Relevant bibliographies by topics / Sjögren’s disease

Contents

  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers

Academic literature on the topic 'Sjögren’s disease'

Author: Grafiati
Published: 31 May 2025
Last updated: 31 July 2025

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Journal articles on the topic "Sjögren’s disease"

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Gunawan, Giovanny Azalia, Adinda Ayu Dyah Rahadina, and Budi Prasetyo. "Comprehensive management of pregnant woman with Sjögren’s syndrome." Majalah Obstetri & Ginekologi 30, no. 3 (2022): 134–38. http://dx.doi.org/10.20473/mog.v30i32022.134-138.

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HIGHLIGHTS 1. Sjögren’s syndrome is a chronic autoimmune disease that attacks the exocrine glands, especially lacrimal and salivary glands. 2. Comprehensive management of pregnant women with Sjögren’s syndrome was described.3. Clinical and laboratory examination, risk assessment and also preconception counseling before planning pregnancy are needed by women with Sjögren’s syndrome. ABSTRACT Objective: To illustrate the comprehensive management of pregnant women with Sjögren syndrome. Case Report: A 24 years old women came to Dr. Soetomo General Academic Hospital, Surabaya, Indonesia, due to Sj
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Nalbant, Merve, Gamze Akbaş, and Yunus Özcan. "Panniculitis; A Rare Cutaneous Mafestation of Sjögren’s Syndrome." Medical Science and Discovery 10, no. 10 (2023): 942–44. http://dx.doi.org/10.36472/msd.v10i10.1087.

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Objective: Panniculitis, an inflammatory disorder primarily affecting subcutaneous adipose tissue, is frequently associated with inflammatory rheumatic diseases. Panniculitis is an uncommon cutaneous manifestation of Sjögren's syndrome (SS), an autoimmune disease primarily known for causing dry eyes and mouth. Case: We report the case of a 56-year-old female initially diagnosed with rheumatoid arthritis, who later met the 2016 ACR-EULAR criteria for primary Sjögren’s syndrome. Following several treatments, she developed nodular lesions in the interscapular area, which were later diagnosed as s
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Ghafoor, M. "Sjögren’s Before Sjögren: Did Henrik Sjögren (1899–1986) Really Discover Sjögren’s Disease?" Journal of Maxillofacial and Oral Surgery 11, no. 3 (2011): 373–74. http://dx.doi.org/10.1007/s12663-011-0303-0.

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Heros Aureliano Antunes da Silva Maia, Gabriela Afonso Pereira, José César Batista Filho, and Viviane Machicado Cavalcante. "Síndrome de Sjögren: um Diagnóstico Diferencial de Polirradiculopatia Desmielinizante Inflamatória Crônica." Revista Científica Hospital Santa Izabel 8, no. 1 (2024): 34–39. http://dx.doi.org/10.35753/rchsi.v8i1.513.

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A Síndrome de Sjögren é uma doença autoimune caracterizada pelo acometimento das glândulas exócrinas e está relacionada à síndrome seca e diversas manifestações sistêmicas, dentre elas alterações neurológicas. Este trabalho tem como objetivo relatar o caso de um paciente com história de polineuropatia crônica, cuja investigação permitiu identificar achados compatíveis com o diagnóstico de Síndrome de Sjögren.Palavras-chave: Síndrome de Sjögren; Polirradiculoneuropatia Desmielinizante Inflamatória Crônica; Pulsoterapia. Sjögren’s Syndrome is na autoimmune disease characterized by involvement of
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Javed, A., R. Balabanov, BGW Arnason, et al. "Minor salivary gland inflammation in Devic’s disease and longitudinally extensive myelitis." Multiple Sclerosis Journal 14, no. 6 (2008): 809–14. http://dx.doi.org/10.1177/1352458508088941.

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Devic’s disease is often considered as a variant of multiple sclerosis (MS). However, evidence suggests that Devic’s disease may be distinct from MS. Devic’s disease can coexist with connective tissue diseases, particularly Sjögren’s disease, but this association is rare with MS. Diagnosis of Sjögren’s disease in patients with neurological symptoms is often difficult. During early stages of Sjögren’s disease, patients may not fulfill all criteria for Sjögren’s disease. A high percentage of patients with Sjögren’s disease have inflammatory infiltrates in minor salivary glands, and this may be a
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Okawa, Yuko, and Kenji Ihara. "Sensorineural Hearing Loss in Sjögren’s Syndrome." International Journal of Molecular Sciences 23, no. 19 (2022): 11181. http://dx.doi.org/10.3390/ijms231911181.

