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Now showing items 231-240 of 468
Hyperform Balloon-Assisted Endovascular Neck Bypass Technique To Perform Balloon Or Stentassisted Treatment Of Cerebral Aneurysms
(Amer Soc Neuroradiology, 2007)
We describe a technique to bypass aneurysm neck using the HyperForm balloon to perform balloon- or stent-assisted enclovascular treatment of complex large or giant aneurysms with very wide neck in which other methods would ...
Laparoscopic Presacral Neurolysis for Endometriosis-Related Pelvic Pain
(Oxford Univ Press, 2003)
BACKGROUND: Some patients with endometriosis are candidates for sympathectomy of the superior hypogastric plexus. The objective of this paper is to describe our technique of laparoscopic presacral neurolysis for sympathectomy ...
Automated Discrimination of Psychotropic Drugs in Mice Via Computer Vision-Based Analysis
(Elsevier Science Bv, 2009)
We developed an inexpensive computer vision-based method utilizing an algorithm which differentiates drug-induced behavioral alterations. The mice were observed in an open-field arena and their activity was recorded for ...
Estrogen And Aging Affect Synaptic Distribution Of Phosphorylated Lim Kinase (Plimk) In Ca1 Region Of Female Rat Hippocampus
(Pergamon-Elsevier Science Ltd, 2008)
17 beta-Estradiol (E) increases axospinous synapse density in the hippocampal CA1 region of young female rats, but not in aged rats. This may be linked to age-related alterations in signaling pathways activated by synaptic ...
The Role Of Nitric Oxide In The Electrical Field Stimulation-Induced Contractions Of Sphincter Of Oddi And Gallbladder Strips In Guinea Pigs
(Japanese Pharmacological Soc, 2006)
The aim of this study was to investigate the modulatory role of nitric oxide (NO) in the electrical field stimulation (EFS)-induced contractions of isolated sphincter of Oddi (SO) and gallbladder strips from guinea pigs. ...
Clinically Abnormal Case With Paternally Derived Partial Trisomy 8P23.3 To 8P12 Including Maternal Isodisomy Of 8P23.3: A Case Report
(2009)
Background Because of low copy repeats (LCRs) and common inversion polymorphisms, the human chromosome 8p is prone to a number of recurrent rearrangements. Each of these rearrangements is associated with several phenotypic ...
Congenital Contractural Arachnodactyly (Beals Syndrome)
(2006)
Congenital contractural arachnodactyly (Beals syndrome) is an autosomal dominantly inherited connective tissue disorder characterized by multiple flexion contractures, arachnodactyly, severe kyphoscoliosis, abnormal pinnae ...
Molecular And Clinical Spectrum Of Type I Plasminogen Deficiency: A Series Of 50 Patients
(Amer Soc Hematology, 2006)
Severe type I plasminogen (PLG) deficiency has been causally linked to a rare chronic inflammatory disease of the mucous membranes that may be life threatening. Here we report clinical manifestations, PLG plasma levels, ...
Mutations In The Very Low-Density Lipoprotein Receptor Vldlr Cause Cerebellar Hypoplasia And Quadrupedal Locomotion In Humans
(Natl Acad Sciences, 2008)
Quadrupedal gait in humans, also known as Unertan syndrome, is a rare phenotype associated with dysarthric speech, mental retardation, and varying degrees of cerebrocerebellar hypoplasia. Four large consanguineous kindreds ...