Results 41 to 50 of about 1,177,850 (201)

Neuropsychiatric disturbances in atypical Parkinsonian disorders [PDF]

open access: yes, 2018
Multiple system atrophy (MSA), progressive supranuclear palsy (PSP), and corticobasal degeneration (CBD) are the most common atypical parkinsonisms. These disorders are characterized by varying combinations of autonomic, cerebellar and pyramidal system ...
Belvisi, Daniele   +6 more
core   +1 more source

Characterization of an Inherited Neurologic Syndrome in Toyger Cats with Forebrain Commissural Malformations, Ventriculomegaly and Interhemispheric Cysts. [PDF]

open access: yes, 2016
BackgroundIn children, frequent congenital malformations with concomitant agenesis of the corpus callosum are diagnosed by neuroimaging in association with other cerebral malformations, including interhemispheric cysts and ventriculomegaly.
Creighton, EK   +5 more
core  

Abnormal resting-state functional connectivity in progressive supranuclear palsy and corticobasal syndrome [PDF]

open access: yes, 2017
Background: Pathological and MRI-based evidence suggests that multiple brain structures are likely to be involved in functional disconnection between brain areas. Few studies have investigated resting-state functional connectivity (rsFC) in progressive
Berardelli, Alfredo   +9 more
core   +2 more sources

Co-Occurrence of Multiple Endocrine Abnormalities Induced by the DIHS/DRESS

open access: yesInternational Journal of Endocrinology, 2019
Background. Drug-induced hypersensitivity syndrome/drug reaction with eosinophilia and systemic symptoms (DIHS/DRESS) is a severe adverse reaction caused by specific drugs.
Mingqun Deng   +5 more
doaj   +1 more source

Prothrombotic coagulation abnormalities in patients with newly diagnosed multiple myeloma

open access: yesHaematologica, 2007
Prothrombotic coagulation abnormalities were analyzed in patients with untreated multiple myeloma. Increases in factor VIII, in von Willebrand factor and a decrease in protein S were observed and these changes were strongly associated with disease stage.
Johannes J.A. Auwerda   +3 more
doaj   +1 more source

Corticobasal syndrome: neuroimaging and neurophysiological advances [PDF]

open access: yes, 2019
Corticobasal degeneration (CBD) is a neurodegenerative condition characterized by 4R-tau protein deposition in several brain regions that clinically manifests itself as a heterogeneous atypical parkinsonism typically expressing in the adulthood.
Asci, Francesco   +9 more
core   +1 more source

Foraminiferal test abnormalities in the western Baltic Sea [PDF]

open access: yes, 2008
Abnormal tests were commonly found in recent benthic foraminiferal assemblages in two fjords of the Kiel Bay, the western Baltic Sea. We assessed 18 different types of abnormalities, which were classified into five groups: chamber, apertural, umbilical ...
Polovodova, Irina, Schönfeld, Joachim
core   +1 more source

Multiple Electrolyte Abnormalities after Pamidronate Administration

open access: yesNephron, 1998
Pamidronate constitutes a major advance in the treatment of tumor-associated hypercalcemia. However, transient electrolyte abnormalities have been reported after pamidronate administration. We describe here a patient with multiple myeloma and severe hypercalcemia who developed transient but significant electrolyte disturbances (mainly hypophosphatemia ...
Elisaf, M. S.   +2 more
openaire   +3 more sources

Voxel-Based Meta-Analysis of Gray Matter Abnormalities in Multiple System Atrophy

open access: yesFrontiers in Aging Neuroscience, 2020
Purpose: This study aimed to identify consistent gray matter volume (GMV) changes in the two subtypes of multiple system atrophy (MSA), including parkinsonism subtype (MSA-P), and cerebellar subtype (MSA-C), by conducting a voxel-wise meta-analysis of ...
Junyu Lin   +4 more
doaj   +1 more source

Congenital microcephaly [PDF]

open access: yes, 2014
The underlying etiologies of genetic congenital microcephaly are complex and multifactorial. Recently, with the exponential growth in the identification and characterization of novel genetic causes of congenital microcephaly, there has been a ...
Agha   +129 more
core   +1 more source

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