Brown BI - Search Results

1

Glycogen debranching enzyme: purification, antibody characterization, and immunoblot analyses of type III glycogen storage disease.

Chen YT, He JK, Ding JH, Brown BI. Chen YT, et al. Among authors: brown bi. Am J Hum Genet. 1987 Dec;41(6):1002-15. Am J Hum Genet. 1987. PMID: 2961257 Free PMC article.

2

Definitive prenatal diagnosis for type III glycogen storage disease.

Yang BZ, Ding JH, Brown BI, Chen YT. Yang BZ, et al. Among authors: brown bi. Am J Hum Genet. 1990 Oct;47(4):735-9. Am J Hum Genet. 1990. PMID: 2220811 Free PMC article.

3

Immunoblot analyses of glycogen debranching enzyme in different subtypes of glycogen storage disease type III.

Ding JH, de Barsy T, Brown BI, Coleman RA, Chen YT. Ding JH, et al. Among authors: brown bi. J Pediatr. 1990 Jan;116(1):95-100. doi: 10.1016/s0022-3476(05)81652-x. J Pediatr. 1990. PMID: 2295969

4

Glycogen storage disease in adults.

Talente GM, Coleman RA, Alter C, Baker L, Brown BI, Cannon RA, Chen YT, Crigler JF Jr, Ferreira P, Haworth JC, Herman GE, Issenman RM, Keating JP, Linde R, Roe TF, Senior B, Wolfsdorf JI. Talente GM, et al. Among authors: brown bi. Ann Intern Med. 1994 Feb 1;120(3):218-26. doi: 10.7326/0003-4819-120-3-199402010-00008. Ann Intern Med. 1994. PMID: 8273986 Review.

5

Branching enzyme activity of cultured amniocytes and chorionic villi: prenatal testing for type IV glycogen storage disease.

Brown BI, Brown DH. Brown BI, et al. Am J Hum Genet. 1989 Mar;44(3):378-81. Am J Hum Genet. 1989. PMID: 2521770 Free PMC article.

6

X-linked glycogen storage disease. A cause of hypotonia, hyperuricemia, and growth retardation.

Keating JP, Brown BI, White NH, DiMauro S. Keating JP, et al. Among authors: brown bi. Am J Dis Child. 1985 Jun;139(6):609-13. doi: 10.1001/archpedi.1985.02140080079037. Am J Dis Child. 1985. PMID: 3859203

7

Studies of the residual glycogen branching enzyme activity present in human skin fibroblasts from patients with type IV glycogen storage disease.

Brown DH, Brown BI. Brown DH, et al. Among authors: brown bi. Biochem Biophys Res Commun. 1983 Mar 16;111(2):636-43. doi: 10.1016/0006-291x(83)90354-6. Biochem Biophys Res Commun. 1983. PMID: 6220706

8

Structure of the polysaccharide formed by incubating glycogen with D-[14C]glucose in the presence of the glycogen debranching enzyme [amylo-(1 linked to 6)-glucosidase-4-alpha-glucanotransferase].

Brown DH, Sprinkle DJ, Brown BI. Brown DH, et al. Among authors: brown bi. Carbohydr Res. 1978 Mar;61:265-77. doi: 10.1016/s0008-6215(00)84487-0. Carbohydr Res. 1978. PMID: 274178

9

Glycogen storage disease type IB.

Buchino JJ, Brown BI, Volk DM. Buchino JJ, et al. Among authors: brown bi. Arch Pathol Lab Med. 1983 Jun;107(6):283-5. Arch Pathol Lab Med. 1983. PMID: 6303265

10

Type IV glycogen storage disease: branching enzyme deficiency in skin fibroblasts and possible heterozygote detection.

Howell RR, Kaback MM, Brown BI. Howell RR, et al. Among authors: brown bi. J Pediatr. 1971 Apr;78(4):638-42. doi: 10.1016/s0022-3476(71)80466-3. J Pediatr. 1971. PMID: 5278749 No abstract available.

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