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European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
September 18, 2012
Neonatal vocal cord paralysis-an early presentation of hereditary neuralgic amyotrophy due to a mutation in the SEPT9 gene
E Leshinsky-Silver, M Ginzberg, R Dabby, et al.
Seizure
|
December 8, 2009
Neuropsychological aspects of benign childhood epilepsy with centrotemporal spikes
H Goldberg-Stern, O M Gonen, M Sadeh, et al.
Acta Neurologica Scandinavica
|
September 19, 2008
Treatment of status epilepticus and acute repetitive seizures with i.v. valproic acid vs phenytoin
R Gilad, N Izkovitz, R Dabby, et al.
Journal of Child Neurology
|
February 24, 2001
Cerebellar involvement in Langerhans' cell histiocytosis: a progressive neuropsychiatric disease
A Shuper, B Stark, Y Yaniv, et al.
Neuromuscular Disorders : NMD
|
September 1, 1993
Clinical features of oculopharyngeal muscular dystrophy among Bukhara Jews
S C Blumen, P Nisipeanu, M Sadeh, et al.
Neurology
|
May 14, 2003
Hereditary inclusion body myopathy: the Middle Eastern genetic cluster
Z Argov, I Eisenberg, G Grabov-Nardini, et al.
Magnetic Resonance in Medicine
|
February 1, 1997
In vivo 23Na NMR studies of myotonic dystrophy
T Kushnir, T Knubovets, Y Itzchak, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
April 24, 2002
Serum leptin level in women with idiopathic intracranial hypertension
Y Lampl, Y Eshel, A Kessler, et al.
Neurology
|
May 1, 1996
Intranuclear inclusions in oculopharyngeal muscular dystrophy among Bukhara Jews
S C Blumen, M Sadeh, A D Korczyn, et al.
Seminars in Arthritis and Rheumatism
|
May 8, 1998
High incidence of malignancies in patients with dermatomyositis and polymyositis: an 11-year analysis
C R Maoz, P Langevitz, A Livneh, et al.
Page
of 12
Search research articles
Search
Showing results (91-100 of 119) with videos related to
Sort By:
Page
of 12
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
September 18, 2012
Neonatal vocal cord paralysis-an early presentation of hereditary neuralgic amyotrophy due to a mutation in the SEPT9 gene
E Leshinsky-Silver, M Ginzberg, R Dabby, et al.
Seizure
|
December 8, 2009
Neuropsychological aspects of benign childhood epilepsy with centrotemporal spikes
H Goldberg-Stern, O M Gonen, M Sadeh, et al.
Acta Neurologica Scandinavica
|
September 19, 2008
Treatment of status epilepticus and acute repetitive seizures with i.v. valproic acid vs phenytoin
R Gilad, N Izkovitz, R Dabby, et al.
Journal of Child Neurology
|
February 24, 2001
Cerebellar involvement in Langerhans' cell histiocytosis: a progressive neuropsychiatric disease
A Shuper, B Stark, Y Yaniv, et al.
Neuromuscular Disorders : NMD
|
September 1, 1993
Clinical features of oculopharyngeal muscular dystrophy among Bukhara Jews
S C Blumen, P Nisipeanu, M Sadeh, et al.
Neurology
|
May 14, 2003
Hereditary inclusion body myopathy: the Middle Eastern genetic cluster
Z Argov, I Eisenberg, G Grabov-Nardini, et al.
Magnetic Resonance in Medicine
|
February 1, 1997
In vivo 23Na NMR studies of myotonic dystrophy
T Kushnir, T Knubovets, Y Itzchak, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
April 24, 2002
Serum leptin level in women with idiopathic intracranial hypertension
Y Lampl, Y Eshel, A Kessler, et al.
Neurology
|
May 1, 1996
Intranuclear inclusions in oculopharyngeal muscular dystrophy among Bukhara Jews
S C Blumen, M Sadeh, A D Korczyn, et al.
Seminars in Arthritis and Rheumatism
|
May 8, 1998
High incidence of malignancies in patients with dermatomyositis and polymyositis: an 11-year analysis
C R Maoz, P Langevitz, A Livneh, et al.
Page
of 12