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3. Assessing mNIS+7Ionis and international neurologists' proficiency in a familial amyloidotic polyneuropathy trial

6. Inotersen preserves or improves quality of life in hereditary transthyretin amyloidosis

8. Phase 1/2 Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamic Effects of AOC 1020 Administered Intravenously to Adult Patients with Facioscapulohumeral Muscular Dystrophy (FORTITUDE) Trial Design (P3-8.007)

9. DNA polymorphisms associated with lactase persistence, self‐perceived symptoms of lactose intolerance, milk and dairy consumption, and ancestry, in the Uruguayan population

10. Inhibition of Macrophage Ca2+-independent Phospholipase A2 by Bromoenol Lactone and Trifluoromethyl Ketones (∗)

11. Study Design of AOC 1001-CS1, a Phase 1/2 Clinical Trial Evaluating the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of AOC 1001 Administered Intravenously to Adult Patients with Myotonic Dystrophy Type 1 (DM1) (MARINA) (S23.006)

12. Filogeografía de mitogenomas indígenas de Uruguay

17. mNIS+7 and lower limb function in inotersen treatment of hereditary transthyretin‐mediated amyloidosis

18. Neuropathy symptom and change: Inotersen treatment of hereditary transthyretin amyloidosis

20. Inotersen preserves or improves quality of life in hereditary transthyretin amyloidosis

22. Nonidentity of the alpha-neurotoxin binding sites on the nicotinic acetylcholine receptor revealed by modification in alpha-neurotoxin and receptor structures

23. Inhibition of calcium-independent phospholipase A2 prevents arachidonic acid incorporation and phospholipid remodeling on P388D1 macrophages

24. Burden of hereditary transthyretin amyloidosis on quality of life

25. Responsiveness of Neuropathy Symptom and Change (NSC) Score Components in Inotersen Treatment of Hereditary Transthyretin Amyloidosis Polyneuropathy (P3.9-060)

26. Ancestría genética y estratificación social en Montevideo, Uruguay.

27. Inotersen Treatment for Patients with Hereditary Transthyretin Amyloidosis

28. Hereditary transthyretin amyloidosis: baseline characteristics of patients in the NEURO-TTR trial

30. Open Label Extension of the Phase 3 Study NEURO-TTR to Assess the Long-term Efficacy and Safety of Inotersen in Patients With Hereditary Transthyretin Amyloidosis (P1.324)

31. Safety and Efficacy of Inotersen in Patients With Hereditary Transthyretin Amyloidosis With Polyneuropathy (NEURO-TTR) (N2.001)

32. Burden of Hereditary Transthyretin Amyloidosis With Polyneuropathy in Patients Enrolled in the Phase 3 Study NEURO-TTR (P1.331)

33. Inotersen Improves Norfolk Quality of Life-Diabetic Neuropathy Measures in Patients With Hereditary Transthyretin Amyloidosis with Polyneuropathy in the Phase 3 Study NEURO-TTR (S5.006)

34. INOTERSEN IMPROVES QUALITY OF LIFE IN PATIENTS WITH HEREDITARY TRANSTHYRETIN AMYLOIDOSIS WITH POLYNEUROPATHY AND CARDIOMYOPATHY: RESULTS OF THE PHASE 3 STUDY NEURO-TTR

35. Evaluation of Therapeutic Oligonucleotides for Familial Amyloid Polyneuropathy in Patient-Derived Hepatocyte-Like Cells

37. Suppressing transthyretin production in mice, monkeys and humans using 2nd-Generation antisense oligonucleotides

38. Tu1724 In Vitro Study of the 2nd-Generation Antisense Oligonucleotide ISIS-TTRRX in Familial Amyloid Polyneuropathy-Specific Induced Pluripotent Stem Cell-Derived Hepatocyte-Like Cells

41. Breast cancer risk and genetic ancestry: a case–control study in Uruguay

45. Expression of eIF4E relevant biomarkers detected in circulating tumor cells from metastatic NSCLC and prostate cancer patients using antibody-independent ApoStream technology.

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