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Volumn 29, Issue 4, 2008, Pages 378-381

Placental Involvement in Glycogen Storage Disease Type IV

Author keywords

Glycogen storage disease IV; Histopathology; Placenta; Polyglucosan bodies; Prenatal diagnosis

Indexed keywords

ADULT; ARTICLE; CASE REPORT; CELL INCLUSION; DIAGNOSTIC PROCEDURE; FEMALE; FETUS; GENETIC ANALYSIS; GESTATIONAL AGE; GLYCOGEN STORAGE DISEASE TYPE 4; HISTOLOGY; HISTOPATHOLOGY; HUMAN; HUMAN TISSUE; PLACENTA; PRENATAL DIAGNOSIS; PRIORITY JOURNAL; TROPHOBLAST;

EID: 40949148540     PISSN: 01434004     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.placenta.2008.01.005     Document Type: Article
Times cited : (27)

References (11)
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    • Moses, S.W.1    Parvari, R.2
  • 2
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    • Clinical and genetic heterogeneity of branching enzyme deficiency (glycogenosis type IV)
    • Bruno C., van Diggelen O.P., Cassandrini D., Gimpelev M., Giuffre B., Donati M.A., et al. Clinical and genetic heterogeneity of branching enzyme deficiency (glycogenosis type IV). Neurology 63 (2004) 1053-1058
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  • 3
    • 33744461812 scopus 로고    scopus 로고
    • Neonatal neuromuscular variant of glycogen storage disease type IV: histopathological findings leading to the diagnosis
    • Konstantinidou A.E., Anninos H., Gyftodimou Y., Petersen M.B., Karadimas C., Fotopoulos S., et al. Neonatal neuromuscular variant of glycogen storage disease type IV: histopathological findings leading to the diagnosis. Histopathology 48 (2006) 878-880
    • (2006) Histopathology , vol.48 , pp. 878-880
    • Konstantinidou, A.E.1    Anninos, H.2    Gyftodimou, Y.3    Petersen, M.B.4    Karadimas, C.5    Fotopoulos, S.6
  • 6
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    • Neonatal type IV glycogen storage disease associated with "null" mutations in glycogen branching enzyme
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    • (2004) J Pediatr , vol.145 , pp. 705-709
    • Janecke, A.R.1    Dertinger, S.2    Ketelsen, U.P.3    Bereuter, L.4    Simma, B.5    Muller, T.6
  • 7
    • 0033543480 scopus 로고    scopus 로고
    • Early-onset fetal hydrops and muscle degeneration in siblings due to a novel variant of type IV glycogenosis
    • Cox P.M., Brueton L.A., Murphy K.W., Worthington V.C., Bjelogrlic P., Lazda E.J., et al. Early-onset fetal hydrops and muscle degeneration in siblings due to a novel variant of type IV glycogenosis. Am J Med Genet 86 (1999) 187-193
    • (1999) Am J Med Genet , vol.86 , pp. 187-193
    • Cox, P.M.1    Brueton, L.A.2    Murphy, K.W.3    Worthington, V.C.4    Bjelogrlic, P.5    Lazda, E.J.6
  • 8
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    • Fetal type IV glycogen storage disease: clinical, enzymatic, and genetic data of a pure muscular form with variable and early antenatal manifestations in the same family
    • L'herminé-Coulomb A., Beuzen F., Bouvier R., Rolland M.O., Froissart R., Menez F., et al. Fetal type IV glycogen storage disease: clinical, enzymatic, and genetic data of a pure muscular form with variable and early antenatal manifestations in the same family. Am J Med Genet 139 (2005) 118-122
    • (2005) Am J Med Genet , vol.139 , pp. 118-122
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  • 11
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    • Chorionic villus ultrastructure in type II glycogen storage disease (Pompe's disease)
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.