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Select item 102166411.

Cerebrospinal Fluid–Basic Concepts Review

Natalia Czarniak, Joanna Kamińska, Joanna Matowicka-Karna, Olga Martyna Koper-Lenkiewicz

Biomedicines. 2023 May; 11(5): 1461. Published online 2023 May 17. doi: 10.3390/biomedicines11051461

PMCID:: PMC10216641

Article PDF–4.7M

Select item 79165612.

Cerebrospinal Fluid Biomarkers of Alzheimer’s Disease: Current Evidence and Future Perspectives

Donovan A. McGrowder, Fabian Miller, Kurt Vaz, Chukwuemeka Nwokocha, Cameil Wilson-Clarke, Melisa Anderson-Cross, Jabari Brown, Lennox Anderson-Jackson, Lowen Williams, Lyndon Latore, Rory Thompson, Ruby Alexander-Lindo

Brain Sci. 2021 Feb; 11(2): 215. Published online 2021 Feb 10. doi: 10.3390/brainsci11020215

PMCID:: PMC7916561

Article PDF–2.1M

Select item 88971543.

Fluid transport in the brain

Martin Kaag Rasmussen, Humberto Mestre, Maiken Nedergaard

Physiol Rev. 2022 Apr 1; 102(2): 1025–1151. Published online 2021 May 5. doi: 10.1152/physrev.00031.2020

PMCID:: PMC8897154

Article

Select item 62060304.

Rapid pathogen identification using a novel microarray-based assay with purulent meningitis in cerebrospinal fluid

Yuting Hou, Xu Zhang, Xiaolin Hou, Ruofen Wu, Yanbai Wang, Xuexian He, Libin Wang, Zhenhai Wang

Sci Rep. 2018; 8: 15965. Published online 2018 Oct 29. doi: 10.1038/s41598-018-34051-0

PMCID:: PMC6206030

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Select item 94065675.

Basic Analysis of the Cerebrospinal Fluid: An Important Framework for Laboratory Diagnostics of the Impairment of the Central Nervous System

Petr Kelbich, Karel Hrach, Jan Spicka, Petr Vachata, Tomas Radovnicky, Eva Hanuljakova, Jan Krejsek

Curr Issues Mol Biol. 2022 Aug; 44(8): 3666–3680. Published online 2022 Aug 14. doi: 10.3390/cimb44080251

PMCID:: PMC9406567

Article PDF–1.6M

Select item 80044966.

Cerebrospinal fluid outflow: a review of the historical and contemporary evidence for arachnoid villi, perineural routes, and dural lymphatics

Steven T. Proulx

Cell Mol Life Sci. 2021; 78(6): 2429–2457. Published online 2021 Jan 11. doi: 10.1007/s00018-020-03706-5

PMCID:: PMC8004496

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Select item 80559057.

Zika-exposed microcephalic neonates exhibit higher degree of inflammatory imbalance in cerebrospinal fluid

Gustavo C. Nascimento-Carvalho, Eduardo C. Nascimento-Carvalho, Clara L. Ramos, Ana-Luisa Vilas-Boas, Otávio A. Moreno-Carvalho, Caian L. Vinhaes, Beatriz Barreto-Duarte, Artur T. L. Queiroz, Bruno B. Andrade, Cristiana M. Nascimento-Carvalho

Sci Rep. 2021; 11: 8474. Published online 2021 Apr 19. doi: 10.1038/s41598-021-87895-4

PMCID:: PMC8055905

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Select item 97533058.

Measurements of cerebrospinal fluid production: a review of the limitations and advantages of current methodologies

Guojun Liu, Antonio Ladrón-de-Guevara, Yara Izhiman, Maiken Nedergaard, Ting Du

Fluids Barriers CNS. 2022; 19: 101. Published online 2022 Dec 15. doi: 10.1186/s12987-022-00382-4

PMCID:: PMC9753305

Article PDF–3.2M

Select item 49456009.

