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kw.\*:("Becker muscular dystrophy")

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Becker muscular dystrophy (BMD) and Klinefelter's syndrome: a possible cause of variable expression of BMD within a pedigreeSUTHERS, G. K; MANSON, J. I; STERN, L. M et al.Journal of medical genetics. 1989, Vol 26, Num 4, pp 251-254, issn 0022-2593, 4 p.Article

Genetic counseling in Becker type X-linked muscular dystrophy. II. Practical considerationsGRIMM, T.American journal of medical genetics. 1984, Vol 18, Num 4, pp 719-723, issn 0148-7299Article

UNUSUAL INHERITANCE OF BECKER TYPE MUSCULAR DYSTROPHY.AGUILAR L; LISKER R; GARCIA RAMOS G et al.1978; J. MED. GENET.; G.B.; DA. 1978; VOL. 15; NO 2; PP. 116-118; BIBL. 5 REF.Article

SULLA DISTROFIA MUSCOLARE BENIGNA DI BECKER. CONSIDERAZIONI SU UNA FAMIGLIA. = SUR LA DYSTROPHIE MUSCULAIRE BENIGNE DE BECKER. CONSIDERATIONS SUR UNE FAMILLEARMOCIDA G; COTTINI R; FINAVERA L et al.1978; MINERVA MED.; ITA; DA. 1978; VOL. 69; NO 25; PP. 1745-1748; ABS. ANGL.; BIBL. 1 P.Article

PSEUDOHYPERTROPHY OF MUSCLES OF THENAR EMINENCE IN X-LINKED MUSCULAR DYSTROPHY (BECKER TYPE)BODDIE HG; WADE J.1980; POSTGRAD. MED. J.; GBR; DA. 1980; VOL. 56; NO 652; PP. 115-116; BIBL. 7 REF.Article

Homozygous Female Becker Muscular DystrophyFUJII, Katsunori; MINAMI, Narihiro; HAYASHI, Yukiko et al.American journal of medical genetics. Part A. 2009, Vol 149, Num 5, pp 1052-1055, issn 1552-4825, 4 p.Article

Absence of neuronal nitric oxide synthase (nNOS) as a pathological marker for the diagnosis of Becker muscular dystrophy with rod domain deletionsTORELLI, S; BROWN, S. C; JIMENEZ-MALLEBRERA, C et al.Neuropathology and applied neurobiology (Print). 2004, Vol 30, Num 5, pp 540-545, issn 0305-1846, 6 p.Article

Weight reduction in boys with muscular dystrophyEDWARDS, R. H. T; ROUND, J. M; JACKSON, M. J et al.Developmental medicine and child neurology (Print). 1984, Vol 26, Num 3, pp 384-390, issn 0012-1622Article

Cardiac manifestations and their management in Becker's muscular dystrophyORLOV, Y. S. K; BRODSKY, M. A; ALLEN, B. J et al.The American heart journal. 1994, Vol 128, Num 1, pp 193-196, issn 0002-8703Article

Variation of serum myoglobin levels in normal individuals with reference to the use of myoglobin measurements for the detection of women carrying genes for the X-linked muscular dystrophiesNICHOLSON, L. V. B; WALLS, T. J.Journal of the neurological sciences. 1983, Vol 62, Num 1-3, pp 41-58, issn 0022-510XArticle

PROSPECTIVE STUDY OF X-LINKED PROGRESSIVE MUSCULAR DYSTROPHY IN CAMPANIANIGRO G; LIMONGELLI FM; GIUGLIANO MAA et al.1983; MUSCLE AND NERVE; ISSN 0148-639X; USA; DA. 1983; VOL. 6; NO 4; PP. 253-262; BIBL. 66 REF.Article

KARDIOMYOPATHIE BEI SKELETTMUSKELERKRANKUNGEN. EINE KASUISTISCHE MITTEILUNG = CARDIOMYOPATHIE DANS LES MYOPATHIES. UNE CONTRIBUTION CASUISTIQUELOOS U; BOXLER K; GRUBE E et al.1983; HERZ. KREISLAUF; ISSN 0046-7324; DEU; DA. 1983; VOL. 15; NO 1; PP. 18-21; ABS. ENG; BIBL. 30 REF.Article

BILATERAL PATELLAR SUBLUXATION SECONDARY TO BECKER MUSCULAR DYSTROPHYKHAN RH; MACNICOL MF.1982; J. BONE JT. SURG. (AM. VOL.); ISSN 0021-9355; USA; DA. 1982; VOL. 64A; PP. 777-778; BIBL. 10 REF.Article

