The blood-brain barrier and immune function and dysfunction

Microbial translocation is a cause of systemic immune activation in chronic HIV infection

Brenchley, J. M., Price, D. A., Schacker, T. W., Asher, T. E., Silvestri, G., Rao, S., Kazzaz, Z., Bornstein, E., Lambotte, O., Altmann, D., et al. (2006) · Nature Medicine · doi:10.1038/nm1511 · Cited by 3,559

FINE STRUCTURAL LOCALIZATION OF A BLOOD-BRAIN BARRIER TO EXOGENOUS PEROXIDASE

Reese, T. S., & Karnovsky, M. J. (1967) · The Journal of Cell Biology · doi:10.1083/jcb.34.1.207 · Cited by 2,629

Systemic LPS causes chronic neuroinflammation and progressive neurodegeneration

Qin, L., Wu, X., Block, M. L., Liu, Y., Breese, G. R., Hong, J., Knapp, D. J., & Crews, F. T. (2007) · Glia · doi:10.1002/glia.20467 · Cited by 2,144

Multiplicity of cerebrospinal fluid functions: new challenges in health and disease

Johanson, C. E., Duncan, J. A., Klinge, P. M., Brinker, T., Stopa, E. G., & Silverberg, G. D. (2008) · Cerebrospinal Fluid Research · doi:10.1186/1743-8454-5-10 · Cited by 861

Passage of cytokines across the blood–brain barrier

Banks, W. A., Kastin, A. J., & Broadwell, R. D. (1996) · Neuroimmunomodulation · doi:10.1159/000097202 · Cited by 778

Chylomicrons promote intestinal absorption of lipopolysaccharides

Ghoshal, S., Witta, J., Zhong, J., de Villiers, W., & Eckhardt, E. (2009) · Journal of Lipid Research · doi:10.1194/jlr.m800156-jlr200 · Cited by 662

Brain-immune communication pathways

Quan, N., & Banks, W. A. (2007) · Brain, Behavior, and Immunity · doi:10.1016/j.bbi.2007.05.005 · Cited by 626

Physiology of the cerebro-spinal fluid

(1967) · Postgraduate Medical Journal · doi:10.1136/pgmj.43.501.508 · Cited by 620

Energy intake is associated with endotoxemia in apparently healthy men

Amar, J., Burcelin, R., Ruidavets, J. B., Cani, P. D., Fauvel, J., Alessi, M., Chamontin, B., & Ferrières, J. (2008) · American Journal of Clinical Nutrition · doi:10.1093/ajcn/87.5.1219 · Cited by 610

The gut-brain barrier in major depression: intestinal mucosal dysfunction with an increased translocation of LPS from gram negative enterobacteria (leaky gut) plays a role in the inflammatory pathophysiology of depression.

Maes, M. H. J., Kubera, M., & Leunis, J. (2008) · PubMed · Cited by 609

Potential Regulation Mechanisms of P-gp in the Blood-Brain Barrier in Hypoxia

Ding, Y., Wang, R., Zhang, J., Zhao, A., Lu, H., Li, W., Wang, C., & Yuan, X. (2019) · Current Pharmaceutical Design · doi:10.2174/1381612825666190610140153 · Cited by 20

Gut permeability and mimicry of the Glutamate Ionotropic Receptor NMDA type Subunit Associated with protein 1 (GRINA) as potential mechanisms related to a subgroup of people with schizophrenia with elevated antigliadin antibodies (AGA IgG)

Čiháková, D., Eaton, W. W., Talor, M. V., Harkus, U. H., Demyanovich, H. K., Rodriguez, K. M., Feldman, S. M., & Kelly, D. L. (2019) · Schizophrenia Research · doi:10.1016/j.schres.2019.01.007 · Cited by 19

What Is Our Understanding of the Influence of Gut Microbiota on the Pathophysiology of Parkinson’s Disease?

