Ventricular Volume Dynamics During the Development of Adult Chronic Communicating Hydrocephalus in a Rodent Model
The pathophysiology of normal-pressure hydrocephalus and the correlation with its symptomatology is not well understood. To monitor and evaluate the enlargement patterns of the ventricular system for each ventricle and its correlation with the presenting symptoms. Bilateral kaolin injection into the...
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Veröffentlicht in: | World neurosurgery 2018-12, Vol.120, p.e1120-e1127 |
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creator | Vivas-Buitrago, Tito Pinilla-Monsalve, Gabriel Jusué-Torres, Ignacio Oishi, Kumiko Robison, Jamie Crawford, Joshua A. Pletnikov, Mikhail Xu, Jiadi Baledént, Olivier Lokossou, Armelle Hung, Alice L. Blitz, Ari M. Lu, Jennifer Herzka, Daniel A. Guerrero-Cazares, Hugo Oishi, Kenichi Mori, Susumu Quiñones-Hinojosa, Alfredo Rigamonti, Daniele |
description | The pathophysiology of normal-pressure hydrocephalus and the correlation with its symptomatology is not well understood.
To monitor and evaluate the enlargement patterns of the ventricular system for each ventricle and its correlation with the presenting symptoms.
Bilateral kaolin injection into the subarachnoid space overlying the cranial convexities was done in 18 adult rats. Magnetic resonance imaging was performed on an 11.7-T scanner 15, 60, 90, and 120 days after injection. Volumes of the ventricular system were measured for each ventricle and correlated with biweekly behavioral findings.
There was a progressive increase in the ventricular volume for the lateral ventricles since day 15 in the kaolin-injected animals. There was a nonsignificant trend in volume growth for the third ventricle, but its enlargement was synchronous with the lateral ventricles. No significant change for the fourth ventricle. No symptoms were detected in the first 60 days. Association was found between the ventricular volume and locomotor changes. In addition, the odds of locomotor symptoms increased by 3% for every additional cubic millimeter of volume in the left (P < 0.001) and right (P = 0.023) ventricles, and for the total magnetic resonance imaging volume by 1% (P = 0.013).
Expansion of the lateral ventricles maintained similar proportions over time, accompanied by a synchronous third ventricular expansion with less proportion and a nonsignificant fourth enlargement. Lateral ventricles enlarged most in those animals that were to develop late locomotor deterioration. Further research using this animal model combined with different radiologic imaging techniques, such as diffusion tensor imaging and perfusion studies, is recommended.
•Ventricular volumetric analysis of adult chronic communicating hydrocephalus in an animal model.•11.7 Tesla Brain MRI acquisition in Sprague-Dawley rats.•Kaolin injection into the subarachnoid space over the convexities.•Simultaneous expansion of the lateral ventricles with synchronous enlargement of third and non-significant fourth changes.•Lateral ventricles enlarged most in those animals that were to develop late locomotor deterioration. |
doi_str_mv | 10.1016/j.wneu.2018.08.241 |
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To monitor and evaluate the enlargement patterns of the ventricular system for each ventricle and its correlation with the presenting symptoms.
Bilateral kaolin injection into the subarachnoid space overlying the cranial convexities was done in 18 adult rats. Magnetic resonance imaging was performed on an 11.7-T scanner 15, 60, 90, and 120 days after injection. Volumes of the ventricular system were measured for each ventricle and correlated with biweekly behavioral findings.
There was a progressive increase in the ventricular volume for the lateral ventricles since day 15 in the kaolin-injected animals. There was a nonsignificant trend in volume growth for the third ventricle, but its enlargement was synchronous with the lateral ventricles. No significant change for the fourth ventricle. No symptoms were detected in the first 60 days. Association was found between the ventricular volume and locomotor changes. In addition, the odds of locomotor symptoms increased by 3% for every additional cubic millimeter of volume in the left (P < 0.001) and right (P = 0.023) ventricles, and for the total magnetic resonance imaging volume by 1% (P = 0.013).