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Sjögren’s syndrome is a chronic autoimmune disease characterized by systemic dysfunction of exocrine glands, mainly the salivary and lachrymal glands. Sjögren’s syndrome consists of two forms: primary Sjögren’s syndrome, which is characterized by dry eyes and dry mouth without autoimmune diseases; and secondary Sjögren’s syndrome, which is characterized by symptoms associated with other autoimmune diseases, such as systemic lupus erythematosus. Disease severities vary considerably from mild glandular dryness to severe glandular involvement with numerous extraglandular and systemic features. Se
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Gennari, Juliana D’Agostino, and Louise d’Abadia Morais. "Síndrome de Sjögren: ESSDAI, fluxo salivar, escore oftalmológico e olho seco." Revista Paulista de Reumatologia, no. 2022 jan-mar;21(1) (March 31, 2022): 35–47. http://dx.doi.org/10.46833/reumatologiasp.2022.21.1.35-47.

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A síndrome de Sjögren primária (SSp) é uma doença inflamatória e crônica que pode apresentar manifestações glandulares e sistêmicas (presentes entre 20% e 40% dos casos). Para melhor avaliação dos pacientes com essa doença, métricas que avaliam essas manifestações podem ser utilizadas, dentre elas temos o EULAR Sjögren’s syndrome patient report index (ESSPRI), que avalia sintomas de secura, fadiga e dor articular; o EULAR Sjögren’s syndrome disease activity index (ESSDAI), que avalia atividade sistêmica da doença, resposta ao tratamento e prognóstico; já os índices de dano são representados pe
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Islam, Asif, Fatima Khurshid, Muhammad Ahmad Khan, Muhammad Yaser Imran, Samara Siddique, and Tooba Fatima. "An Intriguing Combination: Sjogren Syndrome Coexisting with Hodgkin Lymphoma." International Journal of Advanced Multidisciplinary Research and Studies 4, no. 1 (2024): 934–37. http://dx.doi.org/10.62225/2583049x.2024.4.1.2315.

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While Hodgkin's lymphoma is a lymphoid malignancy, Sjögren’s syndrome is an autoimmune disorder marked by exocrine gland inflammation. Sjögren's syndrome (SS) is a chronic autoimmune condition marked by lymphocytic infiltration of the exocrine glands, primarily the salivary and lachrymal glands, which typically manifests as xerostomia and xerophthalmia. Lymphoma is the most dreaded of these systemic sequelae, which are present in about 50% of individuals with primary SS. These neoplasias are mostly non-Hodgkin and arise from B cells. It is unusual for these two diseases to coexist, and the und
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Mlynáriková, V., D. Mičeková, J. Rovenský, and E. Šteňová. "Sjögren’s syndrome." Acta Facultatis Pharmaceuticae Universitatis Comenianae 62, s11 (2015): 8–14. http://dx.doi.org/10.1515/afpuc-2015-0019.

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Abstract Sjögren’s syndrome is a slowly progressive, inflammatory autoimmune disease primarily affecting exocrine glands. Lymphocytic infiltrates replace functional epithelium and lead to decreased exocrine secretion of salivary and lacrimal glands - xerocrinopathy. Glands of intestinal system and pulmonary tract, skin and vaginal mucosa may also be affected. The most common extraglandular manifestations of primary Sjögren’s syndrome include skin vasculitis, Raynaud’s phenomenon, functional renal abnormalities, neuropathy and arthritis symptoms. This disorder may appear separately as a primary
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Mieliauskaitė, Diana, and Vilius Kontenis. "Sjögren’s Disease and Gastroesophageal Reflux Disease: What Is Their Evidence-Based Link?" Medicina 60, no. 11 (2024): 1894. http://dx.doi.org/10.3390/medicina60111894.

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Sjögren’s disease (SjD), or primary Sjögren’s syndrome (pSS), is a heterogeneous chronic autoimmune disorder with multiple clinical manifestations that can develop into non-Hodgkin’s lymphoma in mucosa-associated lymphoid tissue. SjD is one of the autoimmune diseases with the maximum delayed diagnosis due to its insidious onset, heterogeneous clinical features and varied course. It is increasingly recognized that extraglandular manifestations represent a clinical challenge for patients with SjD. The European League Against Rheumatism (EULAR) Sjögren’s Syndrome (SS) Disease Activity Index (ESSD
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Dissertations / Theses on the topic "Sjögren’s disease"

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Bettacchioli, Eléonore. "Identification de signatures biologiques pour la stratification des patients atteints de maladies auto-immunes systémiques." Electronic Thesis or Diss., Brest, 2025. http://www.theses.fr/2025BRES0013.