Hill, A. E., Wade‐Martins, R., & Burnet, P. W. J. (2021) · Frontiers in Neuroscience · doi:10.3389/fnins.2021.708587 · Cited by 19

Modulatory Effects of Dietary Amino Acids on Neurodegenerative Diseases

Rajagopal, S., Sangam, S. R., Singh, S., & Rao, J. V. (2016) · Advances in neurobiology · doi:10.1007/978-3-319-28383-8_22 · Cited by 19

Recent advances in nanotechnology based drug delivery to the brain

Lin, L., Liu, Q., Song, L., Liu, F.-F., & Sha, J.-X. (2010) · Cytotechnology · doi:10.1007/s10616-010-9295-8 · Cited by 19

HIV-associated neurocognitive disorder: key implications of the microbiota-gut-brain axis

Hu, A., Zaongo, S. D., Harypursat, V., Wang, X., Ouyang, J., & Chen, Y. (2024) · Frontiers in Microbiology · doi:10.3389/fmicb.2024.1428239 · Cited by 18

Neuromodulatory effect of troxerutin against doxorubicin and cyclophosphamide-induced cognitive impairment in rats: Potential crosstalk between gut–brain and NLRP3 inflammasome axes

Gamal, N. K., El‐Naga, R. N., Ayoub, I. M., & George, M. Y. (2025) · International Immunopharmacology · doi:10.1016/j.intimp.2025.114216 · Cited by 18

Role of Blood-Brain barrier in bacterial translocation

Aborode, A. T., Adesola, R. O., Scott, G. Y., Adepoju, V. A., Akan, O. D., Ogunyemi, A. D., Adetunji, A. P.-G., Arogundade, F. Q., Kwaku, S. D., Emmanuel, A. O., et al. (2025) · Neuroscience · doi:10.1016/j.neuroscience.2025.06.037 · Cited by 18

Altered Gray Matter Volumes and Plasma IL-6 Level in Major Depressive Disorder Patients with Suicidal Ideation

Guo, Y., Jiang, X., Jia, L., Zhu, Y., Han, X., Wu, Y., Liu, W., Zhao, W., Zhu, H., Wang, D., et al. (2022) · NeuroImage Clinical · doi:10.1016/j.nicl.2023.103403 · Cited by 18

Increased production of inflammatory cytokines by circulating monocytes in mesial temporal lobe epilepsy: A possible role in drug resistance

Milano, C., Montali, M., Barachini, S., Burzi, I. S., Pratesi, F., Petrozzi, L., Chico, L., Morganti, R., Gambino, G., Rossi, L., et al. (2023) · Journal of Neuroimmunology · doi:10.1016/j.jneuroim.2023.578272 · Cited by 20

Advancing Blood–Brain Barrier-on-a-Chip Models Through Numerical Simulations

Carvalho, V. M., Rodrigues, R. O., Shin, S. R., Lima, R. A., & Teixeira, S. (2024) · BioChip Journal · doi:10.1007/s13206-024-00168-w · Cited by 18

Epileptic seizures as a manifestation of cow’s milk allergy: a studied relationship and description of our pediatric experience

Falsaperla, R., Pavone, P., Sopo, S. M., Mahmood, F., Scalia, F., Corsello, G., Lubrano, R., & Vitaliti, G. (2014) · Expert Review of Clinical Immunology · doi:10.1586/1744666x.2014.977259 · Cited by 18

Chronic exposure to low doses of ozone produces a state of oxidative stress and blood-brain barrier damage in the hippocampus of rat

Rivas-Arancibia, S., Hernández-Zimbrón, L. F., Rodrı́guez-Martı́nez, E., Borgonio-Pérez, G., Velumani, V., & Dúran-Bedolla, J. (2013) · Advances in Bioscience and Biotechnology · doi:10.4236/abb.2013.411a2004 · Cited by 17

Mecanismos de disfunção da barreira hematoencefálica no paciente criticamente enfermo: ênfase no papel das metaloproteinases de matriz

Rojas, H. A., Ritter, C., & Dal‐Pizzol, F. (2011) · Revista Brasileira de Terapia Intensiva · doi:10.1590/s0103-507x2011000200016 · Cited by 18

Could the Gut Microbiota Serve as a Therapeutic Target in Ischemic Stroke?

