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kw.\*:("GLYCOGENOSIS V MC ARDLE")

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DOMINANT INHERITANCE OF MCARDLE SYNDROME.CHUI LA; MUNSAT TL.1976; ARCH. NEUROL.; U.S.A.; DA. 1976; VOL. 33; NO 9; PP. 636-641; BIBL. 36 REF.Article

RESEARCH ON MOLECULAR MECHANISMS OF MCARDLE'S DISEASE (MUSCLE GLYCOGEN PHOSPHORYLASE DEFICIENCY). USE OF NEW PROTEIN MAPPING AND IMMUNOLOGICAL TECHNIQUESDAEGELEN PROUX D; KAHN A; MARIE J et al.1981; ANN. HUM. GENET.; ISSN 0003-4800; GBR; DA. 1981; VOL. 45; PART. 2; PP. 113-120; BIBL. 17 REF.Article

MUSCLE PHOSPHORYLASE DEFICIENCY IN CHILDHOODSENGERS RCA; STADHOUDERS AM; JASPAR HHJ et al.1980; EUROP. J. PEDIATR.; DEU; DA. 1980; VOL. 134; NO 2; PP. 161-165; BIBL. 12 REF.Article

LACTATE PRODUCTION IN MCARDLE'S DISEASE.BAKSI AK; COCHRANE P; BUXTON PH et al.1977; POSTGRAD. MED. J.; G.B.; DA. 1977; VOL. 53; NO 617; PP. 161-164; BIBL. 6 REF.Article

MYOPHOSPHORYLASE DEFICIENCY: TWO DIFFERENT MOLECULAR ETIOLOGIES.FEIT H; BROOKE MH.1976; NEUROLOGY; U.S.A.; DA. 1976; VOL. 26; NO 10; PP. 963-967; BIBL. 15 REF.Article

MCARDLE'S DISEASE: A STUDY ON THE MOLECULAR BASIS OF TWO DIFFERENT ETIOLOGIES OF MYOPHOSPHORYLASE DEFICIENCYKOSTER JF; SLEE RG; JENNEKENS FGI et al.1979; CLIN. CHIM. ACTA; NLD; DA. 1979; VOL. 94; NO 3; PP. 229-235; BIBL. 19 REF.Article

Insuffisance rénale aiguë au cours d'une glycogénose de Mac Ardle = Acute renal failure in Mc Ardle's diseaseDE PRECIGOUT, V; DUPON, M; LACUT, J. Y et al.La Presse médicale (1983). 1989, Vol 18, Num 34, pp 1709-1710, issn 0755-4982, 2 p.Article

EXERCISE HYPERVENTILATION IN PATIENTS WITH MCARDLE'S DISEASEHAGBERG JM; COYLE EF; CARROLL JE et al.1982; J. APPL. PHYSIOL.: RESPIR. ENVIRON. EXERC. PHYSIOL.; ISSN 0161-7567; USA; DA. 1982; VOL. 52; NO 4; PP. 991-994; BIBL. 31 REF.Article

TC-99 M PYROPHOSPHATE MUSCLE LABELING IN MCARDLE SYNDROMESWIFT TR; BROWN M.1978; J. NUCL. MED.; USA; DA. 1978; VOL. 19; NO 3; PP. 295-297; BIBL. 10 REF.Article

MALADIE DE MAC ARDLE. A PROPOS D'UNE OBSERVATION ATYPIQUE: DISCUSSION CLINIQUE ET PHYSIOPATHOLOGIQUEMARCELLIN MARIE JOSEPHE.sd; FRA; DA. S.D.; 93; 52 P.: ILL; 30 CM; BIBL. 78 REF.; TH.: MED./GRENOBLE 1/1979Thesis

MALADIE DE MAC ARDLE. REVUE DU SYNDROME A PROPOS D'UNE NOUVELLE OBSERVATIONBARRAUD CAPDEPON MARTINE.1979; ; FRA; DA. 1979; 476; 73 P.: ILL.-PL.; 30 CM; BIBL. 88 REF.; TH.: MED./BORDEAUX 2/1979Thesis

