These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
180 related articles for article (PubMed ID: 9427152)
1. A case of the carbohydrate-deficient glycoprotein syndrome type 1 (CDGS type 1) with normal phosphomannomutase activity. Charlwood J; Clayton P; Johnson A; Keir G; Mian N; Winchester B J Inherit Metab Dis; 1997 Nov; 20(6):817-26. PubMed ID: 9427152 [TBL] [Abstract][Full Text] [Related]
2. Molecular basis of carbohydrate-deficient glycoprotein syndromes type I with normal phosphomannomutase activity. Freeze HH; Aebi M Biochim Biophys Acta; 1999 Oct; 1455(2-3):167-78. PubMed ID: 10571010 [TBL] [Abstract][Full Text] [Related]
3. Abnormal metabolism of mannose in families with carbohydrate-deficient glycoprotein syndrome type 1. Panneerselvam K; Etchison JR; Skovby F; Freeze HH Biochem Mol Med; 1997 Aug; 61(2):161-7. PubMed ID: 9259981 [TBL] [Abstract][Full Text] [Related]
4. Hypoglycosylation of a brain glycoprotein (beta-trace protein) in CDG syndromes due to phosphomannomutase deficiency and N-acetylglucosaminyl-transferase II deficiency. Pohl S; Hoffmann A; Rüdiger A; Nimtz M; Jaeken J; Conradt HS Glycobiology; 1997 Dec; 7(8):1077-84. PubMed ID: 9455908 [TBL] [Abstract][Full Text] [Related]
5. Carbohydrate-deficient glycoprotein syndrome type 1: correction of the glycosylation defect by deprivation of glucose or supplementation of mannose. Körner C; Lehle L; von Figura K Glycoconj J; 1998 May; 15(5):499-505. PubMed ID: 9881752 [TBL] [Abstract][Full Text] [Related]
6. Abnormal synthesis of dolichol-linked oligosaccharides in carbohydrate-deficient glycoprotein syndrome. Krasnewich DM; Holt GD; Brantly M; Skovby F; Redwine J; Gahl WA Glycobiology; 1995 Jul; 5(5):503-10. PubMed ID: 8563136 [TBL] [Abstract][Full Text] [Related]
8. Carbohydrate-deficient glycoprotein syndrome type V: deficiency of dolichyl-P-Glc:Man9GlcNAc2-PP-dolichyl glucosyltransferase. Körner C; Knauer R; Holzbach U; Hanefeld F; Lehle L; von Figura K Proc Natl Acad Sci U S A; 1998 Oct; 95(22):13200-5. PubMed ID: 9789065 [TBL] [Abstract][Full Text] [Related]
9. Carbohydrate-deficient glycoprotein syndromes: inborn errors of protein glycosylation. Keir G; Winchester BG; Clayton P Ann Clin Biochem; 1999 Jan; 36 ( Pt 1)():20-36. PubMed ID: 10370757 [TBL] [Abstract][Full Text] [Related]
10. Carbohydrate-deficient glycoprotein syndrome type IA (phosphomannomutase-deficiency). Carchon H; Van Schaftingen E; Matthijs G; Jaeken J Biochim Biophys Acta; 1999 Oct; 1455(2-3):155-65. PubMed ID: 10571009 [TBL] [Abstract][Full Text] [Related]
11. High residual activity of PMM2 in patients' fibroblasts: possible pitfall in the diagnosis of CDG-Ia (phosphomannomutase deficiency). Grünewald S; Schollen E; Van Schaftingen E; Jaeken J; Matthijs G Am J Hum Genet; 2001 Feb; 68(2):347-54. PubMed ID: 11156536 [TBL] [Abstract][Full Text] [Related]
12. Genotypes and phenotypes of patients in the UK with carbohydrate-deficient glycoprotein syndrome type 1. Imtiaz F; Worthington V; Champion M; Beesley C; Charlwood J; Clayton P; Keir G; Mian N; Winchester B J Inherit Metab Dis; 2000 Mar; 23(2):162-74. PubMed ID: 10801058 [TBL] [Abstract][Full Text] [Related]
13. Phosphomannomutase deficiency is the main cause of carbohydrate-deficient glycoprotein syndrome with type I isoelectrofocusing pattern of serum sialotransferrins. Jaeken J; Artigas J; Barone R; Fiumara A; de Koning TJ; Poll-The BT; de Rijk-van Andel JF; Hoffmann GF; Assmann B; Mayatepek E; Pineda M; Vilaseca MA; Saudubray JM; Schlüter B; Wevers R; Van Schaftingen E J Inherit Metab Dis; 1997 Jul; 20(3):447-9. PubMed ID: 9266378 [No Abstract] [Full Text] [Related]
15. Diagnostic value of Western blotting in carbohydrate-deficient glycoprotein syndrome. Seta N; Barnier A; Hochedez F; Besnard MA; Durand G Clin Chim Acta; 1996 Oct; 254(2):131-40. PubMed ID: 8896901 [TBL] [Abstract][Full Text] [Related]
16. Phosphomannomutase activity in congenital disorders of glycosylation type Ia determined by direct analysis of the interconversion of mannose-1-phosphate to mannose-6-phosphate by high-pH anion-exchange chromatography with pulsed amperometric detection. Orvisky E; Stubblefield B; Long RT; Martin BM; Sidransky E; Krasnewich D Anal Biochem; 2003 Jun; 317(1):12-8. PubMed ID: 12729595 [TBL] [Abstract][Full Text] [Related]
17. Neurological presentation of a congenital disorder of glycosylation CDG-Ia: implications for diagnosis and genetic counseling. Drouin-Garraud V; Belgrand M; Grünewald S; Seta N; Dacher JN; Hénocq A; Matthijs G; Cormier-Daire V; Frébourg T; Saugier-Veber P Am J Med Genet; 2001 Jun; 101(1):46-9. PubMed ID: 11343337 [TBL] [Abstract][Full Text] [Related]
18. Congenital disorder of glycosylation type Ia in a Malaysian family: clinical outcome and description of a novel PMM2 mutation. Thong MK; Fietz M; Nicholls C; Lee MH; Asma O J Inherit Metab Dis; 2009 Dec; 32 Suppl 1():S41-4. PubMed ID: 19165618 [TBL] [Abstract][Full Text] [Related]
19. A novel carbohydrate-deficient glycoprotein syndrome characterized by a deficiency in glucosylation of the dolichol-linked oligosaccharide. Burda P; Borsig L; de Rijk-van Andel J; Wevers R; Jaeken J; Carchon H; Berger EG; Aebi M J Clin Invest; 1998 Aug; 102(4):647-52. PubMed ID: 9710431 [TBL] [Abstract][Full Text] [Related]
20. Effect of mutations found in carbohydrate-deficient glycoprotein syndrome type IA on the activity of phosphomannomutase 2. Pirard M; Matthijs G; Heykants L; Schollen E; Grünewald S; Jaeken J; van Schaftingen E FEBS Lett; 1999 Jun; 452(3):319-22. PubMed ID: 10386614 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]