Cardiac Resynchronization Therapy in the Medicare Population - NCBI Bookshelf 
    https://www.ncbi.nlm.nih.gov/books/NBK310316
    ... failure. Cardiol J. 2009:545–552. [ PubMed : 19950091 ] Cabrera-Bueno F, Molina-Mora MJ, Alzueta J, Pena- ... pilot study. Europace. 2010:78–83. [ PubMed : 19897503 ] Cabrera-Bueno F, Fernandez-Pastor J, Molina-Mora MJ, ...
  9. Prolidase Deficiency - GeneReviews® - NCBI Bookshelf 
    https://www.ncbi.nlm.nih.gov/books/NBK299584
    ... 10 :18. [ PMC free article : PMC3623899 ] [ PubMed : 22726576 ] Cabrera HN, Giovanna PD, Bozzini NF, Forlino A. Prolidase ... two siblings with prolidase deficiency. Clin Rheumatol. 1993; 12 :410–4. [ PubMed : 8258246 ] Clare A, FitzHenley M, ...
  10. von Willebrand Disease - GeneReviews® - NCBI Bookshelf 
    https://www.ncbi.nlm.nih.gov/books/NBK7014
    ... Trillo Á, Lourés E, Cid AR, Bonanad S, Cabrera N, Moret A, Parra R, Mingot-Castellano ME, ... 3: the first case of maternal uniparental disomy 12. Haematologica. 2011; 96 :1567–8. [ PMC free article : ...
previous · 1 · 2 · next