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M Auranen

Showing results (1-10 of 14) with videos related to

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Duodecim; Laaketieteellinen Aikakauskirja|January 1, 1997
[Gene errors in muscular diseases]H Somer, M Auranen
Duodecim; Laaketieteellinen Aikakauskirja|May 23, 2002
[First gene connected to autism spectrum disorders has been found]M Auranen, R Vanhala, I Järvelä
Kidney International|September 29, 2001
Further evidence for linkage of autosomal-dominant medullary cystic kidney disease on chromosome 1q21M Auranen, S Ala-Mello, J A Turunen, et al.
Molecular Psychiatry|July 13, 2000
Analysis of autism susceptibility gene loci on chromosomes 1p, 4p, 6q, 7q, 13q, 15q, 16p, 17q, 19q and 22q in Finnish multiplex familiesM Auranen, T Nieminen, S Majuri, et al.
Annals of Neurology|May 11, 2000
X-linked vacuolar myopathies: two separate loci and refined genetic mappingM Auranen, M Villanova, F Muntoni, et al.
Neurology|March 14, 2001
MECP2 gene analysis in classical Rett syndrome and in patients with Rett-like featuresM Auranen, R Vanhala, M Vosman, et al.
Molecular Psychiatry|September 30, 2003
Evidence for allelic association on chromosome 3q25-27 in families with autism spectrum disorders originating from a subisolate of FinlandM Auranen, T Varilo, R Alen, et al.
Neuromuscular Disorders : NMD|April 24, 2017
Patient with multiple acyl-CoA dehydrogenation deficiency disease and FLAD1 mutations benefits from riboflavin therapyM Auranen, A Paetau, P Piirilä, et al.
Acta Neurologica Scandinavica|July 31, 2015
Intrafamilial clinical variability in individuals carrying the CHCHD10 mutation Gly66ValP Pasanen, L Myllykangas, M Pöyhönen, et al.
Neuromuscular Disorders : NMD|March 11, 2000
Muscle membrane-skeleton protein changes and histopathological characterization of muscle-eye-brain diseaseM Auranen, J Rapola, H Pihko, et al.
Pageof 2

Showing results (1-10 of 14) with videos related to

Sort By:
Pageof 2
Duodecim; Laaketieteellinen Aikakauskirja|January 1, 1997
[Gene errors in muscular diseases]H Somer, M Auranen
Duodecim; Laaketieteellinen Aikakauskirja|May 23, 2002
[First gene connected to autism spectrum disorders has been found]M Auranen, R Vanhala, I Järvelä
Kidney International|September 29, 2001
Further evidence for linkage of autosomal-dominant medullary cystic kidney disease on chromosome 1q21M Auranen, S Ala-Mello, J A Turunen, et al.
Molecular Psychiatry|July 13, 2000
Analysis of autism susceptibility gene loci on chromosomes 1p, 4p, 6q, 7q, 13q, 15q, 16p, 17q, 19q and 22q in Finnish multiplex familiesM Auranen, T Nieminen, S Majuri, et al.
Annals of Neurology|May 11, 2000
X-linked vacuolar myopathies: two separate loci and refined genetic mappingM Auranen, M Villanova, F Muntoni, et al.
Neurology|March 14, 2001
MECP2 gene analysis in classical Rett syndrome and in patients with Rett-like featuresM Auranen, R Vanhala, M Vosman, et al.
Molecular Psychiatry|September 30, 2003
Evidence for allelic association on chromosome 3q25-27 in families with autism spectrum disorders originating from a subisolate of FinlandM Auranen, T Varilo, R Alen, et al.
Neuromuscular Disorders : NMD|April 24, 2017
Patient with multiple acyl-CoA dehydrogenation deficiency disease and FLAD1 mutations benefits from riboflavin therapyM Auranen, A Paetau, P Piirilä, et al.
Acta Neurologica Scandinavica|July 31, 2015
Intrafamilial clinical variability in individuals carrying the CHCHD10 mutation Gly66ValP Pasanen, L Myllykangas, M Pöyhönen, et al.
Neuromuscular Disorders : NMD|March 11, 2000
Muscle membrane-skeleton protein changes and histopathological characterization of muscle-eye-brain diseaseM Auranen, J Rapola, H Pihko, et al.
Pageof 2