BECKER'S X-LINKED MUSCULAR DYSTROPHY HISTOLOGICAL, ENZYME-HISTOCHEMICAL, AND ULTRASTRUCTURAL STUDIES OF TWO CASES, ORIGINALLY REPORTED BY BECKERGOEBEL HH; PRANGE H; GULLOTTA F et al.1979; ACTA NEUROPATHOL.; DEU; DA. 1979; VOL. 46; NO 1-2; PP. 69-77; BIBL. 15 REF.Article

AN UNUSUAL FAMILY OF BENIGN "X" LINKED MUSCULAR DYSTROPHY WITH CARDIAC INVOLVEMENT.WADIA RS; WADGAONKAR SU; AMIN RB et al.1976; J. MED. GENET.; G.B.; DA. 1976; VOL. 13; NO 5; PP. 352-356; BIBL. 12 REF.Article

INTRAFAMILIAL VARIABILITY OF X-LINKED PROGRESSIVE MUSCULAR DISTROPHY. MILD AND ACUTE FORM OF X-LINKED MUSCULAR DISTROPHY IN THE SAME FAMILY.HAUSMANOWA PETRUSEWICZ I; BORKOWSKA J.1978; J. NEUROL.; GERM.; DA. 1978; VOL. 218; NO 1; PP. 43-50; BIBL. 17 REF.Article

X-LINKED GENE LOCI AND MUSCULAR DYSTROPHYGROUNDS MD.1981; AUST. J. EXP. BIOL. MED. SCI.; ISSN 0004-945X; AUS; DA. 1981; VOL. 59; NO 5; PP. 617-622; BIBL. 2 P.Article

TROPOMYOSIN AND TROPONIN C FROM HUMAN FETAL, ADULT, AND DYSTROPHIC SKELETAL MUSCLEROMERO HERRERA AE; LIESKA NG.1982; MUSCLE AND NERVE; ISSN 0148-639X; USA; DA. 1982; VOL. 5; NO 9; PP. 707-712; BIBL. 37 REF.Article

MUSKELDYSTROPHIE: DUCHENNE- UND BECKER-KIENER-TYP = DYSTROPHIE MUSCULAIRE: LES FORMES DE DUCHENNE ET DE BECKER-KIENERKUHN E.1979; DTSCHE MED. WSCHR.; DEU; DA. 1979; VOL. 104; NO 51; PP. 1817-1820; BIBL. 61 REF.Article

Mutation spectrum leading to an attenuated phenotype in dystrophinopathiesTUFFERY-GIRAUD, Sylvie; SAQUET, Céline; THOREL, Delphine et al.European journal of human genetics. 2005, Vol 13, Num 12, pp 1254-1260, issn 1018-4813, 7 p.Article

BECKER MUSCULAR DYSTROPHY DUE TO AN INVERSION OF EXONS 23 AND 24 OF THE DMD GENEFLANIGAN, Kevin M; DUNN, Diane; AARON LARSEN, C et al.Muscle & nerve. 2011, Vol 44, Num 5, pp 822-825, issn 0148-639X, 4 p.Article

Endurance training improves fitness and strength in patients with Becker muscular dystrophy. CommentaryZEVIANI, Massimo; SVEEN, Marie Louise; JEPPESEN, Tina D et al.Brain. 2008, Vol 131, issn 0006-8950, 2809-2811, 2824-2831 [11 p.], 11Article

Quantification of dystrophin immunofluorescence in dystrophinopathy muscle specimensTAYLOR, L. E; KAMINOH, Y. J; RODESCH, C. K et al.Neuropathology and applied neurobiology (Print). 2012, Vol 38, Num 6, pp 591-601, issn 0305-1846, 11 p.Article

MUSCLE METABOLIC ALTERATIONS ASSESSED BY 31-PHOSPHORUS MAGNETIC RESONANCE SPECTROSCOPY IN MILD BECKER MUSCULAR DYSTROPHYTOSETTI, Michela; LINSALATA, Stefania; BATTINI, Roberta et al.Muscle & nerve. 2011, Vol 44, Num 5, pp 816-819, issn 0148-639X, 4 p.Article

Origins and early descriptions of Duchenne muscular dystrophyTYLER, Kenneth L.Muscle & nerve. 2003, Vol 28, Num 4, pp 402-422, issn 0148-639X, 21 p.Article

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