Expansion of the lateral ventricles maintained similar proportions over time, accompanied by a synchronous third ventricular expansion with less proportion and a nonsignificant fourth enlargement. Lateral ventricles enlarged most in those animals that were to develop late locomotor deterioration. Further research using this animal model combined with different radiologic imaging techniques, such as diffusion tensor imaging and perfusion studies, is recommended.
•Ventricular volumetric analysis of adult chronic communicating hydrocephalus in an animal model.•11.7 Tesla Brain MRI acquisition in Sprague-Dawley rats.•Kaolin injection into the subarachnoid space over the convexities.•Simultaneous expansion of the lateral ventricles with synchronous enlargement of third and non-significant fourth changes.•Lateral ventricles enlarged most in those animals that were to develop late locomotor deterioration.</description><identifier>ISSN: 1878-8750</identifier><identifier>EISSN: 1878-8769</identifier><identifier>DOI: 10.1016/j.wneu.2018.08.241</identifier><identifier>PMID: 30217783</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Animal model ; Animals ; Behavioral changes ; Cerebral Ventricles - diagnostic imaging ; Cerebral Ventricles - pathology ; Cerebral Ventricles - physiopathology ; Disease Models, Animal ; Disease Progression ; Female ; Hydrocephalus - diagnostic imaging ; Hydrocephalus - pathology ; Hydrocephalus - physiopathology ; Kaolin ; Life Sciences ; Magnetic Resonance Imaging ; Normal pressure hydrocephalus ; Organ Size ; Rats, Sprague-Dawley ; Ventricular volume enlargement ; Volumetric measurement</subject><ispartof>World neurosurgery, 2018-12, Vol.120, p.e1120-e1127</ispartof><rights>2018 Elsevier Inc.</rights><rights>Copyright © 2018 Elsevier Inc. All rights reserved.</rights><rights>Distributed under a Creative Commons Attribution 4.0 International License</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c390t-fed747ae8938a6148c13931c04471fdc93e37872d86237edc611d672ca0f23593</citedby><cites>FETCH-LOGICAL-c390t-fed747ae8938a6148c13931c04471fdc93e37872d86237edc611d672ca0f23593</cites><orcidid>0000-0001-6028-6440</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.wneu.2018.08.241$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>230,314,780,784,885,3541,27915,27916,45986</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30217783$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://u-picardie.hal.science/hal-03599026$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>Vivas-Buitrago, Tito</creatorcontrib><creatorcontrib>Pinilla-Monsalve, Gabriel</creatorcontrib><creatorcontrib>Jusué-Torres, Ignacio</creatorcontrib><creatorcontrib>Oishi, Kumiko</creatorcontrib><creatorcontrib>Robison, Jamie</creatorcontrib><creatorcontrib>Crawford, Joshua A.</creatorcontrib><creatorcontrib>Pletnikov, Mikhail</creatorcontrib><creatorcontrib>Xu, Jiadi</creatorcontrib><creatorcontrib>Baledént, Olivier</creatorcontrib><creatorcontrib>Lokossou, Armelle</creatorcontrib><creatorcontrib>Hung, Alice L.</creatorcontrib><creatorcontrib>Blitz, Ari M.</creatorcontrib><creatorcontrib>Lu, Jennifer</creatorcontrib><creatorcontrib>Herzka, Daniel A.</creatorcontrib><creatorcontrib>Guerrero-Cazares, Hugo</creatorcontrib><creatorcontrib>Oishi, Kenichi</creatorcontrib><creatorcontrib>Mori, Susumu</creatorcontrib><creatorcontrib>Quiñones-Hinojosa, Alfredo</creatorcontrib><creatorcontrib>Rigamonti, Daniele</creatorcontrib><title>Ventricular Volume Dynamics During the Development of Adult Chronic Communicating Hydrocephalus in a Rodent Model</title><title>World neurosurgery</title><addtitle>World Neurosurg</addtitle><description>The pathophysiology of normal-pressure hydrocephalus and the correlation with its symptomatology is not well understood.
