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Applied Optics|March 25, 2008
Heiligenschein and related phenomena in divergent lightJ O Mattsson, L BärringJournal of Neural Transmission. Parkinson'S Disease and Dementia Section|January 1, 1993
Screening of amyloid precursor protein gene mutation (APP 717 Val-->Ile) in Swedish families with Alzheimer's diseaseE Almqvist, S Lake, K Axelman, et al.Clinical Genetics|March 22, 2001
The "flap" endonuclease gene FEN1 is excluded as a candidate gene implicated in the CAG repeat expansion underlying Huntington diseaseC J Otto, E Almqvist, M R Hayden, et al.American Journal of Human Genetics|May 1, 1997
The likelihood of being affected with Huntington disease by a particular age, for a specific CAG sizeR R Brinkman, M M Mezei, J Theilmann, et al.The British Journal of Surgery|May 28, 2011
Cohort study of patients with adrenal lesions discovered incidentallyA Muth, L Hammarstedt, M Hellström, et al.Neuroscience Letters|April 16, 1993
Low frequency of the APP 670/671 mutation in familial Alzheimer's disease in SwedenL Lannfelt, M Viitanen, K Johansson, et al.Journal of Neural Transmission. Parkinson'S Disease and Dementia Section|January 1, 1994
A comparison of multiplex and simplex families with Alzheimer's disease/senile dementia of Alzheimer type within a well defined populationI Alafuzoff, E Almqvist, R Adolfsson, et al.American Journal of Medical Genetics|January 24, 1998
Reactions to predictive testing in Huntington disease: case reports of coping with a new genetic statusT B Wahlin, A Lundin, L Bäckman, et al.American Journal of Human Genetics|August 1, 1995
Sex-dependent mechanisms for expansions and contractions of the CAG repeat on affected Huntington disease chromosomesB Kremer, E Almqvist, J Theilmann, et al.Pageof 3