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Journal of Neuroimmunology|September 4, 2013
Immunological perspectives of temporal lobe seizuresSuvi Liimatainen, Kai Lehtimäki, Lehtimäki Kai, et al.Neuromuscular Disorders : NMD|March 8, 2011
Four new Finnish families with LGMD1D; refinement of the clinical phenotype and the linked 7q36 locusPeter Hackman, Satu Sandell, Jaakko Sarparanta, et al.Journal of Neurology|March 3, 2022
Comprehensive transcriptomic analysis shows disturbed calcium homeostasis and deregulation of T lymphocyte apoptosis in inclusion body myositisMridul Johari, Anna Vihola, Johanna Palmio, et al.The American Journal of Pathology|June 8, 2014
Abnormal splicing of NEDD4 in myotonic dystrophy type 2: possible link to statin adverse reactionsMark Screen, Per Harald Jonson, Olayinka Raheem, et al.American Journal of Human Genetics|January 19, 2024
The shared ancestry between the C9orf72 hexanucleotide repeat expansion and intermediate-length alleles using haplotype sharing trees and HAPTKOsma S Rautila, Karri Kaivola, Harri Rautila, et al.Neurology. Genetics|April 12, 2016
PFKM gene defect and glycogen storage disease GSDVII with misleading enzyme histochemistryMari Auranen, Johanna Palmio, Emil Ylikallio, et al.Annals of Medicine|June 28, 2023
Risk of vascular diseases in patients with dermatitis herpetiformis and coeliac disease: a long-term cohort studyNoora Nilsson, Joonas Leivo, Pekka Collin, et al.Scandinavian Journal of Gastroenterology|February 28, 2026
Cohort study of neurological and psychiatric morbidity in dermatitis herpetiformis and celiac diseaseNoora Nilsson, Teea Salmi, Merja Viikki, et al.Frontiers in Neurology|June 16, 2016
Unique Exercise Lactate Profile in Muscle Phosphofructokinase Deficiency (Tarui Disease); Difference Compared with McArdle DiseasePäivi Piirilä, Minna E Similä, Johanna Palmio, et al.Neurology|March 3, 2019
Myasthenic congenital myopathy from recessive mutations at a single residue in NaV1.4Nathaniel Elia, Johanna Palmio, Marisol Sampedro Castañeda, et al.Pageof 7