To monitor and evaluate the enlargement patterns of the ventricular system for each ventricle and its correlation with the presenting symptoms.
Bilateral kaolin injection into the subarachnoid space overlying the cranial convexities was done in 18 adult rats. Magnetic resonance imaging was performed on an 11.7-T scanner 15, 60, 90, and 120 days after injection. Volumes of the ventricular system were measured for each ventricle and correlated with biweekly behavioral findings.
There was a progressive increase in the ventricular volume for the lateral ventricles since day 15 in the kaolin-injected animals. There was a nonsignificant trend in volume growth for the third ventricle, but its enlargement was synchronous with the lateral ventricles. No significant change for the fourth ventricle. No symptoms were detected in the first 60 days. Association was found between the ventricular volume and locomotor changes. In addition, the odds of locomotor symptoms increased by 3% for every additional cubic millimeter of volume in the left (P < 0.001) and right (P = 0.023) ventricles, and for the total magnetic resonance imaging volume by 1% (P = 0.013).
Expansion of the lateral ventricles maintained similar proportions over time, accompanied by a synchronous third ventricular expansion with less proportion and a nonsignificant fourth enlargement. Lateral ventricles enlarged most in those animals that were to develop late locomotor deterioration. Further research using this animal model combined with different radiologic imaging techniques, such as diffusion tensor imaging and perfusion studies, is recommended.
•Ventricular volumetric analysis of adult chronic communicating hydrocephalus in an animal model.•11.7 Tesla Brain MRI acquisition in Sprague-Dawley rats.•Kaolin injection into the subarachnoid space over the convexities.•Simultaneous expansion of the lateral ventricles with synchronous enlargement of third and non-significant fourth changes.•Lateral ventricles enlarged most in those animals that were to develop late locomotor deterioration.</description><subject>Animal model</subject><subject>Animals</subject><subject>Behavioral changes</subject><subject>Cerebral Ventricles - diagnostic imaging</subject><subject>Cerebral Ventricles - pathology</subject><subject>Cerebral Ventricles - physiopathology</subject><subject>Disease Models, Animal</subject><subject>Disease Progression</subject><subject>Female</subject><subject>Hydrocephalus - diagnostic imaging</subject><subject>Hydrocephalus - pathology</subject><subject>Hydrocephalus - physiopathology</subject><subject>Kaolin</subject><subject>Life Sciences</subject><subject>Magnetic Resonance Imaging</subject><subject>Normal pressure hydrocephalus</subject><subject>Organ Size</subject><subject>Rats, Sprague-Dawley</subject><subject>Ventricular volume enlargement</subject><subject>Volumetric measurement</subject><issn>1878-8750</issn><issn>1878-8769</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kU9rGzEQxUVpSEKSL5BD0bE9eKM_65UWejFOGwccAqXNVajSbC2jXTnSysXfvlqc-pi5zDD83mOYh9AtJRUltLnbVn8HyBUjVFZEVqymH9AllULOpGjaj6d5Ti7QTUpbUorTWgp-ji44YVQIyS_R6wsMY3Qmex3xS_C5B3x_GHTvTML3ObrhDx43ZQd78GHXFxqHDi9s9iNebmIYnMHL0Pe5DHqc8NXBxmBgt9E-J-wGrPGPYCfhU2n-Gp112ie4eetX6Nf3bz-Xq9n6-eFxuVjPDG_JOOvAilpokC2XuimHG8pbTg2pa0E7a1oOXEjBrGwYF2BNQ6ltBDOadIzPW36Fvhx9yx1qF12v40EF7dRqsVbTjhSqJazZ08J-PrK7GF4zpFH1LhnwXg8QclKMkjmpeU0nW3ZETQwpRehO3pSoKRm1VVMyakpGEalKMkX06c0__-7BniT_cyjA1yMA5SN7B1El42AwYF0EMyob3Hv-_wA18p7C</recordid><startdate>20181201</startdate><enddate>20181201</enddate><creator>Vivas-Buitrago, Tito</creator><creator>Pinilla-Monsalve, Gabriel</creator><creator>Jusué-Torres, Ignacio</creator><creator>Oishi, Kumiko</creator><creator>Robison, Jamie</creator><creator>Crawford, Joshua A.