| Publication |
Sentence |
Publish Date |
Extraction Date |
Species |
| Tomohiro Matsuda, Mami Hanaoka, Noriya Enomoto, Tadashi Yamaguchi, Takeshi Miyamoto, Hitoshi Niki, Kazuhito Matsuzak. Combined Mechanical Thrombectomy for Multiple Cerebral Venous Sinus Thrombosis Involving the Straight Sinus: A Case Report. NMC case report journal. vol 11. 2024-09-03. PMID:39224239. |
magnetic resonance imaging (mri) revealed thrombosis of the bilateral internal cerebral veins, vein of galen, sts, torcular herophili (th), and right transverse sinus (ts), as well as edema mainly in the left thalamus, basal ganglia, and corpus callosum. |
2024-09-03 |
2024-09-05 |
Not clear |
| Anya Topiwala, Thomas E Nichols, Logan Z J Williams, Emma C Robinson, Fidel Alfaro-Almagro, Bernd Taschler, Chaoyue Wang, Christopher P Nelson, Karla L Miller, Veryan Codd, Nilesh J Samani, Stephen M Smit. Telomere length and brain imaging phenotypes in UK Biobank. PloS one. vol 18. issue 3. 2023-03-22. PMID:36947528. |
longer ltl is associated with: i) larger global and subcortical grey matter volumes including the hippocampus, ii) lower t1-weighted grey-white tissue contrast in sensory cortices, iii) white-matter microstructure measures in corpus callosum and association fibres, iv) lower volume of white matter hyperintensities, and v) lower basal ganglia iron. |
2023-03-22 |
2023-08-14 |
human |
| Reham Khalaf-Nazzal, James Fasham, Katherine A Inskeep, Lauren E Blizzard, Joseph S Leslie, Matthew N Wakeling, Nishanka Ubeyratna, Tadahiro Mitani, Jennifer L Griffith, Wisam Baker, Fida' Al-Hijawi, Karen C Keough, Alper Gezdirici, Loren Pena, Christine G Spaeth, Peter D Turnpenny, Joseph R Walsh, Randall Ray, Amber Neilson, Evguenia Kouranova, Xiaoxia Cui, David T Curiel, Davut Pehlivan, Zeynep Coban Akdemir, Jennifer E Posey, James R Lupski, William B Dobyns, Rolf W Stottmann, Andrew H Crosby, Emma L Bapl. Bi-allelic CAMSAP1 variants cause a clinically recognizable neuronal migration disorder. American journal of human genetics. 2022-10-25. PMID:36283405. |
the neuroradiological phenotype comprises a highly recognizable combination of classic lissencephaly with a posterior more severe than anterior gradient similar to pafah1b1(lis1)-related lissencephaly and severe hypoplasia or absence of the corpus callosum; dysplasia of the basal ganglia, hippocampus, and midbrain; and cerebellar hypodysplasia, similar to the tubulinopathies, a group of monogenic tubulin-associated disorders of cortical dysgenesis. |
2022-10-25 |
2023-08-14 |
mouse |
| Yunjia Cai, Linan Ren, Xinming Liu, Chen Li, Xiaokun Gang, Guixia Wan. Thyroid storm complicated by corpus callosum infarction in a young patient: A case report and literature review. Medicine. vol 101. issue 34. 2022-08-31. PMID:36042649. |
previous studies have shown that hyperthyroidism complicated by cerebral infarction mainly occurs in the intracranial basal ganglia; however, there are no reports of corpus callosum infarction. |
2022-08-31 |
2023-08-14 |
Not clear |
| Mary C Whitman, Brenda J Barry, Caroline D Robson, Flavia M Facio, Carol Van Ryzin, Wai-Man Chan, Tanya J Lehky, Audrey Thurm, Christopher Zalewski, Kelly A King, Carmen Brewer, Konstantinia Almpani, Janice S Lee, Angela Delaney, Edmond J FitzGibbon, Paul R Lee, Camilo Toro, Scott M Paul, Omar A Abdul-Rahman, Bryn D Webb, Ethylin Wang Jabs, Hans Ulrik Moller, Dorte Ancher Larsen, Jayne H Antony, Christopher Troedson, Alan Ma, Glad Ragnhild, Katrine V Wirgenes, Emma Tham, Malin Kvarnung, Timothy James Maarup, Sarah MacKinnon, David G Hunter, Francis S Collins, Irini Manoli, Elizabeth C Engl. TUBB3 Arg262His causes a recognizable syndrome including CFEOM3, facial palsy, joint contractures, and early-onset peripheral neuropathy. Human genetics. vol 140. issue 12. 2021-11-08. PMID:34652576. |
