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Neurology
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July 6, 2000
Ataxia, deafness, leukodystrophy: inherited disorder of the white matter in three related patients
V Leuzzi, A Rinna, M Gallucci, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
February 1, 1995
Patients with clinically definite multiple sclerosis, white matter abnormalities on MRI, and normal CSF: if not multiple sclerosis, what is it?
C Fieschi, C Gasperini, G Ristori, et al.
Journal of Inherited Metabolic Disease
|
July 15, 2000
Oxidative abnormalities in Menkes disease
C Rizzo, E Bertini, F Piemonte, et al.
Human Genetics
|
October 1, 1991
Mitochondrial DNA mutation in an Italian family with Leber hereditary optic neuropathy
C Carducci, V Leuzzi, M Scuderi, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
March 20, 1999
Childhood demyelinating diseases with a prolonged remitting course and their relation to Schilder's disease: report of two cases
V Leuzzi, G Lyon, M R Cilio, et al.
Brain & Development
|
May 1, 1996
Evolution of daytime quiet sleep components in early treated phenylketonuric infants
G F De Giorgis, E Nonnis, F Crocioni, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1996
Screening of mtDNA mutations in Italian LHON pedigrees
C Carducci, A M De Negri, V Leuzzi, et al.
European Journal of Neurology
|
November 29, 2013
Diagnostic problems in "clinically definite" multiple sclerosis patients with normal CSF and multiple MRI abnormalities
C Fieschi, C Gasperini, G Ristori, et al.
AJNR. American Journal of Neuroradiology
|
March 14, 2007
Treatment monitoring of brain creatine deficiency syndromes: a 1H- and 31P-MR spectroscopy study
M C Bianchi, M Tosetti, R Battini, et al.
Epilepsy & Behavior : E&B
|
February 22, 2023
Psychogenic non-epileptic seizures and functional motor disorders in developmental age: A comparison of clinical and psychopathological features
F Gigliotti, F Di Santo, S Cesario, et al.
Page
of 7
Search research articles
Search
Showing results (31-40 of 64) with videos related to
Sort By:
Page
of 7
Neurology
|
July 6, 2000
Ataxia, deafness, leukodystrophy: inherited disorder of the white matter in three related patients
V Leuzzi, A Rinna, M Gallucci, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
February 1, 1995
Patients with clinically definite multiple sclerosis, white matter abnormalities on MRI, and normal CSF: if not multiple sclerosis, what is it?
C Fieschi, C Gasperini, G Ristori, et al.
Journal of Inherited Metabolic Disease
|
July 15, 2000
Oxidative abnormalities in Menkes disease
C Rizzo, E Bertini, F Piemonte, et al.
Human Genetics
|
October 1, 1991
Mitochondrial DNA mutation in an Italian family with Leber hereditary optic neuropathy
C Carducci, V Leuzzi, M Scuderi, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
March 20, 1999
Childhood demyelinating diseases with a prolonged remitting course and their relation to Schilder's disease: report of two cases
V Leuzzi, G Lyon, M R Cilio, et al.
Brain & Development
|
May 1, 1996
Evolution of daytime quiet sleep components in early treated phenylketonuric infants
G F De Giorgis, E Nonnis, F Crocioni, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1996
Screening of mtDNA mutations in Italian LHON pedigrees
C Carducci, A M De Negri, V Leuzzi, et al.
European Journal of Neurology
|
November 29, 2013
Diagnostic problems in "clinically definite" multiple sclerosis patients with normal CSF and multiple MRI abnormalities
C Fieschi, C Gasperini, G Ristori, et al.
AJNR. American Journal of Neuroradiology
|
March 14, 2007
Treatment monitoring of brain creatine deficiency syndromes: a 1H- and 31P-MR spectroscopy study
M C Bianchi, M Tosetti, R Battini, et al.
Epilepsy & Behavior : E&B
|
February 22, 2023
Psychogenic non-epileptic seizures and functional motor disorders in developmental age: A comparison of clinical and psychopathological features
F Gigliotti, F Di Santo, S Cesario, et al.
Page
of 7