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Results of search for 'au:"Raymackers, J M"'
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Authors
Ackermans, N
Bonnier, C
Boulanger, S
Celio, M R
Colson-Van Schoor, M
Cosnard, G
Davies, K E
De Backer, F
Debaix, H
Delpech, A
Duprez, T
Duprez, T P
Dupuis, M
Evrard, P
Fisher, R
Gailly, P
Gillis, J M
Gressens, P
Raymackers, J M
Schwaller, B
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Topics
Animals
Brain
Calcium
Female
Humans
Magnetic Resonance Imaging
Mice
Mice, Inbred mdx
Muscle Fibers, Fast-Twitch
Muscular Dystrophy, Duchenne
Mutation
Myosin Heavy Chains
Parvalbumins
Phenotype
Time Factors
complications
deficiency
genetics
metabolism
pathology
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English
Your search returned 7 results.
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1.
Hereditary axonal neuropathy related to MME gene mutation in a family with fetomaternal alloimmune glomerulonephritis.
[electronic resource]
by
Dupuis, M
Raymackers, J M
Ackermans, N
Boulanger, S
Verellen-Dumoulin, C
Producer:
20201026
In:
Acta neurologica Belgica
vol. 120
Online resources:
Available from publisher's website
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No items available.
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2.
Glycine antagonist and NO synthase inhibitor protect the developing mouse brain against neonatal excitotoxic lesions.
[electronic resource]
by
Marret, S
Bonnier, C
Raymackers, J M
Delpech, A
Evrard, P
Gressens, P
Producer:
19990622
In:
Pediatric research
vol. 45
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Available from publisher's website
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3.
Resolution of early diffusion-weighted and FLAIR MRI abnormalities in a patient with TIA.
[electronic resource]
by
Lecouvet, F E
Duprez, T P
Raymackers, J M
Peeters, A
Cosnard, G
Producer:
19990506
In:
Neurology
vol. 52
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4.
Discrepant time course of cranial and spinal subdural collections in a case of SIH treated by EBP.
[electronic resource]
by
Raymackers, J M
Duprez, T
Jeanjean, A
Le Polain de Waroux, B
Sindic, C J
Producer:
20020715
In:
European radiology
vol. 11
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5.
Prevention of pathology in mdx mice by expression of utrophin: analysis using an inducible transgenic expression system.
[electronic resource]
by
Squire, S
Raymackers, J M
Vandebrouck, C
Potter, A
Tinsley, J
Fisher, R
Gillis, J M
Davies, K E
Producer:
20030711
In:
Human molecular genetics
vol. 11
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6.
Tetanus relaxation of fast skeletal muscles of the mouse made parvalbumin deficient by gene inactivation.
[electronic resource]
by
Raymackers, J M
Gailly, P
Schoor, M C
Pette, D
Schwaller, B
Hunziker, W
Celio, M R
Gillis, J M
Producer:
20001107
In:
The Journal of physiology
vol. 527 Pt 2
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7.
Consequence of parvalbumin deficiency in the mdx mouse: histological, biochemical and mechanical phenotype of a new double mutant.
[electronic resource]
by
Raymackers, J M
Debaix, H
Colson-Van Schoor, M
De Backer, F
Tajeddine, N
Schwaller, B
Gailly, P
Gillis, J M
Producer:
20031006
In:
Neuromuscular disorders : NMD
vol. 13
Online resources:
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