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kw.\*:("FIBRE MUSCULAIRE TYPE I")

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''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

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

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

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

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

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

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

DESPROPORCION CONGENITA DE LOS TIPOS DE FIBRAS: ESTUDIO DE UNA FAMILIA = DISPROPORTION CONGENITALE DES DEUX TYPES DE FIBRE MUSCULAIRE: ETUDE D'UNE FAMILLEGOBERNADO JM; RIVA C; ZARAGOZA E et al.1980; ARCH. NEUROBIOL.; ESP; DA. 1980; VOL. 43; NO 3; PP. 147-164; ABS. ENG; BIBL. 3 P.Article

EINE SELTENE MYOPATHIE: DIE SOG. KONGENITALE FASERTYP-DISPROPORTION = UNE MYOPATHIE RARE: LA MYOPATHIE CONGENITALE PAR DISPROPORTION DES FIBRES MUSCULAIRESLOESSNER J; ZIEGAN J; OERTEL G et al.1979; Z. GES. INNERE MED. GRENZGEB.; DDR; DA. 1979; VOL. 34; NO 22; PP. 685-687; ABS. RUS/ENGArticle

MUSCLE FIBER HYPOTROPHY WITH INTACT NEUROMUSCULAR JUNCTIONS. A STUDY OF A PATIENT WITH CONGENITAL NEUROMUSCULAR DISEASE AND OPHTHALMOPLEGIA.BENDER AN; BENDER MB.1977; NEUROLOGY; U.S.A.; DA. 1977; VOL. 27; NO 3; PP. 206-212; BIBL. 41 REF.Article

MYOTUBULAR (CENTRONUCLEAR) (NEURO-) MYOPATHY. I. CLINICAL, GENETICAL AND MORPHOLOGICAL STUDIES.RADU H; KILLYEN I; IONESCU V et al.1977; EUROP. NEUROL.; SWITZ.; DA. 1977; VOL. 15; NO 5; PP. 285-300; BIBL. 2 P.Article

SIMULTANEOUS DETERMINATION OF SKELETAL MUSCLE FIBER, TYPES I, IIA, AND IIB BY HISTOCHEMISTRY.TUNELL GL; HART MN.1977; ARCH. NEUROL.; U.S.A.; DA. 1977; VOL. 34; NO 3; PP. 171-173; BIBL. 5 REF.Article

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

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

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

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