Zhang, J., Tang, Q., & Zhu, L. (2021) · Evidence-based Complementary and Alternative Medicine · doi:10.1155/2021/1391384 · Cited by 17

Identification of highly connected hub genes in the protective response program of human macrophages and microglia activated by alpha B‐crystallin

Holtman, I. R., Bsibsi, M., Gerritsen, W. H., Boddeke, H. W. G. M., Eggen, B. J. L., van der Valk, P., Kipp, M., van Noort, J. M., & Amor, S. (2017) · Glia · doi:10.1002/glia.23104 · Cited by 18

Interferons: A molecular switch between damage and repair in ageing and Alzheimer’s disease

Gorlé, N., & Vandenbroucke, R. E. (2019) · Mechanisms of Ageing and Development · doi:10.1016/j.mad.2019.111148 · Cited by 18

Executive functioning in pediatric cystic fibrosis: A preliminary study and conceptual model

Borschuk, A. P., Molitor, S. J., Everhart, R. S., Siracusa, C. M., & Filigno, S. S. (2020) · Pediatric Pulmonology · doi:10.1002/ppul.24648 · Cited by 16

CNS Targets of Adipokines

Beall, C., Hanna, L., & Ellacott, K. L. J. (2017) · Comprehensive physiology · doi:10.1002/cphy.c160045 · Cited by 16

The clinical features and potential mechanisms of cognitive disorders in peripheral autoimmune and inflammatory diseases

Fan, K.-Q., Huang, T., Yu, J.-S., Li, Y., & Jin, J. (2022) · Fundamental Research · doi:10.1016/j.fmre.2022.12.005 · Cited by 18

The role of cytokines in memory consolidation

Малашенкова, И. К., Krynskiy, S., Khailov, N. A., Kazanova, G. V., Velichkovsky, B. B., & Didkovsky, N. A. (2016) · Biology Bulletin Reviews · doi:10.1134/s2079086416020055 · Cited by 15

The combination of postnatal maternal separation and social stress in young adulthood does not lead to enhanced inflammatory pain sensitivity and depression-related behavior in rats

Genty, J., Nomigni, M. T., Anton, F., & Hanesch, U. (2018) · PLoS ONE · doi:10.1371/journal.pone.0202599 · Cited by 15

Anti-inflammatory agent, OKN-007, reverses long-term neuroinflammatory responses in a rat encephalopathy model as assessed by multi-parametric MRI: implications for aging-associated neuroinflammation

Towner, R. A., Saunders, D., Smith, N., Gulej, R., McKenzie, T., Lawrence, B., & Morton, K. A. (2019) · GeroScience · doi:10.1007/s11357-019-00094-y · Cited by 15

From Bench to Bedside: New Frontiers in Understanding and Treating Postoperative Delirium

Monge, K. M., Shapiro, A. L. B., Coughlan, C. M., Mungo, B., Schulick, R. D., Pratap, A., Kovacs, E. J., & Idrovo, J. (2025) · Journal of Clinical Medicine · doi:10.3390/jcm14238418 · Cited by 19

The blood–brain barrier, TWEAK, and neuropsychiatric involvement in human systemic lupus erythematosus and primary Sjögren’s syndrome

Lauvsnes, M. B., Tjensvoll, A. B., Maroni, S. S., Kvivik, I., Grimstad, T. B., Greve, O. J., Harboe, E., Gøransson, L. G., Putterman, C., & Omdal, R. (2018) · Lupus · doi:10.1177/0961203318804895 · Cited by 14

Stress‐related suppression of peripheral cytokines predicts future relapse in alcohol‐dependent individuals with and without subclinical depression

Fox, H. C., Milivojevic, V., MacDougall, A., LaVallee, H., Simpson, C. A., Angarita, G. A., & Sinha, R. (2019) · Addiction Biology · doi:10.1111/adb.12832 · Cited by 15

Can stress promote the pathophysiology of brain metastases? A critical review of biobehavioral mechanisms

Seiler, A., Sood, A. K., Jenewein, J., & Fagundes, C. P. (2019) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2019.12.013 · Cited by 14

Plexin-A1 is required for Toll-like receptor-mediated microglial activation in the development of lipopolysaccharide-induced encephalopathy

