Novel presenilin 1 mutation with profound neurofibrillary pathology in an indigenous Southern African family with early‐onset Alzheimer’s disease

By Heckmann Jeannine M.  

Brain, Vol. 127, Iss. 1, 2004-01 ,pp. : 133-142

Oxford University Press

Access to resources Recommend Favorite

Prominent behavioural and psychiatric symptoms in early-onset Alzheimer’s disease in a sib pair with the presenilin-1 gene R269G mutation

By Doran M.   Larner A.  

European Archives of Psychiatry and Clinical Neuroscience, Vol. 254, Iss. 3, 2004-06 ,pp. : 187-189

Springer Publishing Company

Access to resources Recommend Favorite

Presenilin 1 gene mutation (M139I) in a patient with an early-onset Alzheimer’s disease: clinical characteristics and genetic identification

By Kim Hee-Jin   Kim Hyun   Ki Chang-Seok   Kim Seung  

Neurological Sciences, Vol. 31, Iss. 6, 2010-12 ,pp. : 781-783

Springer Publishing Company

Access to resources Recommend Favorite

A case of atypical early-onset Alzheimer’s disease carrying the missense mutation Thr354Ile in exon 10 of the PSEN1 gene

By Marini Sandro   Lucidi Giulia   Tedde Andrea   Bessi Valentina   Nacmias Benedetta  

Neurological Sciences, Vol. 34, Iss. 9, 2013-09 ,pp. : 1691-1692

Springer Publishing Company

Access to resources Recommend Favorite

Late onset familial Alzheimer's disease: novel presenilin 2 mutation and PS1 E318G polymorphism

By Bernardi L.  

Journal of Neurology, Vol. 255, Iss. 4, 2008-04 ,pp. : 604-606

Springer Publishing Company

Access to resources Recommend Favorite