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Results 1 to 25 of 1790

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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

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

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

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

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

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

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

Expression of muscle cell surface antigen 5.1H11 in infantile or juvenile spinal muscular atrophyWALSH, F. S; MOORE, S. E.Neurology. 1986, Vol 36, Num 8, pp 1140-1142, issn 0028-3878Article

Fatty acid oxidation abnormalities in childhood-onset spinal muscular atrophy: primary or secondary defect(s)?TEIN, I; SLOANE, A. E; DONNER, E. J et al.Pediatric neurology. 1995, Vol 12, Num 1, pp 21-30, issn 0887-8994Article

Smad3 Induces Atrogin-1, Inhibits mTOR and Protein Synthesis, and Promotes Muscle Atrophy In VivoGOODMAN, Craig A; MCNALLY, Rachel M; HOFFMANN, F. Michael et al.Molecular endocrinology (Baltimore, Md.). 2013, Vol 27, Num 11, pp 1946-1957, issn 0888-8809, 12 p.Article

Les amyotrophies spinales de l'adulte = Spinal muscular atrophies are heterogeneous groupCAMU, W.Revue neurologique (Paris). 2004, Vol 160, Num 2, pp 225-228, issn 0035-3787, 4 p.Conference Paper

Progressive neurogenic muscle atrophy with fasciculation in mice treated with IDPNUEBAYASHI, Y; YANO, I; YASE, Y et al.Journal of the neurological sciences. 1987, Vol 78, Num 1, pp 79-86, issn 0022-510XArticle

Phrenic neuropathy due to neuralgic amyotrophyTSAO, Bryan E; OSTROVSKIY, Denis A; WILBOURN, Asa J et al.Neurology. 2006, Vol 66, Num 10, pp 1582-1584, issn 0028-3878, 3 p.Article

Dystrophy, abiotrophy, amyotrophyPEARCE, J. M. S.European neurology. 2005, Vol 54, Num 1, issn 0014-3022, p. 54Article

Development of ophthalmoplegia in amyotrophic lateral sclerosis during long-term use of respiratorsMIZUTANI, T; AKI, M; SHIOZAWA, R et al.Journal of the neurological sciences. 1990, Vol 99, Num 2-3, pp 311-319, issn 0022-510XArticle

La maladie d'Hirayama = Hirayama's diseaseWANG, F; GÖBELS, C; TOMASELLA, M et al.La Lettre du neurologue. 2011, Vol 15, Num 7, issn 1276-9339, 247-254 [7 p.]Article

Mechanism of Attenuation of Skeletal Muscle Atrophy by Zinc-α2-GlycoproteinRUSSELL, Steven T; TISDALE, Michael J.Endocrinology (Philadelphia). 2010, Vol 151, Num 10, pp 4696-4704, issn 0013-7227, 9 p.Article

Persisting muscle atrophy two years after replacement of the hipRASCH, A; BYSTRÖM, A. H; DALEN, N et al.Journal of bone and joint surgery. British volume (Print). 2009, Vol 91, Num 5, pp 583-588, issn 0301-620X, 6 p.Article

Summary of work group I : Population-based studiesGUO, S. S; HARRIS, T; STUDENSKI, S et al.Muscle & nerve. 1997, pp S114-S116, issn 0148-639X, SUP5Conference Paper

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