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kw.\*:("GLYCOGENOSIS IV ANDERSEN")

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TYPE IV GLYCOGEN-STORAGE DISEASE. LIGHT-MICROSCOPIC ELECTRON-MICROSCOPIC, AND ENZYMATIC STUDY.BANNAYAN GA; DEAN WJ; HOWELL RR et al.1976; AMER. J. CLIN. PATHOL.; U.S.A.; DA. 1976; VOL. 66; NO 4; PP. 702-709; BIBL. 19 REF.Article

RECTAL BIOPSY IN TYPE 4 GLYCOGENOSIS.CANTIN M; BROCHU P; TURGEON KNAACK C et al.1976; ARCH. PATHOL. LAB. MED.; U.S.A.; DA. 1976; VOL. 100; NO 8; PP. 422-426; BIBL. 25 REF.Article

NERVOUS SYSTEM INVOLVEMENT IN TYPE IV GLYCOGENOSISMCMASTER KR; POWERS JM; HENNIGAR GR JR et al.1979; ARCH. PATHOL. LAB. MED.; USA; DA. 1979; VOL. 103; NO 3; PP. 105-111; BIBL. 25 REF.Article

ZUR DIAGNOSTIK DER GLYKOGENOSEN: GLYKOGENOSE TYP IV = DIAGNOSTIC DES GLYCOGENOSES: GLYCOGENOSES DE TYPE IVBUEHRDEL P; WOHLRAB F; ZIMMERMANN G et al.1980; DTSCHE GESUNDH.-WES.; DDR; DA. 1980; VOL. 35; NO 9; PP. 336-340; ABS. RUS/ENG; BIBL. 21 REF.Article

INTEREST OF FINE STRUCTURAL ANALYSIS OF DEEP-FROZEN OR FORMALINE-FIXED, PARAFFIN-EMBEDDED BIOPSY AND AUTOPSY SPECIMEN. DEMONSTRATION IN THREE BROTHERS WITH GLYCOGENOSIS TYPE IV (AMYLOPECTINOSIS)HUBNER G.1980; BIOL. CELL.; FRA; DA. 1980; VOL. 37; NO 3; PP. 313-318; BIBL. 4 REF.Article

Modes de transmission de la glycogénose type VI = Glycogenosis IV Andersen: transmission modeDE BARSY, T; VAN DEN HOVE-LEDERER, B; VAN HOOF, F et al.Acta gastro-enterologica belgica (Ed. multilingue). 1984, Vol 47, Num 2, issn 0001-5644, 123Article

An adult case of Andersen's disease t Type IV glycogenosis. A clinical, histochemical, ultrastructural and biochemical studyFERGUSON, I. T; MAHON, M; CUMMING, W. J. K et al.Journal of the neurological sciences. 1983, Vol 60, Num 3, pp 337-351, issn 0022-510XArticle

DONNEES RECENTES SUR LA MALADIE DE LA FORA: A PROPOS DE 17 OBSERVATIONSMOUREN MC; ROGER J.1979; ARCH. FR. PEDIATR.; FRA; DA. 1979; VOL. 36; NO 3; PP. 268-277; ABS. ENG; BIBL. 16 REF.Article

ETUDE D'UNE OBSERVATION DE GLYCOGENOSE DE TYPE IVKIRGO JEAN LOUP.sd; FRA; DA. S.D.; 169; 65 P.; 30 CM; BIBL. 38 P.; TH.: MED./PARIS 5/1978Thesis

DIAGNOSTIC PRECOCE DE LA GLYCOGENOSE TYPE IV ET DETECTION DES HETEROZYGOTES.SAINT ROME G; ROY CC; LESCOP J et al.1976; UN. MED. CANADA; CANADA; DA. 1976; VOL. 105; NO 8; PP. 1223-1227; ABS. ANGL.; BIBL. 20 REF.Article

A DISTINCT FORM OF ADULT POLYGLUCOSAN BODY DISEASE WITH MASSIVE INVOLVEMENT OF CENTRAL AND PERIPHERAL NEURONAL PROCESSES AND ASTROCYTES. A REPORT OF FOUR CASES AND A REVIEW OF THE OCCURRENCE OF POLYGLUCOSAN BODIES IN OTHER CONDITIONS SUCH AS LAFORA'S DISEASE AND NORMAL AGEINGROBITAILLE Y; CARPENTER S; KARPATI G et al.1980; BRAIN; GBR; DA. 1980; VOL. 103; NO 2; PP. 315-336; BIBL. 4 P.Article

