Results 131 to 140 of about 2,561 (186)
Some of the next articles are maybe not open access.

New findings in the ataxia of Charlevoix–Saguenay

Journal of Neurology, 2011
The aim of the study was to enhance our understanding of the pathogenesis of the ataxia of Charlevoix-Saguenay, based on the findings presented herein. Five patients with a molecular diagnosis of this disease underwent clinical, radiological, ophthalmologic and electrophysiological examinations.
José, Gazulla   +11 more
openaire   +2 more sources

Sill Processes in the Saguenay Fjord

2020
<p>The Saguenay Fjord is a 110 km long and 250 m deep (max depth) multi-silled glacial valley that connects the Saguenay River at its head with the St. Lawrence Estuary at its mouth. The bathymetry is characterized with 3 sills: a shallow 20-m deep sill at the mouth, an intermediate 60-m deep 20 km landward sill and a deep 120-m ...
Jérôme Guay   +5 more
openaire   +1 more source

Saguenay Risk Management

2017
The city of Saguenay, in the province of Quebec, is located in an area with a hilly topography and where sensitive marine clays are predominant. The slopes throughout the city are either former riverbanks or scarps of old large retrogressive landslides and their height can vary from a few meters to dozens of meters.
Janelle Potvin   +5 more
openaire   +1 more source

Le Panache du Saguenay

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
openaire   +1 more source

The Saguenay earthquake

1989
Aussi disponsible en francais: Séisme au ...
Allen, D. E., Maurenbrecher, A. H. P.
openaire   +1 more source

Autosomal recessive spastic ataxia of Charlevoix–Saguenay

Neuromuscular Disorders, 1998
A 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
openaire   +2 more sources

PSEUDODOMINANT INHERITANCE OF SPASTIC ATAXIA OF CHARLEVOIX-SAGUENAY

Neurology, 2010
Spastic ataxia of Charlevoix-Saguenay (ARSACS, MIM 270550) is an early-onset neurodegenerative disease characterized by mild to moderate early-onset ataxia, spastic paraparesis, sensory motor neuropathy in the lower limbs, and almost invariably atrophy of the upper cerebellar vermis on brain MRI.1 Autosomal recessively inherited mutations in SACS have ...
Terracciano, A.   +7 more
openaire   +3 more sources

Variabilité génétique au Saguenay

1999
Mémoire numérisé par la Direction des bibliothèques de l'Université de Montréal.
openaire   +1 more source

Mercury diagenesis in the Saguenay Fjord

2005
This item was digitized as part of a project to share McGill's intellectual legacy with the public. If you are the copyright holder or a relative of the copyright holder who is deceased, you may request withdrawal by emailing escholarship.library@mcgill.ca.
openaire   +1 more source

Autosomal recessive spastic ataxia of Charlevoix‐Saguenay

Neuropathology, 2006
Autosomal 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.
openaire   +2 more sources

Home - About - Disclaimer - Privacy