Ito, T., Yoshida, K., Negishi, T., Miyajima, M., Takamatsu, H., Kikutani, H., Kumanogoh, A., & Yukawa, K. (2014) · International Journal of Molecular Medicine · doi:10.3892/ijmm.2014.1690 · Cited by 14

Interleukin 6 deficiency affects spontaneous activity of mice in age- and sex-dependent manner

Aniszewska, A., Szymański, J., Winnicka, M. M., & Turlejski, K. (2014) · Acta Neurobiologiae Experimentalis · doi:10.55782/ane-2014-2005 · Cited by 14

Critical Role of Monocyte Recruitment in Optic Nerve Damage Induced by Experimental Optic Neuritis

Aranda, M. L., Guerrieri, D., Piñero, G., Fleitas, M. F. G., Altschuler, F., Diéguez, H. H., Sarmiento, M. I. K., Chianelli, M. S., Sande, P. H., Dorfman, D., et al. (2019) · Molecular Neurobiology · doi:10.1007/s12035-019-1608-0 · Cited by 13

Cytokine expression profiles in children and adolescents with tic disorders

Kütük, M. Ö., Tufan, A. E., Kılıçaslan, F., Gökçen, C., Aksu, G. G., Yektaş, Ç., Kandemir, H., Celik, F., Mutluer, T., Büber, A., et al. (2024) · Scientific Reports · doi:10.1038/s41598-024-62121-z · Cited by 13

The role of cerebrospinal fluid metabolites in mediating the impact of lipids on Late-Onset Alzheimer’s Disease: a two-step mendelian randomization analysis

Jie, J., Gong, Y., Hu, H., & Liu, S. (2024) · Journal of Translational Medicine · doi:10.1186/s12967-024-05796-2 · Cited by 13

Attention-Deficit/Hyperactivity Disorder in Atopic Dermatitis: An Appraisal of the Current Literature

Nygaard, U., Riis, J. L., Deleuran, M. S., & Vestergaard, C. (2016) · Pediatric Allergy Immunology and Pulmonology · doi:10.1089/ped.2016.0705 · Cited by 13

Investigation of the Feasibility of Ventricular Delivery of Resveratrol to the Microelectrode Tissue Interface

Kim, Y., Ereifej, E. S., Schwartzman, W. E., Meade, S. M., Chen, K., Rayyan, J., He, F., Aluri, V., Mueller, N. N., Bhambra, R., et al. (2021) · Micromachines · doi:10.3390/mi12121446 · Cited by 13

Semaphorin 3A-Plexin-A1 signaling through ERK activation is crucial for Toll-like receptor-induced NO production in BV-2 microglial cells

Ito, T., Morita, T., Yoshida, K., Negishi, T., & Yukawa, K. (2014) · International Journal of Molecular Medicine · doi:10.3892/ijmm.2014.1727 · Cited by 13

Future Directions of Cytokine Hypothesis in Depression: ‘NLRP3 inflamazomu’

Şahin, C., & Arıcıoğlu, F. (2013) · Klinik Psikofarmakoloji Bülteni-Bulletin of Clinical Psychopharmacology · doi:10.5455/bcp.20130927070724 · Cited by 13

Vibrio vulnificus MO6-24/O Lipopolysaccharide Stimulates Superoxide Anion, Thromboxane B2, Matrix Metalloproteinase-9, Cytokine and Chemokine Release by Rat Brain Microglia in Vitro

Mayer, A. M. S., Hall, M. L. M., Holland, M. A., Castro, C. D., Molinaro, A., Aldulescu, M., Frenkel, J., Ottenhoff, L., Rowley, D. C., & Powell, J. (2014) · Marine Drugs · doi:10.3390/md12041732 · Cited by 13

Single-cell dissection of the human cerebrovasculature in health and diseasePreprint

García, F., Sun, N., Lee, H., Godlewski, B. R., Galani, K., Mantero, J. C., Bennett, D. A., Şahin, M., Kellis, M., & Heiman, M. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.04.26.440975 · Cited by 13

Ligand-receptor interactions: A key to understanding microglia and astrocyte roles in epilepsy

