Results 201 to 210 of about 70,292 (240)
An Unusual Case of Extrapontine Myelinolysis in a Post-partum Woman with Hypernatremia. [PDF]
Rathore A +6 more
europepmc +1 more source
The Role of Lipid Alteration in Multiple Sclerosis. [PDF]
Damiza-Detmer A +2 more
europepmc +1 more source
Isolated Sixth Cranial Nerve Palsy as the First Presenting Sign of MOG Antibody-Associated Disease in a Three-Year-Old Child. [PDF]
Healey C +3 more
europepmc +1 more source
Tumefactive Demyelinating Lesion Mimicking Low-Grade Astrocytoma with a T2/FLAIR Mismatch Sign: A Case Report and Review of the Literature. [PDF]
Karhu M +6 more
europepmc +1 more source
The CEMIP Hyaluronidase is Elevated in Oligodendrocyte Progenitor Cells and Inhibits Oligodendrocyte Maturation. [PDF]
Peters A +8 more
europepmc +1 more source
Some of the next articles are maybe not open access.
Related searches:
Related searches:
Annals of Diagnostic Pathology, 2002
Demyelinating disease presenting as a solitary contrast-enhancing mass poses a diagnostic challenge for both radiologists and surgical pathologists. We report the cases of two female patients, aged 23 and 37 years, who exhibited the clinical and radiologic features of a space-occupying mass strongly suggestive of neoplasia.
Irma E, Erana-Rojas +3 more
openaire +2 more sources
Demyelinating disease presenting as a solitary contrast-enhancing mass poses a diagnostic challenge for both radiologists and surgical pathologists. We report the cases of two female patients, aged 23 and 37 years, who exhibited the clinical and radiologic features of a space-occupying mass strongly suggestive of neoplasia.
Irma E, Erana-Rojas +3 more
openaire +2 more sources
Current Opinion in Neurology, 2003
To review recent advances in heritable demyelinating neuropathies and their genotype-phenotype correlations.Two themes dominated the literature on demyelinating neuropathies in the past 2 years: (1) the dissection of the localization and roles of new molecules in the axon-Schwann cell unit, including periaxin and connexin32, which are mutated in ...
Lan, Zhou, John W, Griffin
openaire +2 more sources
To review recent advances in heritable demyelinating neuropathies and their genotype-phenotype correlations.Two themes dominated the literature on demyelinating neuropathies in the past 2 years: (1) the dissection of the localization and roles of new molecules in the axon-Schwann cell unit, including periaxin and connexin32, which are mutated in ...
Lan, Zhou, John W, Griffin
openaire +2 more sources
Continuum, 2016
This review summarizes a general approach to pediatric demyelination as well as specific features of each of the acquired demyelinating syndromes to help clinicians in their evaluation of children with these disorders. Case studies are included to illustrate the expanding phenotype of many of these syndromes.With the creation of consensus definitions ...
Sona, Narula, Brenda, Banwell
openaire +2 more sources
This review summarizes a general approach to pediatric demyelination as well as specific features of each of the acquired demyelinating syndromes to help clinicians in their evaluation of children with these disorders. Case studies are included to illustrate the expanding phenotype of many of these syndromes.With the creation of consensus definitions ...
Sona, Narula, Brenda, Banwell
openaire +2 more sources