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Les maladies auto-immunes telles que la maladie de Sjögren (SjD) et le lupus érythémateux systémique (LES) posent des défis majeurs liés à une grande hétérogénéité clinique et biologique. Au travers d’analyses multi-omiques, cette thèse présente des objectifs multiples : (i) Caractériser le profil clinique et biologique des patients atteints de SjD selon leur profil d’auto-anticorps, (ii) Créer un outil en ligne facilitant l'accès et l'interprétation des données de transcriptomique du LES, et (iii) Analyser les interactions cellulaires dans le tissu rénal du LES. Dans la SjD, la stratification
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Jazzar, Ahoud Abdulaziz A. "Biomarkers of salivary gland disease in Sjögren's syndrome." Thesis, King's College London (University of London), 2017. https://kclpure.kcl.ac.uk/portal/en/theses/biomarkers-of-salivary-gland-disease-in-sjoegrens-syndrome(a889fe46-ad28-4403-8099-9668eaa13c1f).html.

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Sjögren’s syndrome (SS) is a systemic, chronic, autoimmune inflammatory disease that affects the exocrine glands. The absence of early diagnostic markers contributes to delays in its diagnosis. Furthermore, SS patients have an increased incidence of lymphoma and there is a need for biomarkers to identify its development. To enable a better understanding of disease activity and progression, the following aims were undertaken; 1. Investigate the potential use of the salivary gland assessment tests (whole flow rates (WFR), parotid flow rates (PFR), clinical oral dryness score (CODS) and ultrasoun
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Vasaitis, Lilian. "Lymphoma studies in patients with Sjögren's syndrome." Doctoral thesis, Uppsala universitet, Institutionen för medicinska vetenskaper, 2017. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-320220.

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Patients with primary Sjögren’s syndrome (pSS) are at increased risk of developing malignant lymphoma. The studies in this thesis aim at broadening our understanding of the association between these two conditions. Germinal centre (GC)-like structures were found in minor salivary gland biopsies taken at the time of pSS diagnosis in 25% of 175 studied patients. Lymphoma development was observed in 86% of the GC-positive pSS patients and 14% of the GC-negative patients. GC-like structures in salivary gland biopsies at pSS diagnosis might identify pSS patients at high risk for later lymphoma deve
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Aasarød, Knut. "Renal involvement in inflammatory rheumatic disease : a study of renal disease in Wegener's granulomatosis and in primary Sjögren's syndrome." Doctoral thesis, Norwegian University of Science and Technology, Faculty of Medicine, 2001. http://urn.kb.se/resolve?urn=urn:nbn:no:ntnu:diva-1471.

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Finnsson, Johannes. "Radiological studies of LMNB1-related autosomal dominant leukodystrophy and Marinesco-Sjögren syndrome." Doctoral thesis, Uppsala universitet, Radiologi, 2016. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-303171.

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There are approximately 6000 to 8000 rare diseases, each with a prevalence of less than 1 / 10 000, but in aggregate affecting 6 to 8% of the population. It is important to evaluate disease development and progression to know the natural course of any disease. This information can be utilized in diagnostics and in assessing effects of therapeutic interventions as they become available. This thesis describes the natural clinical history and evolution of imaging findings of two rare diseases over approximately two decades. Papers I, II and III present clinical, magnetic resonance imaging (MRI),
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Li, Baihui. "Autophagie comme cible thérapeutique potentielle pour le syndrome de Sjögren." Thesis, Strasbourg, 2017. http://www.theses.fr/2017STRAJ042.

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Le syndrome de Sjögren (SS) est l'une des maladies autoimmunes (MAI) systémiques les plus fréquentes chez l’Homme. Cette maladie est caractérisée par une infiltration lymphocytaire dans les glandes exocrines conduisant à des symptômes dits de « yeux secs » et à la bouche sèche. Il n’existe actuellement aucun traitement curatif pour cette maladie. Le peptide P140 a été démontrée comme un outil thérapeutique efficace chez les patients atteints d'un lupus érythémateux disséminé (LED) et des souris modèles développant un lupus.L'autophagie est une voie intracellulaire conservée qui joue un rôle ce
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Soyfoo, Muhammad Shahnawaz. "Contribution to the diagnosis and pathophysiology of Sjögren's syndrome." Doctoral thesis, Universite Libre de Bruxelles, 2012. http://hdl.handle.net/2013/ULB-DIPOT:oai:dipot.ulb.ac.be:2013/209588.

