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Journal of Child Neurology
|
May 28, 2004
Mitochondrial DNA deletion in a child with megaloblastic anemia and recurrent encephalopathy
Cigdem Inan Akman, Carolyn M Sue, Sara Shanske, et al.
Journal of Child Neurology
|
March 30, 2005
Clinical and genetic features in two families with MELAS and the T3271C mutation in mitochondrial DNA
Stacey K H Tay, Sara Shanske, Carol Crowe, et al.
La Clinica Terapeutica
|
June 17, 2025
Sudden Gastrointestinal Deaths of a Child due to a Fecaloma: a Multilevel Forensic Pathological Approach
G V Lacasella, S De Simone, M Karaboue, et al.
Spine Deformity
|
February 7, 2020
A dual-team approach benefits standard-volume surgeons, but has minimal impact on outcomes for a high-volume surgeon in AIS patients
Vishal Sarwahi, Jesse Galina, Stephen Wendolowski, et al.
Journal of Neurology
|
June 3, 2026
Progressive disability but survival advantage in anti-Hu/ANNA1 paraneoplastic neurological syndromes
Kimberly A DiMauro, Nicolas R Thompson, Brittany Lapin, et al.
Annals of Neurology
|
September 1, 1991
Short-chain L-3-hydroxyacyl-CoA dehydrogenase deficiency in muscle: a new cause for recurrent myoglobinuria and encephalopathy
I Tein, D C De Vivo, D E Hale, et al.
BMC Research Notes
|
December 6, 2017
The p75<sup>NTR</sup>-mediated effect of nerve growth factor in L6C5 myogenic cells
Alessandra de Perini, Ivan Dimauro, Guglielmo Duranti, et al.
Neuromuscular Disorders : NMD
|
October 26, 2002
Molecular genetic study of myophosphorylase deficiency (McArdle's disease) in two Yemenite-Jewish families
Georgios M Hadjigeorgiou, Menachem Sadeh, Olimpia Musumeci, et al.
Journal of Pediatric Orthopedics
|
June 20, 2015
Uniplanar Versus Taylor Spatial Frame External Fixation For Pediatric Diaphyseal Tibia Fractures: A Comparison of Cost and Complications
Benjamin J Shore, Jon-Paul P DiMauro, David D Spence, et al.
Muscle & Nerve
|
October 27, 1997
Biochemical and genetic studies in a family with mitochondrial myopathy
T D Heiman-Patterson, Z Argov, J M Chavin, et al.
Page
of 95
Search research articles
Search
Showing results (591-600 of 942) with videos related to
Sort By:
Page
of 95
Journal of Child Neurology
|
May 28, 2004
Mitochondrial DNA deletion in a child with megaloblastic anemia and recurrent encephalopathy
Cigdem Inan Akman, Carolyn M Sue, Sara Shanske, et al.
Journal of Child Neurology
|
March 30, 2005
Clinical and genetic features in two families with MELAS and the T3271C mutation in mitochondrial DNA
Stacey K H Tay, Sara Shanske, Carol Crowe, et al.
La Clinica Terapeutica
|
June 17, 2025
Sudden Gastrointestinal Deaths of a Child due to a Fecaloma: a Multilevel Forensic Pathological Approach
G V Lacasella, S De Simone, M Karaboue, et al.
Spine Deformity
|
February 7, 2020
A dual-team approach benefits standard-volume surgeons, but has minimal impact on outcomes for a high-volume surgeon in AIS patients
Vishal Sarwahi, Jesse Galina, Stephen Wendolowski, et al.
Journal of Neurology
|
June 3, 2026
Progressive disability but survival advantage in anti-Hu/ANNA1 paraneoplastic neurological syndromes
Kimberly A DiMauro, Nicolas R Thompson, Brittany Lapin, et al.
Annals of Neurology
|
September 1, 1991
Short-chain L-3-hydroxyacyl-CoA dehydrogenase deficiency in muscle: a new cause for recurrent myoglobinuria and encephalopathy
I Tein, D C De Vivo, D E Hale, et al.
BMC Research Notes
|
December 6, 2017
The p75<sup>NTR</sup>-mediated effect of nerve growth factor in L6C5 myogenic cells
Alessandra de Perini, Ivan Dimauro, Guglielmo Duranti, et al.
Neuromuscular Disorders : NMD
|
October 26, 2002
Molecular genetic study of myophosphorylase deficiency (McArdle's disease) in two Yemenite-Jewish families
Georgios M Hadjigeorgiou, Menachem Sadeh, Olimpia Musumeci, et al.
Journal of Pediatric Orthopedics
|
June 20, 2015
Uniplanar Versus Taylor Spatial Frame External Fixation For Pediatric Diaphyseal Tibia Fractures: A Comparison of Cost and Complications
Benjamin J Shore, Jon-Paul P DiMauro, David D Spence, et al.
Muscle & Nerve
|
October 27, 1997
Biochemical and genetic studies in a family with mitochondrial myopathy
T D Heiman-Patterson, Z Argov, J M Chavin, et al.
Page
of 95