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https://www.readbyqxmd.com/read/27891561/citrus-psorosis-virus-coat-protein-derived-hairpin-construct-confers-stable-transgenic-resistance-in-citrus-against-psorosis-a-and-b-syndromes
#1
A De Francesco, N Costa, M L García
Citrus psorosis virus (CPsV) is the causal agent of psorosis, a serious and widespread citrus disease. Two syndromes of psorosis, PsA and PsB, have been described. PsB is the most aggressive and rampant form. Previously, we obtained Pineapple sweet orange plants transformed with a hairpin construct derived from the CPsV coat protein gene (ihpCP). Some of these plants were resistant to CPsV 90-1-1, a PsA isolate homologous to the transgene. In this study, we found that expression of the ihpCP transgene and siRNA production in lines ihpCP-10 and -15 were stable with time and propagation...
November 28, 2016: Transgenic Research
https://www.readbyqxmd.com/read/27886403/rapid-test-for-lung-maturity-based-on-spectroscopy-of-gastric-aspirate-predicted-respiratory-distress-syndrome-with-high-sensitivity
#2
Henrik Verder, Christian Heiring, Howard Clark, David Sweet, Torben E Jessen, Finn Ebbesen, Lars J Björklund, Bengt Andreasson, Lars Bender, Aksel Bertelsen, Marianne Dahl, Christian Eschen, Jesper Fenger-Grøn, Stine F Hoffmann, Agnar Höskuldsson, Maria Bruusgaard-Mouritsen, Fredrik Lundberg, Anthony D Postle, Peter Schousboe, Peter Schmidt, Hristo Stanchev, Lars Sørensen
AIM: Respiratory distress syndrome (RDS) is a major cause of mortality and morbidity in premature infants. By the time symptoms appear it may already be too late to prevent a severe course, with bronchopulmonary dysplasia or mortality. We aimed to develop a rapid test of lung maturity for targeting surfactant supplementation. METHODS: Concentrations of the most surface-active lung phospholipid dipalmitoylphosphatidylcholine and sphingomyelin in gastric aspirates from premature infants were measured by mass spectrometry and expressed as the lecithin/sphingomyelin ratio (L/S)...
November 25, 2016: Acta Paediatrica
https://www.readbyqxmd.com/read/27882877/dermpath-clinic-drug-induced-sweet-syndrome
#3
Pauline Hoelt, Kinda Fattouh, Axel-Patrice Villani
No abstract text is available yet for this article.
November 23, 2016: European Journal of Dermatology: EJD
https://www.readbyqxmd.com/read/27851623/1989-a-fatal-case-of-hydralazine-induced-sweet-syndrome
#4
Areej Mazhar, Jelena Arnautovic
No abstract text is available yet for this article.
December 2016: Critical Care Medicine
https://www.readbyqxmd.com/read/27851357/1722-ecmo-for-severe-ards-in-a-patient-with-acute-myelogenous-leukemia-and-sweet-syndrome
#5
Nikhil Huprikar, James Lantry, Justin Reis, Jeffrey DellaVolpe
No abstract text is available yet for this article.
December 2016: Critical Care Medicine
https://www.readbyqxmd.com/read/27843926/single-nail-involvement-as-first-sign-of-sweet-s-syndrome
#6
EDITORIAL
Giulia Rech, Riccardo Balestri, Michelangelo La Placa, Michela Magnano, Carlo Renè Girardelli
No abstract text is available yet for this article.
September 2016: Skin Appendage Disorders
https://www.readbyqxmd.com/read/27830291/-cutaneous-involvement-in-chronic-inflammatory-bowel-disease-crohn-s-disease-and-ulcerative-colitis
#7
REVIEW
L Richter, K Rappersberger
BACKGROUND: Over recent decades, both the incidence and prevalence of chronic inflammatory bowel disease have continued to rise in industrialized countries; the disease is frequently associated with extracutaneous involvement and comorbidity. OBJECTIVES: The purpose of this work was to investigate the frequency and specificity of mucocutaneous manifestations in Crohn's disease (CD) and ulcerative colitis (UC). MATERIALS AND METHODS: An extensive search in peer-reviewed journals via PubMed was performed; presented is a summary and analysis of various studies and data, including data of patients treated at our department...