all fourteen subjects share a recognizable set of brain malformations, including hypoplasia of the corpus callosum and anterior commissure, basal ganglia malformations, absent olfactory bulbs and sulci, and subtle cerebellar malformations. |
2021-11-08 |
2023-08-13 |
human |
| Monique Boukobza, Carsten Ehmer, Frédéric Baud, Jean-Pierre Laiss. "Unusual Pattern of Cerebral Microbleeds and Petechial Hemorrhages after Veno-Arterial Extracorporeal Membrane Oxygenation Support. A Report of 2 Cases". Journal of stroke and cerebrovascular diseases : the official journal of National Stroke Association. vol 30. issue 7. 2021-06-15. PMID:33866273. |
mri 30 days later showed widespread petechial hemorrhages in the subcortical and deep white matter (wm) (optic radiations, corpus callosum, predominantly in the splenium, internal and external capsules), caudate nuclei, basal ganglia, frontal and parietal cortex and in infratentorial structures. |
2021-06-15 |
2023-08-13 |
Not clear |
| Rui Liu, Xing-Ping Qin, Yang Zhuang, Ya Zhang, Hua-Bao Liao, Jun-Chun Tang, Meng-Xian Pan, Fei-Fei Zeng, Yang Lei, Rui-Xue Lei, Shu Wang, An-Chun Liu, Juan Chen, Zhi-Feng Zhang, Dan Zhao, Song-Lin Wu, Ren-Zhong Liu, Ze-Fen Wang, Qi Wa. Glioblastoma recurrence correlates with NLGN3 levels. Cancer medicine. 2021-01-09. PMID:29777576. |
together, this study suggests that increased levels of nlgn3 in the deep brain region under the gbm pathological circumstances may contribute to gbm recurrence in the basal ganglia, thalamus, and corpus callosum. |
2021-01-09 |
2023-08-13 |
mouse |
| Antonella Sferra, Stefania Petrini, Emanuele Bellacchio, Francesco Nicita, Francesco Scibelli, Maria Lisa Dentici, Paolo Alfieri, Gianluca Cestra, Enrico Silvio Bertini, Ginevra Zann. TUBB Variants Underlying Different Phenotypes Result in Altered Vesicle Trafficking and Microtubule Dynamics. International journal of molecular sciences. vol 21. issue 4. 2020-11-30. PMID:32085672. |
we used a combination of immunocytochemical and cellular approaches to explore, on patients' derived fibroblasts, the functional consequences of two tubb variants: the novel mutation (p.n52s), associated with basal ganglia and cerebellar dysgenesis, and the previously reported variant (p.m73t), linked to microcephaly, corpus callosum agenesis and csc-kt skin phenotype. |
2020-11-30 |
2023-08-13 |
human |
| Trina Mitchell, Derek B Archer, Winston T Chu, Stephen A Coombes, Song Lai, Bradley J Wilkes, Nikolaus R McFarland, Michael S Okun, Mieniecia L Black, Ellen Herschel, Tanya Simuni, Cynthia Comella, Tao Xie, Hong Li, Todd B Parrish, Ajay S Kurani, Daniel M Corcos, David E Vaillancour. Neurite orientation dispersion and density imaging (NODDI) and free-water imaging in Parkinsonism. Human brain mapping. vol 40. issue 17. 2020-04-16. PMID:31403737. |
noddi (using multi-shell; isotropic volume [viso]; intracellular volume [vic]; orientation dispersion [odi]) and fw imaging (using single-shell; fw; free-water corrected fractional anisotropy [fat]) were compared with 44 pd, 21 multiple system atrophy parkinsonian variant (msap), 26 progressive supranuclear palsy (psp), and 24 healthy control subjects in the basal ganglia, midbrain/thalamus, cerebellum, and corpus callosum. |
2020-04-16 |
2023-08-13 |
human |
| Sarah N Mattson, Edward P Rile. Prenatal Exposure to Alcohol: What the Images Reveal. Alcohol health and research world. vol 19. issue 4. 2020-01-08. PMID:31798069. |
