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Journal articles on the topic 'Lupus (constellation)'

Author: Grafiati

Published: 20 February 2023

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1

Fischer, Karl A. F. "Al‘suphi’s Star-Atlases and Middle Europe." International Astronomical Union Colloquium 91 (1987): 165–67. http://dx.doi.org/10.1017/s0252921100105998.

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The oldest European mythological figures of the star constellations originate from the Farnesian Globe of the 3rd century B.C. The “Centaurus” with the Therion “Lupus” is the most important constellation from which I derive all the series specified. Centaurus holds the wolf with one hand on the hind leg; in the other hand he holds a lance with which he cuts the wolf’s throat. This constellation is incorrectly drawn in the first publication of the Farnesian Globe by Bianchini. These antique figures were the pattern for Cod. Vind. 5415, probably by John Dorn, a Dominican, who made also the globe

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2

Luo, Yiming, Yumeng Wen, Ana Belen Arevalo Molina, Punya Dahal, Lorenz Leuprecht, and Makda Bsrat. "Macrophage Activation Syndrome, Glomerulonephritis, Pericarditis, and Retinal Vasculitis as Initial Presentation of Systemic Lupus Erythematosus." Case Reports in Medicine 2018 (September 26, 2018): 1–5. http://dx.doi.org/10.1155/2018/5979386.

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Macrophage activation syndrome (MAS) is a rare manifestation of systemic lupus erythematosus (SLE) with potentially life-threatening consequences. To the best of our knowledge, this is the first case reported in literature for a constellation of MAS, glomerulonephritis, pericarditis, and retinal vasculitis as initial presentation of SLE. Despite extensive multisystem involvement of his disease, the patient responded well to initial steroid treatment, with mycophenolate mofetil successfully added as a steroid-sparing agent. Our case highlights the importance of multispecialty collaboration in t

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3

Alzughayyar, Tareq Z., Jihad Samer Zalloum, Mohammad N. Elqadi, et al. "Systemic Lupus Erythematosus with Multiple Autoimmune Disease Presented with Extensive Peripheral Gangrene." Case Reports in Rheumatology 2020 (March 10, 2020): 1–5. http://dx.doi.org/10.1155/2020/8278275.

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Systemic lupus erythematosus (SLE) is an autoimmune disease and can be associated with other autoimmune diseases. SLE usually presents with skin change and rarely presents with gangrene. SLE gangrene usually involves the digits of upper extremities. We report the first case of SLE associated with an extremely rare constellation of neuromyelitis Optica (NMO) and diabetes mellitus type 1, presented with a rare form of the SLE gangrene which involves bilateral lower extremities up to midlegs, a case that has not yet been reported in the literature. Although SLE gangrene may respond to immunosuppr

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4

Alvarado Verduzco, Hector, and Anjali Acharya. "Acute Kidney Injury, Recurrent Seizures, and Thrombocytopenia in a Young Patient with Lupus Nephritis: A Diagnostic Dilemma." Case Reports in Nephrology 2016 (2016): 1–8. http://dx.doi.org/10.1155/2016/7104098.

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Introduction. Posterior reversible encephalopathy syndrome (PRES) is a constellation of clinical and radiologic findings. Fluctuations in blood pressure, seizures, and reversible brain MRI findings mainly in posterior cerebral white matter are the main manifestations. PRES has been associated with multiple conditions such as autoimmune disorders, pregnancy, organ transplant, and thrombotic microangiopathy (TMA). Case Presentation. A 22-year-old woman with history of Systemic Lupus Erythematous complicated with chronic kidney disease secondary to lupus nephritis class IV presented with recurren

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Ghadiri, Nima, and Miles Stanford. "Case of vaso-occlusive retinopathy in Kikuchi-Fujimoto and lupus overlap syndrome." BMJ Case Reports 14, no. 5 (2021): e240752. http://dx.doi.org/10.1136/bcr-2020-240752.