December 2016: Der Hautarzt; Zeitschrift Für Dermatologie, Venerologie, und Verwandte Gebiete
https://www.readbyqxmd.com/read/27823912/-chronic-recurrent-annular-neutrophilic-dermatosis
#8
A Croci-Torti, B Guillot, V Rigau, D Bessis
BACKGROUND: Chronic recurrent annular neutrophilic dermatosis (CRAND) is a rare form of neutrophilic dermatosis characterised by chronic annular progression, histological impairment similar to that seen in Sweet's syndrome and the absence of association with generalised signs, abnormal laboratory values or underlying systemic disease. Herein we report two new cases. PATIENTS AND METHODS: Case n(o) 1. A 41-year-old woman had presented with four annular lesions on the forearms and neckline which she had had for one year...
November 4, 2016: Annales de Dermatologie et de Vénéréologie
https://www.readbyqxmd.com/read/27812416/baseline-reef-health-surveys-at-bangka-island-north-sulawesi-indonesia-reveal-new-threats
#9
Massimo Ponti, Francesca Fratangeli, Nicolò Dondi, Marco Segre Reinach, Clara Serra, Michael J Sweet
Worldwide coral reef decline appears to be accompanied by an increase in the spread of hard coral diseases. However, whether this is the result of increased direct and indirect human disturbances and/or an increase in natural stresses remains poorly understood. The provision of baseline surveys for monitoring coral health status lays the foundations to assess the effects of any such anthropogenic and/or natural effects on reefs. Therefore, the objectives of this present study were to provide a coral health baseline in a poorly studied area, and to investigate possible correlations between coral health and the level of anthropogenic and natural disturbances...
2016: PeerJ
https://www.readbyqxmd.com/read/27803515/pregnancy-associated-sweet-s-syndrome-a-rare-clinical-entity
#10
Madhavi Sankar, Karthikeyan Kaliaperumal
No abstract text is available yet for this article.
October 2016: Journal of Obstetrics and Gynaecology of India
https://www.readbyqxmd.com/read/27796411/-pyoderma-gangrenosum-and-sweet-s-syndrome-cutaneous-manifestations-of-autoinflammatory-disorders
#11
B Meier, J-T Maul, L E French
Pyoderma gangrenosum and Sweet's syndrome are rare diseases that belong to the group of neutrophilic dermatoses and share several common characteristics. Although the two disorders differ clinically from each other, both diseases show pronounced dermal infiltration of neutrophils without evidence of primary vasculitis and respond well to immunosuppressive drugs. In addition, both diseases are often associated with other systemic and hematological disorders. Recent findings show that the neutrophil dermatoses can be considered as cutaneous manifestations of autoinflammation, demonstrating an interesting new aspect in the development of the diseases and additional therapeutic avenues...
December 2016: Der Hautarzt; Zeitschrift Für Dermatologie, Venerologie, und Verwandte Gebiete
https://www.readbyqxmd.com/read/27759696/xanthomatized-neutrophilic-dermatosis-in-a-patient-with-myelodysplastic-syndrome
#12
Gina J Ferris, Stephanie Fabbro, Alejandro Gru, Jessica Kaffenberger
We present an original case report of a 58-year-old man with a history of histiocytoid Sweet and myelodysplastic syndrome who presented with a new onset of tender plaques on his oral commissures. A biopsy revealed a dense dermal neutrophilic infiltrate, leukocytoclasis without frank vasculitis, and, most notably, the presence of many xanthomatized cells. Clinical presentation and histologic features were most consistent with an acute neutrophilic dermatosis, which we believe to be a xanthomized variant of Sweet syndrome...
October 18, 2016: American Journal of Dermatopathology
https://www.readbyqxmd.com/read/27749403/elevated-18f-fdg-uptake-in-skeletal-muscles-rather-than-cutaneous-foci-in-a-patient-with-sweet-s-syndrome
#13
Shengming Deng, Bin Zhang, Xiuli Sui, Shibiao Sang, Wei Zhang
A 64-year-old man was admitted to our hospital with a history of recurrent fever lasting 2 months. The initial physical examination for the patient showed normal cutaneous signs. An elevated uptake of tracer in skeletal muscles was observed by F-FDG PET/CT imaging. Three weeks later, a multitude of painful erythematous maculopapules appeared over his face, chest, and back. Pathological examination of a skin lesion showed papillary dermal edema with predominantly dense neutrophilic infiltrate in the dermis with no evidence of vasculitis, which was consistent with Sweet's syndrome...