MUSCLE METABOLIC STUDIES OF A GIRL WITH MCARDLE-LIKE SYMPTOMSERIKSSON BO; HANSSON O; KARLSSON J et al.1978; MED. AND SPORT; CHE; DA. 1978; VOL. 11; PP. 65-71; BIBL. 2 P.Article

MCARDLE'S SYNDROME. FINE STRUCTURAL CHANGES IN MUSCLE.KORENYI BOTH A; SMITH BH; BARUAH JK et al.1977; ACTA NEUROPATOL.; ALLEM.; DA. 1977; VOL. 40; NO 1; PP. 11-19; BIBL. 51 REF.Article

MALADIE DE MAC ARDLE. A PROPOS D'UN CAS FAMILIAL. II. ETUDE BIO-ENERGETIQUE.ECLACHE JP; QUARD S; FLANDROIS R et al.1977; LYON MED.; FR.; DA. 1977; VOL. 238; NO 15; PP. 151-157; ABS. ANGL.; BIBL. 15 REF.Article

EXAMINATION OF A CASE OF SUSPECTED MC ARDLE'S SYNDROME BY 31P NUCLEAR MAGNETIC RESONANCEROSS BD; RADDA GK; GADIAN DG et al.1981; N. ENGL. J. MED.; ISSN 0028-4793; USA; DA. 1981; VOL. 304; NO 22; PP. 1338-1342; BIBL. 13 REF.Article

METABOLISME GLUCIDIQUE PENDANT L'EXERCICE MUSCULAIRE DANS LA MALADIE DE MCARDLEKRZENTOWSKI G; PALLIKARAKIS N; PIRNAY F et al.1979; ACTA CLIN. BELG.; BEL; DA. 1979; VOL. 34; NO 3; PP. 151-157; ABS. ENG/DUT; BIBL. 19 REF.Article

UNE CAUSE RARE D'INADAPTATION A L'EFFORT: LA MALADIE DE MAC ARDLEGARCIN JM; VERGES PASCAL M; CANICAVE JC et al.1979; MED. ET ARMEES; FRA; DA. 1979; VOL. 7; NO 6; PP. 549-553; BIBL. 10 REF.Article

POST-TETANIC MECHANICAL TENSION AND EVOKED ACTION POTENTIALS IN MCARDLE'S DISEASE.BRANDT NJ; BUCHTHAL F; EBBESEN F et al.1977; J. NEUROL. NEUROSURG. PSYCHIATRY; G.B.; DA. 1977; VOL. 40; NO 9; PP. 920-925; BIBL. 21 REF.Article

LATE-ONSET MCARDLE'S DISEASE WITH UNUSUAL ELECTROMYOGRAPHIC FINDINGSPOURMAND R; SANDERS DB; CORWIN HM et al.1983; ARCHIVES OF NEUROLOGY (CHICAGO); ISSN 0003-9942; USA; DA. 1983; VOL. 40; NO 6; PP. 374-377; BIBL. 25 REF.Article

McArdle's disease presenting with rhabdomyolysisHAINS, A. D. B; PANNALL, P. R; BOURNE, A. J et al.Australian and New Zealand journal of medicine. 1984, Vol 14, Num 5, pp 681-684, issn 0004-8291Article

Excess purine degradation in exercising muscles of patients with glycogen storage disease types V and VIIMINEO, I; KONO, N; SHIMIZU, T et al.The Journal of clinical investigation. 1985, Vol 76, Num 2, pp 556-560, issn 0021-9738Article

Type V glycogen storage diseaseWILLIAMS, J; HOSKING, G.Archives of disease in childhood. 1985, Vol 60, Num 12, pp 1184-1186, issn 0003-9888Article

McArdle's disease. Problems of anaesthetic management for Caesarean sectionCOLEMAN, P.Anaesthesia. 1984, Vol 39, Num 8, pp 784-787, issn 0003-2409Article

Molecular heterogeneity of McArdle diseaseDAEGELEN, D; GAUTRON, S; MENNECIER, F et al.Journal of inherited metabolic disease. 1986, Vol 9, pp 287-290, issn 0141-8955, suppl. 2Conference Paper

Myopathy in McArdlés syndrome: improvement with a high-protein dietSLONIM, A. E; GOANS, P. J.The New England journal of medicine. 1985, Vol 312, Num 6, pp 355-359, issn 0028-4793Article

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