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A 35-year-old woman presented with a constellation of systemic symptoms: rashes, weight loss, arthralgia and mouth ulcers. Six months afterwards, she experienced bilateral and sequential reduction in vision, and was found to have bilateral vaso-occlusive retinopathy, with critical macular ischaemia in the left eye. Her serological markers were consistent with a diagnosis of lupus. A lymph node biopsy confirmed Kikuchi-Fujimoto disease, a benign condition of unknown cause characterised by fever, cervical and axillary lymphadenopathy. Given that this overlap syndrome was associated with a number

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Goldhar, Hart A., Paloma O’Meara, and Lana A. Castellucci. "A case of antiphospholipid syndrome presenting cryptogenically as Budd-Chiari syndrome, then fulminantly as Libman-Sacks endocarditis." BMJ Case Reports 12, no. 5 (2019): e227450. http://dx.doi.org/10.1136/bcr-2018-227450.

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A 58 year-old left-handed woman was transferred to our hospital with an evolving left middle cerebral artery stroke, severe thrombocytopenia and elevated inflammatory markers. She had a history of chronic Budd-Chiari syndrome (BCS) 16 months prior, attributed to a calcified web in the inferior vena cava that was stented. No thrombophilia testing was performed at that time. The current presentation demonstrated dense right-sided facial and arm paresis and neglect. Erythrocyte sedimentation rate and C-reactive protein were elevated, an autoimmune workup was consistent with a new diagnosis of sys

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Satish, Suchitha, Pallavi Deka, and Manjunath Sanjeev Shetty. "A clinico-pathological study of lupus nephritis based on the International Society of Nephrology-Renal Pathology Society 2003 classification system." Journal of Laboratory Physicians 9, no. 03 (2017): 149–55. http://dx.doi.org/10.4103/jlp.jlp_44_16.

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Abstract INTRODUCTION: Lupus nephritis (LN) is a major complication of systemic lupus erythematosus (SLE). Renal involvement is a major determinant of the prognosis of SLE. The histological classification of LN is a key factor in determining the renal survival of patients with LN. Prompt recognition and treatment of renal disease are important, as early response to therapy is correlated with better outcome and renal biopsy plays an important role in achieving this. OBJECTIVES: The objective of this study was to correlate the clinical and laboratory findings with histopathological classes of LN

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8

Ford, Vanessa, Cassandra Mooney, Meera Shah, and Elan Jenkins. "Leukocytoclastic Vasculitis as the Presenting Symptom of Crohn’s Disease in an Adolescent." Journal of Investigative Medicine High Impact Case Reports 8 (January 2020): 232470962094760. http://dx.doi.org/10.1177/2324709620947608.

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Leukocytoclastic vasculitis (LCV) is a rare vascular inflammatory condition that affects post-capillary venules. Its incidence in the pediatric population is unknown. However, its incidence has been shown to increase with age. The causes of LCV can be varied, ranging from drugs to infections to systemic disease. LCV as a presenting symptom of inflammatory bowel disease (IBD) is rare, especially in the pediatric population. A 15-year-old female with a family history of systemic lupus erythematosus was transferred to our hospital with a month-long history of rash, joint swelling and tenderness,

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Mariampillai, Anusiyanthan Isaac, Michael Garrison, and Alice A. Zervoudakis. "Rituximab for Prevention of Recurrent Pregnancy Related Thrombotic Thrombocytopenic Purpura in High Risk Patients with Previous Episodes of Thrombotic Thrombocytopenic Purpura during Pregnancy." Blood 128, no. 22 (2016): 4940. http://dx.doi.org/10.1182/blood.v128.22.4940.4940.

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Abstract Introduction We describe the use of rituximab for the successful prophylaxis and delivery of a multiparous female with a history of pregnancy related thrombotic thrombocytopenic purpura (TTP) now presenting with a high risk of relapse during subsequent pregnancy. Case Presentation A 33 year-old African American female with a history of post-partum TTP diagnosed two years prior was referred to the hematology clinic for suspected recurrence of her TTP at 22 weeks gestation. Two years ago the patient had presented with symptoms of severe headache and hypertension which began 1 week after

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Barbero Mota, M., J. L. Gamboa, J. M. Still, C. M. Stein, V. K. Kawai, and T. A. Lasko. "POS0114 COMPUTATIONAL IDENTIFICATION OF SLE PATIENT RECORDS USING DATA-DRIVEN CLINICAL FINGERPRINTS." Annals of the Rheumatic Diseases 81, Suppl 1 (2022): 282.2–282. http://dx.doi.org/10.1136/annrheumdis-2022-eular.954.

