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1. Next-generation phenotyping integrated in a national framework for patients with ultrarare disorders improves genetic diagnostics and yields new molecular findings

3. 5qSMA: standardised retrospective natural history assessment in 268 patients with four copies of SMN2

7. The promise of behavioral tracking systems for advancing primate animal welfare

10. The expanding clinical and genetic spectrum of DYNC1H1-related disorders

11. Improved upper limb function in non-ambulant children with SMA type 2 and 3 during nusinersen treatment: a prospective 3-years SMArtCARE registry study

14. Clinical Effectiveness of Newborn Screening for Spinal Muscular Atrophy: A Nonrandomized Controlled Trial.

17. Politische Gedichte

23. Next-generation phenotyping integrated in a national framework for patients with ultra-rare disorders improves genetic diagnostics and yields new molecular findings

24. Implementation of 2D Barcode Medication Labels and Smart Pumps in Pediatric Acute Care: Lessons Learned

25. Newbornscreening SMA – From Pilot Project to Nationwide Screening in Germany

27. Implementation of 2D barcode medication labels and smart pumps in pediatric acute care: Lessons learned

29. Positive effect of the combination of multilevel contracture release and glucocorticoid treatment in Duchenne muscular dystrophy

30. Treatment of uncertain malignant potential breast lesions (B3) with 3 different pathways: 3 years experience in Breast Screening Program

31. Cathepsin D as biomarker in cerebrospinal fluid of nusinersen-treated patients with spinal muscular atrophy

33. Gene replacement therapy with onasemnogene abeparvovec in children with spinal muscular atrophy aged 24 months or younger and bodyweight up to 15 kg: an observational cohort study

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