</creator><creator>Pletnikov, Mikhail</creator><creator>Xu, Jiadi</creator><creator>Baledént, Olivier</creator><creator>Lokossou, Armelle</creator><creator>Hung, Alice L.</creator><creator>Blitz, Ari M.</creator><creator>Lu, Jennifer</creator><creator>Herzka, Daniel A.</creator><creator>Guerrero-Cazares, Hugo</creator><creator>Oishi, Kenichi</creator><creator>Mori, Susumu</creator><creator>Quiñones-Hinojosa, Alfredo</creator><creator>Rigamonti, Daniele</creator><general>Elsevier Inc</general><general>Elsevier</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>1XC</scope><orcidid>https://orcid.org/0000-0001-6028-6440</orcidid></search><sort><creationdate>20181201</creationdate><title>Ventricular Volume Dynamics During the Development of Adult Chronic Communicating Hydrocephalus in a Rodent Model</title><author>Vivas-Buitrago, Tito ; Pinilla-Monsalve, Gabriel ; Jusué-Torres, Ignacio ; Oishi, Kumiko ; Robison, Jamie ; Crawford, Joshua A. ; Pletnikov, Mikhail ; Xu, Jiadi ; Baledént, Olivier ; Lokossou, Armelle ; Hung, Alice L. ; Blitz, Ari M. ; Lu, Jennifer ; Herzka, Daniel A. ; Guerrero-Cazares, Hugo ; Oishi, Kenichi ; Mori, Susumu ; Quiñones-Hinojosa, Alfredo ; Rigamonti, Daniele</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c390t-fed747ae8938a6148c13931c04471fdc93e37872d86237edc611d672ca0f23593</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Animal model</topic><topic>Animals</topic><topic>Behavioral changes</topic><topic>Cerebral Ventricles - diagnostic imaging</topic><topic>Cerebral Ventricles - pathology</topic><topic>Cerebral Ventricles - physiopathology</topic><topic>Disease Models, Animal</topic><topic>Disease Progression</topic><topic>Female</topic><topic>Hydrocephalus - diagnostic imaging</topic><topic>Hydrocephalus - pathology</topic><topic>Hydrocephalus - physiopathology</topic><topic>Kaolin</topic><topic>Life Sciences</topic><topic>Magnetic Resonance Imaging</topic><topic>Normal pressure hydrocephalus</topic><topic>Organ Size</topic><topic>Rats, Sprague-Dawley</topic><topic>Ventricular volume enlargement</topic><topic>Volumetric measurement</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Vivas-Buitrago, Tito</creatorcontrib><creatorcontrib>Pinilla-Monsalve, Gabriel</creatorcontrib><creatorcontrib>Jusué-Torres, Ignacio</creatorcontrib><creatorcontrib>Oishi, Kumiko</creatorcontrib><creatorcontrib>Robison, Jamie</creatorcontrib><creatorcontrib>Crawford, Joshua A.</creatorcontrib><creatorcontrib>Pletnikov, Mikhail</creatorcontrib><creatorcontrib>Xu, Jiadi</creatorcontrib><creatorcontrib>Baledént, Olivier</creatorcontrib><creatorcontrib>Lokossou, Armelle</creatorcontrib><creatorcontrib>Hung, Alice L.</creatorcontrib><creatorcontrib>Blitz, Ari M.</creatorcontrib><creatorcontrib>Lu, Jennifer</creatorcontrib><creatorcontrib>Herzka, Daniel A.</creatorcontrib><creatorcontrib>Guerrero-Cazares, Hugo</creatorcontrib><creatorcontrib>Oishi, Kenichi</creatorcontrib><creatorcontrib>Mori, Susumu</creatorcontrib><creatorcontrib>Quiñones-Hinojosa, Alfredo</creatorcontrib><creatorcontrib>Rigamonti, Daniele</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>Hyper Article en Ligne (HAL)</collection><jtitle>World neurosurgery</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Vivas-Buitrago, Tito</au><au>Pinilla-Monsalve, Gabriel</au><au>Jusué-Torres, Ignacio</au><au>Oishi, Kumiko</au><au>Robison, Jamie</au><au>Crawford, Joshua A.</au><au>Pletnikov, Mikhail</au><au>Xu, Jiadi</au><au>Baledént, Olivier</au><au>Lokossou, Armelle</au><au>Hung, Alice L.</au><au>Blitz, Ari M.