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X-linked myotubular myopathy mimics hereditary spastic paraplegia in two female manifesting carriers of pathogenic MTM1 variant
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Published in European journal of medical genetics (01.11.2020)
Published in European journal of medical genetics (01.11.2020)
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Exploring Spinal Cord Protection by Remote Ischemic Preconditioning: An Experimental Study
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Biallelic loss-of-function P4HTM gene variants cause hypotonia, hypoventilation, intellectual disability, dysautonomia, epilepsy, and eye abnormalities (HIDEA syndrome)
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The terminal prostaglandin synthases mPGES-1, mPGES-2, and cPGES are all overexpressed in human gliomas
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Encephalopsin (OPN3) protein abundance in the adult mouse brain
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Published in Journal of Comparative Physiology (01.11.2012)
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The distribution of melanopsin (OPN4) protein in the human brain
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Published in Chronobiology international (02.01.2017)
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Neonatal Alexander Disease: Novel GFAP Mutation and Comparison to Previously Published Cases
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Published in Neuropediatrics (01.08.2018)
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Published in BMC neurology (18.05.2017)
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Neuropathological characterization of two siblings carrying the MAPT S305S mutation demonstrates features resembling argyrophilic grain disease
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Published in Acta neuropathologica (01.02.2014)
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Prostatic acid phosphatase is not a prostate specific target
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Immunohistochemical Analysis of the Spinal Cord Ischemia- Effect of Remote Ischemic Preconditioning in a Porcine Model
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Tuppurainen, Karoliina, Mäkinen, Johanna M, Junttila, Oili, Liakka, Annikki, Kyllönen, Atte P, Tuominen, Hannu, Karttunen, Tuomo J, Mäkinen, Markus J
Published in The Journal of pathology (01.11.2005)
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Published in Molecular genetics & genomic medicine (01.09.2020)
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