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Journal of Inherited Metabolic Disease
|
January 1, 1988
Adrenomyeloneurodystrophy with late cerebral involvement and evidence of a multiple autoimmune disorder
A Federico, M T Dotti, P Annunziata, et al.
Journal of Submicroscopic Cytology and Pathology
|
July 1, 1997
A rare association of myasthenia gravis and mitochondrial myopathy: a clinical, biochemical and morphologic study of one case
K Plewnia, M T Dotti, A Malandrini, et al.
Journal of the Neurological Sciences
|
June 2, 2017
Neuroendocrine lung cancer in a patient with limbic encephalopathy due to anti-Hu antibodies: A rare association not to be missed
A R Pati, C Battisti, S A Tripodi, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
July 1, 1996
The A to G transition at nt 3243 of the mitochondrial tRNALeu(UUR) may cause an MERRF syndrome
G M Fabrizi, E Cardaioli, G S Grieco, et al.
Journal of Neurology
|
August 11, 2012
Polyneuropathy in cerebrotendinous xanthomatosis and response to treatment with chenodeoxycholic acid
F Ginanneschi, A Mignarri, M Mondelli, et al.
Neurology
|
September 15, 2005
Motor-sensory neuropathy with minifascicle formation in a woman with normal karyotype
A Malandrini, S Gambelli, M Muglia, et al.
Acta Neurologica Scandinavica
|
August 12, 2014
Clinical, familial, and neuroimaging features of CADASIL-like patients
S Nannucci, F Pescini, B Bertaccini, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
October 26, 2010
Clinical relevance of brain volume changes in patients with cerebrotendinous xanthomatosis
S Guerrera, M L Stromillo, A Mignarri, et al.
Neurology
|
August 3, 1999
Association of trisomy 9p and band heterotopia
A Federico, P Tomasetti, M Zollino, et al.
Journal of Lipid Research
|
July 1, 1996
Cerebrotendinous xanthomatosis caused by two new mutations of the sterol-27-hydroxylase gene that disrupt mRNA splicing
R Garuti, N Lelli, M Barozzini, et al.
Page
of 15
Search research articles
Search
Showing results (101-110 of 144) with videos related to
Sort By:
Page
of 15
Journal of Inherited Metabolic Disease
|
January 1, 1988
Adrenomyeloneurodystrophy with late cerebral involvement and evidence of a multiple autoimmune disorder
A Federico, M T Dotti, P Annunziata, et al.
Journal of Submicroscopic Cytology and Pathology
|
July 1, 1997
A rare association of myasthenia gravis and mitochondrial myopathy: a clinical, biochemical and morphologic study of one case
K Plewnia, M T Dotti, A Malandrini, et al.
Journal of the Neurological Sciences
|
June 2, 2017
Neuroendocrine lung cancer in a patient with limbic encephalopathy due to anti-Hu antibodies: A rare association not to be missed
A R Pati, C Battisti, S A Tripodi, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
July 1, 1996
The A to G transition at nt 3243 of the mitochondrial tRNALeu(UUR) may cause an MERRF syndrome
G M Fabrizi, E Cardaioli, G S Grieco, et al.
Journal of Neurology
|
August 11, 2012
Polyneuropathy in cerebrotendinous xanthomatosis and response to treatment with chenodeoxycholic acid
F Ginanneschi, A Mignarri, M Mondelli, et al.
Neurology
|
September 15, 2005
Motor-sensory neuropathy with minifascicle formation in a woman with normal karyotype
A Malandrini, S Gambelli, M Muglia, et al.
Acta Neurologica Scandinavica
|
August 12, 2014
Clinical, familial, and neuroimaging features of CADASIL-like patients
S Nannucci, F Pescini, B Bertaccini, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
October 26, 2010
Clinical relevance of brain volume changes in patients with cerebrotendinous xanthomatosis
S Guerrera, M L Stromillo, A Mignarri, et al.
Neurology
|
August 3, 1999
Association of trisomy 9p and band heterotopia
A Federico, P Tomasetti, M Zollino, et al.
Journal of Lipid Research
|
July 1, 1996
Cerebrotendinous xanthomatosis caused by two new mutations of the sterol-27-hydroxylase gene that disrupt mRNA splicing
R Garuti, N Lelli, M Barozzini, et al.
Page
of 15