Search research articles
Contact Us
Filters
Showing results (541-550 of 942) with videos related to
Page
of 95
Sort By:
Neuromuscular Disorders : NMD
|
January 1, 1991
An adult-onset myopathy characterized by a double ring appearance of muscle fibers
C L Coulter, W A Marks, J B Bodensteiner, et al.
Medical Science Monitor : International Medical Journal of Experimental and Clinical Research
|
February 23, 2002
The course of vision disturbances in a patient with the MELAS syndrome
Maria Pachalska, Salvatore DiMauro, Maria Formińska-Kapuścik, et al.
Headache
|
June 24, 2004
Study of mitochondrial DNA mutations in patients with migraine with prolonged aura
Todd D Rozen, Sara Shanske, David Otaegui, et al.
Animal : an International Journal of Animal Bioscience
|
May 17, 2013
Effect of extruded linseed supplementation on blood metabolic profile and milk performance of Saanen goats
A Nudda, G Battacone, A S Atzori, et al.
Physical Review Letters
|
June 12, 2026
Terahertz-Assisted Multiband High-Harmonic Spectroscopy
Sha Li, Lun Yue, Yaguo Tang, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
|
November 23, 2018
MR evaluation of encephalic leukoaraiosis in sudden sensorineural hearing loss (SSNHL) patients
Franca Dicuonzo, Stefano Purciariello, Aurora De Marco, et al.
Journal of the Neurological Sciences
|
August 1, 1980
Myoadenylate deaminase deficiency--muscle biopsy and muscle culture in a patient with gout
S DiMauro, A F Miranda, A P Hays, et al.
Muscle & Nerve
|
August 2, 2006
Exercise-induced cramp, myoglobinuria, and tubular aggregates in phosphoglycerate mutase deficiency
Shin J Oh, Kyung-Seok Park, Hewitt F Ryan, et al.
Physical Review Letters
|
May 23, 2006
High-energy cutoff in the spectrum of strong-field nonsequential double ionization
J S Parker, B J S Doherty, K T Taylor, et al.
Neuromuscular Disorders : NMD
|
October 26, 2002
Mitochondrial myopathy and ophthalmoplegia in a sporadic patient with the G12315A mutation in mitochondrial DNA
Charalampos L Karadimas, Leonardo Salviati, Sabrina Sacconi, et al.
Page
of 95
Search research articles
Search
Showing results (541-550 of 942) with videos related to
Sort By:
Page
of 95
Neuromuscular Disorders : NMD
|
January 1, 1991
An adult-onset myopathy characterized by a double ring appearance of muscle fibers
C L Coulter, W A Marks, J B Bodensteiner, et al.
Medical Science Monitor : International Medical Journal of Experimental and Clinical Research
|
February 23, 2002
The course of vision disturbances in a patient with the MELAS syndrome
Maria Pachalska, Salvatore DiMauro, Maria Formińska-Kapuścik, et al.
Headache
|
June 24, 2004
Study of mitochondrial DNA mutations in patients with migraine with prolonged aura
Todd D Rozen, Sara Shanske, David Otaegui, et al.
Animal : an International Journal of Animal Bioscience
|
May 17, 2013
Effect of extruded linseed supplementation on blood metabolic profile and milk performance of Saanen goats
A Nudda, G Battacone, A S Atzori, et al.
Physical Review Letters
|
June 12, 2026
Terahertz-Assisted Multiband High-Harmonic Spectroscopy
Sha Li, Lun Yue, Yaguo Tang, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
|
November 23, 2018
MR evaluation of encephalic leukoaraiosis in sudden sensorineural hearing loss (SSNHL) patients
Franca Dicuonzo, Stefano Purciariello, Aurora De Marco, et al.
Journal of the Neurological Sciences
|
August 1, 1980
Myoadenylate deaminase deficiency--muscle biopsy and muscle culture in a patient with gout
S DiMauro, A F Miranda, A P Hays, et al.
Muscle & Nerve
|
August 2, 2006
Exercise-induced cramp, myoglobinuria, and tubular aggregates in phosphoglycerate mutase deficiency
Shin J Oh, Kyung-Seok Park, Hewitt F Ryan, et al.
Physical Review Letters
|
May 23, 2006
High-energy cutoff in the spectrum of strong-field nonsequential double ionization
J S Parker, B J S Doherty, K T Taylor, et al.
Neuromuscular Disorders : NMD
|
October 26, 2002
Mitochondrial myopathy and ophthalmoplegia in a sporadic patient with the G12315A mutation in mitochondrial DNA
Charalampos L Karadimas, Leonardo Salviati, Sabrina Sacconi, et al.
Page
of 95