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Annals of Neurology
|
May 11, 2000
X-linked vacuolar myopathies: two separate loci and refined genetic mapping
M Auranen, M Villanova, F Muntoni, et al.
Revue Neurologique
|
January 5, 2001
["MELAS" (A3243G) mutation of mitochondrial DNA: a study of the relationships between the clinical phenotype in 19 patients and morphological and molecular data]
P Laforêt, F Ziegler, D Sternberg, et al.
Annals of Neurology
|
May 1, 1995
X-linked vacuolated myopathy: complement membrane attack complex on surface membrane of injured muscle fibers
M Villanova, J P Louboutin, D Chateau, et al.
Journal of the Neurological Sciences
|
March 1, 1974
Histochemical and ultrastructural study of muscle biopsies in 3 cases of dystrophia myotonica in the newborn child
E Farkas, F M Tomé, M Fardeau, et al.
Journal of the Neurological Sciences
|
October 1, 1996
Paramyotonia congenita: genotype to phenotype correlations in two families and report of a new mutation in the sodium channel gene
E Plassart, B Eymard, L Maurs, et al.
Neuromuscular Disorders : NMD
|
September 1, 1993
Malignant hyperthermia and central core disease: analysis of two families with heterogeneous clinical expression
N B Romero, Y Nivoche, J Lunardi, et al.
Revue Neurologique
|
June 1, 1978
[A new familial muscular disorder demonstrated by the intra-sarcoplasmic accumulation of a granulo-filamentous material which is dense on electron microscopy (author's transl)]
M Fardeau, J Godet-Guillain, F M Tome, et al.
Revue Neurologique
|
June 1, 1977
[Anatomo-clinical study of a case of "ophthalmoplegia plus" with analysis of muscular, central nervous, ocular, myocardial, and thyroid lesions]
P Castaigne, F Lhermitte, R Escourolle, et al.
Revue Neurologique
|
January 1, 1989
[Familial myopathy with "cytoplasmic body" (or "spheroid") type inclusions, disclosed by respiratory insufficiency]
F Chapon, F Viader, M Fardeau, et al.
Human Genetics
|
March 1, 1988
Nebulin seen in DMD males including one patient with a large DNA deletion encompassing the DMD gene
J J Pernelle, P Chafey, J Chelly, et al.
Page
of 29
Search research articles
Search
Showing results (161-170 of 289) with videos related to
Sort By:
Page
of 29
Annals of Neurology
|
May 11, 2000
X-linked vacuolar myopathies: two separate loci and refined genetic mapping
M Auranen, M Villanova, F Muntoni, et al.
Revue Neurologique
|
January 5, 2001
["MELAS" (A3243G) mutation of mitochondrial DNA: a study of the relationships between the clinical phenotype in 19 patients and morphological and molecular data]
P Laforêt, F Ziegler, D Sternberg, et al.
Annals of Neurology
|
May 1, 1995
X-linked vacuolated myopathy: complement membrane attack complex on surface membrane of injured muscle fibers
M Villanova, J P Louboutin, D Chateau, et al.
Journal of the Neurological Sciences
|
March 1, 1974
Histochemical and ultrastructural study of muscle biopsies in 3 cases of dystrophia myotonica in the newborn child
E Farkas, F M Tomé, M Fardeau, et al.
Journal of the Neurological Sciences
|
October 1, 1996
Paramyotonia congenita: genotype to phenotype correlations in two families and report of a new mutation in the sodium channel gene
E Plassart, B Eymard, L Maurs, et al.
Neuromuscular Disorders : NMD
|
September 1, 1993
Malignant hyperthermia and central core disease: analysis of two families with heterogeneous clinical expression
N B Romero, Y Nivoche, J Lunardi, et al.
Revue Neurologique
|
June 1, 1978
[A new familial muscular disorder demonstrated by the intra-sarcoplasmic accumulation of a granulo-filamentous material which is dense on electron microscopy (author's transl)]
M Fardeau, J Godet-Guillain, F M Tome, et al.
Revue Neurologique
|
June 1, 1977
[Anatomo-clinical study of a case of "ophthalmoplegia plus" with analysis of muscular, central nervous, ocular, myocardial, and thyroid lesions]
P Castaigne, F Lhermitte, R Escourolle, et al.
Revue Neurologique
|
January 1, 1989
[Familial myopathy with "cytoplasmic body" (or "spheroid") type inclusions, disclosed by respiratory insufficiency]
F Chapon, F Viader, M Fardeau, et al.
Human Genetics
|
March 1, 1988
Nebulin seen in DMD males including one patient with a large DNA deletion encompassing the DMD gene
J J Pernelle, P Chafey, J Chelly, et al.
Page
of 29