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1. Efficacy and Safety of Vamorolone Over 48 Weeks in Boys With Duchenne Muscular Dystrophy: A Randomized Controlled Trial.

2. An autosomal dominant neurological disorder caused by de novo variants in FAR1 resulting in uncontrolled synthesis of ether lipids.

3. Clinical RNA sequencing clarifies variants of uncertain significance identified by prior testing

6. Efficacy and Safety of Vamorolone vs Placebo and Prednisone Among Boys With Duchenne Muscular Dystrophy

7. Clinical, neurological, and electrophysiological features of nodding syndrome in Kitgum, Uganda: an observational case series

8. Midwest farm ground values increased over 2021, new report finds

9. Correction to: An autosomal dominant neurological disorder caused by de novo variants in FAR1 resulting in uncontrolled synthesis of ether lipids

10. A Population‐based Study of Scoliosis among Males Diagnosed with a Dystrophinopathy Identified by the Muscular Dystrophy Surveillance, Tracking, and Research Network ( MD STAR net )

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

13. Correction to:An autosomal dominant neurological disorder caused by de novo variants in FAR1 resulting in uncontrolled synthesis of ether lipids (Genetics in Medicine, (2021), 23, 4, (740-750), 10.1038/s41436-020-01027-3)

14. Association of variants in the SPTLC1 gene with juvenile amyotrophic lateral sclerosis

15. Association of Variants in the SPTLC1 Gene With Juvenile Amyotrophic Lateral Sclerosis

16. Defining the clinical, molecular and imaging spectrum of adaptor protein complex 4-associated hereditary spastic paraplegia

18. Kentucky students split on instructions during COVID-19

19. Defining the clinical, molecular and imaging spectrum of adaptor protein complex 4-associated hereditary spastic paraplegia

22. A population‐based study of scoliosis among males diagnosed with a dystrophinopathy identified by the Muscular Dystrophy Surveillance, Tracking, and Research Network (MD STARnet).

23. Fundraising in cyberspace: the current state of Internet law, fundraising and revenue generation

24. Association of Variants in the SPTLC1 Gene With Juvenile Amyotrophic Lateral Sclerosis

25. Fundraising in cyberspace: the law of Internet charitable fundraising and revenue generation

26. An autosomal dominant neurological disorder caused by de novo variants in FAR1resulting in uncontrolled synthesis of ether lipids

28. Opportunities in high technology

30. Cause marketing: how far can the quid pro quo go?

31. Evidence-Based Decision Support for Neurological Diagnosis Reduces Errors and Unnecessary Workup

34. Evidence-Based Decision Support for Neurological Diagnosis Reduces Errors and Unnecessary Workup.

35. Correction to: An autosomal dominant neurological disorder caused by de novo variants in FAR1resulting in uncontrolled synthesis of ether lipids

36. What You Need to Know When Your Charity Clients Engage in Multi-State Fundraising Activities.

37. Childhood Graves Disease Masquerading as Myasthenia Gravis.

40. Wanted: uniform registration

41. 2017 NHL draft to be held in Chicago.

42. Sally Beauty Doubles Profit.

44. Transfusion in elderly patients with myocardial infarction.

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