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Investigating the Causes of the Response of the Thermohaline Circulation to Past and Future Climate Changes

Journal of climate, 2006-04, Vol.19 (8), p.1365-1387

2006

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The pathological basis of temporal lobe epilepsy in childhood

Neurology, 2003-01, Vol.60 (2), p.191-195

2003

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Vulnerable neuronal subsets in Alzheimer's and Pick's disease are distinguished by their τ isoform distribution and phosphorylation

Annals of neurology, 1998-02, Vol.43 (2), p.193-204

1998

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Warming of the subpolar Atlantic triggered by freshwater discharge at the continental boundary

Geophysical research letters, 2007-08, Vol.34 (15), p.L15604-n/a

2007

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A novel autosomal recessive limb-girdle muscular dystrophy with quadriceps atrophy maps to 11p13–p12

Brain (London, England : 1878), 2007-02, Vol.130 (2), p.368-380

2007

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Cellular distribution of insulin-like growth factor-II/mannose-6-phosphate receptor in normal human brain and its alteration in Alzheimer's disease pathology

Neurobiology of aging, 2006-02, Vol.27 (2), p.199-210

2006

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Changes in fall-related mortality in older adults in Quebec, 1981-2009

Chronic diseases and injuries in Canada, 2013-09, Vol.33 (4), p.226-235

2013

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Surface characteristics, equipment height, and the occurrence and severity of playground injuries

Injury prevention, 2001-03, Vol.7 (1), p.35-40

2001

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Founder Mutation for α-sarcoglycan-LGMD2D in a Magdalen Islands Acadian Cluster

Canadian journal of neurological sciences, 2011-09, Vol.38 (5), p.747-752

2011

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Long term effects of a home visit to prevent childhood injury: three year follow up of a randomized trial

Injury prevention, 2005-04, Vol.11 (2), p.106-109

2005

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Pituitary choriocarcinoma in an adolescent male: Tumor-derived CG and GH delay diagnosis

Growth hormone & IGF research, 2011-06, Vol.21 (3), p.181-184

2011

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A new form of congenital muscular dystrophy with joint hyperlaxity maps to 3p23-21

Brain (London, England : 1878), 2006-08, Vol.129 (8), p.2077-2084

2006

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Fetal magnetic resonance imaging in the prenatal diagnosis of cerebellar hemorrhage

Ultrasound in obstetrics & gynecology, 2006-01, Vol.27 (1), p.78-80

2006

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Insulin-like growth factor-I and its receptor in the frontal cortex, hippocampus, and cerebellum of normal human and Alzheimer disease brains

Synapse (New York, N.Y.), 2000-12, Vol.38 (4), p.450-459

2000

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Comparative Alterations of Nicotinic and Muscarinic Binding Sites in Alzheimer's and Parkinson's Diseases

Journal of neurochemistry, 1992-02, Vol.58 (2), p.529-541

1992

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Early childhood prolonged febrile convulsions, atrophy and sclerosis of mesial structures, and temporal lobe epilepsy: an MRI volumetric study

Neurology, 1993-06, Vol.43 (6), p.1083-1083

1993

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O.23 Anoctamin 5 (ANO5) subcellular localization in skeletal muscle

Neuromuscular disorders : NMD, 2011-10, Vol.21 (9), p.750-751

2011

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P27 Pituitary choriocarcinoma in an adolescent: tumor-derived CG and GHv delay presentation

Growth hormone & IGF research, 2010, Vol.20, p.S49-S49

2010

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Validation of sub-grid-scale mixing schemes using CFCs in a global ocean model

Geophysical research letters, 1995-11, Vol.22 (21), p.2917-2920

1995

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Atrophy of mesial structures in patients with temporal lobe epilepsy: Cause or consequence of repeated seizures?

Annals of neurology, 1993-12, Vol.34 (6), p.795-801

1993

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Chronic encephalitis and epilepsy in adults and adolescents: a variant of Rasmussen's syndrome?

Neurology, 1997-02, Vol.48 (2), p.418-424

1997

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O.9 Recessive mutations in the putative calcium-activated chloride channel Anoctamin 5 cause proximal LGMD2L and distal MMD3 muscular dystrophies

Neuromuscular disorders : NMD, 2010-10, Vol.20 (9), p.637-637

2010

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Double pathology in Rasmussen's syndrome: a window on the etiology?

Neurology, 1998-03, Vol.50 (3), p.731-735

1998

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LRPPRC mutations cause a phenotypically distinct form of Leigh syndrome with cytochrome c oxidase deficiency

Journal of medical genetics, 2011-03, Vol.48 (3), p.183-189

2011

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P13 Identification of a novel group of muscular dystrophies, the Anoctaminopathies, caused by recessive mutations in the putative calcium activated chloride channel, ANO5

Neuromuscular disorders : NMD, 2010, Vol.20, p.S8-S8

2010

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Investigating the Causes of the Response of the Thermohaline Circulation to Past and Future Climate Changes

The pathological basis of temporal lobe epilepsy in childhood

Vulnerable neuronal subsets in Alzheimer's and Pick's disease are distinguished by their τ isoform distribution and phosphorylation

Warming of the subpolar Atlantic triggered by freshwater discharge at the continental boundary

A novel autosomal recessive limb-girdle muscular dystrophy with quadriceps atrophy maps to 11p13–p12

Cellular distribution of insulin-like growth factor-II/mannose-6-phosphate receptor in normal human brain and its alteration in Alzheimer's disease pathology

Changes in fall-related mortality in older adults in Quebec, 1981-2009

Surface characteristics, equipment height, and the occurrence and severity of playground injuries

Founder Mutation for α-sarcoglycan-LGMD2D in a Magdalen Islands Acadian Cluster

Long term effects of a home visit to prevent childhood injury: three year follow up of a randomized trial

Pituitary choriocarcinoma in an adolescent male: Tumor-derived CG and GH delay diagnosis

A new form of congenital muscular dystrophy with joint hyperlaxity maps to 3p23-21

Fetal magnetic resonance imaging in the prenatal diagnosis of cerebellar hemorrhage

Insulin-like growth factor-I and its receptor in the frontal cortex, hippocampus, and cerebellum of normal human and Alzheimer disease brains

Comparative Alterations of Nicotinic and Muscarinic Binding Sites in Alzheimer's and Parkinson's Diseases

Early childhood prolonged febrile convulsions, atrophy and sclerosis of mesial structures, and temporal lobe epilepsy: an MRI volumetric study

O.23 Anoctamin 5 (ANO5) subcellular localization in skeletal muscle

P27 Pituitary choriocarcinoma in an adolescent: tumor-derived CG and GHv delay presentation

Validation of sub-grid-scale mixing schemes using CFCs in a global ocean model

Atrophy of mesial structures in patients with temporal lobe epilepsy: Cause or consequence of repeated seizures?

Chronic encephalitis and epilepsy in adults and adolescents: a variant of Rasmussen's syndrome?

O.9 Recessive mutations in the putative calcium-activated chloride channel Anoctamin 5 cause proximal LGMD2L and distal MMD3 muscular dystrophies

Double pathology in Rasmussen's syndrome: a window on the etiology?

LRPPRC mutations cause a phenotypically distinct form of Leigh syndrome with cytochrome c oxidase deficiency

P13 Identification of a novel group of muscular dystrophies, the Anoctaminopathies, caused by recessive mutations in the putative calcium activated chloride channel, ANO5

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