Research into the Physiology of Cerebrospinal Fluid Reaches a New Horizon: Intimate Exchange between Cerebrospinal Fluid and Interstitial Fluid May Contribute to Maintenance of Homeostasis in the Central Nervous System

Mitsunori MATSUMAE, Osamu SATO, Akihiro HIRAYAMA, Naokazu HAYASHI, Ken TAKIZAWA, Hideki ATSUMI, Takatoshi SORIMACHI

Neurol Med Chir (Tokyo) 2016 Jul; 56(7): 416–441. Published online 2016 May 27. doi: 10.2176/nmc.ra.2016-0020

Correction in:: Neurol Med Chir (Tokyo). 2018 May; 58(5): 228.

PMCID:: PMC4945600

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Select item 1075686010.

Recommendations for reproducibility of cerebrospinal fluid extracellular vesicle studies

Ursula S. Sandau, Setty M. Magaña, Júlia Costa, John P. Nolan, Tsuneya Ikezu, Laura J. Vella, Hannah K. Jackson, Lissette Retana Moreira, Paola Loreto Palacio, Andrew F. Hill, Joseph F. Quinn, Kendall R. Van Keuren‐Jensen, Trevor J. McFarland, Joanna Palade, Eric A. Sribnick, Huaqi Su, Kostas Vekrellis, Beth Coyle, You Yang, Juan M. Falcón‐Perez, Rienk Nieuwland, Julie A. Saugstad, International Society for Extracellular Vesicles Cerebrospinal Fluid Task Force

J Extracell Vesicles. 2024 Jan; 13(1): 12397. Published online 2023 Dec 29. doi: 10.1002/jev2.12397

Correction in:: J Extracell Vesicles. 2024 Jan; 13(1): 12405.

PMCID:: PMC10756860

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Select item 921766511.

Lumbar Stenosis Spinal Surgery-Associated Cerebrospinal Fluid Leak Without Headache: An Autobiographical Case Report

Philip R Cohen, Stephen M Dorros

Cureus. 2022 May; 14(5): e25253. Published online 2022 May 23. doi: 10.7759/cureus.25253

PMCID:: PMC9217665

Article PDF–940K

Select item 284208912.

CEREBROSPINAL FLUID STASIS AND ITS CLINICAL SIGNIFICANCE

James M. Whedon, Donald Glassey

Altern Ther Health Med. Author manuscript; available in PMC 2010 Mar 19.

Published in final edited form as: Altern Ther Health Med. 2009 May–Jun; 15(3): 54–60.

PMCID:: PMC2842089

Article PDF–51K

Select item 591632413.

Cerebrospinal fluid and blood biomarkers for neurodegenerative dementias: An update of the Consensus of the Task Force on Biological Markers in Psychiatry of the World Federation of Societies of Biological Psychiatry

Piotr Lewczuk, Peter Riederer, Sid E. O’Bryant, Marcel M. Verbeek, Bruno Dubois, Pieter Jelle Visser, Kurt A. Jellinger, Sebastiaan Engelborghs, Alfredo Ramirez, Lucilla Parnetti, Clifford R. Jack, Jr, Charlotte E. Teunissen, Harald Hampel, Alberto Lleó, Frank Jessen, Lidia Glodzik, Mony J. de Leon, Anne M. Fagan, José Luis Molinuevo, Willemijn J. Jansen, Bengt Winblad, Leslie M. Shaw, Ulf Andreasson, Markus Otto, Brit Mollenhauer, Jens Wiltfang, Martin R. Turner, Inga Zerr, Ron Handels, Alexander G. Thompson, Gunilla Johansson, Natalia Ermann, John Q. Trojanowski, Ilker Karaca, Holger Wagner, Patrick Oeckl, Linda van Waalwijk van Doorn, Maria Bjerke, Dimitrios Kapogiannis, H. Bea Kuiperij, Lucia Farotti, Yi Li, Brian A. Gordon, Stéphane Epelbaum, Stephanie J. B. Vos, Catharina J. M. Klijn, William E. Van Nostrand, Carolina Minguillon, Matthias Schmitz, Carla Gallo, Andrea Lopez Mato, Florence Thibaut, Simone Lista, Daniel Alcolea, Henrik Zetterberg, Kaj Blennow, Johannes Kornhuber, Peter Riederer, Carla Gallo, Dimitrios Kapogiannis, Andrea Lopez Mato, Florence Thibaut

World J Biol Psychiatry. Author manuscript; available in PMC 2019 Jun 1.

