Results 91 to 100 of about 8,444 (208)
Análise da melhor alternativa terapêutica para malformações arteriovenosas durais intracranianas [PDF]
, 2005 The material for this research consisted of 93 patients with dural arteriovenous malformations (DAVMs) who were studied retrospectively with regards to therapeutic success and failure, who had undergone either neurosurgery, or embolization or a ...
Caldas, José Guilherme Mendes Pereira +2 more
core +4 more sources
Molecular Diagnosis in a Specialised Neurogenetic Clinic With Access to Whole‐Genome Sequencing
Acta Neurologica Scandinavica, Volume 2026, Issue 1, 2026.Background Rare diseases, collectively affecting 1 in 17 people in the United Kingdom and Ireland, require coordinated care. Specialised multidisciplinary clinics offer a streamlined approach for diagnosis and management of rare neurogenetic disorders.
Patrick B. Moloney +2 more
wiley +1 more source
Cerebral Cavernous Malformations
Indian Journal of Dermatology, 2021 Igor Vazquez-Osorio +4 more
openaire +5 more sources
Advances in the biology of cerebral cavernous malformations
Surgical Neurology International, 2010 To provide a review of current, high-impact scientific findings pertaining to the biology of cerebral cavernous malformations (CCMs).A comprehensive literature review was conducted using PubMed to examine the current literature regarding the molecular biology and pathophysiology of CCMs.In this literature review, a comprehensive approach is taken to ...
Hauptman, Jason S. +4 more
openaire +6 more sources
Efficacy and Mechanism EvaluationBackground Symptomatic cerebral cavernous malformations are a rare sporadic or familial disease, which may cause haemorrhagic strokes or epileptic seizures.
Rustam Al-Shahi Salman +10 more
doaj +1 more source
Unexpected distribution of KRIT1 inside the nucleus: new insight in a complex molecular pathway
European Journal of Histochemistry, 2014 KRIT1 is an 84kDa protein that lacks any relevant catalytic domains, associated with the cerebral cavernous malformation disease. We have investigated by means of ultrastructural immunocytochemistry the nuclear distribution of KRIT1 in different cell ...
S. Marzo, V. Galimberti, M. Biggiogera
doaj +1 more source
Acta Neurologica Scandinavica, Volume 2026, Issue 1, 2026.Objectives Peak width of skeletonized mean diffusivity (PSMD) serves as a new biomarker for diffuse white matter microstructural damage. This study is aimed at quantifying PSMD in patients with status epilepticus (SE) to investigate white matter microstructural abnormalities and their potential association with small vessel disease (SVD) mechanisms in ...
Jinseung Kim +4 more
wiley +1 more source
Two Cases of Oculomotor Nerve Palsy in Idiopathic Intracranial Hypertension and a Literature Review
Case Reports in Neurological Medicine, Volume 2026, Issue 1, 2026.Idiopathic intracranial hypertension (IIH) is characterized by elevated intracranial pressure in the absence of a secondary cause. Classically, it presents with headache, visual obscurations, pulsatile tinnitus, and diplopia, most commonly due to abducens nerve palsy. Involvement of other cranial nerves is rare.
Parth A. Patel +3 more
wiley +1 more source
Angiomas cavernosos cerebrales múltiples tipo IV en paciente de 7 años [PDF]
, 2014 This is a presentation of a clinical case of an unusual pathology due to multiple manifestation of benign cerebral vascular angiocavernomas. Generally described in the literature for the presence of unique masses at a supratentorial level.
Cevallos Castañeda, Edison Ramiro
core
Cranial nerve cavernous malformations causing trigeminal neuralgia and chiasmal apoplexy: report of 2 cases and review of literature [PDF]
, 2012 Objective: To verify whether fluorescence in situ hybridization (FISH) of cells from the buccal epithelium could be employed to detect cryptomosaicism with a 45,X lineage in 46,XY patients.
Andrade, Juliana Gabriel Ribeiro de +5 more
core +6 more sources