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Matti J. Haltia, MD

Affiliations: 
Pathology University of Helsinki, Helsingfors, Finland 
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http://research.med.helsinki.fi/neuro/Tienari/publications.htm

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Cross-listing: Neuropathology Tree

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Chen Z, Yan Yau W, Jaunmuktane Z, et al. (2020) Neuronal intranuclear inclusion disease is genetically heterogeneous. Annals of Clinical and Translational Neurology
Kiuru-Enari SMK, Haltia M. (2013) Hereditary gelsolin amyloidosis. Handbook of Clinical Neurology. 115: 659-681
Haltia M, Goebel HH. (2013) The neuronal ceroid-lipofuscinoses: a historical introduction. Biochimica Et Biophysica Acta. 1832: 1795-800
Airaksinen EM, Iivanainen M, Karli P, et al. (2009) Hereditary recurrent brachial plexus neuropathy with dysmorphic features. Acta Neurologica Scandinavica. 71: 309-316
Haltia M, Tarkkanen A, Somer H, et al. (2009) Neuronal intranuclear inclusion disease. Clinical ophthalmological features and ophthalmic pathology. Acta Ophthalmologica. 64: 637-643
Sulkava R, Haltia M, Paetau A, et al. (2009) Clinical And Neuropathological Features In Alzheimer'S Disease Acta Neurologica Scandinavica. 65: 294-295
Koskiniemi M, Donner M, Majuri H, et al. (2009) Progressive myoclonus epilepsy. A clinical and histopathological study. Acta Neurologica Scandinavica. 50: 307-332
Santavuori P, Haltia M, Rapola J. (2008) Infantile Type of So‐called Neuronal Ceroid‐lipofuscinosis Developmental Medicine & Child Neurology. 16: 644-653
Salonen R, Somer M, Haltia M, et al. (2008) Progressive encephalopathy with edema, hypsarrhythmia, and optic atrophy (PEHO syndrome). Clinical Genetics. 39: 287-293
Haltia M. (2006) The neuronal ceroid-lipofuscinoses: from past to present. Biochimica Et Biophysica Acta. 1762: 850-856
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