Pean A - Search Results

1

Sulphoxidation and sulphation capacity in patients with primary biliary cirrhosis.

Davies MH, Ngong JM, Pean A, Vickers CR, Waring RH, Elias E. Davies MH, et al. Among authors: pean a. J Hepatol. 1995 May;22(5):551-60. doi: 10.1016/0168-8278(95)80450-1. J Hepatol. 1995. PMID: 7650336

2

Pathways of cysteine metabolism in MND/ALS.

Pean A, Steventon GB, Waring RH, Foster H, Sturman S, Williams AC. Pean A, et al. J Neurol Sci. 1994 Jul;124 Suppl:59-61. doi: 10.1016/0022-510x(94)90179-1. J Neurol Sci. 1994. PMID: 7807143

3

Toxicity of sulphur-containing compounds to neuronal cell lines.

Pean AR, Parsons RB, Waring RH, Williams AC, Ramsden DB. Pean AR, et al. J Neurol Sci. 1995 May;129 Suppl:107-8. doi: 10.1016/0022-510x(95)00078-g. J Neurol Sci. 1995. PMID: 7595598

4

Effects of immediate telephone follow-up with providers on sweat chloride test timing after cystic fibrosis newborn screening identifies a single mutation.

La Pean A, Farrell MH, Eskra KL, Farrell PM. La Pean A, et al. J Pediatr. 2013 Mar;162(3):522-9. doi: 10.1016/j.jpeds.2012.08.055. Epub 2012 Oct 24. J Pediatr. 2013. PMID: 23102590 Free PMC article.

5

A qualitative secondary evaluation of statewide follow-up interviews for abnormal newborn screening results for cystic fibrosis and sickle cell hemoglobinopathy.

La Pean A, Collins JL, Christopher SA, Eskra KL, Roedl SJ, Tluczek A, Farrell MH. La Pean A, et al. Genet Med. 2012 Feb;14(2):207-14. doi: 10.1038/gim.0b013e31822dd7b8. Genet Med. 2012. PMID: 22261754 Free PMC article.

6

Factors that influence parents' experiences with results disclosure after newborn screening identifies genetic carrier status for cystic fibrosis or sickle cell hemoglobinopathy.

Collins JL, La Pean A, O'Tool F, Eskra KL, Roedl SJ, Tluczek A, Farrell MH. Collins JL, et al. Among authors: la pean a. Patient Educ Couns. 2013 Mar;90(3):378-85. doi: 10.1016/j.pec.2011.12.007. Epub 2012 Jan 11. Patient Educ Couns. 2013. PMID: 22240007 Free PMC article.

7

Improving communication between doctors and parents after newborn screening.

Farrell MH, Christopher SA, Tluczek A, Kennedy-Parker K, La Pean A, Eskra K, Collins J, Hoffman G, Panepinto J, Farrell PM. Farrell MH, et al. Among authors: la pean a. WMJ. 2011 Oct;110(5):221-7. WMJ. 2011. PMID: 22164579 Free PMC article.

8

Genetic testing and counseling for hereditary neurological diseases in Mali.

Meilleur KG, Coulibaly S, Traoré M, Landouré G, La Pean A, Sangaré M, Mochel F, Traoré S, Fischbeck KH, Han HR. Meilleur KG, et al. Among authors: la pean a. J Community Genet. 2011 Mar;2(1):33-42. doi: 10.1007/s12687-011-0038-0. Epub 2011 Feb 22. J Community Genet. 2011. PMID: 22109722 Free PMC article.

9

Clinical and genetic analysis of spinocerebellar ataxia in Mali.

Traoré M, Coulibaly T, Meilleur KG, La Pean A, Sangaré M, Landouré G, Mochel F, Karambé M, Guinto CO, Fischbeck KH. Traoré M, et al. Among authors: la pean a. Eur J Neurol. 2011 Oct;18(10):1269-71. doi: 10.1111/j.1468-1331.2011.03376.x. Epub 2011 Mar 21. Eur J Neurol. 2011. PMID: 21418439 Free PMC article.

10

Efficacy and safety of dutasteride in patients with spinal and bulbar muscular atrophy: a randomised placebo-controlled trial.

Fernández-Rhodes LE, Kokkinis AD, White MJ, Watts CA, Auh S, Jeffries NO, Shrader JA, Lehky TJ, Li L, Ryder JE, Levy EW, Solomon BI, Harris-Love MO, La Pean A, Schindler AB, Chen C, Di Prospero NA, Fischbeck KH. Fernández-Rhodes LE, et al. Among authors: la pean a. Lancet Neurol. 2011 Feb;10(2):140-7. doi: 10.1016/S1474-4422(10)70321-5. Epub 2011 Jan 6. Lancet Neurol. 2011. PMID: 21216197 Free PMC article. Clinical Trial.

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