566 results on '"Jones, Patricia A."'
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2. Clinician-Level Knowledge and Barriers to Hepatocellular Carcinoma Surveillance
3. Cover
4. Multiple Barriers Impede Screening for Hepatitis Delta: An Internet-Based Survey of Healthcare Providers
5. A Portfolio Analysis of the National Institutes of Health, National Institute on Aging's Diversity Administrative Supplement Program
6. Newborn Screening: Current Practice and Our Journey over the Last 60 Years
7. National Institute on Aging's 50th anniversary: Advancing aging research and the health and well‐being of older adults
8. National Institute on Aging efforts toward ensuring representation of diverse older adults in clinical studies
9. Visualization of the intracranial pressure and time burden in childhood brain trauma: What we have learnt one decade on with KidsBrainIT.
10. “We Pledge Ourselves to the Masses of Working Girls”: The Distinctive Mission of the Women's Young Christian Workers Movement in its Founding Decades in England (1940s–1960s)
11. Inter-colony variation in predation, mercury burden and adult survival in a declining seabird
12. Clinical, biochemical, and molecular profiles of three Sri Lankan neonates with pyruvate carboxylase deficiency
13. Low Health Literacy, Lack of Knowledge, and Self-Control Hinder Healthy Lifestyles in Diverse Patients with Steatotic Liver Disease
14. NIA Office of Special Populations
15. ESPO AND BUTLER-WILLIAMS SCIENTIFIC SYMPOSIUM: CAREER DEVELOPMENT TO PROMOTE DIVERSITY, DISCOVERY, AND AGING
16. S1442 Hepatitis Delta Virus Screening Patterns Among Patients With Chronic Hepatitis B
17. Pediatric clinical biochemistry: why is it different?
18. Plant secondary metabolite has dose‐dependent effects on bumblebees
19. Incidence of Etiology-specific Hepatocellular Carcinoma: Diverging Trends and Significant Heterogeneity by Race and Ethnicity
20. Disorder: Phenylketonuria
21. Disorder: Medium-chain acyl-CoA dehydrogenase deficiency
22. Disorder: 3-Methyglutaconic aciduria
23. Disorder: Argininosuccinic acidemia
24. Disorder: Carnitine palmitoyltransferase 1 deficiency
25. List of contributors
26. Disorder: Arginase deficiency
27. Disorder: Lysinuric protein intolerance
28. Disorder: Tyrosinemia types 2 and 3
29. Disorder: Glutaric acidemia type 2
30. False-positive levorphanol (opioid) due to dextromethorphan on urine drug screen by time-of-flight MS
31. Disorder: Citrullinemia and citrin deficiency
32. Disorder: Carnitine-acylcarnitine translocase deficiency
33. Disorder: Methylmalonic aciduria
34. Disorder: Propionic acidemia
35. Disorder: Carnitine palmitoyltransferase 2 deficiency
36. Disorder: Succinic semialdehyde dehydrogenase deficiency
37. Disorder: 3-Methylcrotonyl-CoA-carboxylase deficiency
38. Disorder: Carbamyl phosphate synthetase 1 deficiency and N-acetylglutamate synthase deficiency
39. Disorder: Short chain 3-hydroxyacyl-CoA dehydrogenase deficiency
40. Disorder: Tyrosinemia type 1
41. Disorder: Dihydropyrimidine dehydrogenase deficiency
42. Disorder: Isovaleric aciduria
43. Disorder: 2-Methylbutyrylglycinuria
44. Disorder: Ornithine transcarbamylase deficiency
45. Disorder: Glutathione synthetase deficiency
46. Disorder: Long chain 3-hydroxyacyl-CoA dehydrogenase deficiency
47. Disorder: Glutaric acidemia type 1
48. Disorder: Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome
49. Disorder: Pyruvate dehydrogenase deficiency
50. Disorder: Biotin: Biotinidase deficiency and holocarboxylase synthetase deficiency
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