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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.
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.
International Journal of Tissue Reactions
|
January 1, 1992
Serum angiotensin converting enzyme in diabetic retinopathy
C Letizia, P Repossi, M Sellini, et al.
Biological Psychiatry
|
April 3, 1999
A quantified analysis of sleep electroencephalography in anorectic adolescents
L Nobili, M G Baglietto, F De Carli, et al.
Annals of Clinical and Translational Neurology
|
December 7, 2020
Missense PDSS1 mutations in CoenzymeQ10 synthesis cause optic atrophy and sensorineural deafness
Francesca Nardecchia, Agnese De Giorgi, Flavia Palombo, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology
|
July 10, 1999
Modulation of sleep interictal epileptiform discharges in partial epilepsy of childhood
L Nobili, M G Baglietto, M Beelke, et al.
Developmental Medicine and Child Neurology
|
June 21, 2001
Neuropsychological disorders related to interictal epileptic discharges during sleep in benign epilepsy of childhood with centrotemporal or Rolandic spikes
M G Baglietto, F M Battaglia, L Nobili, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology
|
May 29, 1999
Relationship of sleep interictal epileptiform discharges to sigma activity (12-16 Hz) in benign epilepsy of childhood with rolandic spikes
L Nobili, F Ferrillo, M G Baglietto, et al.
Visual Neuroscience
|
July 5, 2008
Psychophysical analysis of contrast processing segregated into magnocellular and parvocellular systems in asymptomatic carriers of 11778 Leber's hereditary optic neuropathy
M Gualtieri, M Bandeira, R D Hamer, et al.
Page
of 7
Search research articles
Search
Showing results (61-70 of 69) with videos related to
Sort By:
Page
of 7
You have reached the last page of results.
This site can display upto 69 results.
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.
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.
International Journal of Tissue Reactions
|
January 1, 1992
Serum angiotensin converting enzyme in diabetic retinopathy
C Letizia, P Repossi, M Sellini, et al.
Biological Psychiatry
|
April 3, 1999
A quantified analysis of sleep electroencephalography in anorectic adolescents
L Nobili, M G Baglietto, F De Carli, et al.
Annals of Clinical and Translational Neurology
|
December 7, 2020
Missense PDSS1 mutations in CoenzymeQ10 synthesis cause optic atrophy and sensorineural deafness
Francesca Nardecchia, Agnese De Giorgi, Flavia Palombo, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology
|
July 10, 1999
Modulation of sleep interictal epileptiform discharges in partial epilepsy of childhood
L Nobili, M G Baglietto, M Beelke, et al.
Developmental Medicine and Child Neurology
|
June 21, 2001
Neuropsychological disorders related to interictal epileptic discharges during sleep in benign epilepsy of childhood with centrotemporal or Rolandic spikes
M G Baglietto, F M Battaglia, L Nobili, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology
|
May 29, 1999
Relationship of sleep interictal epileptiform discharges to sigma activity (12-16 Hz) in benign epilepsy of childhood with rolandic spikes
L Nobili, F Ferrillo, M G Baglietto, et al.
Visual Neuroscience
|
July 5, 2008
Psychophysical analysis of contrast processing segregated into magnocellular and parvocellular systems in asymptomatic carriers of 11778 Leber's hereditary optic neuropathy
M Gualtieri, M Bandeira, R D Hamer, et al.
Page
of 7