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Neuropediatrics
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August 18, 2001
Presence of delayed myelination and macrocephaly in the sister of a patient with vacuolating leukoencephalopathy with subcortical cysts
R Biancheri, C Pisaturo, M V Perrone, et al.
Neuropediatrics
|
May 7, 2010
Enhancing cranial nerves and cauda equina: an emerging magnetic resonance imaging pattern in metachromatic leukodystrophy and krabbe disease
G Morana, R Biancheri, M Dirocco, et al.
Giornale Italiano Di Medicina Del Lavoro Ed Ergonomia
|
February 15, 2013
[Occupational health and safety and gender differences: need for the identification of an adequate risk assessment]
G Ficini, E Caponi, S Cervia, et al.
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery
|
July 7, 1999
Unusually prolonged survival and childhood-onset epilepsy in a case of alobar holoprosencephaly
E Veneselli, R Biancheri, M Di Rocco, et al.
AJNR. American Journal of Neuroradiology
|
June 23, 2012
The shrunken, bright cerebellum: a characteristic MRI finding in congenital disorders of glycosylation type 1a
P Feraco, M Mirabelli-Badenier, M Severino, et al.
Neuropediatrics
|
April 21, 2001
Cobalamin (Cbl) C/D deficiency: clinical, neurophysiological and neuroradiologic findings in 14 cases
R Biancheri, R Cerone, M C Schiaffino, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology
|
May 5, 2001
Hypersomnia in the Prader Willi syndrome: clinical-electrophysiological features and underlying factors
R Manni, L Politini, L Nobili, et al.
AJNR. American Journal of Neuroradiology
|
March 10, 2001
Early-onset combined methylmalonic aciduria and homocystinuria: neuroradiologic findings
A Rossi, R Cerone, R Biancheri, et al.
AJNR. American Journal of Neuroradiology
|
November 3, 2007
Hypomyelination and congenital cataract: neuroimaging features of a novel inherited white matter disorder
A Rossi, R Biancheri, F Zara, et al.
Clinical Genetics
|
January 15, 2008
Genotype-phenotype correlation in five Pelizaeus-Merzbacher disease patients with PLP1 gene duplications
S Regis, R Biancheri, E Bertini, et al.
Page
of 4
Search research articles
Search
Showing results (11-20 of 36) with videos related to
Sort By:
Page
of 4
Neuropediatrics
|
August 18, 2001
Presence of delayed myelination and macrocephaly in the sister of a patient with vacuolating leukoencephalopathy with subcortical cysts
R Biancheri, C Pisaturo, M V Perrone, et al.
Neuropediatrics
|
May 7, 2010
Enhancing cranial nerves and cauda equina: an emerging magnetic resonance imaging pattern in metachromatic leukodystrophy and krabbe disease
G Morana, R Biancheri, M Dirocco, et al.
Giornale Italiano Di Medicina Del Lavoro Ed Ergonomia
|
February 15, 2013
[Occupational health and safety and gender differences: need for the identification of an adequate risk assessment]
G Ficini, E Caponi, S Cervia, et al.
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery
|
July 7, 1999
Unusually prolonged survival and childhood-onset epilepsy in a case of alobar holoprosencephaly
E Veneselli, R Biancheri, M Di Rocco, et al.
AJNR. American Journal of Neuroradiology
|
June 23, 2012
The shrunken, bright cerebellum: a characteristic MRI finding in congenital disorders of glycosylation type 1a
P Feraco, M Mirabelli-Badenier, M Severino, et al.
Neuropediatrics
|
April 21, 2001
Cobalamin (Cbl) C/D deficiency: clinical, neurophysiological and neuroradiologic findings in 14 cases
R Biancheri, R Cerone, M C Schiaffino, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology
|
May 5, 2001
Hypersomnia in the Prader Willi syndrome: clinical-electrophysiological features and underlying factors
R Manni, L Politini, L Nobili, et al.
AJNR. American Journal of Neuroradiology
|
March 10, 2001
Early-onset combined methylmalonic aciduria and homocystinuria: neuroradiologic findings
A Rossi, R Cerone, R Biancheri, et al.
AJNR. American Journal of Neuroradiology
|
November 3, 2007
Hypomyelination and congenital cataract: neuroimaging features of a novel inherited white matter disorder
A Rossi, R Biancheri, F Zara, et al.
Clinical Genetics
|
January 15, 2008
Genotype-phenotype correlation in five Pelizaeus-Merzbacher disease patients with PLP1 gene duplications
S Regis, R Biancheri, E Bertini, et al.
Page
of 4