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Annals of the New York Academy of Sciences
|
December 10, 1999
The autosomal recessive form of CMT disease linked to 5q31-q33
A Guilbot, M Kessali, N Ravisé, et al.
Rheumatology (Oxford, England)
|
June 6, 2002
Renal microaneurysms in three cases of hepatitis C virus-related vasculitis
N Costedoat-Chalumeau, P Cacoub, T Maisonobe, et al.
Annals of the New York Academy of Sciences
|
November 1, 2017
The Autosomal Recessive Form of CMT Disease Linked to 5q31-q33
A Guilbot, M Kessali, N Ravisé, et al.
La Revue De Medecine Interne
|
June 17, 2018
[Acute myositis in a 53 year-old man]
C David, A Michon, A Passeron, et al.
Revue Neurologique
|
February 24, 2004
[Myopathy-lipomatosis associated with A8344G mitochondrial DNA mutation]
K Auré, D Sternberg, T Maisonobe, et al.
Revue Neurologique
|
October 17, 1998
[Pure motor neuropathy after radiation therapy: 6 cases]
T Lalu, B Mercier, N Birouk, et al.
Neuromuscular Disorders : NMD
|
June 19, 2001
The frequency of 17p11.2 duplication and Connexin 32 mutations in 282 Charcot-Marie-Tooth families in relation to the mode of inheritance and motor nerve conduction velocity
O Dubourg, S Tardieu, N Birouk, et al.
Arthritis Care & Research
|
October 29, 2010
Hepatitis C virus-associated polyarteritis nodosa
D Saadoun, B Terrier, O Semoun, et al.
Brain Research
|
May 4, 2000
Further evidence for a central reorganisation of synaptic connectivity in patients with hypoglossal-facial anastomosis in man
F Tankéré, T Maisonobe, L Naccache, et al.
Brain : a Journal of Neurology
|
September 26, 2001
Clinical, electrophysiological and molecular genetic characteristics of 93 patients with X-linked Charcot-Marie-Tooth disease
O Dubourg, S Tardieu, N Birouk, et al.
Page
of 13
Search research articles
Search
Showing results (71-80 of 122) with videos related to
Sort By:
Page
of 13
Annals of the New York Academy of Sciences
|
December 10, 1999
The autosomal recessive form of CMT disease linked to 5q31-q33
A Guilbot, M Kessali, N Ravisé, et al.
Rheumatology (Oxford, England)
|
June 6, 2002
Renal microaneurysms in three cases of hepatitis C virus-related vasculitis
N Costedoat-Chalumeau, P Cacoub, T Maisonobe, et al.
Annals of the New York Academy of Sciences
|
November 1, 2017
The Autosomal Recessive Form of CMT Disease Linked to 5q31-q33
A Guilbot, M Kessali, N Ravisé, et al.
La Revue De Medecine Interne
|
June 17, 2018
[Acute myositis in a 53 year-old man]
C David, A Michon, A Passeron, et al.
Revue Neurologique
|
February 24, 2004
[Myopathy-lipomatosis associated with A8344G mitochondrial DNA mutation]
K Auré, D Sternberg, T Maisonobe, et al.
Revue Neurologique
|
October 17, 1998
[Pure motor neuropathy after radiation therapy: 6 cases]
T Lalu, B Mercier, N Birouk, et al.
Neuromuscular Disorders : NMD
|
June 19, 2001
The frequency of 17p11.2 duplication and Connexin 32 mutations in 282 Charcot-Marie-Tooth families in relation to the mode of inheritance and motor nerve conduction velocity
O Dubourg, S Tardieu, N Birouk, et al.
Arthritis Care & Research
|
October 29, 2010
Hepatitis C virus-associated polyarteritis nodosa
D Saadoun, B Terrier, O Semoun, et al.
Brain Research
|
May 4, 2000
Further evidence for a central reorganisation of synaptic connectivity in patients with hypoglossal-facial anastomosis in man
F Tankéré, T Maisonobe, L Naccache, et al.
Brain : a Journal of Neurology
|
September 26, 2001
Clinical, electrophysiological and molecular genetic characteristics of 93 patients with X-linked Charcot-Marie-Tooth disease
O Dubourg, S Tardieu, N Birouk, et al.
Page
of 13