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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

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

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

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

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

Hepatocellular carcinoma in glycogen storage disease type IVDE MOOR, R. A; SCHWEIZER, J. J; VAN HOEK, B et al.Archives of disease in childhood. 2000, Vol 82, Num 6, pp 479-480, issn 0003-9888Article

Glycogénose type IV variante congénitale : A propos d'une observation anatomo-clinique = Type IV glycogenosis. Congenital variant. Report of a caseURO-COSTE, E; LELONG-TISSIER, M.-C; MAIRE, I et al.Annales de pathologie (Paris). 1996, Vol 16, Num 6, pp 449-452, issn 0242-6498Article

Cardiomyopathie sévère révélant une amylopectinose : deux observations chez des adolescents d'une même fratrie = Severe cardiomyopathy revealing type IV glycogen storage diseaseDE LA BLANCHARDIERE, A; VAYSSIER, C; DUBOC, D et al.La Presse médicale (1983). 1994, Vol 23, Num 24, pp 1124-1127, issn 0755-4982Article

Prenatal diagnosis of glycogen storage disease type IV using PCR-based DNA mutation analysisJIANJUN SHEN; LIU, H.-M; MCCONKIE-ROSELL, A et al.Prenatal diagnosis. 1999, Vol 19, Num 9, pp 837-839, issn 0197-3851Article

Hepatocellular adenoma in glycogen storage disease type IVALSHAK, N. S; COCJIN, J; PODESTA, L et al.Archives of pathology & laboratory medicine (1976). 1994, Vol 118, Num 1, pp 88-91, issn 0363-0153Article

Acid maltase deficiency and related myopathiesAMATO, A. A.Neurologic clinics. 2000, Vol 18, Num 1, pp vi-vii, issn 0733-8619, 17 p.Article

Concimitant branching enzyme and phosphorylase deficiencies an unusual glycogenosis with extensive neuronal polyglucosan storageHERRICK, M. K; TWISS, J. L; VLADUTIU, G. D et al.Journal of neuropathology and experimental neurology. 1994, Vol 53, Num 3, pp 239-246, issn 0022-3069Article

Juvenile hereditary polyglucosan body disease with complete branching enzyme deficiency (type IV glycogenosis)SCHRÖDER, J. M; MAY, R; SHIN, Y. S et al.Acta neuropathologica. 1993, Vol 85, Num 4, pp 419-430, issn 0001-6322Article

Early-onset fetal hydrops and muscle degeneration in siblings due to a novel variant of type IV glycogenosisCOX, P. M; BRUETON, L. A; MURPHY, K. W et al.American journal of medical genetics. 1999, Vol 86, Num 2, pp 187-193, issn 0148-7299Article

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