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Biochimica Et Biophysica Acta|August 16, 2006
The neuronal ceroid-lipofuscinoses: from past to presentMatti HaltiaJournal of Neuropathology and Experimental Neurology|January 17, 2003
The neuronal ceroid-lipofuscinosesMatti HaltiaHandbook of Clinical Neurology|August 13, 2013
Hereditary gelsolin amyloidosisSari Kiuru-Enari, Matti HaltiaBiochimica Et Biophysica Acta|September 11, 2012
The neuronal ceroid-lipofuscinoses: a historical introductionMatti Haltia, Hans H GoebelDuodecim; Laaketieteellinen Aikakauskirja|July 6, 2010
[Hereditary gelsolin amyloidosis--40 years of Meretoja disease]Sari Kiuru-Enari, Matti HaltiaJournal of Neuropathology and Experimental Neurology|June 20, 2002
Neuromuscular pathology in hereditary gelsolin amyloidosisSari Kiuru-Enari, Hannu Somer, Anna-Maria Seppäläinen, et al.Brain Pathology (Zurich, Switzerland)|December 21, 2004
Hippocampal pathology in the human neuronal ceroid-lipofuscinoses: distinct patterns of storage deposition, neurodegeneration and glial activationJaana Tyynelä, Jonathan D Cooper, M Nadeem Khan, et al.Brain : a Journal of Neurology|May 4, 2006
Cathepsin D deficiency underlies congenital human neuronal ceroid-lipofuscinosisEija Siintola, Sanna Partanen, Petter Strömme, et al.The Journal of Experimental Medicine|August 20, 2003
DAP12/TREM2 deficiency results in impaired osteoclast differentiation and osteoporotic featuresJuha Paloneva, Jami Mandelin, Anna Kiialainen, et al.Journal of the Neurological Sciences|February 5, 2004
Neuropsychological functions in variant Alzheimer's disease with spastic paraparesisAuli Verkkoniemi, Raija Ylikoski, Juha O Rinne, et al.Pageof 2