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Relevant bibliographies by topics / Lupus (constellation)

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Journal articles

Academic literature on the topic 'Lupus (constellation)'

Author: Grafiati

Published: 20 February 2023

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Journal articles on the topic "Lupus (constellation)"

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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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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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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6

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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7

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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