Wolf B - Search Results

1

Characterization of seizures associated with biotinidase deficiency.

Salbert BA, Pellock JM, Wolf B. Salbert BA, et al. Among authors: wolf b. Neurology. 1993 Jul;43(7):1351-5. doi: 10.1212/wnl.43.7.1351. Neurology. 1993. PMID: 8327137

2

Ophthalmologic findings in biotinidase deficiency.

Salbert BA, Astruc J, Wolf B. Salbert BA, et al. Among authors: wolf b. Ophthalmologica. 1993;206(4):177-81. doi: 10.1159/000310387. Ophthalmologica. 1993. PMID: 8278163

3

Progressive bilateral nasal alar collapse: a dominantly inherited trait.

Cole H, Bodurtha J, Salbert BA, Wolf B. Cole H, et al. Among authors: wolf b. Am J Med Genet. 1992 Jan 1;42(1):88-9. doi: 10.1002/ajmg.1320420117. Am J Med Genet. 1992. PMID: 1308370

4

Biochemical and immunologic characterization of serum biotinidase in partial biotinidase deficiency.

Hart PS, Hymes J, Wolf B. Hart PS, et al. Among authors: wolf b. Pediatr Res. 1992 Mar;31(3):261-5. doi: 10.1203/00006450-199203000-00013. Pediatr Res. 1992. PMID: 1561012

5

Biochemical and immunological characterization of serum biotinidase in profound biotinidase deficiency.

Hart PS, Hymes J, Wolf B. Hart PS, et al. Among authors: wolf b. Am J Hum Genet. 1992 Jan;50(1):126-36. Am J Hum Genet. 1992. PMID: 1729884 Free PMC article.

6

Worldwide survey of neonatal screening for biotinidase deficiency.

Wolf B. Wolf B. J Inherit Metab Dis. 1991;14(6):923-7. doi: 10.1007/BF01800475. J Inherit Metab Dis. 1991. PMID: 1779651

7

Partial biotinidase deficiency: clinical and biochemical features.

McVoy JR, Levy HL, Lawler M, Schmidt MA, Ebers DD, Hart PS, Pettit DD, Blitzer MG, Wolf B. McVoy JR, et al. Among authors: wolf b. J Pediatr. 1990 Jan;116(1):78-83. doi: 10.1016/s0022-3476(05)81649-x. J Pediatr. 1990. PMID: 2295967

8

Nonketotic hyperglycinemia in two retarded adults: a mild form of infantile nonketotic hyperglycinemia.

Flannery DB, Pellock J, Bousounis D, Hunt P, Nance C, Wolf B. Flannery DB, et al. Among authors: wolf b. Neurology. 1983 Aug;33(8):1064-6. doi: 10.1212/wnl.33.8.1064. Neurology. 1983. PMID: 6683804

9

Mutational hotspot in the human biotinidase gene causes profound biotinidase deficiency.

Pomponio RJ, Reynolds TR, Cole H, Buck GA, Wolf B. Pomponio RJ, et al. Among authors: wolf b. Nat Genet. 1995 Sep;11(1):96-8. doi: 10.1038/ng0995-96. Nat Genet. 1995. PMID: 7550325

10

Mutation (Q456H) is the most common cause of profound biotinidase deficiency in children ascertained by newborn screening in the United States.

Norrgard KJ, Pomponio RJ, Swango KL, Hymes J, Reynolds TR, Buck GA, Wolf B. Norrgard KJ, et al. Among authors: wolf b. Biochem Mol Med. 1997 Jun;61(1):22-7. doi: 10.1006/bmme.1997.2597. Biochem Mol Med. 1997. PMID: 9232193

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