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Le syndrome de Sjögren (SS) est une maladie auto-immunitaire caractérisée par une infiltration lymphocytaire des glandes exocrines menant le plus souvent, à une xérophtalmie et à une xérostomie. La physiopathologie de la maladie est complexe et malgré les progrès realisés, il existe beaucoup de questions à repondre. Classiquement, le syndrome sec qui caractérise la maladie résulterait d’un double processus où dans un premier temps, la glande serait envahie par des cellules lymphoplasmocytaires puis secondairement détruite. Des avancées récentes dans la physiopathologie de la maladie ont démont
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Imgenberg-Kreuz, Juliana. "Epigenetic and Gene Expression Signatures in Systemic Inflammatory Autoimmune Diseases." Doctoral thesis, Uppsala universitet, Molekylär medicin, 2017. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-310388.

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Autoimmune diseases are clinical manifestations of a loss-of-tolerance of the immune system against the body’s own substances and healthy tissues. Primary Sjögren’s syndrome (pSS) and systemic lupus erythematosus (SLE) are two chronic inflammatory autoimmune diseases characterized by autoantibody production and an activated type I interferon system. Although the precise mechanisms leading to autoimmune processes are not well defined, recent studies suggest that aberrant DNA methylation and gene expression patterns may play a central role in the pathogenesis of these disorders. The aim of this
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Niemelä, R. (Raija). "Imaging of salivary glands and assessment of autonomic nervous system function in primary Sjögren's syndrome." Doctoral thesis, University of Oulu, 2004. http://urn.fi/urn:isbn:9514272757.

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Abstract The purpose of the present study was to find reliable non-invasive methods for imaging salivary glands and diagnosing primary Sj?gren's syndrome (SS) and to evaluate autonomic function and central nervous system (CNS) disorders in patients with primary SS. The patient population consisted of consecutive patients with primary SS, who fulfilled the International classification criteria for primary SS, from the Division of Rheumatology, Department of Internal Medicine in Oulu University Hospital. Magnetic resonance (MR) imaging and MR sialography of parotid glands were performed on 27 p
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Serrano, Érica Vieira. "Adaptação transcultural do Eular Sjögren s Syndrome Disease Activity Index(ESSDAI) para a Língua Portuguesa Brasileira." Universidade Federal do Espírito Santo, 2012. http://repositorio.ufes.br/handle/10/5494.

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Made available in DSpace on 2016-08-30T10:50:13Z (GMT). No. of bitstreams: 1 tese_6197_2011_Erica Serrano.pdf: 772975 bytes, checksum: d76dc5832c1174a3d28b433ca9851c73 (MD5) Previous issue date: 2012-11-05<br>Introdução: O EULAR Sjögren's Syndrome Disease Activity Index (ESSDAI) é um índice composto para avaliar a atividade sistêmica da Síndrome de Sjögren primária (SSP), criado em 2009 na língua inglesa, ainda sem adaptação cultural para a língua portuguesa. Objetivo: Realizar a adaptação transcultural do ESSDAI para a língua portuguesa brasileira. Método: Estudo observacional transversal d
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Books on the topic "Sjögren’s disease"

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C, Horsfall Angela, Isenberg David, and University College, London. Dept. of Molecular Pathology., eds. Autoimmune diseases, focus on Sjögren's syndrome. BIOS Scientific Publishers, 1994.

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van der Waal, Isaäc. Diseases of the Salivary Glands Including Dry Mouth and Sjögren’s Syndrome. Springer Berlin Heidelberg, 1997. http://dx.doi.org/10.1007/978-3-642-80274-4.

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1950-, Carsons Steven E., and Harris Elaine K, eds. The new Sjogren's syndrome handbook. Oxford University Press, 1998.

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Waal, Isaac van der. Diseases of the salivary glands including dry mouth and Sjögren's syndrome: Diagnosis and treatment. Springer-Verlag, 1996.

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Ng, Wan-Fai, Arjan Vissink, Elke Theander, and Francisco Figueiredo. Sjögren’s syndrome—management. Oxford University Press, 2013. http://dx.doi.org/10.1093/med/9780199642489.003.0128.

