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Alison La Pean

Research Profile

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Mali

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Pediatrics

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Publications

TOP 3
Alison La Pean; Kerry L Eskra; Michael H Farrell; Philip M Farrell
Effects of immediate telephone follow-up with providers on sweat chloride test timing after cystic fibrosis newborn screening identifies a single mutation.
Jenelle L Collins; Kerry L Eskra; Alison La Pean; Faith O'Tool; Sara J Roedl; Audrey Tluczek; Michael H Farrell
Factors that influence parents' experiences with results disclosure after newborn screening identifies genetic carrier status for cystic fibrosis or sickle cell hemoglobinopathy.
Alison La Pean; Sara J Roedl; Audrey Tluczek; Stephanie A Christopher; Jenelle L Collins; Kerry L Eskra; Michael H Farrell
A qualitative secondary evaluation of statewide follow-up interviews for abnormal newborn screening results for cystic fibrosis and sickle cell hemoglobinopathy.

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All Publications

2013: Alison La Pean; Kerry L Eskra; Michael H Farrell; Philip M Farrell
Effects of immediate telephone follow-up with providers on sweat chloride test timing after cystic fibrosis newborn screening identifies a single mutation.
The Journal of pediatrics 2013;162(3):522-9.
2013: Jenelle L Collins; Kerry L Eskra; Alison La Pean; Faith O'Tool; Sara J Roedl; Audrey Tluczek; Michael H Farrell
Factors that influence parents' experiences with results disclosure after newborn screening identifies genetic carrier status for cystic fibrosis or sickle cell hemoglobinopathy.
Patient education and counseling 2013;90(3):378-85.
2012: Alison La Pean; Sara J Roedl; Audrey Tluczek; Stephanie A Christopher; Jenelle L Collins; Kerry L Eskra; Michael H Farrell
A qualitative secondary evaluation of statewide follow-up interviews for abnormal newborn screening results for cystic fibrosis and sickle cell hemoglobinopathy.
Genetics in medicine : official journal of the American College of Medical Genetics 2012;14(2):207-14.
2011: M Traoré; T Coulibaly; C O Guinto; M Karambé; Alison La Pean; G Landouré; K G Meilleur; Fanny Mochel; M Sangaré; Kenneth H Fischbeck
Clinical and genetic analysis of spinocerebellar ataxia in Mali.
European journal of neurology : the official journal of the European Federation of Neurological Societies 2011;18(10):1269-71.
2011: Lindsay E Fernández-Rhodes; Angela D Kokkinis; Michelle J White; Charlotte A Watts; Sungyoung Auh; Neal O Jeffries; Joseph A Shrader; TJ Lehky; Li Li; Jennifer E Ryder; Ellen W Levy; Beth I Solomon; Michael Harris-Love; Alison La Pean; Alice B Schindler; Cheunju Chen; Nicholas A Di Prospero; Kenneth H Fischbeck
Efficacy and safety of dutasteride in patients with spinal and bulbar muscular atrophy: a randomised placebo-controlled trial.
Lancet neurology 2011;10(2):140-7.
2010: K G Meilleur; M Traoré; M Sangaré; A Britton; G Landouré; S Coulibaly; B Niaré; Fanny Mochel; Alison La Pean; I Rafferty; C Watts; D Shriner; Marguerite T Littleton-Kearney; Craig Blackstone; Andrew Singleton; Kenneth H Fischbeck
Hereditary spastic paraplegia and amyotrophy associated with a novel locus on chromosome 19.
Neurogenetics 2010;11(3):313-8.
2009: Lindsay E Rhodes; Brandi K Freeman; Sungyoung Auh; Angela D Kokkinis; Alison La Pean; Cheunju Chen; TJ Lehky; Joseph A Shrader; Ellen W Levy; Michael Harris-Love; Nicholas A Di Prospero; Kenneth H Fischbeck
Clinical features of spinal and bulbar muscular atrophy.
Brain : a journal of neurology 2009;132(Pt 12):3242-51.
2008: Alison La Pean; Neal Jeffries; Chelsea Grow; Bernard Ravina; Nicholas A Di Prospero
Predictors of progression in patients with Friedreich ataxia.
Movement disorders : official journal of the Movement Disorder Society 2008;23(14):2026-32.
2005: Alison La Pean; Michael H Farrell
Initially misleading communication of carrier results after newborn genetic screening.
Pediatrics 2005;116(6):1499-505.
2005: Michael H Farrell; Alison La Pean; Lynnea Ladouceur
Content of communication by pediatric residents after newborn genetic screening.
Pediatrics 2005;116(6):1492-8.
2003: Huilin Qi; Dean J Aguiar; Shelly M Williams; Alison La Pean; Wei Pan; Catherine M Verfaillie
Identification of genes responsible for osteoblast differentiation from human mesodermal progenitor cells.
Proceedings of the National Academy of Sciences of the United States of America 2003;100(6):3305-10.