Filters
Results 1 - 10 of 1917
Results 1 - 10 of 1917.
Search took: 0.028 seconds
Sort by: date | relevance |
Bajaj, Manish; Jangid, Hemant; Vats, AK; Meena, ML, E-mail: mbj_rnt@hotmail.com2010
AbstractAbstract
[en] A 36-year-old man presented with headache and right upper and lower limb weakness for 10 days. MRI revealed absence of the odontoid process of the C2 vertebral body, with resultant atlantoaxial dislocation along with myelomalacic changes involving the cervicomedullary junction
Primary Subject
Source
Available from http://dx.doi.org/10.4103/0971-3026.63050; Available from http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2890915; PMCID: PMC2890915; PMID: 20607020; PUBLISHER-ID: IJRI-20-109; OAI: oai:pubmedcentral.nih.gov:2890915; Copyright (c) Indian Journal of Radiology and Imaging; This is an open-access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.; Country of input: International Atomic Energy Agency (IAEA)
Record Type
Journal Article
Journal
Indian Journal of Radiology and Imaging - New Series (Print); ISSN 0971-3026;
; v. 20(2); p. 109-111

Country of publication
Reference NumberReference Number
INIS VolumeINIS Volume
INIS IssueINIS Issue
External URLExternal URL
Kundum, Prasad R; Gupta, Arun K; Thottom, Prasad V; Jana, Manisha, E-mail: manishajana@gmail.com2010
AbstractAbstract
[en] Congenital posterior urethral diverticulum is an uncommon anomaly, sometimes complicated by infection or calculi formation. A conventional voiding cystourethrogram (VCUG) is the most commonly used diagnostic modality. Dynamic magnetic resonance imaging (MRI) has not been frequently described in this entity. We describe a case of posterior urethral diverticulum complicated with secondary calculi, where the patient was evaluated using dynamic MRI and conventional VCUG
Primary Subject
Source
Available from http://dx.doi.org/10.4103/0971-3026.73536; Available from http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3056630; PMCID: PMC3056630; PMID: 21423908; PUBLISHER-ID: IJRI-20-300; OAI: oai:pubmedcentral.nih.gov:3056630; Copyright (c) Indian Journal of Radiology and Imaging; This is an open-access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.; Country of input: International Atomic Energy Agency (IAEA)
Record Type
Journal Article
Journal
Indian Journal of Radiology and Imaging - New Series (Print); ISSN 0971-3026;
; v. 20(4); p. 300-303

Country of publication
Reference NumberReference Number
INIS VolumeINIS Volume
INIS IssueINIS Issue
External URLExternal URL
Funayama, Emi; Yamamoto, Yuhei; Oyama, Akihiko; Murao, Naoki; Hayashi, Toshihiko; Maeda, Taku; Furukawa, Hiroshi; Osawa, Masayuki, E-mail: emi-f@bc.iij4u.or.jp2019
AbstractAbstract
No abstract available
Primary Subject
Source
Copyright (c) 2019 Springer-Verlag London Ltd., part of Springer Nature; Country of input: International Atomic Energy Agency (IAEA)
Record Type
Journal Article
Journal
Lasers in Medical Science (Online); ISSN 1435-604X;
; v. 34(9); p. 1925-1928

Country of publication
Reference NumberReference Number
INIS VolumeINIS Volume
INIS IssueINIS Issue
Rajeswaran, Rangasami; Murthy, Jyotsna; Chandrasekharan, Anupama; Joseph, Santhosh, E-mail: rrajeswaran@rediffmail.com2008
AbstractAbstract
[en] Congenital infiltrating lipomatosis of the face is a rare condition characterized by diffuse fatty infiltration of the facial soft tissues. There may be muscle involvement along with associated bony hyperplasia. It is a type of lipomatous tumor that is congenital in origin; it is rare and seen usually in childhood. We recently saw an 11-year-old girl with this condition. She presented with a swelling of the right side of the face that had been present since birth; there were typical findings on plain radiographs, CT, and MRI. The patient underwent cosmetic surgery. Histopathological examination showed mature adipocytes without any capsule
Primary Subject
Source
Available from http://dx.doi.org/10.4103/0971-3026.43847; Available from http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2747453; PMCID: PMC2747453; PMID: 19774187; PUBLISHER-ID: IJRI-18-306; OAI: oai:pubmedcentral.nih.gov:2747453; Copyright (c) Indian Journal of Radiology and Imaging; This is an open-access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.; Country of input: International Atomic Energy Agency (IAEA)
Record Type
Journal Article
Journal
Indian Journal of Radiology and Imaging - New Series (Print); ISSN 0971-3026;
; v. 18(4); p. 306-309

