kw.\*:("Fibre musculaire type I")
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Nonprogressive congenital neuromuscular disease with uniform type 1 fiberSHIN JOONG OH; DANON, M. J.Archives of neurology (Chicago). 1983, Vol 40, Num 3, pp 147-150, issn 0003-9942Article
''MYOTUBULAR MYOPATHY'' AND ''TYPE I FIBER ATROPHY'' IN A FAMILY = "MYOPATHIE MYOTUBULAIRE" ET "ATROPHIE DES FIBRES DU TYPE I" DANS UNE FAMILLEKINOSHITA M; SATOYOSHI E; MATSUO N et al.1975; J. NEUROL. SCI.; NETHERL.; DA. 1975; VOL. 26; NO 4; PP. 575-582; BIBL. 21 REF.Article
ACTIVITY PATTERNS OF HUMAN SKELETAL MUSCLES: RELATION TO MUSCLE FIBER TYPE COMPOSITION.MONSTER AW; CHAN HC; O'CONNOR D et al.1978; SCIENCE; U.S.A.; DA. 1978; VOL. 200; NO 4339; PP. 314-317; BIBL. 18 REF.Article
DISPROPORTION CONGENITALE DES DIFFERENTS TYPES DE FIBRE MUSCULAIRE, AVEC PETITESSE RELATIVE DES FIBRES DE TYPE I. DOCUMENTS MORPHOLOGIQUES CONCERNANT LES BIOPSIES MUSCULAIRES PRELEVEES CHEZ LES TROIS MEMBRES D'UNE MEME FAMILLEFARDEAU M; HARPEY JP; CAILLE B et al.1975; REV. NEUROL.; FR.; DA. 1975; VOL. 131; NO 11; PP. 745-766; ABS. ANGL.; BIBL. 1 P. 1/2Article
CONGENITAL MYOPATHY WITH CYTOPLASMIC BODIESGOEBEL HH; SCHLOON H; LENARD HG et al.1981; NEUROPEDIATRICS; ISSN 0174-304X; DEU; DA. 1981; VOL. 12; NO 2; PP. 166-180; ABS. GER; BIBL. 15 REF.Article
FASERTYPENDISPROPORTION, EINE FORM DER SOGENANNTEN KONGENITALEN NICHTPROGRESSIVEN MYOPATHIEN = LA DISPROPORTION DE FIBRES MUSCULAIRES DE TYPE I, FORME DE MYOPATHIE NON PROGRESSIVEBERGER M; SCHROEDER JM; GIBBELS E et al.1979; FORTSCHR. NEUROL. PSYCHIATR. GRENZGEB.; DEU; DA. 1979; VOL. 47; NO 9; PP. 466-478; ABS. ENG; BIBL. 3 P.Article
DISUSE ATROPHY OF HUMAN SKELETAL MUSCLE: AN ENZYME HISTOCHEMICAL STUDYLINDBOE CF; PLATOU CS.1982; ACTA NEUROPATHOL.; ISSN 0001-6322; DEU; DA. 1982; VOL. 56; NO 4; PP. 241-244; BIBL. 18 REF.Article
Infantile myopathy with type 1 fibre specific hypertrophyYOUNG, J. A; ANDERSON, J. M.Developmental medicine and child neurology (Print). 1987, Vol 29, Num 5, pp 680-685, issn 0012-1622Article
Muscle fiber types in thoracic erector spinae muscles: fiber types in idiopathic and other forms of scoliosisBYLUND, P; JANSSON, E; DAHLBERG, E et al.Clinical orthopaedics and related research. 1987, Num 214, pp 222-227, issn 0009-921XArticle
THE METALLOPROTEINASE-DISINTEGRIN ADAM10 IS EXCLUSIVELY EXPRESSED BY TYPE I MUSCLE FIBERSDEHMEL, Thomas; GOEBEL, Hans Hilmar; HARTUNG, Hans-Peter et al.Muscle & nerve. 2008, Vol 38, Num 2, pp 1049-1051, issn 0148-639X, 3 p.Article
Hypotrophy of type I fibres with central nuclei: recovery 4 years after diagnosisRICOY, J. R; CABELLO, A.Journal of neurology, neurosurgery and psychiatry. 1985, Vol 48, Num 2, pp 167-171, issn 0022-3050Article
Respiratory capacity of developing chick red and white skeletal muscleBARNES, W. S; MASSON, S. M.Comparative biochemistry and physiology. A. Comparative physiology. 1983, Vol 75, Num 3, pp 491-495, issn 0300-9629Article
