Publications by authors named "Satu Sandell"

Claim this Profile
D
Discontinuation of carbamazepine due to concerns of long-term consequences of enzyme induction.
Jussi Mäkinen, Sirpa Rainesalo, Jani Raitanen, Jukka Saarinen, Satu Sandell

Epilepsia Open· September 2018

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
P
Pain in SCN4A Mutated P.A1156T muscle sodium channelopathy-a postal survey.
Kimmo Suokas, Johanna Palmio, Satu Sandell, Bjarne Udd, Aki Hietaharju

Muscle Nerve· June 2018

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
D
Distal myopathies in Finnish patients.
Johanna Palmio, Manu Jokela, Satu Sandell, Tiina Suominen, Sini Penttilä

Duodecim· January 2018

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
C
Critical neural targets for (the level of) human consciousness: Arousal arrest and unconsciousness after sumatriptan administration.
Jaakko W Långsjö, Kai Lehtimäki, Jyrki Ruohonen, Anne Sajanti, Satu Sandell

Brain Inj· January 2018

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
P
Predominantly myalgic phenotype caused by the c.3466G>A p.A1156T mutation in gene.
Johanna Palmio, Satu Sandell, Michael G Hanna, Roope Männikkö, Sini Penttilä

Neurology· April 2017

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
mutations and motor neuron disease: the distribution in Finnish patients.
Sini Penttilä, Manu Jokela, Anna Maija Saukkonen, Jari Toivanen, Johanna Palmio, Satu Sandell

J Neurol Neurosurg Psychiatry· March 2017

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
U
Unique Exercise Lactate Profile in Muscle Phosphofructokinase Deficiency (Tarui Disease); Difference Compared with McArdle Disease.
Päivi Piirilä, Minna E Similä, Johanna Palmio, Tomi Wuorimaa, Emil Ylikallio, Satu Sandell

Front Neurol· June 2016

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
D
Diagnostically important muscle pathology in DNAJB6 mutated LGMD1D.
Satu Sandell, Sanna Huovinen, Johanna Palmio, Olayinka Raheem, Mikaela Lindfors

Acta Neuropathol Commun· February 2016

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
N
Novel mutations in DNAJB6 gene cause a very severe early-onset limb-girdle muscular dystrophy 1D disease.
Johanna Palmio, Per Harald Jonson, Anni Evilä, Mari Auranen, Volker Straub, Satu Sandell

Neuromuscul Disord· November 2015

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
S
Spontaneous activity in electromyography may differentiate certain benign lower motor neuron disease forms from amyotrophic lateral sclerosis.
Manu E Jokela, Satu K Jääskeläinen, Satu Sandell, Johanna Palmio, Sini Penttilä

J Neurol Sci· August 2015

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
P
PFKM gene defect and glycogen storage disease GSDVII with misleading enzyme histochemistry.
Mari Auranen, Johanna Palmio, Emil Ylikallio, Sanna Huovinen, Anders Paetau, Satu Sandell

Neurol Genet· June 2015

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
Atypical phenotypes in titinopathies explained by second titin mutations.
Anni Evilä, Anna Vihola, Jaakko Sarparanta, Olayinka Raheem, Johanna Palmio, Satu Sandell

Ann Neurol· February 2014

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
[
[The expanding spectrum of LGMD--recently discovered disease genes are important also in Finnish patients].
Manu Jokela, Johanna Palmio, Satu Sandell, Sini Penttilä, Tiina Suominen

Duodecim· December 2013

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
N
New immunohistochemical method for improved myotonia and chloride channel mutation diagnostics.
Olayinka Raheem, Sini Penttilä, Tiina Suominen, Mika Kaakinen, James Burge, Satu Sandell

Neurology· November 2012

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
M
Mutations affecting the cytoplasmic functions of the co-chaperone DNAJB6 cause limb-girdle muscular dystrophy.
Jaakko Sarparanta, Per Harald Jonson, Christelle Golzio, Satu Sandell, Helena Luque

Nat Genet· February 2012

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
D
Distinct distal myopathy phenotype caused by VCP gene mutation in a Finnish family.
Johanna Palmio, Satu Sandell, Tiina Suominen, Sini Penttilä, Olayinka Raheem

Neuromuscul Disord· August 2011

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
F
Four new Finnish families with LGMD1D; refinement of the clinical phenotype and the linked 7q36 locus.
Peter Hackman, Satu Sandell, Jaakko Sarparanta, Helena Luque, Sanna Huovinen

Neuromuscul Disord· May 2011

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
T
The enigma of 7q36 linked autosomal dominant limb girdle muscular dystrophy.
Satu Sandell, Sanna Huovinen, Jaakko Sarparanta, Helena Luque, Olayinka Raheem

J Neurol Neurosurg Psychiatry· August 2010

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis