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1. Diagnosis and management of glycogen storage disease type IV, including adult polyglucosan body disease: A clinical practice resource

3. How and when does personal life orientation predict well-being?

6. A systematic global stocktake of evidence on human adaptation to climate change

7. Neuroimaging findings in infantile Pompe patients treated with enzyme replacement therapy

14. Clinical and Molecular Variability in Patients with PHKA2 Variants and Liver Phosphorylase b Kinase Deficiency

16. Diagnosis and management of glycogen storage diseases type VI and IX: a clinical practice resource of the American College of Medical Genetics and Genomics (ACMG)

26. O18: A path forward for patients with glycogen branching enzyme deficiency: Consensus on diagnosing and managing glycogen storage disease type IV*

32. PRKAG2 mutations presenting in infancy

35. Predicting Intraindividual Changes in Teacher Burnout: The Role of Perceived School Environment and Motivational Factors

37. A RETROSPECTIVE LONGITUDINAL STUDY AND COMPREHENSIVE REVIEW OF ADULT PATIENTS WITH GLYCOGEN STORAGE DISEASE TYPE III

40. Girls Action Network

43. A retrospective longitudinal study and comprehensive review of adult patients with glycogen storage disease type III

47. Targeted long-read sequencing identifies missing disease-causing variation

48. The effects on public health of climate change adaptation responses: a systematic review of evidence from low- and middle-income countries

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