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Plos One
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May 3, 2016
Internal Jugular Vein Cross-Sectional Area and Cerebrospinal Fluid Pulsatility in the Aqueduct of Sylvius: A Comparative Study between Healthy Subjects and Multiple Sclerosis Patients
Clive B Beggs, Christopher Magnano, Pavel Belov, et al.
Clinical Neuroscience (New York, N.Y.)
|
January 1, 1995
Oxidative phosphorylation diseases and cerebellar ataxia
J M Shoffner, A Kaufman, D Koontz, et al.
Journal of Mental Deficiency Research
|
December 1, 1985
Serum carnosinase deficiency: a non-disabling phenotype?
M Cohen, P L Hartlage, N Krawiecki, et al.
Cellular Signalling
|
October 21, 2004
Cypermethrin blocks a mitochondria-dependent apoptotic signal initiated by deficient N-linked glycosylation within the endoplasmic reticulum
Katherine E Niederer, Daniel K Morrow, Justin L Gettings, et al.
Epilepsy & Behavior : E&B
|
October 4, 2011
Caregiver measures for seizure control, efficacy, and tolerability of antiepileptic drugs for childhood epilepsy: results of a preference survey
M Scott Perry, Charlotte Swint, Jonathan Hawley, et al.
AJNR. American Journal of Neuroradiology
|
December 9, 2017
Lower Arterial Cross-Sectional Area of Carotid and Vertebral Arteries and Higher Frequency of Secondary Neck Vessels Are Associated with Multiple Sclerosis
P Belov, D Jakimovski, J Krawiecki, et al.
Neurology
|
September 1, 1989
Evidence in a lethal infantile mitochondrial disease for a nuclear mutation affecting respiratory complexes I and IV
X Zheng, J M Shoffner, M T Lott, et al.
Medical and Pediatric Oncology
|
August 1, 1997
Systematic approach for detection of endocrine disorders in children treated for brain tumors
L R Meacham, T T Ghim, I R Crocker, et al.
Neurology
|
November 1, 1992
Subacute necrotizing encephalopathy: oxidative phosphorylation defects and the ATPase 6 point mutation
J M Shoffner, P M Fernhoff, N S Krawiecki, et al.
Annals of Neurology
|
September 27, 2002
Aggregation of actin and cofilin in identical twins with juvenile-onset dystonia
Marla Gearing, Jorge L Juncos, Vincent Procaccio, et al.
Page
of 6
Search research articles
Search
Showing results (41-50 of 53) with videos related to
Sort By:
Page
of 6
Plos One
|
May 3, 2016
Internal Jugular Vein Cross-Sectional Area and Cerebrospinal Fluid Pulsatility in the Aqueduct of Sylvius: A Comparative Study between Healthy Subjects and Multiple Sclerosis Patients
Clive B Beggs, Christopher Magnano, Pavel Belov, et al.
Clinical Neuroscience (New York, N.Y.)
|
January 1, 1995
Oxidative phosphorylation diseases and cerebellar ataxia
J M Shoffner, A Kaufman, D Koontz, et al.
Journal of Mental Deficiency Research
|
December 1, 1985
Serum carnosinase deficiency: a non-disabling phenotype?
M Cohen, P L Hartlage, N Krawiecki, et al.
Cellular Signalling
|
October 21, 2004
Cypermethrin blocks a mitochondria-dependent apoptotic signal initiated by deficient N-linked glycosylation within the endoplasmic reticulum
Katherine E Niederer, Daniel K Morrow, Justin L Gettings, et al.
Epilepsy & Behavior : E&B
|
October 4, 2011
Caregiver measures for seizure control, efficacy, and tolerability of antiepileptic drugs for childhood epilepsy: results of a preference survey
M Scott Perry, Charlotte Swint, Jonathan Hawley, et al.
AJNR. American Journal of Neuroradiology
|
December 9, 2017
Lower Arterial Cross-Sectional Area of Carotid and Vertebral Arteries and Higher Frequency of Secondary Neck Vessels Are Associated with Multiple Sclerosis
P Belov, D Jakimovski, J Krawiecki, et al.
Neurology
|
September 1, 1989
Evidence in a lethal infantile mitochondrial disease for a nuclear mutation affecting respiratory complexes I and IV
X Zheng, J M Shoffner, M T Lott, et al.
Medical and Pediatric Oncology
|
August 1, 1997
Systematic approach for detection of endocrine disorders in children treated for brain tumors
L R Meacham, T T Ghim, I R Crocker, et al.
Neurology
|
November 1, 1992
Subacute necrotizing encephalopathy: oxidative phosphorylation defects and the ATPase 6 point mutation
J M Shoffner, P M Fernhoff, N S Krawiecki, et al.
Annals of Neurology
|
September 27, 2002
Aggregation of actin and cofilin in identical twins with juvenile-onset dystonia
Marla Gearing, Jorge L Juncos, Vincent Procaccio, et al.
Page
of 6