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Results 1 to 25 of 2711

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On becoming an authorityARING, C. D.Archives of neurology (Chicago). 1990, Vol 47, Num 1, pp 91-93, issn 0003-9942Conference Paper

An unusual case of myasthenia gravis in an elderly patient with severe muscular atrophyVELLODI, C; TALLIS, R. C.Gerontology (Basel). 1988, Vol 34, Num 4, pp 209-211, issn 0304-324XArticle

Les amyotrophies spinales de l'enfant = Spinal amyotrophy in childrenSERRATRICE, G.La Semaine des hôpitaux de Paris. 1986, Vol 62, Num 21, pp 1551-1567, issn 0037-1777Article

Becker's allelic model to explain unusual pedigree with spinal muscular atrophyZERRES, K; STEPHAN, M; KEHREN, U et al.Clinical genetics. 1987, Vol 31, Num 4, pp 276-277, issn 0009-9163Article

Spinal muscular atrophy in African childrenMOOSA, A; DAWOOD, A.Neuropediatrics. 1990, Vol 21, Num 1, pp 27-31, issn 0174-304XArticle

Neuralgic AmyotrophyKOSTER, Jelle B.The New England journal of medicine. 2010, Vol 362, Num 24, issn 0028-4793, p. 2304Article

Une myatonie congénitale à révélation tardive. L'amyotrophie spinale infantile pseudo-myopathique = Kugelberg Welander infantile spinal amyotrophyLE FUR, J.-M; LEROY, J.-P; PARENT, P et al.Revue internationale de pédiatrie. 1987, Num 167, pp 13-15, issn 0048-8135Article

Gene for chronic proximal spinal muscular atrophies maps to chromosome 5qMELKI, J; ABDELHAK, S; FONTAN, D et al.Nature (London). 1990, Vol 344, Num 6268, pp 767-768, issn 0028-0836, 2 p.Article

Muscle atrophy is not always sarcopeniaHEPPLE, Russell T.Journal of applied physiology (1985). 2012, Vol 113, Num 2, pp 677-679, issn 8750-7587, 3 p.Article

Mutations in SEPT9 cause hereditary neuralgic amyotrophyKUHLENBÄUMER, Gregor; HANNIBAL, Mark C; HALFTER, Hartmut et al.Nature genetics. 2005, Vol 37, Num 10, pp 1044-1046, issn 1061-4036, 3 p.Article

Muscle changes in aging : Muscle loss with aging: Is it reversible?BASU, R; BASU, A; NAIR, K. S et al.The Journal of nutrition, health & aging. 2002, Vol 6, Num 5, pp 336-341, issn 1279-7707, 6 p.Article

Respiratory muscle dysfunction in hereditary motor sensory neuropathy, type IEICHACKER, P. Q; SPIRO, A; SHERMAN, M et al.Archives of internal medicine (1960). 1988, Vol 148, Num 8, pp 1739-1740, issn 0003-9926Article

The application of nerve conduction and clinical studies to genetic counseling in hereditary motor and sensory neuropathy type IBERCIANO, J; COMBARROS, O; CALLEJA, J et al.Muscle & nerve. 1989, Vol 12, Num 4, pp 302-306, issn 0148-639X, 5 p.Article

Assessment of quadriceps femoris muscle atrophy and hypertrophy in neuromuscular disease in childrenHECKMATT, J. Z; PIER, N; DUBOWITZ, V et al.Journal of clinical ultrasound. 1988, Vol 16, Num 3, pp 177-181, issn 0091-2751Article

Somatosensory evoked potentials in spinal muscular atrophies and hereditary motor sensory neuropathiesEGERHAZI, A; DIOSZEGHY, P; MECHLER, F et al.Electromyography and clinical neurophysiology. 1988, Vol 28, Num 5, pp 285-288, issn 0301-150XArticle

Spontaneous motor unit firing in spinal muscular atrophy of childhoodHAUSMANOWA-PETRUSEWICZ, I; FRIEDMAN, A; KOWALSKI, J et al.Electromyography and clinical neurophysiology. 1987, Vol 27, Num 5, pp 259-264, issn 0301-150XArticle

Hereditary distal dominant amyotrophy followed by spastic paraplegiaSUNOHARA, N; TOMI, H; KISHIBAYASHI, J et al.Internal medicine (Tokyo. 1992). 1993, Vol 32, Num 11, pp 825-831, issn 0918-2918Article

Promotion of ambulation of patients with spinal muscular atrophy by early fitting of knee-ankle-foot orthosesGRANATA, C; CORNELIO, F; BONFIGLIOLI, S et al.Developmental medicine and child neurology (Print). 1987, Vol 29, Num 2, pp 221-224, issn 0012-1622Article

Electromyographic findings in different forms of infantile and juvenile proximal spinal muscular atrophyHAUSMANOWA-PETRUSEWICZ, I; KARNANSKA, A.Muscle & nerve. 1986, Vol 9, Num 1, pp 37-46, issn 0148-639XArticle

Etude nosologique de 25 cas d'amyotrophie monomélique chronique = A nosologic study of 25 cases of chronic monomalic amyotrophySERRATRICE, G; PELLISSIER, J. F; POUGET, J et al.Revue neurologique (Paris). 1987, Vol 143, Num 3, pp 201-210, issn 0035-3787Article

Genetic linkage studies in hereditary motor and sensory neuropathies. RepliesLEBLHUBER, F; REISECKER, F; MAYR, W. R et al.Journal of neurology. 1986, Vol 233, Num 5, pp 317-319, issn 0340-5354Article

Cell adhesion molecule N-CAM is expressed by denervated myofibres in Werdnig-Hoffman and Kugelberg-Welander type spinal muscular atrophiesWALSH, F. S; MOORE, S. E; LAKE, B. D et al.Journal of neurology, neurosurgery and psychiatry. 1987, Vol 50, Num 4, pp 439-442, issn 0022-3050Article

Long-term follow-up of spinal fusion in spinal muscular atrophyPIASECKI, J. O; MAHINPOUR, S; LEVINE, D. B et al.Clinical orthopaedics and related research. 1986, Num 207, pp 44-54, issn 0009-921XArticle

Chronic neurogenic quadriceps amyotrophiesSERRATRICE, G; POU-SERRADEL, A; PELLISSIER, J. F et al.Journal of neurology. 1985, Vol 232, Num 3, pp 150-153, issn 0340-5354Article

The application of the nearest neighbor decision rule in the evaluation of electromyogram in spinal muscular atrophy (SMA) of childhoodHAUSMANOWA-PETRUSEWICZ, I; JOZWIK, P. D. A.Electromyography and clinical neurophysiology. 1986, Vol 26, Num 8, pp 689-703, issn 0301-150XArticle

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