October 5, 2016: Clinical Nuclear Medicine
https://www.readbyqxmd.com/read/27728737/sweet-s-syndrome-a-rare-case-study
#14
Ruju Gala, Priyank Dumade, Kshiteeja Jain, Nikhil Saxena, Rakesh Mp
No abstract text is available yet for this article.
January 2016: Journal of the Association of Physicians of India
https://www.readbyqxmd.com/read/27728558/aml-presenting-as-sweet-s-syndrome-with-leukemia-cutis
#15
V Santosh Kumar
No abstract text is available yet for this article.
January 2016: Journal of the Association of Physicians of India
https://www.readbyqxmd.com/read/27726871/-vesiculobullous-sweet-s-syndrome
#16
P Janssens, C Courtin, A Saint-Remy, M-N Voogeleer, P Ngendahayo, B Bouffioux
No abstract text is available yet for this article.
October 7, 2016: Annales de Dermatologie et de Vénéréologie
https://www.readbyqxmd.com/read/27720691/acute-myeloid-leukemia-presenting-with-sweet-syndrome-a-case-report-and-review-of-the-literature
#17
Shu-Huey Chen, Yung-Ting Kuo, Yen-Lin Liu, Bo-Jung Chen, Yuan-Chieh Lu, James S Miser
No abstract text is available yet for this article.
August 5, 2016: Pediatrics and Neonatology
https://www.readbyqxmd.com/read/27681337/a-not-so-sweet-diagnosis%C3%A2-%C3%A2-leukocytoclastic-vasculitis-masquerading-as-squamous-cell-carcinoma
#18
Mussa Mensa, Zita M Jessop, Nick Wilson-Jones, Iain S Whitaker
Leukocytoclastic vasculitis (LCV) is a rare small-vessel vasculitis characterised by neutrophilic inflammation of post-capillary venules. Incidence varies from 3 to 4.5 per 100 000 people per year. Patients typically present with painful, itchy purpura and erythema, although clinical manifestations can vary making diagnosis a challenge. We report the case of a 75-year-old man with a history of a previously completely excised and grafted squamous cell carcinoma (SCC) on the dorsum of his hand, who presented with an acutely swollen, erythematous and ulcerated lesion adjacent to the graft site...
September 29, 2016: International Wound Journal
https://www.readbyqxmd.com/read/27663147/sweet-syndrome-long-term-follow-up-of-138-patients
#19
J Marcoval, C Martín-Callizo, F Valentí-Medina, M Bonfill-Ortí, L Martínez-Molina
BACKGROUND: Several studies support a strong association of Sweet syndrome (SS) with malignancy. However, only a few studies analysing the clinical features of malignancy-associated SS have been published in recent years. AIM: To retrospectively study the clinical features of SS that could predict the development of associated malignancies and to analyse the development of malignant neoplasia during long-term follow-up of patients with SS. METHODS: Clinical features of the patients diagnosed with SS syndrome between 1987 and 2013 at Bellvitge Hospital (Barcelona, Spain) were retrospectively analysed...
October 2016: Clinical and Experimental Dermatology
https://www.readbyqxmd.com/read/27659797/neuro-sweet-syndrome-a-systematic-review-a-rare-complication-of-sweet-syndrome
#20
Francesco Drago, Giulia Ciccarese, Arianna Fay Agnoletti, Francesca Sarocchi, Aurora Parodi
Sweet's syndrome (SS) is an inflammatory disease characterized by fever, leucocytosis and distinctive skin lesions that histologically consist of a dermal infiltrate of neutrophils with nuclear fragmentation. Aseptic neutrophilic inflammation may occur also in other organs. Central nervous system involvement in SS, Neuro-Sweet's syndrome (NSS), is rare and reported especially among Asian patients. A systematic review of the literature has been performed to find articles reporting cases of SS with neurological involvement...
September 22, 2016: Acta Neurologica Belgica
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