Type IV glycogen storage diseaseSUNATI SAHOO; BLUMBERG, Andrea K; SENGUPTA, Elizabeth et al.Archives of pathology & laboratory medicine (1976). 2002, Vol 126, Num 5, pp 630-631, issn 0363-0153Article

Abnormal oligosaccharide pattern in glycogen storage disease type IIIGALVIN-PARTON, P; HOMMES, F. A.Journal of inherited metabolic disease. 1996, Vol 19, Num 3, pp 383-384, issn 0141-8955Article

Hypoglycemia in type IV glycogenosis: hepatic improvement in two patients with nutritional managementGREENE, H. L; GHISHAN, F. K; BROWN, B et al.The Journal of pediatrics. 1988, Vol 112, Num 1, pp 55-58, issn 0022-3476Article

Dicarboxylicaciduria and secondary carnitine deficiency in glycogenosis type IVMAASWINKEL-MOOY, P. D; POORTHUIS, B. J. H. M; VAN GELDEREN, H. H et al.Archives of disease in childhood. 1987, Vol 62, Num 10, pp 1066-1067, issn 0003-9888Article

A juvenile variant of glycogenosis IV (Andersen disease)GUERRA, A. S; VAN DIGGELEN, O. P; CARNEIRO, F et al.European journal of pediatrics. 1986, Vol 145, Num 3, pp 179-181, issn 0340-6199Article

LABORATORY DIAGNOSIS OF THE NEUROMUSCULAR GLYCOGEN STORAGE DISEASESFARMER PM.1982; ANNALS OF CLINICAL AND LABORATORY SCIENCE; ISSN 0091-7370; USA; DA. 1982; VOL. 12; NO 6; PP. 431-438; BIBL. 62 REF.Article

Liver transplantation for type IV glycogen storage diseaseSELBY, R; STARZI, T. E; YUNIS, E et al.The New England journal of medicine. 1991, Vol 324, Num 1, pp 39-42, issn 0028-4793, 4 p.Article

Branching enzyme in erythrocytes. Detection of type IV glycogenosis homozygotes and heterozygotesSHIN, Y. S; STEIGÜBER, H; KLEMM, P et al.Journal of inherited metabolic disease. 1988, Vol 11, pp 252-254, issn 0141-8955, suppl. 2Article

A mild juvenile variant of type IV glycogenosisREUSCHE, E; AKSU, F; GOEBEL, H. H et al.Brain & development (Tokyo. 1979). 1992, Vol 14, Num 1, pp 36-43, issn 0387-7604Article

Clinical and laboratory findings in four patients with the non-progressive hepatic form of type IV glycogen storage diseaseMCONKIE-ROSELL, A; WILSON, C; PICCOLI, D. A et al.Journal of inherited metabolic disease. 1996, Vol 19, Num 1, pp 51-58, issn 0141-8955Article

Progressive cardiac failure following orthotopic liver transplantation for type IV glycogenosisSOKAL, E. M; VAN HOOF, F; ALBERTI, D et al.European journal of pediatrics. 1992, Vol 151, Num 3, pp 200-203, issn 0340-6199Conference Paper

Branching enzyme activity of cultured amniocytes and chorionic villi: prenatal testing for type IV glycogen storage diseaseBROWN, B. I; BROWN, D. H.American journal of human genetics. 1989, Vol 44, Num 3, pp 378-381, issn 0002-9297Article

Type IV glycogen storage disease : first reported case in ThailandVICHITRA HEMSRICHART; KLEOPHANT THAKERNGPOL; SAYOOMPORN KARALAK et al.Chot Mai Het Thang Phaet. 1989, Vol 72, Num 12, pp 696-700, issn 0125-2208Article

Liver-spleen scintigraphy in glycogen storage disease (glycogenoses)HEYMAN, S.Clinical nuclear medicine. 1985, Vol 10, Num 12, pp 839-843, issn 0363-9762Article

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