145 results on '"Fialho, D"'
Search Results
2. Clinical, genetic and electrophysiological study of skeletal muscle channelopathies : new insights into myotonia congenita and Andersen-Tawil syndrome
3. Notas breves acerca das restrições dos acordos parassociais em matéria de administração
4. A (síndrome de) alienação parental: uma nova forma de patriarcado?
5. Breves notas acerca do rapto internacional de crianças e seus instrumentos de resolução
6. Andersen-Tawil syndrome: deep phenotyping reveals significant cardiac and neuromuscular morbidity
7. The long exercise test as a functional marker of periodic paralysis
8. Translating genetic and functional data into clinical practice: a series of 223 families with myotonia
9. A publicidade dirigida a menores e os novos limites em velhos hábitos no direito à alimentação
10. (Des)ilusão europeia ou oportunidade, tal Fénix renascida?
11. A positive McManis test in a series of patients with muscle disease but without periodic paralysis: 10
12. O Exercício das Responsabilidades Parentais em Residência Alternada
13. Andersen-Tawil Syndrome Presenting with Complete Heart Block
14. Treatment of chronic inflammatory demyelinating polyradiculoneuropathy with methotrexate
15. Predicting response to treatment in chronic inflammatory demyelinating polyradiculoneuropathy
16. Evidence for a role of sensory pathway abnormalities in the pathophysiology of childhood dystonia: T051
17. The non-dystrophic myotonias: molecular pathogenesis, diagnosis and treatment
18. Notas breves acerca das restrições dos acordos parassociais em matéria de administração
19. Os acordos parassociais: reflexão dogmática e jurisprudencial
20. Chloride channel myotonia: exon 8 hot-spot for dominant-negative interactions
21. The primary periodic paralyses: diagnosis, pathogenesis and treatment
22. A (síndrome de) alienação parental: uma nova forma de patriarcado?
23. Breves notas acerca do rapto internacional de crianças e seus instrumentos de resolução
24. P.98RCT of 2mg bumetanide for hypokalaemic periodic paralysis
25. P.101Defining the phenotype of Andersen-Tawil syndrome: the largest reported series
26. Atypical periodic paralysis and myalgia: A novel RYR1 phenotype
27. An audit of acetazolamide use in genetic channelopathies
28. RCT of bumetanide in hypokalaemic periodic paralysis (HypoPP) using abductor digiti minimi compound muscle action potential (CMAP) as an objective outcome measure
29. Large scale validation of functional expression of ClC-1 variants in genetic counselling of myotonia congenital
30. RCT of Bumetanide in Hypokalaemic Periodic Paralysis (HypoPP) using abductor digiti minimi compound muscle action potential (CMAP) as an objective outcome measure
31. Somatosensory evoked potentials in children with dystonia help predict outcome from deep brain stimulation
32. Improving genetic diagnosis and counselling for patients with myotoniacongenita
33. The Proliferation of Developing Country Classifications
34. Pelas ruas do Rio de Janeiro. Dois (ou três?) olhares estrangeiros: Henry Chamberlain e Jean-Baptiste Debret
35. Bumetanide in hypokalaemic periodic paralysis: a randomised, double-blind, placebo controlled phase II clinical trial with a crossover design
36. NMJ&C02 - An audit of acetazolamide use in genetic channelopathies
37. NMJ&C03 - RCT of bumetanide in hypokalaemic periodic paralysis (HypoPP) using abductor digiti minimi compound muscle action potential (CMAP) as an objective outcome measure
38. Caveolinopathy presenting with muscle pain and rhabdomyolysis
39. (Des)ilusão europeia ou oportunidade, tal Fénix renascida?
40. Aplicação da espectroscopia NIR na determinação de alguns parâmetros de qualidade em ameixas
41. Contribuição para a construção de um modelo matemático da produção da pêra 'Rocha'
42. P.230 - Large scale validation of functional expression of ClC-1 variants in genetic counselling of myotonia congenital
43. NMJ+C05 - Improving genetic diagnosis and counselling for patients with myotoniacongenita
44. P.373 - Bumetanide in hypokalaemic periodic paralysis: a randomised, double-blind, placebo controlled phase II clinical trial with a crossover design
45. A new explanation for recessive myotonia congenita: exon deletions and duplications in CLCN1.
46. What causes paramyotonia in the United Kingdom? Common and new SCN4A mutations revealed.
47. Prevalence study of genetically defined skeletal muscle channelopathies in England
48. NIR CASE DEVICE USE IN A PACKING HOUSE AND THE PREDICTION OF POSTHARVEST QUALITY OF 'ROCHA' PEAR AND 'GALA' APPLE
49. Clinical and Molecular Characterization of Non-Dystrophic Myotonia (P05.181)
50. EEG Abnormalities in the Episodic Ataxias (P05.029)
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