Published in final edited form as: World J Biol Psychiatry. 2018 Jun; 19(4): 244–328. Published online 2017 Oct 27. doi: 10.1080/15622975.2017.1375556

PMCID:: PMC5916324

Article PDF–1.8M

Select item 1058801414.

The value of elevated cerebrospinal fluid lactate concentrations in post-neurosurgical bacterial meningitis

Qin Wang, YongFang Wang, Yan Yang, YanXi Kong, Yuan Peng

BMC Neurol. 2023; 23: 377. Published online 2023 Oct 20. doi: 10.1186/s12883-023-03428-8

PMCID:: PMC10588014

Article PDF–1003K

Select item 992589215.

Cerebrospinal fluid kappa free light chains for the diagnosis of multiple sclerosis: A systematic review and meta-analysis

Harald Hegen, Janette Walde, Klaus Berek, Georgina Arrambide, Sharmilee Gnanapavan, Batia Kaplan, Michael Khalil, Ruba Saadeh, Charlotte Teunissen, Hayrettin Tumani, Luisa M Villar, Maria Alice V Willrich, Henrik Zetterberg, Florian Deisenhammer

Mult Scler. 2023 Feb; 29(2): 169–181. Published online 2022 Dec 1. doi: 10.1177/13524585221134213

PMCID:: PMC9925892

Article PDF–1.8M

Select item 806578216.

Development of the Cerebrospinal Fluid in Early Stage after Hemorrhage in the Central Nervous System

Petr Kelbich, Aleš Hejčl, Jan Krejsek, Tomáš Radovnický, Inka Matuchová, Jan Lodin, Jan Špička, Martin Sameš, Jan Procházka, Eva Hanuljaková, Petr Vachata

Life (Basel) 2021 Apr; 11(4): 300. Published online 2021 Apr 1. doi: 10.3390/life11040300

PMCID:: PMC8065782

Article PDF–2.6M

Select item 760095717.

Can Aspartate Aminotransferase in the Cerebrospinal Fluid Be a Reliable Predictive Parameter?

Petr Kelbich, Tomáš Radovnický, Iva Selke-Krulichová, Jan Lodin, Inka Matuchová, Martin Sameš, Jan Procházka, Jan Krejsek, Eva Hanuljaková, Aleš Hejčl

Brain Sci. 2020 Oct; 10(10): 698. Published online 2020 Oct 1. doi: 10.3390/brainsci10100698

PMCID:: PMC7600957

Article PDF–505K

Select item 940535218.

Cerebrospinal Fluid System Infection in Children with Cancer: A Retrospective Analysis over 14 Years in a Major European Pediatric Cancer Center

Antonia Diederichs, Evelyn Pawlik, Anke Barnbrock, Stefan Schöning, Jürgen Konczalla, Tobias Finger, Thomas Lehrnbecher, Stephan Göttig, Konrad Bochennek

Antibiotics (Basel) 2022 Aug; 11(8): 1113. Published online 2022 Aug 17. doi: 10.3390/antibiotics11081113

PMCID:: PMC9405352

Article PDF–1.9M

Select item 750355319.

Cerebrospinal Fluid Mitochondrial DNA in Rapid and Slow Progressive Forms of Alzheimer’s Disease

Petar Podlesniy, Franc Llorens, Margalida Puigròs, Nuria Serra, Diego Sepúlveda-Falla, Christian Schmidt, Peter Hermann, Inga Zerr, Ramon Trullas

Int J Mol Sci. 2020 Sep; 21(17): 6298. Published online 2020 Aug 31. doi: 10.3390/ijms21176298

PMCID:: PMC7503553

Article PDF–1.4M

Select item 452868420.

Relevance of retrovirus quantification in cerebrospinal fluid for neurologic diagnosis

Carolina Rosadas, Marzia Puccioni-Sohler

J Biomed Sci. 2015; 22(1): 66. Published online 2015 Aug 8. doi: 10.1186/s12929-015-0170-y

PMCID:: PMC4528684

Article PDF–775K

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Figure 1:CF global metabolomics profiles are altered by SHSe.

