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Human ontogensis. III, Cell death in fetal muscleFIDZIANSKA, A; GOEBEL, H. H.Acta neuropathologica. 1991, Vol 81, Num 5, pp 572-577, issn 0001-6322Article

Tubuloreticular structures (TRS) and cylindric confronting cisternae (CCC) in childhood dermatomyositisFIDZIANSKA, A; GOEBEL, H. H.Acta neuropathologica. 1989, Vol 79, Num 3, pp 310-316, issn 0001-6322Article

CAP DISEASE: NEW CONGENITAL MYOPATHYFIDZIANSKA A; BADURSKA B; RYNIEWICZ B et al.1981; NEUROLOGY; ISSN 0028-3878; USA; DA. 1981; VOL. 31; NO 9; PP. 1113-1120; BIBL. 22 REF.Article

Phagocytic capacity of human muscle fibersFIDZIANSKA, A; GOEBEL, H. H.Human pathology. 1992, Vol 23, Num 9, pp 1044-1047, issn 0046-8177Article

CONGENITAL MUSCULAR DYSTROPHY (CMD): A COLLAGEN FORMATIVE DISEASE.FIDZIANSKA A; GOEBEL HH; LENARD HG et al.1982; J. NEUROL. SCI.; ISSN 0022-510X; NLD; DA. 1982; VOL. 55; NO 1; PP. 79-90; BIBL. 1 P.Article

Congenital myopathy with tubular aggregates and tubulofilamentous IBM-type inclusionsFIDZIANSKA, A; KAMINSKA, A; RYNIEWICZ, B et al.Neuropediatrics. 2005, Vol 36, Num 1, pp 35-39, issn 0174-304X, 5 p.Article

An ultrastructural study of the vascular and muscular basement membrane in Duchenne-type dystrophyFIDZIANSKA, A; GLINKA, Z; WALSKI, M et al.Clinical neuropathology. 1987, Vol 6, Num 6, pp 257-261, issn 0722-5091Article

Ultrastructural abnormality of sarcolemmal nuclei in Emery-Dreifuss muscular dystrophy (EDMD)FIDZIANSKA, A; TONIOLO, D; HAUSMANOWA-PETRUSEWICZ, I et al.Journal of the neurological sciences. 1998, Vol 159, Num 1, pp 88-93, issn 0022-510XArticle

MALLORY BODY-LIKE INCLUSIONS IN A HEREDITARY CONGENITAL NEUROMUSCULAR DISEASEFIDZIANSKA A; GOEBEL HG; OSBORN M et al.1983; MUSCLE AND NERVE; ISSN 0148-639X; USA; DA. 1983; VOL. 6; NO 3; PP. 195-200; BIBL. 24 REF.Article

Myopathic form of arthrogryposis and microcirculation lesionFIDZIANSKA, A; GOEBEL, H. H; BURCK-LEHMANN, U et al.Journal of the neurological sciences. 1989, Vol 92, Num 2-3, pp 337-348, issn 0022-510X, 12 p.Article

Lipid storage myopathy in Kearns-Sayre syndromeNIEBROJ-DOBOSZ, I; RYNIEWICZ, B; FIDZIANSKA, A et al.Neurology. 1985, Vol 35, Num 11, pp 1582-1586, issn 0028-3878Article

Is central core disease with structural core a fetal defect?FIDZIANSKA, A; NIEBROJ-DOBOSZ, I; BADURSKA, B et al.Journal of neurology. 1984, Vol 231, Num 4, pp 212-219, issn 0340-5354Article

CADASIL: new cases and new questionsRAFALOWSKA, J; FIDZIANSKA, A; DZIEWULSKA, D et al.Acta neuropathologica. 2003, Vol 106, Num 6, pp 569-574, issn 0001-6322, 6 p.Article

Macroemg in manifesting carriers of Duchenne Muscular DystrophySZMIDT-SALKOWSKA, E; ROWINSKA-MARCINSKA, K; FIDZIANSKA, A et al.Electromyography and clinical neurophysiology. 1999, Vol 39, Num 2, pp 87-92, issn 0301-150XArticle

Atypical motor unit potentials in Emery-Dreifuss muscular dystrophy (EDMD)ROWINSKA-MARCINSKA, K; SZMIDT-SAŁKOWSKA, E; FIDZIANSKA, A et al.Clinical neurophysiology. 2005, Vol 116, Num 11, pp 2520-2527, issn 1388-2457, 8 p.Article

A dystrophin missense mutation showing persistence of dystrophin and dystrophin-associated proteins yet a severe phenotypeGOLDBERG, L. R; HAUSMANOWA-PETRUSEWICZ, I; FIDZIANSKA, A et al.Annals of neurology. 1998, Vol 44, Num 6, pp 971-976, issn 0364-5134Article

An X:autosome translocation stabilizes truncated dystrophin : implications for lack of truncated dystrophins in Duchenne muscular dystrophyFIDZIANSKA, A; MORRONE, A; PEGORARO, E et al.Neuropediatrics. 1995, Vol 26, Num 3, pp 163-167, issn 0174-304XArticle

Calpain III mutation analysis of a heterogeneous limb- girdle muscular dystrophy populationCHOU, F.-L; ANGELINI, C; DAENTL, D et al.Neurology. 1999, Vol 52, Num 5, pp 1015-1020, issn 0028-3878Article

Hyperkalemic periodic paralysis : rapid molecular diagnosis and relationship of genotype to phenotype in 12 familiesFEERO, W. G; WANG, J; WESSEL, H. B et al.Neurology. 1993, Vol 43, Num 4, pp 668-673, issn 0028-3878Article

In vivo and in vitro examination of the functional significances of novel lamin gene mutations in heart failure patientsSYLVIUS, N; BILINSKA, Z. T; DYACK, S et al.Journal of medical genetics. 2005, Vol 42, Num 8, pp 639-647, issn 0022-2593, 9 p.Article

Molecular genetic and genetic correlations in sodium channelopathies : lack of founder effect and evidence for a second geneWANG, J; ZHOU, J; SILLEN, A et al.American journal of human genetics. 1993, Vol 52, Num 6, pp 1074-1084, issn 0002-9297Article