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Journal of Inherited Metabolic Disease|February 24, 2001
Tyrosine hydroxylase deficiency unresponsive to L-dopa treatment with unusual clinical and biochemical presentationP DE Lonlay, M C Nassogne, A H van Gennip, et al.
American Journal of Public Health|April 20, 2013
Improvements in health care use associated with community coalitions: long-term results of the allies against asthma initiativeNoreen M Clark, Laurie L Lachance, M Beth Benedict, et al.
The Journal of Asthma : Official Journal of the Association for the Care of Asthma|February 21, 2014
Asthma coalition effects on vulnerable sub groups of children: the most frequent users of health care and the youngestLaurie Lachance, M Beth Benedict, Linda Jo Doctor, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|February 28, 2002
[Neurofibromatosis 1: recommendations for management]S Pinson, A Créange, S Barbarot, et al.
American Journal of Medical Genetics|July 11, 1997
The spectrum of congenital anomalies of the VATER association: an international studyL D Botto, M J Khoury, P Mastroiacovo, et al.
Neurobiology of Disease|July 6, 2019
Time course and magnitude of alpha-synuclein inclusion formation and nigrostriatal degeneration in the rat model of synucleinopathy triggered by intrastriatal α-synuclein preformed fibrilsJoseph R Patterson, Megan F Duffy, Christopher J Kemp, et al.
NPJ Parkinson'S Disease|May 24, 2022
Beta2-adrenoreceptor agonist clenbuterol produces transient decreases in alpha-synuclein mRNA but no long-term reduction in proteinJoseph R Patterson, Warren D Hirst, Jacob W Howe, et al.
Frontiers in Neuroscience|April 16, 2025
Intrastriatal injection of alpha-synuclein preformed fibrils to rats results in L-DOPA reversible sensorimotor impairments and alterations in non-motor functionSheila M Fleming, Sophia Scott, Edward J Hamad, et al.
NPJ Parkinson'S Disease|January 3, 2024
Transcriptomic profiling of early synucleinopathy in rats induced with preformed fibrilsJoseph R Patterson, Joseph Kochmanski, Anna C Stoll, et al.
Clinical Genetics|March 26, 2018
Wiedemann-Steiner syndrome as a major cause of syndromic intellectual disability: A study of 33 French casesS Baer, A Afenjar, T Smol, et al.
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