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Neuropediatrics
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August 26, 2004
Congenital myasthenic syndrome due to rapsyn deficiency: three cases with arthrogryposis and bulbar symptoms
C Ioos, A Barois, P Richard, et al.
Biomedicine & Pharmacotherapy = Biomedecine & Pharmacotherapie
|
January 1, 1994
Serine proteases and their serpin inhibitors in Alzheimer's disease
G J Ho, I V Smirnova, M Akaaboune, et al.
Comptes Rendus Des Seances De La Societe De Biologie Et De Ses Filiales
|
January 1, 1994
[Muscular reconstruction by myogenic cell graft]
H Alameddine, M Dehaupas, J P Louboutin, et al.
Neuro-Chirurgie
|
February 13, 2009
[Experimental and pathological changes of the neuromuscular junction]
J Koenig, S Bauché, A Ben Ammar, et al.
The Journal of Comparative Neurology
|
August 12, 1998
Developmental regulation of the serpin, protease nexin I, localization during activity-dependent polyneuronal synapse elimination in mouse skeletal muscle
M Akaaboune, D Hantaï, I Smirnova, et al.
Neuro-Chirurgie
|
February 24, 2009
[Structural and molecular organization, development and maturation of the neuromuscular junction]
P Rigoard, K Buffenoir, S Bauche, et al.
Experimental Cell Research
|
February 13, 2001
Thrombin receptor induction by injury-related factors in human skeletal muscle cells
C Mbebi, T Rohn, M A Doyennette, et al.
Molecular and Cellular Neurosciences
|
June 14, 2000
Developmental regulation of amyloid precursor protein at the neuromuscular junction in mouse skeletal muscle
M Akaaboune, B Allinquant, H Farza, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
March 18, 2009
Novel epsilon subunit mutation of the muscle acetylcholine receptor causing a slow-channel congenital myasthenic syndrome
O Outteryck, P Richard, A Lacour, et al.
Journal of the Neurological Sciences
|
May 1, 1995
Beneficial effects of insulin-like growth factor-I on wobbler mouse motoneuron disease
D Hantaï, M Akaaboune, C Lagord, et al.
Page
of 6
Search research articles
Search
Showing results (31-40 of 51) with videos related to
Sort By:
Page
of 6
Neuropediatrics
|
August 26, 2004
Congenital myasthenic syndrome due to rapsyn deficiency: three cases with arthrogryposis and bulbar symptoms
C Ioos, A Barois, P Richard, et al.
Biomedicine & Pharmacotherapy = Biomedecine & Pharmacotherapie
|
January 1, 1994
Serine proteases and their serpin inhibitors in Alzheimer's disease
G J Ho, I V Smirnova, M Akaaboune, et al.
Comptes Rendus Des Seances De La Societe De Biologie Et De Ses Filiales
|
January 1, 1994
[Muscular reconstruction by myogenic cell graft]
H Alameddine, M Dehaupas, J P Louboutin, et al.
Neuro-Chirurgie
|
February 13, 2009
[Experimental and pathological changes of the neuromuscular junction]
J Koenig, S Bauché, A Ben Ammar, et al.
The Journal of Comparative Neurology
|
August 12, 1998
Developmental regulation of the serpin, protease nexin I, localization during activity-dependent polyneuronal synapse elimination in mouse skeletal muscle
M Akaaboune, D Hantaï, I Smirnova, et al.
Neuro-Chirurgie
|
February 24, 2009
[Structural and molecular organization, development and maturation of the neuromuscular junction]
P Rigoard, K Buffenoir, S Bauche, et al.
Experimental Cell Research
|
February 13, 2001
Thrombin receptor induction by injury-related factors in human skeletal muscle cells
C Mbebi, T Rohn, M A Doyennette, et al.
Molecular and Cellular Neurosciences
|
June 14, 2000
Developmental regulation of amyloid precursor protein at the neuromuscular junction in mouse skeletal muscle
M Akaaboune, B Allinquant, H Farza, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
March 18, 2009
Novel epsilon subunit mutation of the muscle acetylcholine receptor causing a slow-channel congenital myasthenic syndrome
O Outteryck, P Richard, A Lacour, et al.
Journal of the Neurological Sciences
|
May 1, 1995
Beneficial effects of insulin-like growth factor-I on wobbler mouse motoneuron disease
D Hantaï, M Akaaboune, C Lagord, et al.
Page
of 6