Eisensmith RC - Search Results

1

O'Neill CA, Eisensmith RC, Croke DT, Naughten ER, Cahalane SF, Woo SL. O'Neill CA, et al. Among authors: eisensmith rc. Acta Paediatr Suppl. 1994 Dec;407:43-4. doi: 10.1111/j.1651-2227.1994.tb13448.x. Acta Paediatr Suppl. 1994. PMID: 7766956

2

Population genetics of phenylketonuria.

Eisensmith RC, Woo SL. Eisensmith RC, et al. Acta Paediatr Suppl. 1994 Dec;407:19-26. doi: 10.1111/j.1651-2227.1994.tb13442.x. Acta Paediatr Suppl. 1994. PMID: 7766949 Review.

3

Molecular basis of phenylketonuria and related hyperphenylalaninemias: mutations and polymorphisms in the human phenylalanine hydroxylase gene.

Eisensmith RC, Woo SL. Eisensmith RC, et al. Hum Mutat. 1992;1(1):13-23. doi: 10.1002/humu.1380010104. Hum Mutat. 1992. PMID: 1301187 Review.

4

Molecular characterization of PKU allele prevalent in southern Europe and Ireland.

Dasovich M, Konecki D, Lichter-Konecki U, Eisensmith RC, Güttler F, Naughton E, Mullins C, Giovannini M, Riva E, Woo SL. Dasovich M, et al. Among authors: eisensmith rc. Somat Cell Mol Genet. 1991 May;17(3):303-9. doi: 10.1007/BF01232824. Somat Cell Mol Genet. 1991. PMID: 2047941

5

Gene therapy for phenylketonuria.

Eisensmith RC, Woo SL. Eisensmith RC, et al. Acta Paediatr Suppl. 1994 Dec;407:124-9. doi: 10.1111/j.1651-2227.1994.tb13471.x. Acta Paediatr Suppl. 1994. PMID: 7766948 Review.

6

Identification of three novel PKU mutations among Chinese: evidence for recombination or recurrent mutation at the PAH locus.

Wang T, Okano Y, Eisensmith RC, Lo WH, Huang SZ, Zeng YT, Yuan LF, Liu SR, Woo SL. Wang T, et al. Among authors: eisensmith rc. Genomics. 1992 May;13(1):230-1. doi: 10.1016/0888-7543(92)90229-l. Genomics. 1992. PMID: 1349576

7

Identification of a novel phenylketonuria (PKU) mutation in the Chinese: further evidence for multiple origins of PKU in Asia.

Wang T, Okano Y, Eisensmith RC, Lo WH, Huang SZ, Zeng YT, Woo SL. Wang T, et al. Among authors: eisensmith rc. Am J Hum Genet. 1991 Mar;48(3):628-30. Am J Hum Genet. 1991. PMID: 1998345 Free PMC article.

8

A simple, rapid, and highly informative PCR-based procedure for prenatal diagnosis and carrier screening of phenylketonuria.

Eisensmith RC, Goltsov AA, Woo SL. Eisensmith RC, et al. Prenat Diagn. 1994 Dec;14(12):1113-8. doi: 10.1002/pd.1970141204. Prenat Diagn. 1994. PMID: 7899279

9

Molecular basis of PKU in China.

Lo WH, Wang T, Eisensmith R, Woo SL. Lo WH, et al. Chin Med Sci J. 1993 Sep;8(3):180-5. Chin Med Sci J. 1993. PMID: 8142636 No abstract available.

10

Updated listing of haplotypes at the human phenylalanine hydroxylase (PAH) locus.

Eisensmith RC, Woo SL. Eisensmith RC, et al. Am J Hum Genet. 1992 Dec;51(6):1445-8. Am J Hum Genet. 1992. PMID: 1361103 Free PMC article. No abstract available.

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