Country of publication
Reference NumberReference Number
INIS VolumeINIS Volume
INIS IssueINIS Issue
External URLExternal URL
Kroencke, Thomas; Murnauer, Marcus; Jordan, Frank Alexander; Blodow, Vera; Ruhnke, Hannes; Schaller, Tina; Märkl, Bruno, E-mail: thomas.kroencke@klinikum-augsburg.de2018
AbstractAbstract
[en] In a 50-year-old male with an incidentally discovered hepatocellular carcinoma, a congenital extrahepatic portosystemic shunt with the absence of the portal vein (Abernethy syndrome) was diagnosed by imaging. This study aims to discuss the variant anatomy relevant to this splanchnic vascular malformation, review its association with the development of liver neoplasms, and report the safety and efficacy of TARE followed by resection for a HCC arising in this rare condition.
Primary Subject
Source
Copyright (c) 2018 Springer Science+Business Media, LLC, part of Springer Nature and the Cardiovascular and Interventional Radiological Society of Europe (CIRSE); http://www.springer-ny.com; Country of input: International Atomic Energy Agency (IAEA)
Record Type
Journal Article
Journal
Country of publication
Reference NumberReference Number
INIS VolumeINIS Volume
INIS IssueINIS Issue
Freeman, L.
Conferences [25. Alasbimn Congress 2015; 5. Subimn congress; 2. Latin-American meeting of radiochemical]2015
Conferences [25. Alasbimn Congress 2015; 5. Subimn congress; 2. Latin-American meeting of radiochemical]2015
AbstractAbstract
[en] This lecture is about the lung cases. Primary lung carcinoma, benign bronchogenic tumors, mucous plugs, parenchymal lung or mediastinal disease, congenital HD (post shunt), hyperlucent lungs syndrome, post pneumonectomy, pulmonary embolism
Primary Subject
Source
Asociación Latinoamericana de Sociedades de Biología y Medicina Nuclear-Alasbimn, Montevideo (Uruguay); 1 p; Nov 2015; 37 p; 25. Alasbimn Congress 2015; 25. Congreso Alasbimn 2015; Punta del Este (Uruguay); 18-21 Nov 2015; 5. Subimn congress; 5o. congreso de la Subimn; Punta del Este (Uruguay); 18-21 Nov 2015; 2. Latin-American meeting of radiochemical; 2o. encuentro latinoamericano de radiofarmacia; Punta del Este (Uruguay); 18-21 Nov 2015; Available from: http://www.alasbimn2015.org.uy/
Record Type
Miscellaneous
Literature Type
Conference
Report Number
Country of publication
Reference NumberReference Number
Related RecordRelated Record
INIS VolumeINIS Volume
INIS IssueINIS Issue
External URLExternal URL
Mistry, Kewal A.; Sood, Dinesh; Bhoil, Rohit; Chadha, Veenal; Ahluwalia, Ajay K.; Sood, Saurabh; Suthar, Pokhraj P., E-mail: drpgmc12@gmail.com2015
AbstractAbstract
[en] Tuberous Sclerosis (TSC) also known as Bourneville disease is a neurocutaneous syndrome having an autosomal dominant inheritance pattern, though the condition has a high rate of spontaneous mutation. It is the second most common neurocutaneous syndrome after neurofibromatosis. This disease demonstrates a widespread potential for hamartomatous growths in multiple organ systems. We report a case of a 36-year-old female with TSC presenting as massive hematuria with underlying giant bilateral renal angiomyolipomas (AML) with estimated total tumor burden of more than 8 kg which is to the best of our knowledge the highest ever reported. The patient also had lymphangioleiomyomatosis and lesions in the brain, skin, teeth and bones. TSC has a wide variety of clinical and radiologic manifestations. It should be suspected when some of the common radiological manifestations are found, including CNS involvement, renal and hepatic AMLs and LAM, even if clinical signs are not obvious. Renal AMLs in setting of TSC may reach giant proportions and may present with massive hematuria
Primary Subject
Source
Available from http://dx.doi.org/10.12659/PJR.894741; Available from http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4588676; PMCID: PMC4588676; PMID: 26491490; PUBLISHER-ID: 894741; OAI: oai:pubmedcentral.nih.gov:4588676; Copyright (c) Pol J Radiol, 2015; This is an open access article. Unrestricted non-commercial use is permitted provided the original work is properly cited.; Country of input: International Atomic Energy Agency (IAEA)
Record Type
Journal Article
Journal
Polish Journal of Radiology; ISSN 1733-134X;
; v. 80; p. 435-441