throughout the range of severity, however, overall reduction of the brain is apparent, and in particular, portions of the cerebellum, basal ganglia, and corpus callosum are disproportionately reduced in size among children with fas and pea. |
2020-01-08 |
2023-08-13 |
Not clear |
| Brian R Barnett, Jacqueline M Anderson, Maribel Torres-Velázquez, Sue Y Yi, Paul A Rowley, John-Paul J Y. Exercise ameliorates deficits in neural microstructure in a Disc1 model of psychiatric illness. Magnetic resonance imaging. vol 61. 2020-01-03. PMID:31103832. |
short-term exercise uncovered no significant differences in neural microstructure between sedentary and exercise control animals but did lead to significant differences between sedentary and exercise disc1 svΔ2 animals in neocortex, basal ganglia, corpus callosum, and external capsule, suggesting a positive benefit derived from a short-term exercise regimen. |
2020-01-03 |
2023-08-13 |
rat |
| José Bourbon-Teles, Sonya Bells, Derek K Jones, Elizabeth Coulthard, Anne Rosser, Claudia Metzler-Baddele. Myelin Breakdown in Human Huntington's Disease: Multi-Modal Evidence from Diffusion MRI and Quantitative Magnetization Transfer. Neuroscience. vol 403. 2019-07-08. PMID:28579146. |
microstructural differences were studied in wm pathways of the basal ganglia and motor systems known to be impaired in hd: the corpus callosum, the cortico-spinal tract, the anterior thalamic radiation, fibers between prefrontal cortex and caudate and between supplementary motor area and putamen. |
2019-07-08 |
2023-08-13 |
human |
| Luis Del Carpio-Orante. [Zika, a neurotropic virus?]. Revista medica del Instituto Mexicano del Seguro Social. vol 54. issue 4. 2017-05-03. PMID:27197113. |
in this paper, the neurotropism potential zika virus is discussed, by comparison with viruses both rna and dna are neurotropic known, also it is said that compared with the new viruses that have affected the americas, as the chikungunya, zika has shown great affinity by brain tissue, manifested by a high incidence of acute neurological conditions, such as guillain-barré syndrome, among others, as well as the reported incidence of microcephaly that is abnormally high compared with the previous incidence, which, in a stillborn subject necropsied significant alterations demonstrated in brain tissue, identifying viral material and live virus in the fetoplacental complex, and demonstrating the impact both white matter and gray matter as well as basal ganglia, corpus callosum, ventricles and spinal cord, which could explain the microcephaly that concerns him. |
2017-05-03 |
2023-08-13 |
human |
| Marta Simó, Lucía Vaquero, Pablo Ripollés, Josep Jové, Rafael Fuentes, Felipe Cardenal, Antoni Rodríguez-Fornells, Jordi Brun. Brain damage following prophylactic cranial irradiation in lung cancer survivors. Brain imaging and behavior. vol 10. issue 1. 2016-12-13. PMID:26015269. |
patients showed significant decreases of gmd in basal ganglia bilaterally (putamen and caudate), bilateral thalamus and right insula, together with wm microstructural changes of the entire corpus callosum. |
2016-12-13 |
2023-08-13 |
Not clear |
| Hanneke van Ewijk, Annabeth P Groenman, Marcel P Zwiers, Dirk J Heslenfeld, Stephen V Faraone, Catharina A Hartman, Marjolein Luman, Corina U Greven, Pieter J Hoekstra, Barbara Franke, Jan Buitelaar, Jaap Oosterlaa. Smoking and the developing brain: altered white matter microstructure in attention-deficit/hyperactivity disorder and healthy controls. Human brain mapping. vol 36. issue 3. 2015-10-21. PMID:25484258. |
widespread alterations in fa and md were found for regular smokers compared to irregular and nonsmokers, mainly located in the corpus callosum and wm tracts surrounding the basal ganglia. |
