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208 results on '"A. Pou Serradell"'

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1. European Union-Chinese Relations

2. Sensory neuropathy with bone destruction due to a mutation in the membrane-shaping atlastin GTPase 3

3. Genetic spectrum of hereditary neuropathies with onset in the first year of life

4. Fourth meeting of the European Neurological Society 25–29 June 1994 Barcelona, Spain: Abstracts of Symposia and free communications

7. A novel 3′-splice site mutation in peripheral myelin protein 22 causing hereditary neuropathy with liability to pressure palsies

8. Sensory neuropathy with bone destruction due to a mutation in the membrane-shaping atlastin GTPase 3

10. Myo-leukoencephalopathy in twins: Study of 3243-myopathy, encephalopathy, lactic acidosis, and strokelike episodes mitochondrial DNA mutation

11. Genetic spectrum of hereditary neuropathies with onset in the first year of life

12. Genetic spectrum of hereditary neuropathies with onset in the first year of life

13. Schwannomatosis: dermatological relevance of an unusual form of neurofibromatosis type 2 (NF-2)

14. Tuberous sclerosis complex. Forty-years of follow-up of a patients affected

15. Tuberous sclerosis complex. Forty-years of follow-up of a patients affected

16. Mutations in SEPT9 cause hereditary neuralgic amyotrophy

17. [Oculopharyngeal muscular dystrophy: study of patients from seven Spanish families with different GCG expansions in PABP2 gene]

19. [Crazy laughter: first manifestation of a pontine tumour]

21. [Hereditary neuropathy with liability to pressure palsies: study of six Spanish families]

23. [Familial myopathy with desmin storage seen as a granulo-filamentar, electron-dense material without mutation of the alphabeta-crystallin gene]

24. [Acute posterior cord lesions in multiple sclerosis. An MRI study of the clinical course in 20 cases]

25. [Acquired dysimmune neuropathies. Clinical symptoms and classification]

26. The natural history of hereditary neuralgic amyotrophy in the Dutch population

27. Genetic spectrum of hereditary neuropathies with onset in the first year of life

28. Arterial Cerebral Infarcts in Sickle Cell Trait and Antithrombin III Deficiency

29. Genetic refinement of the hereditary neuralgic amyotrophy (HNA) locus at chromosome 17q25

31. [A 56-year-old man with weakness of the legs]

33. [Bilateral intra-axial involvement of the common oculomotor nerve (III): 2 cases]

34. [Natural evolution of neurocutaneous syndrome in adults]

35. [Painful bilateral lumbar radiculoplexopathy associated with Epstein-Barr virus infection]

37. SPTLC1mutation in twin sisters with hereditary sensory neuropathy type I

38. [Spontaneous remission of cervical epidural hematoma with pathological confirmation]

39. [Deletion of 17p11.2 chromosome in Spanish families with hereditary neuropathy and abnormal sensitivity to pressure]

40. [Spinal cord ischemia indicating aneurysm of the abdominal aorta. Report of three cases]

41. [Isolated angiitis of the central nervous system. Clinical and neuropathological study of 2 cases]

45. Estudio clínico, radiológico, terapéutico y evolutivo, de las fístulas durales raquídeas con drenaje venoso perimedular

47. 3 cases of rare peripheral neuropathies associated with primary Gougerot-Sjögren syndrome

48. [Familial recurrent paralysis of the brachial plexus. Tomaculous neuropathy]

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