Country of publication
Reference NumberReference Number
INIS VolumeINIS Volume
INIS IssueINIS Issue
External URLExternal URL
Zhu, Peiran; Li, Weiwei; Ni, Mengxia; Zhang, Cui; Liu, Shuaimei; Wu, Qiuyue; Jiang, Weijun; Zhang, Jing; Zhang, Mingchao; Li, Xiaojun; Cui, Yingxia; Xue, Chunyan; Xia, Xinyi, E-mail: xiaxynju@163.com2017
AbstractAbstract
[en] αB-crystallin acts as an anti-apoptosis protein in human lens epithelial (HLE) cells. We recently identified a missense mutation in αB-crystallin that changes proline 20 to an arginine (P20R) in a Chinese family with autosomal dominant congenital posterior polar cataract. The impact of the P20R mutation on the anti-apoptosis function remains unclear. To explore the anti-apoptotic activity of αB-crystallin wild type (αB-wt) and its P20R mutant under oxidative stress, HLE cells were transfected with αB-wt and αB-P20R constructs and expression was measured by western blotting. Flow cytometry and terminal deoxynucleotidyl transferase (TdT)-mediated dUTP digoxigenin nick end-labelling (TUNEL) staining were performed to investigate apoptosis. We found that αB-wt performed a dominant role in inhibiting stress-induced apoptosis, but this function was impeded in cells expressing αB-P20R. The P20R mutant of αB-crystallin exhibits diminished anti-apoptotic activity compared with the native protein. - Highlights: • We identified a novel mutation (P20R) in αB-crystallin. • The mutation decreased anti-apoptotic activity in αB-crystallin, which compared with the native protein. • We speculate that the mutation may influence phosphorylation, especially Ser19.
Primary Subject
Source
S0006-291X(16)32181-7; Available from http://dx.doi.org/10.1016/j.bbrc.2016.12.121; Copyright (c) 2016 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.; Country of input: International Atomic Energy Agency (IAEA)
Record Type
Journal Article
Journal
Biochemical and Biophysical Research Communications; ISSN 0006-291X;
; CODEN BBRCA9; v. 483(1); p. 463-467

Country of publication
Reference NumberReference Number
INIS VolumeINIS Volume
INIS IssueINIS Issue
AbstractAbstract
No abstract available
Primary Subject
Source
ECR 2002: 14. European congress of radiology; Vienna (Austria); 1-5 Mar 2002
Record Type
Journal Article
Literature Type
Conference
Journal
Country of publication
Reference NumberReference Number
INIS VolumeINIS Volume
INIS IssueINIS Issue
Walsh, Richard M. Jr.; Roh, Soung-Hun; Gharpure, Anant; Morales-Perez, Claudio L.
SLAC National Accelerator Laboratory, Menlo Park, CA (United States). Funding organisation: USDOE (United States)2018
SLAC National Accelerator Laboratory, Menlo Park, CA (United States). Funding organisation: USDOE (United States)2018
AbstractAbstract
[en] Fast chemical communication in the nervous system is mediated by neurotransmitter-gated ion channels. The prototypical member of this class of cell surface receptors is the cation-selective nicotinic acetylcholine receptor. As with most ligand-gated ion channels, nicotinic receptors assemble as oligomers of subunits, usually as hetero-oligomers and often with variable stoichiometries. This intrinsic heterogeneity in protein composition provides fine tunability in channel properties, which is essential to brain function, but frustrates structural and biophysical characterization. The α4β2 subtype of the nicotinic acetylcholine receptor is the most abundant isoform in the human brain and is the principal target in nicotine addiction. This pentameric ligand-gated ion channel assembles in two stoichiometries of α- and β-subunits (2α:3β and 3α:2β). Both assemblies are functional and have distinct biophysical properties, and an imbalance in the ratio of assemblies is linked to both nicotine addiction and congenital epilepsy. Here we leverage cryo-electron microscopy to obtain structures of both receptor assemblies from a single sample. Antibody fragments specific to β2 were used to ‘break’ symmetry during particle alignment and to obtain high-resolution reconstructions of receptors of both stoichiometries in complex with nicotine. Furthermore, the results reveal principles of subunit assembly and the structural basis of the distinctive biophysical and pharmacological properties of the two different stoichiometries of this receptor.
Primary Subject
Source
OSTIID--1461187; AC02-76SF00515; Available from https://www.osti.gov/servlets/purl/1461187; DOE Accepted Manuscript full text, or the publishers Best Available Version will be available free of charge after the embargo period; arXiv:1801.02427; Country of input: United States
Record Type
Journal Article
Journal
Nature (London); ISSN 0028-0836;
; v. 557(7704); p. 261-265

Country of publication
Reference NumberReference Number
INIS VolumeINIS Volume
INIS IssueINIS Issue
External URLExternal URL
1 | 2 | 3 | Next |