Thergarajan, P., O'Brien, T. J., Jones, N. C., & Ali, I. Y. (2024) · Epilepsy & Behavior · doi:10.1016/j.yebeh.2024.110219 · Cited by 13

Leptomeningeal Carcinomatosis in Chronic Lymphocytic Leukemia: A Case Report and Review of the Literature

Naydenov, A. V., & Taylor, L. P. (2019) · The Oncologist · doi:10.1634/theoncologist.2018-0619 · Cited by 12

On the road to resilience: Epigenetic effects of meditation

Verdone, L., Caserta, M., Ben‐Soussan, T. D., & Venditti, S. (2023) · Vitamins and hormones · doi:10.1016/bs.vh.2022.12.009 · Cited by 12

Extracranial Abscopal Responses after Radiation Therapy for Intracranial Metastases: A Review of the Clinical Literature and Commentary on Mechanism

Gui, C., Kleinberg, L. R., Lim, M. K., & Redmond, K. J. (2019) · Cureus · doi:10.7759/cureus.4207 · Cited by 12

Indole-3-guanylhydrazone hydrochloride mitigates long-term cognitive impairment in a neonatal sepsis model with involvement of MAPK and NFκB pathways

Heimfarth, L., Carvalho, A. M. D. S., Quintans, J. D. S. S., Pereira, E. W. M., Lima, N. T., Carvalho, M. T. B., Barreto, R. D. S. S., Moreira, J. C. F., da Silva‐Júnior, E. F., Schmitt, M., et al. (2019) · Neurochemistry International · doi:10.1016/j.neuint.2019.104647 · Cited by 12

Lipopolysaccharide-Elicited Systemic Inflammation Induces Selective Vulnerability of Cerebral Cortex and Striatum of Developing Glutaryl-CoA Dehydrogenase Deficient (Gcdh−/−) Mice to Oxidative Stress

Seminotti, B., Amaral, A. U., Grings, M., Ribeiro, C. A. J., Leipnitz, G., & Wajner, M. (2020) · Neurotoxicity Research · doi:10.1007/s12640-020-00291-0 · Cited by 12

Regulation of the blood-brain barrier function by peripheral cues in health and disease

Devraj, K., Kulkarni, O. P., & Liebner, S. (2024) · Metabolic Brain Disease · doi:10.1007/s11011-024-01468-8 · Cited by 13

Multifaceted therapeutic potentials of catalpol, an iridoid glycoside: an updated comprehensive review

Hassan, M.-A. M., Fahmy, M. I., Azzam, H. N., Ebrahim, Y. M., El‐Shiekh, R. A., & Aboulmagd, Y. M. (2025) · Inflammopharmacology · doi:10.1007/s10787-025-01694-1 · Cited by 12

Managing CNS involvement in systemic lupus erythematosus

Piga, M., & Mathieu, A. (2011) · International Journal of Clinical Rheumatology · doi:10.2217/ijr.11.44 · Cited by 10

Assessment of salsolinol N-methyltransferase activity in rat peripheral lymphocytes by liquid chromatography–electrospray time-of-flight mass spectrometry

Zhang, Y., Wang, L., Mu, X., Duan, J., Zhu, Y., Qing, H., Li, Y., Xiao, S., & Deng, Y. (2011) · Analytical and Bioanalytical Chemistry · doi:10.1007/s00216-011-4683-2 · Cited by 10

Communication from the periphery to the hypothalamus through the blood–brain barrier: An in vitro platform

Martins, J. P., Alves, C. J., Neto, E., & Lamghari, M. (2015) · International Journal of Pharmaceutics · doi:10.1016/j.ijpharm.2015.12.058 · Cited by 12

The effects of voluntary wheel running on neuroinflammatory status: Role of monocyte chemoattractant protein-1

Spielman, L. J., Estaki, M., Ghosh, S., Gibson, D. L., & Klegeris, A. (2017) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2016.12.009 · Cited by 11

Protective effect of neuropeptide Y2 receptor activation against methamphetamine-induced brain endothelial cell alterations

