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Journal of the Neurological Sciences|December 19, 2008
Derivation and validation of diagnostic criteria for chronic inflammatory demyelinating polyneuropathyC L Koski, M Baumgarten, L S Magder, et al.
Physics in Medicine and Biology|September 20, 2022
Accurate measures of changes in regional lung air volumes from chest x-rays of small animalsD W O'Connell, K S Morgan, G Ruben, et al.
Neurology|January 26, 2005
Distal symmetric polyneuropathy: a definition for clinical research: report of the American Academy of Neurology, the American Association of Electrodiagnostic Medicine, and the American Academy of Physical Medicine and RehabilitationJ D England, G S Gronseth, G Franklin, et al.
Muscle & Nerve|November 13, 2004
Distal symmetrical polyneuropathy: definition for clinical researchJ D England, G S Gronseth, G Franklin, et al.
Ophthalmic Genetics|January 23, 2002
Evaluation of the ELOVL4 gene in patients with age-related macular degenerationR Ayyagari, K Zhang, A Hutchinson, et al.
Nature Genetics|March 1, 1997
A photoreceptor cell-specific ATP-binding transporter gene (ABCR) is mutated in recessive Stargardt macular dystrophyR Allikmets, N Singh, H Sun, et al.
Human Mutation|October 1, 2003
Genotyping microarray (gene chip) for the ABCR (ABCA4) geneK Jaakson, J Zernant, M Külm, et al.
PM & R : the Journal of Injury, Function, and Rehabilitation|July 25, 2009
Practice parameter: the evaluation of distal symmetric polyneuropathy: the role of autonomic testing, nerve biopsy, and skin biopsy (an evidence-based review). Report of the American Academy of Neurology, the American Association of Neuromuscular and Electrodiagnostic Medicine, and the American Academy of Physical Medicine and RehabilitationJ D England, G S Gronseth, G Franklin, et al.
Muscle & Nerve|December 18, 2008
Evaluation of distal symmetric polyneuropathy: the role of autonomic testing, nerve biopsy, and skin biopsy (an evidence-based review)J D England, G S Gronseth, G Franklin, et al.
Molecular Syndromology|December 23, 2011
Mutations in SDCCAG8/NPHP10 Cause Bardet-Biedl Syndrome and Are Associated with Penetrant Renal Disease and Absent PolydactylyE Schaefer, A Zaloszyc, J Lauer, et al.
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