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63 results
  1. Evidence for the recognition of coeliac disease - Coeliac Disease - NCBI Bookshelf 
    https://www.ncbi.nlm.nih.gov/books/NBK343379
    ... a lack of evidence for the signs and symptoms of coeliac disease (CD), and in particular the most commonly recognised presenting signs and symptoms such as gastrointestinal dysfunction, weight loss, and abdominal ...
  2. References - Dementia - NCBI Bookshelf 
    https://www.ncbi.nlm.nih.gov/books/NBK536508
    ... Disease, 42(3):915–37 [ PubMed : 25024323 ] Moulton CD, Hopkins CWP, Bevan-Jones WR (2014) Systematic review of pharmacological treatments for depressive symptoms in Huntington’s disease, Movement disorders, 29(12):1556–61 [ PubMed : 25111961 ] ...
  3. NLM Digital Collections - Index-catalogue of the Library of the Surgeon-General's Office, United States Army. Authors ... 
    Publication: Washington : G.P.O., 1880-1932
    resource.nlm.nih.gov/8104689X43
    ... hydatid disease. Lancet, Lond., 1908, i, 1338—Welsh CD. A.), Chapman (H. G.) & Storey (J. C.) Some applications of the precipitin reaction in the diagnosis of hydatid disease- Md., 1909, i, 1103-1105. Hydatids (Multilocular and ...
  4. HEXA Disorders - GeneReviews® - NCBI Bookshelf 
    https://www.ncbi.nlm.nih.gov/books/NBK1218
    ... 2. Genetic Disorders of Interest in the Differential Diagnosis of Acute Infantile ... disease – ≤6 mos Macrocephaly, head lag, hypotonia, seizures ...
  5. Resources for Genetics Professionals — Genetic Disorders Associated with Founder Variants Common in the Ashkenazi ... 
    https://www.ncbi.nlm.nih.gov/books/NBK535149
    ... Zeiger K. Tay-Sachs disease--carrier screening, prenatal diagnosis, and the ... K, Matalon R. Canavan disease: mutations among Jewish and non-Jewish patients. Am ...
  6. GLB1-Related Disorders - GeneReviews® - NCBI Bookshelf 
    https://www.ncbi.nlm.nih.gov/books/NBK164500
    ... 4. Genetic Disorders of Interest in the Differential Diagnosis of Type I (Infantile) GM1 ... mos Macrocephaly, head lag, hypotonia, seizures Leukoencephalopathy, ↑ ...
  7. Sandhoff Disease - GeneReviews® - NCBI Bookshelf 
    https://www.ncbi.nlm.nih.gov/books/NBK579484
    ... 2. Genetic Disorders of Interest in the Differential Diagnosis of Acute Infantile Sandhoff ... disease ≤6 mos Macrocephaly, head lag, hypotonia, seizures ...
  8. Childhood Ataxia with Central Nervous System Hypomyelination / Vanishing White Matter - GeneReviews® - NCBI Bookshelf 
    https://www.ncbi.nlm.nih.gov/books/NBK1258
    ... metachromatic leukodystrophy) ARSA AR Krabbe disease GALC AR ... Megalencephalic leukoencephalopathy with subcortical cysts HEPACAM MLC1 AR ...
  9. Mitochondrial Neurogastrointestinal Encephalopathy Disease - GeneReviews® - NCBI Bookshelf 
    https://www.ncbi.nlm.nih.gov/books/NBK1179
    ... variants, PLP1 -related disorders , Krabbe disease , Alexander disease , Canavan ... at Initial Diagnosis To establish the extent of disease and needs ...
  10. NLM Digital Collections - Hospital and health administration index (Volume 51) 
    resource.nlm.nih.gov/9601831X1
    ... bias in the referral of patients for the diagnosis of coronary artery disease? An exploratory study. Can Med Assoc J 1995 Mar 15; 152(6):873—80 Jaglal SB, Tu JV, Naylor CD. (Clinical Epidemiology Unit, Sunnybrook Health Sciences Centre, Institute ...
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