Ventura, F., Muga, M., Coelho‐Santos, V., Ribeiro, C., Leitão, R. A., & Silva, A. P. (2020) · Toxicology Letters · doi:10.1016/j.toxlet.2020.09.013 · Cited by 10

Peridontitis as a Risk Factor for Attention Deficit Hyperactivity Disorder: Possible Neuro-inflammatory Mechanisms

WILSON, S. K., & Thomas, J. (2022) · Neurochemical Research · doi:10.1007/s11064-022-03650-9 · Cited by 11

Plasma and cerebrospinal fluid interleukin-1β during lipopolysaccharide-induced systemic inflammation in ewes implanted or not with slow-release melatonin

Skipor, J., Kowalewska, M., Szczepkowska, A., Majewska, A. M., Misztal, T., Jałyński, M., Herman, A. P., & Ząbek, K. (2017) · Journal of Animal Science and Biotechnology/Journal of animal science and biotechnology · doi:10.1186/s40104-017-0206-0 · Cited by 10

Dysbiosis and fecal microbiota transplant: Contemplating progress in health, neurodegeneration and longevity

Ahmadi, S., Hasani, A., Khabbaz, A., Poortahmasebi, V., Hosseini, S., Yasdchi, M., Mehdizadehfar, E., Mousavi, Z. B., Hasani, R., Nabizadeh, E., et al. (2024) · Biogerontology · doi:10.1007/s10522-024-10136-4 · Cited by 9

Proposing Bromo-Epi-Androsterone (BEA) for Post-Traumatic Stress Disorder (PTSD)

Dow, C. T., & Obaid, L. (2025) · Cells · doi:10.3390/cells14141120 · Cited by 11

Dexmedetomidine Alleviates Microglia-Induced Spinal Inflammation and Hyperalgesia in Neonatal Rats by Systemic Lipopolysaccharide Exposure

Wen, W., Gong, X., Cheung, H., Yang, Y., Cai, M., Zheng, J., Tong, X., & Zhang, M. (2021) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2021.725267 · Cited by 11

Severity of Peripheral Infection Differentially Affects Brain Functions in Mice via Microglia-Dependent and -Independent Mechanisms

Le, Y.-P., Saito, K., Parajuli, B., Sakai, K., Kubota, Y., Miyakawa, M., Shinozaki, Y., Shigetomi, E., & Koizumi, S. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms242417597 · Cited by 11

The two-pore domain K+ channel TASK-1 is closely associated with brain barriers and meninges

Kanjhan, R., Pow, D., Noakes, P., & Bellingham, M. (2010) · Journal of Molecular Histology · doi:10.1007/s10735-010-9293-3 · Cited by 10

Combined effects of social stress and liver fluke infection in a mouse model

Avgustinovich, D. F., Marenina, M. K., Zhanaeva, S. Y., Tenditnik, M. V., Katokhin, A. V., Pavlov, K. S., Sivkov, A. Y., Vishnivetskaya, G. B., Lvova, M. N., Tolstikova, T. G., et al. (2016) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2016.01.012 · Cited by 10

Effects of Vitamin E and Q10 Supplementation against Doxorubicin-Induced Neurotoxicity in Rats

Al-Geam, M. A. I., & Al-Shawi, N. N. (2018) · Iraqi Journal of Pharmaceutical Sciences · doi:10.31351/vol27iss2pp24-31 · Cited by 9

Extracranial Abscopal Effects Induced by Brain Radiation in Advanced Lung Cancer

D’Andrea, M. A., & Reddy, G. K. (2019) · American Journal of Clinical Oncology · doi:10.1097/coc.0000000000000623 · Cited by 9

Temporary opening of the blood-brain barrier with the nitrone compound OKN-007.

