Results 91 to 100 of about 1,916 (204)
Inherited cavernous malformations of the central nervous system: clinical and genetic features in 19 Swiss families [PDF]
Cavernous malformations (CCMs) are benign, well-circumscribed, and mulberry-like vascular malformations that may be found in the central nervous system in up to 0.5% of the population. Cavernous malformations can be sporadic or inherited.
Andermann, F. +11 more
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Markov models for clinical decision‐making in radiation oncology: A systematic review
Abstract The intrinsic stochasticity of patients' response to treatment is a major consideration for clinical decision‐making in radiation therapy. Markov models are powerful tools to capture this stochasticity and render effective treatment decisions.
Lucas B McCullum +10 more
wiley +1 more source
Endothelial cell diversity: the many facets of the crystal
Endothelial cells form the inner lining of blood vessels and play crucial roles in angiogenesis. Recent years have seen a surge in the identification of spatiotemporal molecular and functional heterogeneity of ECs. In this review, we highlight many aspects of the diversity of ECs, such as their morphological heterogeneity, the paracrine release of ...
Lorena Perez‐Gutierrez +2 more
wiley +1 more source
Cavernous Malformations of the Brain: Natural History and Surgical Outcomes
Cerebral cavernous malformations (CCM) are rare, benign vascular anomalies of the central nervous system with a prevalence of 0.5–0.8%. While often discovered incidentally, they may present with seizures, headaches, focal neurological deficits, or ...
Noman Ahmed +2 more
doaj +1 more source
Angiopoietin-2 predicts morbidity in adults with Fontan physiology. [PDF]
Morbidity in patients with single-ventricle Fontan circulation is common and includes arrhythmias, edema, and pulmonary arteriovenous malformations (PAVM) among others. We sought to identify biomarkers that may predict such complications.
Aboulhosn, Jamil A +8 more
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Abstract Introduction: Brainstem cerebral cavernous malformations (CCM) are clinically more aggressive compared to superficial CCMs. Due to their location, resection can be challenging, making stereotactic radiosurgery (SRS) an attractive alternative for symptomatic patient.
Dayawansa, Sam +35 more
openaire +4 more sources
Creation of a database for evaluating the effect of genetic intellectual property on genetic diagnostic testing [PDF]
Thesis (S.B.)--Massachusetts Institute of Technology, Dept. of Mechanical Engineering, 2006.Includes bibliographical references (leaves 33-34).In this study, we explore the impact of gene-based patents on the pricing and availability of genetic ...
Murray, Philip (Philip E.)
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FAM222B Is Not a Likely Novel Candidate Gene for Cerebral Cavernous Malformations [PDF]
Cerebral cavernous malformations (CCMs) are prevalent slow-flow vascular lesions which harbour the risk to develop intracranial haemorrhages, focal neurological deficits, and epileptic seizures.
Acker-Palmer, Amparo +12 more
core +1 more source
Background Cerebral cavernous malformations are complex vascular anomalies in the central nervous system associated with a risk of intracranial hemorrhage.
Basel Musmar +9 more
doaj +1 more source
The role of MiR-23b-3p in the epileptogenesis [PDF]
癫痫是指脑部持续存在能导致癫痫反复发作,并出现相应的神经生物学、认知、心理学,以及社会学等方面的后果的脑部疾患。目前miRNA在癫痫发生发展中的作用引起越来越多的重视。miR-23b-3p是具有多种生物学作用的miRNA,如调节神经元增殖、分化和凋亡等,参与多种神经退行性疾病的病理机制。 本研究通过腹腔注射海人酸(Kainicacid,KA)构建小鼠癫痫模型,发作达到Racine标准的4-5级作为实验组纳入标准,对照组注射相同剂量的生理盐水,并应用荧光定量PCR法对皮层和海马组织中miR-23b-3p ...
战连波
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