</au><au>Lu, Jennifer</au><au>Herzka, Daniel A.</au><au>Guerrero-Cazares, Hugo</au><au>Oishi, Kenichi</au><au>Mori, Susumu</au><au>Quiñones-Hinojosa, Alfredo</au><au>Rigamonti, Daniele</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Ventricular Volume Dynamics During the Development of Adult Chronic Communicating Hydrocephalus in a Rodent Model</atitle><jtitle>World neurosurgery</jtitle><addtitle>World Neurosurg</addtitle><date>2018-12-01</date><risdate>2018</risdate><volume>120</volume><spage>e1120</spage><epage>e1127</epage><pages>e1120-e1127</pages><issn>1878-8750</issn><eissn>1878-8769</eissn><abstract>The pathophysiology of normal-pressure hydrocephalus and the correlation with its symptomatology is not well understood.
To monitor and evaluate the enlargement patterns of the ventricular system for each ventricle and its correlation with the presenting symptoms.
Bilateral kaolin injection into the subarachnoid space overlying the cranial convexities was done in 18 adult rats. Magnetic resonance imaging was performed on an 11.7-T scanner 15, 60, 90, and 120 days after injection. Volumes of the ventricular system were measured for each ventricle and correlated with biweekly behavioral findings.
There was a progressive increase in the ventricular volume for the lateral ventricles since day 15 in the kaolin-injected animals. There was a nonsignificant trend in volume growth for the third ventricle, but its enlargement was synchronous with the lateral ventricles. No significant change for the fourth ventricle. No symptoms were detected in the first 60 days. Association was found between the ventricular volume and locomotor changes. In addition, the odds of locomotor symptoms increased by 3% for every additional cubic millimeter of volume in the left (P < 0.001) and right (P = 0.023) ventricles, and for the total magnetic resonance imaging volume by 1% (P = 0.013).
Expansion of the lateral ventricles maintained similar proportions over time, accompanied by a synchronous third ventricular expansion with less proportion and a nonsignificant fourth enlargement. Lateral ventricles enlarged most in those animals that were to develop late locomotor deterioration. Further research using this animal model combined with different radiologic imaging techniques, such as diffusion tensor imaging and perfusion studies, is recommended.
•Ventricular volumetric analysis of adult chronic communicating hydrocephalus in an animal model.•11.7 Tesla Brain MRI acquisition in Sprague-Dawley rats.•Kaolin injection into the subarachnoid space over the convexities.•Simultaneous expansion of the lateral ventricles with synchronous enlargement of third and non-significant fourth changes.•Lateral ventricles enlarged most in those animals that were to develop late locomotor deterioration.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>30217783</pmid><doi>10.1016/j.wneu.2018.08.241</doi><orcidid>https://orcid.org/0000-0001-6028-6440</orcidid></addata></record> |
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subjects | Animal model Animals Behavioral changes Cerebral Ventricles - diagnostic imaging Cerebral Ventricles - pathology Cerebral Ventricles - physiopathology Disease Models, Animal Disease Progression Female Hydrocephalus - diagnostic imaging Hydrocephalus - pathology Hydrocephalus - physiopathology Kaolin Life Sciences Magnetic Resonance Imaging Normal pressure hydrocephalus Organ Size Rats, Sprague-Dawley Ventricular volume enlargement Volumetric measurement |
title | Ventricular Volume Dynamics During the Development of Adult Chronic Communicating Hydrocephalus in a Rodent Model |
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