Towner, R. A., Saunders, D., Lerner, M. R., Silasi‐Mansat, R., Yuan, T., Barber, D., Faakye, J., Nyúl‐Tóth, Á., Csiszár, A., Meerveld, B. G., et al. (2021) · Europe PMC (PubMed Central) · Cited by 9

Comorbidity of ADHD and allergic diseases in early adolescence: The role of parental smoking at home

Wong, R. S. M., Tung, K. T. S., Leung, H. E., Chow, R., Chua, G. T., Ho, M., Tso, W. W. Y., Fung, G. P. G., Tao, V. Q., Kwan, M. Y. W., et al. (2022) · Current Psychology · doi:10.1007/s12144-021-02693-5 · Cited by 9

IL-1β Induction and IL-6 Suppression Are Associated with Aggravated Neuronal Damage in a Lipopolysaccharide-Pretreated Kainic Acid-Induced Rat Pup Seizure Model

Lee, S.-H., Kim, B.-J., Kim, Y. B., Chung, P., Moon, H., Suh, B. C., Yoon, W. T., Jin, D., Park, Y. S., Lee, Y., et al. (2012) · NeuroImmunoModulation · doi:10.1159/000339579 · Cited by 9

Immunology as it Pertains to Drugs of Abuse, AIDS and the Neuroimmune Axis: Mediators and Traffic

Rogers, T. J. (2010) · Journal of Neuroimmune Pharmacology · doi:10.1007/s11481-010-9247-2 · Cited by 9

Food Contamination: An Unexplored Possible Link between Dietary Habits and Parkinson’s Disease

Caioni, G., Cimini, A., & Benedetti, E. (2022) · Nutrients · doi:10.3390/nu14071467 · Cited by 9

Disease mechanisms as subtypes: Microbiome

Bonvegna, S., & Cilia, R. (2023) · Handbook of clinical neurology · doi:10.1016/b978-0-323-85555-6.00006-0 · Cited by 8

MicroRNA signatures in neuroplasticity, neuroinflammation and neurotransmission in association with depression

Choudhary, A., Kumar, A., Jindal, M., Rhuthuparna, M., & Munshi, A. (2024) · Journal of Physiology and Biochemistry · doi:10.1007/s13105-024-01065-4 · Cited by 9

Is the immune neuroendocrine system the connection between epipharyngitis and chronic fatigue syndrome induced by HPV vaccine?

Jara, L. J., Izquierdo, E., & Medina, G. (2016) · Immunologic Research · doi:10.1007/s12026-016-8854-2 · Cited by 8

Co-infection with HIV associated with reduced vulnerability to symptoms of depression during antiviral treatment for hepatitis C

Fialho, R., Pereira, M., Harrison, N. A., Rusted, J. M., & Whale, R. (2017) · Psychiatry Research · doi:10.1016/j.psychres.2017.03.049 · Cited by 8

White matter pathways as both a target and mediator of health behaviors

Porter, A., Leckie, R. L., & Verstynen, T. (2018) · Annals of the New York Academy of Sciences · doi:10.1111/nyas.13708 · Cited by 9

Plasma kinetics and matrix residues of deoxynivalenol (DON) and zearalenone (ZEN) are altered in endotoxaemic pigs independent of LPS entry site

Bannert, E., Tesch, T., Kluess, J., Valenta, H., Frahm, J., Kersten, S., Kahlert, S., Renner, L., Rothkötter, H., & Dänicke, S. (2017) · Mycotoxin Research · doi:10.1007/s12550-017-0276-z · Cited by 8

Ageing and the Autonomic Nervous System

Takla, M., Saadeh, K., Tse, G., Huang, C. L.-H., & Jeevaratnam, K. (2023) · Sub-cellular biochemistry/Subcellular biochemistry · doi:10.1007/978-3-031-26576-1_10 · Cited by 8

Paediatric Atopic Dermatitis: The Unexpected Impact on Life with a Specific Look at the Molecular Level

Artusa, S., Mazzuca, G., PIACENTINI, G. L., Castagnoli, R., Marseglia, G. L., Pietrobelli, A., & Pecoraro, L. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25094778 · Cited by 12

Neurotoxicity of chemotherapy and brain-radiotherapy in cancer: overlapping mechanisms underlying cognitive impairment

Kuil, L. E., Coppola, N., Dietrich, J., & Castel, H. (2025) · Journal of Clinical and Experimental Neuropsychology · doi:10.1080/13803395.2025.2539199 · Cited by 7

Behavioral alterations, brain oxidative stress, and elevated levels of corticosterone associated with a pressure injury model in male mice

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