Results 11 to 20 of about 2,424 (174)
Dyke-Davidoff-Masson syndrome: case report of fetal unilateral ventriculomegaly and hypoplastic left middle cerebral artery [PDF]
, 2013 Prenatal ultrasonographic detection of unilateral cerebral ventriculomegaly arises suspicion of pathological condition related to cerebrospinal fluid flow obstruction or cerebral parenchimal pathology.
CORSELLO, Giovanni +4 more
core +3 more sources
PLoS ONE, 2021 Captive cheetahs often demonstrate a high incidence of diseases in which vitamin A imbalances are implicated. These can occur even under controlled and optimised feeding regimens, which is why surveillance of vitamin A status is mandatory in the ...
Martin J. Schmidt +4 more
doaj +2 more sources
Primary intraosseous meningioma: an osteosclerotic bone tumour mimicking malignancy [PDF]
, 2016 BACKGROUND: Sclerotic tumours of the calvarial bones are rare and may be due to primary and secondary bone tumours as well as extradural tumours of meningeal origin. CASE PRESENTATION: We report a case of primary intraosseous meningioma (PIM) which arose
M. Vlychou +3 more
core +1 more source
CALVARIAL THICKENING AFTER DILANTIN MEDICATION [PDF]
American Journal of Roentgenology, 1970 Increase in the thickness of the calvaria, mainly in the diploic space, was noticed in epileptic patients receiving dilantin for prolonged periods. The younger the patient, the more prominent were the changes. Three white teenage patients are reported with skull roentgenograms before and 3 or more years after the institution of dilantin medication.
openaire +2 more sources
Neurological symptoms and natural course of xeroderma pigmentosum [PDF]
, 2008 We have prospectively followed 16 Finnish xeroderma pigmentosum (XP) patients for up to 23 years. Seven patients were assigned by complementation analysis to the group XP-A, two patients to the XP-C group and one patient to the XP-G group.
Anttinen, Anu +12 more
core +3 more sources
Adult Presentation of Dyke-Davidoff-Masson Syndrome: A Case Report
Case Reports in Neurology, 2016 Dyke-Davidoff-Masson syndrome (DDMS) is a rare disease which is clinically characterized by hemiparesis, seizures, facial asymmetry, and mental retardation.
Ujjawal Roy +3 more
doaj +1 more source
Local origins impart conserved bone type-related differences in human osteoblast behaviour [PDF]
, 2015 Osteogenic behaviour of osteoblasts from trabecular, cortical and subchondral bone were examined to determine any bone type-selective differences in samples from both osteoarthritic (OA) and osteoporotic (OP) patients.
Clarkin, C E +6 more
core +3 more sources
BMC Neurology, 2022 Background As the third most common malignancy of childhood, Neuroblastoma has a great propensity to metastasize to multiple organs. The most common site of metastasis is the bone and bone marrow.
Samin Khoei +2 more
doaj +1 more source
F1000Research, 2021 Dyke-Davidoff-Masson syndrome (DMMS) is a non-inherited rare condition with a clinical constellation of hemiparesis/hemiplegia, facial asymmetry, intellectual disability, and epilepsy.
Mohamed Alshmandi +5 more
doaj +1 more source
Ablation of Tak l in osteoclast progenitor leads to defects in skeletal growth and bone remodeling in mice [PDF]
, 2014 Tak1 is a MAPKKK that can be activated by growth factors and cytokines such as RANKL and BMPs and its downstream pathways include NF-κB and JNK/p38 MAPKs.
Cong, Q +9 more
core +1 more source