Defining disease activity states and clinically meaningful improvement in primary Sjögren's syndrome with EULAR primary Sjögren's syndrome disease activity (ESSDAI) and patient-reported indexes (ESSPRI). Research output: Contribution to journal › Article

Bartolini is the director of the Pediatric Epilepsy Program at Hasbro Children's Hospital and Assistant Professor (Research Scholar) of Pediatrics, Neurology and

A pattern of several… What can we help you find? Enter search terms and tap the Search button. Both ar MDS is caused by a mutation of stem cells in the bone marrow. This mutation can be caused by exposure to radiation, chemotherapy, toxic chemicals or a virus. It is not a genetic disorder, but there are familial links, to blood disorders.

to CLINICAL AND IMMUNOLOGICAL PRIMARY SJOGREN SYNDROME' DISEASE PATTERNS ARE DRIVEN BY GENDER AND AGE AT DIAGNOSIS. Bartoloni E, Gonzazlez-Gay MA, Scire C, et al. Clinical follow-up predictors of disease pattern change in anti-Jo1 positive anti-synthetase syndrome: results from 18 Oct 2020 INTRODUCTION: Anti-synthetase syndrome, considered a subset of dermatomyositis and Bartoloni E, Gonzalez-Gay MA, Scirè C, et al. 14 Aug 2015 There is evidence that interferon is involved in the pathogenesis of primary Sjögren's syndrome (pSS). The interferon-inducible IFI16 protein, Bertolotti's syndrome is a rare disease relating to an enlargement of transverse process of a vertebra leading to chronic back pain.

2015-09-16

Semantic Scholar profile for E. Bartoloni, with 89 highly influential citations and 161 scientific research papers. Cardiovascular disease risk burden in primary Sjögren's syndrome: results of a population‐based multicentre cohort study E. Bartoloni Rheumatology Unit, Department of … Elongation of the styloid process and/or ossification of the stylohyoid ligament can be associated with cervical pharyngeal pain, which may be detected both clinically and radiographically. Eagle's syndrome, stylohyoid syndrome, and pseudostylohyoid syndrome should be considered in the differential diagnosis.

Syndrome Society of Argentina Rheumatology Study Group) were analyzed. For the Quartuccio L, Isola M, Baldini C, Priori R, Bartoloni E, Carubbi. F, et al.

The cardiac component includes dilated cardiomyopathy which can at times cause severe systolic congestive hear After a head injury, many people experience symptoms such as dizziness, headaches, and mood changes as long as a year after the accident.

COVID-19 as part of the hyperferritinemic syndromes: the role of iron depletion therapy Carlo Perricone, Elena Bartoloni , Roberto Bursi, Giacomo Cafaro, Giacomo Maria Guidelli, Yehuda Shoenfeld, Roberto Gerli Sjögren’s syndrome (SS) is an autoimmune systemic disease characterized by B-cell lymphoproliferation and an increased risk of B-cell non-Hodgkin lymphoma (NHL) development, mainly of the mucosa-associated lymphoid tissue (MALT) type, which impacts survival and mortality. 2019-08-04 Alessia Alunno & Elena Bartoloni Sjogren’s Syndrome Novel Insights in Pathogenic, Clinical and Therapeutic Aspects Bartoloni E, Bistoni O, Alunno A, Cavagna L, Nalotto L, Baldini C, et al. .
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Se hela listan på hekint.org "Designad för att hjälpa läkare och annan vårdpersonal i en pressad vardag." Terje Johannessen, professor i allmänmedicin och grundare av NEL och Medibas Loop is the open research network that increases the discoverability and impact of researchers and their work. Loop enables you to stay up-to-date with the latest discoveries and news, connect with researchers and form new collaborations. Aberrant Cytokine Activity in the Host Immune Response to COVID-19 Leads to Cytokine Release Syndrome May 2020 Number of journal articles Biomarker CRS ARDS 1,000 800 600 400 200 0 CTACK Eotaxin FGF basic G-CSF GM-CSF GRO-α HGF IFN-α 2 IFN-γ IL1-ra IL-1 α IL-1β IL-2 IL-2R α IL-3 IL-4 IL-5 IL-6 IL-7 IL-8 IL-9 IL-10 Linaclotide, a potent guanylate cyclase C agonist, is a therapeutic peptide approved in the United States for the treatment of irritable bowel syndrome with constipation and chronic idiopathic constipation. We present for the first time the metabolism, degradation, and disposition of linaclotide in animals and humans.

Bertolotti’s syndrome is a rare cause of back pain and can be treated by a qualified spinal specialist with modern spinal healthcare. Bertolotti syndrome refers to the association between lumbosacral transitional vertebrae and low back pain. Although it may be a consideration in younger patients, the entity is considered controversial and has been both supported and disputed since the Italian radiologist Mario Bertolotti (1876-1957) 10 first described it in 1917. Bertolotti’s syndrome is a frequent anomaly which can be related to lower back pain.
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Att ta folsyra i munnen förbättrar inte symtomen på bräckligt X-syndrom. Baron C, Bartoloni C, Ghirlanda G, Gentiloni N. Megaloblastisk anemi beror på

Some studies advocate surgical resection in selected Treatments for Bertolotti’s Syndrome Fluoroscopically-guided steroid injection and/or local anesthetic blocks at the pseudoarticulation site Radiofrequency ablation (thermal) along the articulation Surgical excision of the large transverse process The prevalence and relevance of traditional cardiovascular risk factors in primary Sjögren's syndrome. Bartoloni E(1), Alunno A(1), Valentini V(1), Valentini E(1), La Paglia GMC(1), Leone MC(1), Cafaro G(1), Marcucci E(1), Bonifacio AF(1), Luccioli F(1), Gerli R(2).

Shrinking lung syndrome är en ovanlig manifestation och ger oförklarad Iaccarino L, Bartoloni E, Carli L, Ceccarelli F, Conti F, De Vita S, et al.

It involves a total or partial unilateral or bilateral fusion of the transverse process of the lowest lumbar vertebra to the sacrum, leading to the formation of a transitional 5th lumbar vertebra. Bartolinit är en infektion i blygdläppen. Det är inte farligt, men kan göra ont och du behöver behandling för att infektionen ska gå över.

2020-08-07 Defining disease activity states and clinically meaningful improvement in primary Sjögren's syndrome with EULAR primary Sjögren's syndrome disease activity (ESSDAI) and patient-reported indexes (ESSPRI). Forskningsoutput: Tidskriftsbidrag › Artikel i vetenskaplig tidskrift 2017-05-15 Kartagener syndrome (KS), a subunit of primary ciliary dyskinesia (PCD), is an autosomal recessive disorder with genetic heterogeneity. KS is caused by ciliary immotility or dysmotility due to ultrastructural abnormalities of respiratory cilia and flagella of spermatozoa and Fallopian tube. Defining disease activity states and clinically meaningful improvement in primary Sjögren's syndrome with EULAR primary Sjögren's syndrome disease activity (ESSDAI) and patient-reported indexes (ESSPRI).