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Journal of Medical Genetics
|
July 17, 2008
Alteration of expression of muscle specific isoforms of the fragile X related protein 1 (FXR1P) in facioscapulohumeral muscular dystrophy patients
L Davidovic, S Sacconi, E G Bechara, et al.
Presse Medicale (Paris, France : 1983)
|
March 3, 1990
[An unusual association of myasthenia and T8 lymphoid leukemia]
G Kaplanski, C Desnuelle, J R Harle, et al.
Genomics
|
September 23, 1997
Cloning and expression analysis of a meiosis-specific MutS homolog: the human MSH4 gene
V Paquis-Flucklinger, S Santucci-Darmanin, R Paul, et al.
Revue Neurologique
|
January 1, 1991
[Slowly progressive myopathy with accumulation of tubular aggregates]
D Figarella-Branger, J F Pellissier, A M Perez-Castillo, et al.
Revue Neurologique
|
January 14, 2014
[Efficacy of autologous peripheral blood stem cell transplantation (auto-PBSCT) on the neuropathic manifestations in POEMS syndrome]
S Gronier, E Delmont, L Legros, et al.
La Revue De Medecine Interne
|
September 1, 1992
[Ptosis and asthenia manifesting a mitochondrial myopathy]
P Disdier, J R Harlé, D Figarella-Branger, et al.
Revue Neurologique
|
April 18, 2026
Treatment pathway, healthcare resource utilization and direct cost of ALS in France: A nationwide claims database study
C Desnuelle, P Couratier, P Corcia, et al.
The American Journal of Medicine
|
February 1, 1992
Polymyalgia rheumatica and mitochondrial myopathy: clinicopathologic and biochemical studies in five cases
J R Harle, J F Pellissier, C Desnuelle, et al.
Revue Neurologique
|
January 1, 1991
[Anomaly in the neurotransmitter amino acids in amyotrophic lateral sclerosis: a therapeutic application]
O Blin, C Desnuelle, C Guelton, et al.
Journees Annuelles De Diabetologie De L'Hotel-Dieu
|
January 1, 1997
[Detection and prevalence of mitochondrial genome mutations in diabetes]
V Paquis-Flucklinger, B Vialettes, B Canivet, et al.
Page
of 12
Search research articles
Search
Showing results (71-80 of 118) with videos related to
Sort By:
Page
of 12
Journal of Medical Genetics
|
July 17, 2008
Alteration of expression of muscle specific isoforms of the fragile X related protein 1 (FXR1P) in facioscapulohumeral muscular dystrophy patients
L Davidovic, S Sacconi, E G Bechara, et al.
Presse Medicale (Paris, France : 1983)
|
March 3, 1990
[An unusual association of myasthenia and T8 lymphoid leukemia]
G Kaplanski, C Desnuelle, J R Harle, et al.
Genomics
|
September 23, 1997
Cloning and expression analysis of a meiosis-specific MutS homolog: the human MSH4 gene
V Paquis-Flucklinger, S Santucci-Darmanin, R Paul, et al.
Revue Neurologique
|
January 1, 1991
[Slowly progressive myopathy with accumulation of tubular aggregates]
D Figarella-Branger, J F Pellissier, A M Perez-Castillo, et al.
Revue Neurologique
|
January 14, 2014
[Efficacy of autologous peripheral blood stem cell transplantation (auto-PBSCT) on the neuropathic manifestations in POEMS syndrome]
S Gronier, E Delmont, L Legros, et al.
La Revue De Medecine Interne
|
September 1, 1992
[Ptosis and asthenia manifesting a mitochondrial myopathy]
P Disdier, J R Harlé, D Figarella-Branger, et al.
Revue Neurologique
|
April 18, 2026
Treatment pathway, healthcare resource utilization and direct cost of ALS in France: A nationwide claims database study
C Desnuelle, P Couratier, P Corcia, et al.
The American Journal of Medicine
|
February 1, 1992
Polymyalgia rheumatica and mitochondrial myopathy: clinicopathologic and biochemical studies in five cases
J R Harle, J F Pellissier, C Desnuelle, et al.
Revue Neurologique
|
January 1, 1991
[Anomaly in the neurotransmitter amino acids in amyotrophic lateral sclerosis: a therapeutic application]
O Blin, C Desnuelle, C Guelton, et al.
Journees Annuelles De Diabetologie De L'Hotel-Dieu
|
January 1, 1997
[Detection and prevalence of mitochondrial genome mutations in diabetes]
V Paquis-Flucklinger, B Vialettes, B Canivet, et al.
Page
of 12