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BackgroundSystemic lupus erythematosus (SLE) is a chronic relapsing autoimmune disorder that is challenging to diagnose due to its heterogeneous presentation of a combination of non-specific clinical manifestations and laboratory findings. This heterogeneity and lack of granularity is a major cause of treatment failure. With the advent of precision medicine, there is a need for accurate methods to identify cases of SLE in large clinical databases, and to recognize constellations of pathological characteristics (or fingerprints) that allow a better understanding of the disease. Computational ph

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11

Ernawati, Ernawati. "PSIKOLOGIS DALAM SENI: KATARSIS SEBAGAI REPRESENTASI DALAM KARYA SENI RUPA." DESKOVI : Art and Design Journal 2, no. 2 (2020): 105. http://dx.doi.org/10.51804/deskovi.v2i2.521.

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Tujuan penelitian ini adalah mengungkap peran aspek psikologis katarsis dalam karya seni rupa. Prinsip seputar psikis dapat dipraktikan dalam karya seni, salahsatunya gerakan seni rupa kontemporer. Kajian karya berdasarkan aspek psikologis, salah satunya katarsis termasuk hal yang krusial untuk dilakukan. Metode pada penelitian ini menerapkan metode kualitatif dengan pendekatan multidisiplin (psikologi seni dan semiotika). Hasil penelitian menunjukkan bahwa Perspektif lebih obyektif karena seniman sebagai kreator berbanding lurus dengan karya yang disajikan. Elemen visual yang dipilih dan disa

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12

Kadia, Tapan M., Hongbing Ma, Ke Zeng, et al. "Phase I Clinical Trial of CK0801 (cord blood regulatory T cells) in Patients with Bone Marrow Failure Syndrome (BMF) Including Aplastic Anemia, Myelodysplasia and Myelofibrosis." Blood 134, Supplement_1 (2019): 1221. http://dx.doi.org/10.1182/blood-2019-127702.

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Background: Aplastic anemia is an autoimmune disease of the bone marrow (BM) characterized by defective and decreased regulatory T cells (Tregs) which results in unchecked cytotoxic T cell mediated bone marrow suppression [1]. In a xenogeneic model of induce BM aplasia, adoptive therapy with cord blood (CB) Tregs reverses such a defect (Fig 1A). Furthermore, as compared to peripheral blood (PB), CB Tregs show a higher expression of Helios, a marker of thymic derived Tregs (Fig 1B) and CB Tregs exert a superior suppression of proliferating conventional T-cells in CFSE assay (Fig 1C). In a xenog

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13

Chang, Chee Keong, Malehah Mohd Noh, Constance Liew Sat Lin, and Alvin Oliver Payus. "Unusual Presentation of Cerebral Lupus: A Case Report of Parkinsonism in Cerebral Lupus." Case Reports in Neurology, September 13, 2021, 591–94. http://dx.doi.org/10.1159/000518912.

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Systemic lupus erythematosus (SLE) is a chronic autoimmune disease with multisystem involvement that follows a relapsing and remitting course. It is characterized by an immune-mediated response to own body defense mechanism and mistakenly attacked healthy cells of the skin, joints, kidneys, blood cells, and nervous system. Cerebral lupus refers to a constellation of neurological and/or behavioral clinical syndromes in patients with SLE. The spectrum of presentation can vary widely ranging from mild symptoms such as headaches, slight cognitive dysfunction, and mood disorders to more serious con

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14

Hamza, Wael Mostafa, and Ahmed Mohammed AlEssa. "Coincidental light chain induced proximal tubulopathy with lupus nephritis: a case report and review of the literature." Journal of Medical Case Reports 15, no. 1 (2021). http://dx.doi.org/10.1186/s13256-021-02990-4.