2015-10-21 |
2023-08-13 |
Not clear |
| Hongmei Meng, Chunkui Zhou, Qingbo Hao, Jiguo Gao, Rensheng Zhang, Zan Wang, Qun Liu, Shaokuan Fan. A rare case of Primary Central Nervous System Lymphoma initially diagnosed as demyelinating encephalopathy. Neuro endocrinology letters. vol 36. issue 2. 2015-09-08. PMID:26071579. |
head mr showed abnormal flaky hypointense t1 and hyperintense t2 signals at right thalamus, splenium of corpus callosum, bilateral cerebral peduncle, pons, medulla oblongata, basal ganglia and right corona radiata. |
2015-09-08 |
2023-08-13 |
Not clear |
| D Amrom, I Tanyalçin, H Verhelst, N Deconinck, G J Brouhard, J-C Décarie, T Vanderhasselt, S Das, F F Hamdan, W Lissens, J L Michaud, A C Janse. Polymicrogyria with dysmorphic basal ganglia? Think tubulin! Clinical genetics. vol 85. issue 2. 2015-03-30. PMID:23495813. |
this report underlines that the association of polymicrogyria with thin or absent corpus callosum, dysmorphic basal ganglia, brainstem and vermis hypoplasia is highly likely to result from mutations in tubb2b and provides further insight in how mutations in tubb2b affect protein function. |
2015-03-30 |
2023-08-12 |
Not clear |
| Gianluca Serafini, Maurizio Pompili, Stefan Borgwardt, Josselin Houenou, Pierre Alexis Geoffroy, Renaud Jardri, Paolo Girardi, Mario Amor. Brain changes in early-onset bipolar and unipolar depressive disorders: a systematic review in children and adolescents. European child & adolescent psychiatry. vol 23. issue 11. 2015-01-06. PMID:25212880. |
reductions in the volume of basal ganglia and the hippocampus appeared more specific for pediatric ud, whereas reduced corpus callosum volume and increased rates of deep wm hyperintensities were more specific for pediatric bd. |
2015-01-06 |
2023-08-13 |
Not clear |
| Daniel Ferreira, Olga Voevodskaya, Kerstin Imrell, Leszek Stawiarz, Gabriela Spulber, Lars-Olof Wahlund, Jan Hillert, Eric Westman, Virginija Danylaité Karrenbaue. Multiple sclerosis patients lacking oligoclonal bands in the cerebrospinal fluid have less global and regional brain atrophy. Journal of neuroimmunology. vol 274. issue 1-2. 2014-11-11. PMID:24999245. |
larger volumes of total csf and white matter (wm) lesions; smaller gray matter (gm) volume in the basal ganglia, diencephalon, cerebellum, and hippocampus; and smaller wm volume in corpus callosum, periventricular-deep wm, brainstem, and cerebellum, were observed in ocb-positives. |
2014-11-11 |
2023-08-13 |
Not clear |
| Christelle Tesson, Magdalena Nawara, Mustafa A M Salih, Rodrigue Rossignol, Maha S Zaki, Mohammed Al Balwi, Rebecca Schule, Cyril Mignot, Emilie Obre, Ahmed Bouhouche, Filippo M Santorelli, Christelle M Durand, Andrés Caballero Oteyza, Khalid H El-Hachimi, Abdulmajeed Al Drees, Naima Bouslam, Foudil Lamari, Salah A Elmalik, Mohammad M Kabiraj, Mohammed Z Seidahmed, Typhaine Esteves, Marion Gaussen, Marie-Lorraine Monin, Gabor Gyapay, Doris Lechner, Michael Gonzalez, Christel Depienne, Fanny Mochel, Julie Lavie, Ludger Schols, Didier Lacombe, Mohamed Yahyaoui, Ibrahim Al Abdulkareem, Stephan Zuchner, Atsushi Yamashita, Ali Benomar, Cyril Goizet, Alexandra Durr, Joseph G Gleeson, Frederic Darios, Alexis Brice, Giovanni Stevani. Alteration of fatty-acid-metabolizing enzymes affects mitochondrial form and function in hereditary spastic paraplegia. American journal of human genetics. vol 91. issue 6. 2013-02-14. PMID:23176821. |
interestingly, three subjects with cyp2u1 mutations presented with a thin corpus callosum, white-matter abnormalities, and/or calcification of the basal ganglia. |
2013-02-14 |
2023-08-12 |
human |