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1. Altered myogenesis and premature senescence underlie human TRIM32-related myopathy

2. Report by the Spanish Foundation for the Brain on the social impact of amyotrophic lateral sclerosis and other neuromuscular disorders

3. Informe de la Fundación Del Cerebro sobre el impacto social de la esclerosis lateral amiotrófica y las enfermedades neuromusculares

4. Acidification-induced cellular changes in Symbiodinium isolated from Mussismilia braziliensis.

5. P.86 Spanish Pompe Registry: Update of the 122 patients included

6. Are metals of antifouling paints transferred to marine biota?

7. P.85 Analysis of Juvenile onset Pompe disease patients included in the Spanish Pompe Registry

9. CLINICAL RESEARCH

10. Traffic of secondary metabolites to cell surface in the red alga Laurencia dendroidea depends on a two-step transport by the cytoskeleton.

11. Heterozygous CAPN3 missense variants causing autosomal-dominant calpainopathy in seven unrelated families

12. Clathriamide, an hexapeptide isolated from the marine sponge Clathria (Clathria) nicoleae

13. Informe de la Fundación Del Cerebro sobre el impacto social de la esclerosis lateral amiotrófica y las enfermedades neuromusculares

14. Report by the Spanish Foundation for the Brain on the social impact of amyotrophic lateral sclerosis and other neuromuscular disorders

15. Cell wall physicochemical properties determine the thallus biomineralization pattern ofPadina gymnospora(Phaeophyceae)

16. POMPE DISEASE

17. LGMD

18. IMAGING

19. A Novel Antifouling Defense Strategy from Red Seaweed: Exocytosis and Deposition of Fatty Acid Derivatives at the Cell Wall Surface

20. Chloroplasts morphology investigation with diverse microscopy approaches and inter-specific variation in Laurencia species (Rhodophyta)

21. Bromopyrrole Alkaloid Inhibitors of the Proteasome Isolated from a Dictyonella sp. Marine Sponge Collected at the Amazon River Mouth

22. Protocolo diagnóstico de la mononeuritis y multineuritis

23. New Insights on the Terpenome of the Red Seaweed Laurencia dendroidea (Florideophyceae, Rhodophyta)

24. Acidification-induced cellular changes in Symbiodinium isolated from Mussismilia braziliensis

25. CONGENITAL MYOPATHIES: NEMALINE AND TITINOPATHIES

26. LIMB-GIRDLE MUSCULAR DYSTROPHY I

27. Diversity of Secondary Metabolites in the Liverwort Syzygiella rubricaulis (<scp>Nees</scp> ) <scp>Stephani</scp> (Jamesoniellaceae, Marchantiophyta) from Neotropical High Mountains

28. Induction of halogenated vesicle transport in cells of the red seaweedLaurencia obtusa

29. Report by the Spanish Foundation for the Brain on the social impact of amyotrophic lateral sclerosis and other neuromuscular disorders

30. Mevalonosomes: specific vacuoles containing the mevalonate pathway in Plocamium brasiliense cortical cells (Rhodophyta)

31. Variable presentation of the clinical phenotype of McArdle's disease in a kindred harbouring a novel compound genotype in the muscle glycogen phosphorylase gene

32. Dystroglycanopathy: Description of the first patient cohort in Spain

33. Diagnostic value of the activity of mitochondrial respiratory chain complex for mitochondrial myopathies

34. A novel MYH7 mutation causing the Laing distal myopathy in Andalucia

36. Sporadic late-onset nemaline myopathy in an aged patient

37. ChemInform Abstract: Crystalline Structure and Thermal Stability of Double Strontium and Barium Carbonates

38. Crystalline structure and thermal stability of double strontium and barium carbonates

39. Are metals of antifouling paints transferred to marine biota?

40. [Present and future of neurology in Spain]

41. Traffic of Secondary Metabolites to Cell Surface in the Red Alga Laurencia dendroidea Depends on a Two-Step Transport by the Cytoskeleton

42. G.P.6.01 Measurements of progression in dysferlin myopathies: A preliminary prospective quantitative study

44. Absolute configuration assignment of marine natural products in Brazil.

45. The Hexokinase 1 5′-UTR Mutation in Charcot–Marie–Tooth 4G Disease Alters Hexokinase 1 Binding to Voltage-Dependent Anion Channel-1 and Leads to Dysfunctional Mitochondrial Calcium Buffering.

46. Clinical and Genetic Analysis of Patients With TK2 Deficiency.

47. Clinical report and genetic analysis of a Chinese family with retinitis pigmentosa 79 caused by a novel loss-of-function HK1 variant.

48. Genomics of Terpene Biosynthesis in Dictyoceratid Sponges (Porifera) - What Do We (Not) Know?

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