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Abstract Background We report a case of light chain proximal tubulopathy associated with lupus nephritis in a patient known to have systemic lupus erythematosus. The kidney can be injured in several ways in any of these disorders. Light chain proximal tubulopathy is a rare form of renal tubular injury that may occur in and complicate plasma cell dyscrasia, characterized by cytoplasmic inclusions of the monoclonal light chain within proximal tubular cells. Lupus nephritis is a common form of renal injury as it occurs in about 25–50% of adult patients with systemic lupus erythematosus. Case pres

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15

Kumar, Kris, Joshua Vogt, Ahmad Masri, et al. "Abstract 13129: Chest Pain and Inflammation: A Story Where Hickam’s Dictum Prevailed." Circulation 142, Suppl_3 (2020). http://dx.doi.org/10.1161/circ.142.suppl_3.13129.

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A 39-year-old male presented with a chief complaint of chest pain that worsened with deep breathing for one day. He was found to be tachycardic, with distant heart sounds and a skin nodule over his right upper extremity. ECG revealed diffuse ST elevations and PR segment depressions with TTE showing a small pericardial effusion. Troponin I was 8.98 ng/mL and NT-proBNP was 981 pg/mL. One day after admission, he developed respiratory distress, and repeat TTE showed a large pericardial effusion with collapse of the RV free wall during diastole with variation of mitral and tricuspid valve inflows c

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16

Mootoo, Amanda, Mark Gibson, and Begoña Lopez. "P33 The successful use of Belimumab in recurrent small bowel obstruction secondary to Lupus Enteritis." Rheumatology Advances in Practice 6, Supplement_1 (2022). http://dx.doi.org/10.1093/rap/rkac067.033.

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Abstract Introduction/Background Lupus enteritis encompasses mesenteric vasculitis, enteric vasculitis, mesenteric arteritis and lupus peritonitis and is an uncommon, potentially life-threatening presentation of SLE. The prevalence in SLE patients ranges from 0.2% to 9.7% and up to 65% in SLE patients presenting with acute abdominal pain. This case brings awareness to the gastrointestinal manifestations of lupus with particular focus on the clinical and radiological features of SLE-related vasculitis of the gastrointestinal tract. It highlights the importance of recognising new ascites and hyd

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17

Solipuram, Swathi, Fabian Wayar, Apeksha Bhattarai, Chandralekha Ashangari, and Amer Suleman. "Abstract 217: Study II - Antinuclear Antibody Levels Study in Postural Orthostatic Tachycardia Syndrome." Circulation Research 121, suppl_1 (2017). http://dx.doi.org/10.1161/res.121.suppl_1.217.

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Background: Postural Orthostatic Tachycardia Syndrome (POTS) is a constellation of signs and symptoms that occurs when the patient stands upright. It affects primarily young women. The antinuclear antibody (ANA) test measures the amount and pattern of antibodies in blood that work against own body (autoimmune reaction). If there are more antibodies in the blood than normal, the test is positive. Previously, we have conducted a research on increased ANA levels and POTS and found that 41% of them had positive results. Taking that one step ahead, the aim of this study is to demonstrate further pa

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18

Yeoh, Su-Ann, Sharfaraz Salam, Gerry Christofi, and Vanessa Morris. "P48 A case of myasthenia gravis presenting to the rheumatology clinic." Rheumatology 59, Supplement_2 (2020). http://dx.doi.org/10.1093/rheumatology/keaa111.047.

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Abstract Background A 32-year-old Lithuanian lady, with a 6-year history of undifferentiated inflammatory arthritis and autoimmune neutropenia, contacted her rheumatologist reporting a constellation of new symptoms. This began with a month’s history of facial weakness and slurred speech. She progressively experienced nasal regurgitation on drinking fluids, reduced exercise tolerance, as well as difficulty chewing, swallowing, and coughing. Her symptoms initially came on in the evening but subsequently appeared earlier in the day. There were no symptoms suggestive of infection. Her arthritis ha

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