A) Synchronized 3D sPLS-DA plots of overall plasma metabolomics profiles. Red dots represent individual non-CF controls, green dots represent CF patients without SHSe, and blue dots represent CF patients with SHSe. B) Synchronized 3D sPLS-DA plots of overall CF plasma metabolomics profiles stratified by age and SHSe. Red dots represent individual CF children without SHSe, dark blue dots represent CF children with SHSe, green dots represent CF infants without SHSe, and light blue dots represent CF infants with SHSe. The top 3 components are presented on the X, Y and Z axes for comparisons in 1A and 1B. C) 2D sPLS-DA plot of overall metabolomics profiles for comparison of CF infants with and without SHSe. CF infants with SHSe are shown in green, and CF infants without SHSe are shown in red. D) 2D sPLS-DA plot of overall metabolomics profiles for comparison of CF children with and without SHSe. CF children with SHSe are shown in green, and CF children without SHSe are shown in red. The top 2 components are presented on the X and Y axes for comparisons in 1C and 1D.

Metabolomics profiling of tobacco exposure in children with cystic fibrosis

J Cyst Fibros. ;19(5):791-800.
FIGURE 1

Collection sites and hydrographic basin of occurrence of Leporinus cf. friderici. Colored circles represent the MOTUs found in this study: L. agassizii (red), L. cf. friderici Amazon 1 (orange), L. cf. friderici Madeira 1 (purple), L. cf. friderici Paraná (light green), L. cf. friderici Paraguay (dark green), L. piau São Francisco (dark blue), L. cf. friderici Upper Tapajós (yellow), and L. cf. friderici Tocantins 1 (light blue). Black dot represents individuals collected as L. cf. friderici Amazon 2; black star represents L. cf. friderici Mearim; black square represents L. cf. friderici Tocantins 2; black polygon represents L. cf. friderici Madeira 2; black triangle represents L. cf. friderici Xingú. A, Prior Sete Quedas waterfalls region and Itaipú dam. B, Teotônio falls in the Madeira River. Map created by Q-GIS (http://www.qgis.org/). The collection site numbers are according to Supplementary Table .

Molecular Evidences of a Hidden Complex Scenario in Leporinus cf. friderici

Front Genet. 2018;9:47.
Fig 2Unweighted UniFrac PCoA plot of healthy and CF microbiota.

Distance comparisons were made for microbiota of: (a) Uninfected control (NIC) and CF baseline, (b) NIC and Exacerbated CF, (c) NIC and After Treatment of Exacerbated CF, (d) NIC and On Treatment of Exacerbated CF, (e) NIC and Before Treatment of Exacerbated CF, (f) CF baseline and Exacerbated CF, (g) Before, During and After Treatment of Exacerbated CF, (h) CF baseline and Before, During, After Treatment of Exacerbated CF. Each point represents a sample from the studies listed in . The color for each sample group can be found on the figure.

Data Mining of Lung Microbiota in Cystic Fibrosis Patients

PLoS One. 2016;11(10):e0164510.
6Intestinal permeability of WT & CF mice and effects of interventions

Mice were fasted overnight and in the morning gavaged with the indigestible tracer rhodaminedextran. After 90 min the mice were killed and the concentration of rhodamine in blood plasma was determined. Con: Control, mice were fed the liquid diet; Abx: Mice were fed the liquid diet supplemented with antibiotics; Lax: Mice were fed standard solid chow and given laxative solution to drink; IAP: Mice were fed the liquid diet supplemented with 13.3 U/ml purified calf IAP; L-Phe: Mice were fed the liquid diet supplemented with 10 mM L-Phe. (*) p=0.00001 CF Con vs WT Con; (+) p=0.040 CF Lax vs CF Con; (+) p= 0.00025 CF IAP vs CF Con; (*) p=0.024 CF L-Phe vs WT L-Phe (n=16 WT Con, 6 WT Abx, 6 WT Lax, 6 WT IAP, 9 WT L-Phe, 15 CF Con, 7 CF Abx, 5 CF Lax, 6 CF IAP, 4 CF L-Phe)

Impaired mucosal barrier function in the small intestine of the cystic fibrosis mouse

J Pediatr Gastroenterol Nutr. ;53(4):371-379.