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Nature Genetics|May 10, 2000
Mutations in TFAP2B cause Char syndrome, a familial form of patent ductus arteriosusM Satoda, F Zhao, G A Diaz, et al.Journal of Medical Genetics|December 1, 1990
Alagille syndrome and deletion of 20pF Anad, J Burn, D Matthews, et al.Brain : a Journal of Neurology|June 16, 2001
The prevalence of progressive supranuclear palsy (Steele-Richardson-Olszewski syndrome) in the UKU Nath, Y Ben-Shlomo, R G Thomson, et al.Acta Gastro-Enterologica Belgica|September 1, 1995
The genetic background of familial adenomatous polyposis. Linkage analysis, the APC gene identification and mutation screeningA Kartheuser, S West, C Walon, et al.International Journal of Geriatric Psychiatry|August 15, 2006
Orthostatic hypotension in Parkinson's disease: association with cognitive decline?Liesl M Allcock, Rose Anne Kenny, Urs Peter Mosimann, et al.Neuroimage|November 6, 2004
The application of statistical parametric mapping to 123I-FP-CIT SPECT in dementia with Lewy bodies, Alzheimer's disease and Parkinson's diseaseSean J Colloby, John T O'Brien, John D Fenwick, et al.Molecules (Basel, Switzerland)|July 9, 2022
Lead Isotopic Constraints on the Provenance of Antarctic Dust and Atmospheric Circulation Patterns Prior to the Mid-Brunhes Event (~430 kyr ago)Changhee Han, Laurie J Burn, Paul Vallelonga, et al.American Journal of Human Genetics|November 1, 1992
Molecular genetic study of the frequency of monosomy 22q11 in DiGeorge syndromeA H Carey, D Kelly, S Halford, et al.International Journal of Geriatric Psychiatry|July 22, 2006
Cholinesterase inhibitors in advanced Dementia with Lewy bodies: increase or stop?Sanjeet Pakrasi, Alan Thomas, Urs P Mosimann, et al.Movement Disorders : Official Journal of the Movement Disorder Society|March 2, 2013
Short latency afferent inhibition: a biomarker for mild cognitive impairment in Parkinson's disease?Alison J Yarnall, Lynn Rochester, Mark R Baker, et al.Pageof 57