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

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

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

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

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

15. POMPE DISEASE

16. LGMD

17. IMAGING

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

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

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

21. Protocolo diagnóstico de la mononeuritis y multineuritis

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

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

24. CONGENITAL MYOPATHIES: NEMALINE AND TITINOPATHIES

25. LIMB-GIRDLE MUSCULAR DYSTROPHY I

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

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

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

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

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

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

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

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

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

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

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

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

39. [Present and future of neurology in Spain]

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

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

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

44. A splice-altering homozygous variant in COX18 causes severe sensory-motor neuropathy with oculofacial apraxia.

45. Decoding the muscle transcriptome of patients with late onset Pompe disease reveals markers of disease progression.

46. The Iberian Roma Population Variant Server (IRPVS).

47. A Laing distal myopathy-associated proline substitution in the β-myosin rod perturbs myosin cross-bridging activity.

48. Correction to: Analysis of muscle magnetic resonance imaging of a large cohort of patient with VCP‑mediated disease reveals characteristic features useful for diagnosis.

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

50. EURO-NMD registry: federated FAIR infrastructure, innovative technologies and concepts of a patient-centred registry for rare neuromuscular disorders.

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