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M Penttinen

Showing results (11-20 of 37) with videos related to

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Acta Oto-Laryngologica|March 1, 1997
Syndecan-1: a new prognostic marker in laryngeal cancerJ O Pulkkinen, M Penttinen, M Jalkanen, et al.
Duodecim; Laaketieteellinen Aikakauskirja|January 1, 1989
[Fabry's disease--a polymorphic generalized disease]E Nikoskelainen, M Penttinen, E Lindahl, et al.
Prenatal Diagnosis|July 27, 1999
Prenatal diagnosis of variant late infantile neuronal ceroid lipofuscinosis (vLINCL[Finnish]; CLN5)J Rapola, J Lähdetie, J Isosomppi, et al.
American Journal of Medical Genetics|March 17, 1997
New progeroid disorderM Penttinen, K M Niemi, H Vinkka-Puhakka, et al.
Human Mutation|January 1, 1997
Tissue distribution of the ND4/11778 mutation in heteroplasmic lineages with Leber hereditary optic neuropathyV Juvonen, E Nikoskelainen, T Lamminen, et al.
The Journal of Endocrinology|May 16, 2014
α-MSH overexpression in the nucleus tractus solitarius decreases fat mass and elevates heart rateK Eerola, P Rinne, A M Penttinen, et al.
Duodecim; Laaketieteellinen Aikakauskirja|January 1, 1997
[Infant sleep apnea behind the life threatening cyanotic episodes, a good response to cpap treatment]T Kirjavainen, J Kirjavainen, O Polo, et al.
British Journal of Rheumatology|December 31, 1997
IgM, IgG and IgA class enterobacterial antibodies in serum and synovial fluid in patients with ankylosing spondylitis and rheumatoid arthritisO Mäki-Ikola, M Penttinen, R Von Essen, et al.
Human Mutation|April 11, 2001
The mutation spectrum of the EDA gene in X-linked anhidrotic ectodermal dysplasiaK Pääkkönen, S Cambiaghi, G Novelli, et al.
Annals of Neurology|September 8, 2000
Clinical and genetic findings in Finnish ataxia patients with the spinocerebellar ataxia 8 repeat expansionV Juvonen, M Hietala, M Päivärinta, et al.
Pageof 4

Showing results (11-20 of 37) with videos related to

Sort By:
Pageof 4
Acta Oto-Laryngologica|March 1, 1997
Syndecan-1: a new prognostic marker in laryngeal cancerJ O Pulkkinen, M Penttinen, M Jalkanen, et al.
Duodecim; Laaketieteellinen Aikakauskirja|January 1, 1989
[Fabry's disease--a polymorphic generalized disease]E Nikoskelainen, M Penttinen, E Lindahl, et al.
Prenatal Diagnosis|July 27, 1999
Prenatal diagnosis of variant late infantile neuronal ceroid lipofuscinosis (vLINCL[Finnish]; CLN5)J Rapola, J Lähdetie, J Isosomppi, et al.
American Journal of Medical Genetics|March 17, 1997
New progeroid disorderM Penttinen, K M Niemi, H Vinkka-Puhakka, et al.
Human Mutation|January 1, 1997
Tissue distribution of the ND4/11778 mutation in heteroplasmic lineages with Leber hereditary optic neuropathyV Juvonen, E Nikoskelainen, T Lamminen, et al.
The Journal of Endocrinology|May 16, 2014
α-MSH overexpression in the nucleus tractus solitarius decreases fat mass and elevates heart rateK Eerola, P Rinne, A M Penttinen, et al.
Duodecim; Laaketieteellinen Aikakauskirja|January 1, 1997
[Infant sleep apnea behind the life threatening cyanotic episodes, a good response to cpap treatment]T Kirjavainen, J Kirjavainen, O Polo, et al.
British Journal of Rheumatology|December 31, 1997
IgM, IgG and IgA class enterobacterial antibodies in serum and synovial fluid in patients with ankylosing spondylitis and rheumatoid arthritisO Mäki-Ikola, M Penttinen, R Von Essen, et al.
Human Mutation|April 11, 2001
The mutation spectrum of the EDA gene in X-linked anhidrotic ectodermal dysplasiaK Pääkkönen, S Cambiaghi, G Novelli, et al.
Annals of Neurology|September 8, 2000
Clinical and genetic findings in Finnish ataxia patients with the spinocerebellar ataxia 8 repeat expansionV Juvonen, M Hietala, M Päivärinta, et al.
Pageof 4