Type IV glycogenosis. Patient with absence of a branching enzyme alpha-1,4-glucan:alpha-1,4-glucan 6-glycosyl transferase
- PMID: 5247008
Type IV glycogenosis. Patient with absence of a branching enzyme alpha-1,4-glucan:alpha-1,4-glucan 6-glycosyl transferase
Similar articles
-
[Considerations on glycogenosis, type 3].Pediatria (Napoli). 1969;77(5):684-708. Pediatria (Napoli). 1969. PMID: 4323634 Italian. No abstract available.
-
[Histologic diagnosis of glucogenosis type IV (amylopectinosis) (author's transl)].Z Kinderheilkd. 1974;117(3):187-203. Z Kinderheilkd. 1974. PMID: 4528211 German. No abstract available.
-
[A study of the abnormal polysaccharide in a child with type IV glycogen storage disease (author's transl)].Arch Fr Pediatr. 1981 Dec;38 Suppl 1:837-41. Arch Fr Pediatr. 1981. PMID: 6949501 French.
-
The liver in inherited metabolic diseases of childhood.Prog Liver Dis. 1972;4:463-88. Prog Liver Dis. 1972. PMID: 4119892 Review. No abstract available.
-
[Differential diagnosis of glycogenoses].Arkh Patol. 1980;42(12):61-71. Arkh Patol. 1980. PMID: 7011274 Review. Russian.
Cited by
-
Polyglucosan body structure in Lafora disease.Carbohydr Polym. 2020 Jul 15;240:116260. doi: 10.1016/j.carbpol.2020.116260. Epub 2020 Apr 14. Carbohydr Polym. 2020. PMID: 32475552 Free PMC article.
-
The histochemical evaluation of the glycogen storage diseases. A review of techniques and their limitations.Histochem J. 1970 Sep;2(5):441-50. doi: 10.1007/BF01004725. Histochem J. 1970. PMID: 4114291 Review. No abstract available.
-
Branching enzyme in erythrocytes. Detection of type IV glycogenosis homozygotes and heterozygotes.J Inherit Metab Dis. 1988;11 Suppl 2:252-4. doi: 10.1007/BF01804250. J Inherit Metab Dis. 1988. PMID: 2972882 No abstract available.
-
Liver transplantation for type I and type IV glycogen storage disease.Eur J Pediatr. 1993;152 Suppl 1(Suppl 1):S71-6. doi: 10.1007/BF02072093. Eur J Pediatr. 1993. PMID: 8319729 Free PMC article.
-
A juvenile variant of glycogenosis IV (Andersen disease).Eur J Pediatr. 1986 Aug;145(3):179-81. doi: 10.1007/BF00446059. Eur J Pediatr. 1986. PMID: 3464425