Format
Sort by
Items per page

Send to

Choose Destination

Links from PubMed

Items: 1 to 20 of 217

1.

Glycogen storage disease type IB.

Buchino JJ, Brown BI, Volk DM.

Arch Pathol Lab Med. 1983 Jun;107(6):283-5.

PMID:
6303265
2.

[Histochemical and ultrastructural study of a case of type 3 glycogenosis].

Chamlian A, Mariani R, Lafon J, Adechy-Benkoel L, Mounition L.

Ann Anat Pathol (Paris). 1971 Jan-Mar;16(1):85-92. French. No abstract available.

PMID:
4327013
3.

Type Ib glycogen storage disease: an in vivo and in vitro study of two cases.

Baussan C, Moatti N, Brivet M, Lemonnier A.

J Inherit Metab Dis. 1984;7 Suppl 2:147-8. No abstract available.

PMID:
6090806
4.

Glycogen storage disease: clinical, biochemical, and molecular heterogeneity.

Shin YS.

Semin Pediatr Neurol. 2006 Jun;13(2):115-20. Review.

PMID:
17027861
5.

A new variant of glycogen storage disease. Type IXc.

Lerner A, Iancu TC, Bashan N, Potashnik R, Moses S.

Am J Dis Child. 1982 May;136(5):406-10.

PMID:
6952760
6.

Impairment of the activity of the hepatic microsomal glucose-6-phosphatase system in three preterm infants.

Hume R, Lyall H, Giles M, Burchell A.

Acta Paediatr. 1992 Aug;81(8):580-4.

PMID:
1327322
7.

Low molecular weight glycogen as a cause of generalized glycogen storage disease.

Krivit W, Sharp HL, Lee JC, Larner J, Edstrom R.

Am J Med. 1973 Jan;54(1):88-97. No abstract available.

PMID:
4345263
8.

Comparative pathology of the canine model of glycogen storage disease type II (Pompe's disease).

Walvoort HC, Dormans JA, van den Ingh TS.

J Inherit Metab Dis. 1985;8(1):38-46.

PMID:
3921759
9.

Glycogen storage disease. Studies related to the mechanism of glycogenosome formation.

Iwamasa T, Ninomiya N, Fukuda S, Hamada T, Hirashima M, Osame M.

Pathol Res Pract. 1983 Mar;176(2-4):236-52.

PMID:
6304667
10.

Studies in glycogen storage disease. IV. Leukocyte phosphorylase in a family with type VI GSD.

Schwartz D, Savin M, Drash A, Field J.

Metabolism. 1970 Mar;19(3):238-45. No abstract available.

PMID:
4313495
11.

Type I glycogen storage diseases: disorders of the glucose-6-phosphatase complex.

Chou JY, Matern D, Mansfield BC, Chen YT.

Curr Mol Med. 2002 Mar;2(2):121-43. Review.

PMID:
11949931
12.

[A study of the abnormal polysaccharide in a child with type IV glycogen storage disease (author's transl)].

Scotto JM, de Barsy T, Hadchouel M, Bernard O.

Arch Fr Pediatr. 1981 Dec;38 Suppl 1:837-41. French.

PMID:
6949501
13.

Type III glycogenosis with multicore structures.

Pellissier JF, de Barsy T, Faugere MC, Rebuffel P.

Muscle Nerve. 1979 Mar-Apr;2(2):124-32.

PMID:
161799
14.

Glycogen storage disease, types I to X: criteria for morphologic diagnosis.

McAdams AJ, Hug G, Bove KE.

Hum Pathol. 1974 Jul;5(4):463-87. No abstract available.

PMID:
4525190
15.

Liver glycogenosis. A biochemical and ultrastructural study.

De Bruijn WC, Fernandes J, Huber J, Koster JF.

Pathol Eur. 1975;10(1):3-15. No abstract available.

PMID:
170575
16.
17.

The histochemical evaluation of the glycogen storage diseases. A review of techniques and their limitations.

Lake BD.

Histochem J. 1970 Sep;2(5):441-50. Review. No abstract available.

PMID:
4114291
18.

An autopsy case of type II glycogenosis.

Asukata I, Aizawa S, Kosakai M, Kirino Y, Ishikawa E.

Acta Pathol Jpn. 1976 Sep;26(5):629-35.

PMID:
1069472
19.

Hepatocyte glycogen accumulation in patients undergoing dietary management of urea cycle defects mimics storage disease.

Miles L, Heubi JE, Bove KE.

J Pediatr Gastroenterol Nutr. 2005 Apr;40(4):471-6.

PMID:
15795597
20.

Identification of a novel mutation (867delA) in the glucose-6-phosphatase gene in two siblings with glycogen storage disease type Ia with different phenotypes.

Rake JP, ten Berge AM, Visser G, Verlind E, Niezen-Koning KE, Buys CH, Smit GP, Scheffer H.

Hum Mutat. 2000 Apr;15(4):381.

PMID:
10737986

Supplemental Content

Support Center