A HISTOLOGICAL AND HISTOCHEMICAL STUDY OF CHANGES OF FIBER TYPES IN EXPERIMENTAL MYOTONIACACCIA MR; PRETO PARVIS V; BRAMBILLA M et al.1979; J. NEUROL.; DEU; DA. 1979; VOL. 220; NO 2; PP. 131-142; ABS. GER; BIBL. 2 P.Article
HISTOCHEMICAL AND ULTRASTRUCTURAL FINDINGS IN A CASE OF CENTRONUCLEAR MYOPATHYPALMUCCI L; BERTOLOTTO A; MONGA G et al.1978; EUROP. NEUROL.; CHE; DA. 1978; VOL. 17; NO 6; PP. 327-332; BIBL. 33 REF.Article
HISTOCHEMICAL TYPE I FIBRES IN THE SOLEUS OF THE RATDEKLEVA A; SIRCA A.1978; J. ANAT.; GBR; DA. 1978; VOL. 127; NO 3; PP. 595-601; BIBL. 2 P.Article
LA DISTROFIA MUSCOLARE MIOTONICA AD INSORGENZA PRECOCE. RELIEVI ISTOENZIMOLOGICI ED ULTRASTRUTTURALI SU BIOPSIE MUSCOLARI. = LA DYSTROPHIE MYOTONIQUE D'APPARITION PRECOCE. CARACTERISTIQUES HISTOENZYMOLOGIQUES ET ULTRASTRUCTURALES SUR BIOPSIES MUSCULAIRESSCELSI R; BESANA D; POGGI P et al.1977; ACTA NEUROL.; ITAL.; DA. 1977; VOL. 32; NO 2; PP. 173-188; ABS. ANGL.; BIBL. 1 P.Article
A PROGRESSIVE CONGENITAL MYOPATHY. INITIAL INVOLVEMENT OF THE DIAPHRAGM WITH TYPE I MUSCLE FIBER ATROPHY.DE REUCK J; HOOFT C; DE COSTER W et al.1977; EUROP. NEUROL.; SWITZ.; DA. 1977; VOL. 15; NO 4; PP. 217-226; BIBL. 1 P. 1/2Article
ETUDE HISTOCHIMIQUE DU NERF FACIAL ET DE QUELQUES MUSCLES CHEZ LES PAPIO PAPIO ATTEINTS DE SPASME FACIALCARLIER E; PELISSIER JF; NAQUET R et al.1975; C.R. SOC. BIOL.; FR.; DA. 1975; VOL. 169; NO 3; PP. 611-615; H.T. 2; ABS. ANGL.; BIBL. 18 REF.Article
WERTIGKEIT DER MUSKELBIOPSIE IN DER DIAGNOSTIK DER DYSTROPHIA MYOTONICA (CURSCHMANN-STEINART) = LA VALEUR DE LA BIOPSIE MUSCULAIRE DANS LE DIAGNOSTIC DE LA DYSTROPHIE MYOTONIQUEPONGRATZ D; SCHULTZ D; KOPPENWALLNER C et al.1979; KLIN. WSCHR.; DEU; DA. 1979; VOL. 57; NO 5; PP. 215-224; ABS. ENG; BIBL. 21 REF.Article
UNILATERAL CALF ENLARGEMENT FOLLOWING S1 RADICULOPATHYMIELKE U; RICKER K; EMSER W et al.1982; MUSCLE NERVE; ISSN 0148-639X; USA; DA. 1982; VOL. 5; NO 6; PP. 434-438; BIBL. 12 REF.Article
TWO POPULATIONS OF TYPE 1 FIBRES IN STRIATED MUSCLE FROM A CASE OF NEUTRAL LIPID STORAGE DISEASEMCKERAN RO; ROYSTON JP; WARD P et al.1979; J. NEUROL. SCI.; NLD; DA. 1979; VOL. 43; NO 1; PP. 1-12; BIBL. 22 REF.Article
ENZYME PATTERNS IN SINGLE HUMAN MUSCLE FIBERSLOWRY CV; KIMMEY JS; FELDER S et al.1978; J. BIOL. CHEM.; USA; DA. 1978; VOL. 253; NO 22; PP. 8269-8277; BIBL. 22 REF.Article
RIGID SPINE SYNDROME. A TYPE I FIBER MYOPATHY.SEAY AR; ZITER FA; PETAJAN JH et al.1977; ARCH. NEUROL.; U.S.A.; DA. 1977; VOL. 34; NO 2; PP. 119-122; BIBL. 13 REF.Article
SELEKTIVE MUSKELFASERTYPANOMALIEN BEI NEUROMUSKULAEREN ERKRANKUNGEN. EINE ANALYSE VON 124 KONSEKUTIVEN HISTOCHEMISCH BEARBEITETEN BIOPSIEN. = ANOMALIES SELECTIVES DES TYPES DE FIBRE MUSCULAIRE DANS LES MALADIES NEUROMUSCULAIRES. ANALYSE DE 124 BIOPSIES AVEC ANALYSE HISTOCHIMIQUETOSI C; JERUSALEM F.1976; J. NEUROL.; GERM.; DA. 1976; VOL. 214; NO 1; PP. 13-34; ABS. ANGL.; BIBL. 2 P.Article
TRICHINELLA THRIVES IN BOTH OXIDATIVE AND GLYCOLYTIC HUMAN MUSCLE FIBRESOCHOA J; PALLIS C.1980; J. NEUROL. NEUROSURG. PSYCHIATRY; GBR; DA. 1980; VOL. 43; NO 3; PP. 281-282; BIBL. 13 REF.Article