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Nucleic Acids Research
|
February 11, 1991
Different mechanisms inferred from sequences of human mitochondrial DNA deletions in ocular myopathies
F Degoul, I Nelson, S Amselem, et al.
Neurology
|
July 23, 2003
Herpes simplex encephalitis relapses in children: differentiation of two neurologic entities
X De Tiège, F Rozenberg, V Des Portes, et al.
Archives of Otolaryngology--Head & Neck Surgery
|
August 1, 1990
Reversible hearing loss in a patient with cryptococcosis
J M Mayer, X Chevalier, E Albert, et al.
Journal of the Neurological Sciences
|
April 29, 1998
A case of mitochondrial encephalomyopathy associated with a muscle coenzyme Q10 deficiency
E Boitier, F Degoul, I Desguerre, et al.
Clinical Genetics
|
October 12, 1999
Aicardi-Goutières syndrome: monogenic recessive disease, genetically heterogeneous disease, or multifactorial disease?
S Fauré, I Bordelais, C Marquette, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
August 3, 1999
[Severe anorexia in infants in Reunion: a new autosomal recessive disease?]
M Renouil, A Fourmaintraux, F Cartault, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
February 20, 2007
[Human herpes virus type 6, etiology of an acute encephalitis in childhood: case report]
A Afenjar, D Rodriguez, F Rozenberg, et al.
Journal of Medical Genetics
|
October 1, 1992
De novo t(X;21)(q28;q11) in a girl with phenotypic features of Williams-Beuren syndrome
L Telvi, J M Pinard, R Ion, et al.
American Journal of Human Genetics
|
December 1, 1994
Genetic heterogeneity of familial hemiplegic migraine
A Joutel, A Ducros, K Vahedi, et al.
Neurology
|
October 1, 1991
Diffuse cortical dysplasia, or the 'double cortex' syndrome: the clinical and epileptic spectrum in 10 patients
A Palmini, F Andermann, J Aicardi, et al.
Page
of 16
Search research articles
Search
Showing results (121-130 of 156) with videos related to
Sort By:
Page
of 16
Nucleic Acids Research
|
February 11, 1991
Different mechanisms inferred from sequences of human mitochondrial DNA deletions in ocular myopathies
F Degoul, I Nelson, S Amselem, et al.
Neurology
|
July 23, 2003
Herpes simplex encephalitis relapses in children: differentiation of two neurologic entities
X De Tiège, F Rozenberg, V Des Portes, et al.
Archives of Otolaryngology--Head & Neck Surgery
|
August 1, 1990
Reversible hearing loss in a patient with cryptococcosis
J M Mayer, X Chevalier, E Albert, et al.
Journal of the Neurological Sciences
|
April 29, 1998
A case of mitochondrial encephalomyopathy associated with a muscle coenzyme Q10 deficiency
E Boitier, F Degoul, I Desguerre, et al.
Clinical Genetics
|
October 12, 1999
Aicardi-Goutières syndrome: monogenic recessive disease, genetically heterogeneous disease, or multifactorial disease?
S Fauré, I Bordelais, C Marquette, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
August 3, 1999
[Severe anorexia in infants in Reunion: a new autosomal recessive disease?]
M Renouil, A Fourmaintraux, F Cartault, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
February 20, 2007
[Human herpes virus type 6, etiology of an acute encephalitis in childhood: case report]
A Afenjar, D Rodriguez, F Rozenberg, et al.
Journal of Medical Genetics
|
October 1, 1992
De novo t(X;21)(q28;q11) in a girl with phenotypic features of Williams-Beuren syndrome
L Telvi, J M Pinard, R Ion, et al.
American Journal of Human Genetics
|
December 1, 1994
Genetic heterogeneity of familial hemiplegic migraine
A Joutel, A Ducros, K Vahedi, et al.
Neurology
|
October 1, 1991
Diffuse cortical dysplasia, or the 'double cortex' syndrome: the clinical and epileptic spectrum in 10 patients
A Palmini, F Andermann, J Aicardi, et al.
Page
of 16