Results 181 to 190 of about 18,524 (210)
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Canadian Journal of Fisheries and Aquatic Sciences, 1983
The large difference between the alkalinity of the fresh waters of the St. Lawrence River (1.475 mmol∙kg−1) and the Saguenay River (0.134 mmol∙kg−1) was used to locate the region on the St. Lawrence estuary which is under the influence of the Saguenay River.
J. Lebel +4 more
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The large difference between the alkalinity of the fresh waters of the St. Lawrence River (1.475 mmol∙kg−1) and the Saguenay River (0.134 mmol∙kg−1) was used to locate the region on the St. Lawrence estuary which is under the influence of the Saguenay River.
J. Lebel +4 more
openaire +1 more source
Autosomal recessive spastic ataxia of Charlevoix–Saguenay
Neuromuscular Disorders, 1998A form of autosomal recessive spastic ataxia unique to the Charlevoix-Saguenay area was clinically identified 20 years ago in patients from that region. This region of Québec, Canada, was once considered a genetic isolate. First noted at gait initiation, signs of ataxia slowly progress along with spasticity of the four limbs, slurred speech, and ...
J P, Bouchard +6 more
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Variabilité génétique au Saguenay
1999Mémoire numérisé par la Direction des bibliothèques de l'Université de Montréal.
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1989
Aussi disponsible en francais: Séisme au ...
Allen, D. E., Maurenbrecher, A. H. P.
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Aussi disponsible en francais: Séisme au ...
Allen, D. E., Maurenbrecher, A. H. P.
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Spastic Ataxia, Charlevoix-Saguenay Type
2014Autosomal recessive spastic ataxia is a genetically heterogeneous group of complex neurodegenerative disorders usually characterized by early onset of cerebellar ataxia, dysarthria, pyramidal tract signs, and peripheral neuropathy; cognition is usually not affected.
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Autosomal recessive spastic ataxia of Charlevoix‐Saguenay
Neuropathology, 2006Autosomal recessive spastic ataxia of Charlevoix‐Saguenay (ARSACS) was originally found among the inhabitants of the Charlevoix‐Saguenay region of Quebec, Canada. This disease is characterized by early‐onset ataxia, spasticity, peripheral neuropathy, finger and foot deformities, and hypermyelination of the retinal nerve fibers.
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