Mian N - Search Results

1

Mass spectrometric analysis of glycans in elucidating the pathogenesis of CDG type IIx.

Mills PB, Mills K, Mian N, Winchester BG, Clayton PT. Mills PB, et al. Among authors: mian n. J Inherit Metab Dis. 2003;26(2-3):119-34. doi: 10.1023/a:1024476915278. J Inherit Metab Dis. 2003. PMID: 12889655 Review.

2

The underglycosylation of plasma alpha 1-antitrypsin in congenital disorders of glycosylation type I is not random.

Mills K, Mills PB, Clayton PT, Mian N, Johnson AW, Winchester BG. Mills K, et al. Among authors: mian n. Glycobiology. 2003 Feb;13(2):73-85. doi: 10.1093/glycob/cwg026. Epub 2002 Dec 17. Glycobiology. 2003. PMID: 12626422

3

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. Charlwood J, et al. Among authors: mian n. J Inherit Metab Dis. 1997 Nov;20(6):817-26. doi: 10.1023/a:1005380003902. J Inherit Metab Dis. 1997. PMID: 9427152

4

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. Imtiaz F, et al. Among authors: mian n. J Inherit Metab Dis. 2000 Mar;23(2):162-74. doi: 10.1023/a:1005669900330. J Inherit Metab Dis. 2000. PMID: 10801058 Clinical Trial.

5

Diagnosis of congenital disorders of glycosylation type-I using protein chip technology.

Mills K, Mills P, Jackson M, Worthington V, Beesley C, Mann A, Clayton P, Grunewald S, Keir G, Young L, Langridge J, Mian N, Winchester B. Mills K, et al. Among authors: mian n. Proteomics. 2006 Apr;6(7):2295-304. doi: 10.1002/pmic.200500682. Proteomics. 2006. PMID: 16552784

6

The carbohydrate-deficient glycoprotein syndrome: an experiment of nature in glycosylation.

Winchester B, Clayton P, Mian N, di-Tomaso E, Dell A, Reason A, Keir G. Winchester B, et al. Among authors: mian n. Biochem Soc Trans. 1995 Feb;23(1):185-8. doi: 10.1042/bst0230185. Biochem Soc Trans. 1995. PMID: 7758727 Review. No abstract available.

7

The identification of abnormal glycoforms of serum transferrin in carbohydrate deficient glycoprotein syndrome type I by capillary zone electrophoresis.

Iourin O, Mattu TS, Mian N, Keir G, Winchester B, Dwek RA, Rudd PM. Iourin O, et al. Among authors: mian n. Glycoconj J. 1996 Dec;13(6):1031-42. doi: 10.1007/BF01053199. Glycoconj J. 1996. PMID: 8981095

8

Defective galactosylation of serum transferrin in galactosemia.

Charlwood J, Clayton P, Keir G, Mian N, Winchester B. Charlwood J, et al. Among authors: mian n. Glycobiology. 1998 Apr;8(4):351-7. doi: 10.1093/glycob/8.4.351. Glycobiology. 1998. PMID: 9499382

9

Prenatal diagnosis of the carbohydrate-deficient glycoprotein syndrome type 1A (CDG1A) by a combination of enzymology and genetic linkage analysis after amniocentesis or chorionic villus sampling.

Charlwood J, Clayton P, Keir G, Mian N, Young E, Winchester B. Charlwood J, et al. Among authors: mian n. Prenat Diagn. 1998 Jul;18(7):693-9. Prenat Diagn. 1998. PMID: 9706650

10

Concerning "Agamanolis disease".

Clayton PT, Mian N. Clayton PT, et al. Among authors: mian n. Am J Med Genet. 1995 Apr 10;56(3):289-90. doi: 10.1002/ajmg.1320560312. Am J Med Genet. 1995. PMID: 7778592 No abstract available.

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