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Management of Sjögren's syndrome (SS) encompasses confirmation of diagnosis, disease assessment, and treatment of glandular and systemic manifestations including special situations such as pregnancy and SS-related lymphoma. The American European Consensus Group classification criteria 2002 are the current gold standard for the diagnosis of SS. Salivary gland sialometry, sialochemistry, and ultrasound and tear osmolarity may be useful adjuncts. Symptoms of SS are non-specific and must be actively explored. When assessing patients with SS, it is important to consider not only objective parameter
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Ng, Wan-Fai, Arjan Vissink, Elke Theander, and Francisco Figueiredo. Sjögren’s syndrome—management. Oxford University Press, 2014. http://dx.doi.org/10.1093/med/9780199642489.003.0128_update_001.

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Management of Sjögren’s syndrome (SS) encompasses confirmation of diagnosis, disease assessment, and treatment of glandular and systemic manifestations including special situations such as pregnancy and SS-related lymphoma. The American European Consensus Group (AECG) classification criteria 2002 are the current gold standard for the diagnosis of SS. Salivary gland sialometry, sialochemistry, and ultrasound and tear osmolarity may be useful adjuncts. Recently, preliminary classification criteria of the American College of Rheumatology have been introduced as an alternative to the AECG criteria
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Bowman, Simon, John Hamburger, Elizabeth Price, and Saaeha Rauz. Sjögren’s syndrome—clinical features. Oxford University Press, 2013. http://dx.doi.org/10.1093/med/9780199642489.003.0127.

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Sjögren's syndrome is a chronic, immune-mediated, condition of unknown aetiology characterized by focal lymphocytic infiltration of exocrine glands associated with dry mouth and eyes. It occurs in its own right (primary Sjögren's syndrome, pSS), or as a late feature of other rheumatic diseases such as rheumatoid arthritis, systemic lupus erythematosus or scleroderma (secondary Sjögren's syndrome). There is a strong female bias. pSS typically affects women in their middle years with an estimated prevalence of 0.1–0.6%. 75% of patients have anti-Ro and/or anti-La antibodies, often with raised im
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Bowman, Simon, John Hamburger, Elizabeth Price, and Saaeha Rauz. Sjögren’s syndrome—clinical features. Oxford University Press, 2016. http://dx.doi.org/10.1093/med/9780199642489.003.0127_update_001.

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Sjögren’s syndrome is a chronic, immune-mediated, condition of unknown aetiology characterized by focal lymphocytic infiltration of exocrine glands associated with dry mouth and eyes. It occurs in its own right (primary Sjögren’s syndrome, pSS), or as a late feature of other rheumatic diseases such as rheumatoid arthritis, systemic lupus erythematosus or scleroderma (secondary Sjögren’s syndrome). There is a strong female bias. pSS typically affects women in their middle years with an estimated prevalence of 0.1–0.6%. 75% of patients have anti-Ro and/or anti-La antibodies, often with raised im
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Wallace, Daniel J., ed. The Sjögren's Book. 5th ed. Oxford University Press, 2022. http://dx.doi.org/10.1093/oso/9780197502112.001.0001.

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Afflicting one in 83 Americans, Sjögren’s is an autoimmune disease that commonly causes dryness of the eyes, mouth, and nose, and can lead to complications such as profound fatigue, depression, and lymphoma. While there is no cure for Sjögren’s, much can be done to alleviate the suffering of patients. This revised handbook offers everything you need to know to cope with this disease. The Sjögren’s Book, fifth edition, is a comprehensive and authoritative guide produced by the Sjögren’s Foundation and its medical advisors and edited by a leading authority on autoimmune disorders. This expanded
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Nageshwaran, Sathiji, Heather C. Wilson, Anthony Dickenson, and David Ledingham. Disorders of peripheral nerves and motor neuron disease. Oxford University Press, 2016. http://dx.doi.org/10.1093/med/9780199664368.003.0007.

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This chapter discusses the clinical features and evidence-based drug treatment regimens of polyneuropathies (Guillain–Barré syndrome (GBS), chronic inflammatory demyelinating polyneuropathy (CIDP), multifocal motor neuropathy, paraproteinaemic neuropathies, and vasculitic neuropathies), mononeuropathies (Bell’s palsy), systemic conditions with peripheral nerve involvement (Sjögren’s and sarcoidosis), and motor neuron disease (MND).
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Book chapters on the topic "Sjögren’s disease"

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Baer, Alan, Vatinee Bunya, Ava Wu, Xavier Mariette, and Frederick Vivino. "Sjögren’s Disease." In A Clinician's Pearls & Myths in Rheumatology. Springer International Publishing, 2023. http://dx.doi.org/10.1007/978-3-031-23488-0_11.

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Khosroshahi, Arezou, John H. Stone, and Vikram Deshpande. "Pancreatic Disease in Sjögren’s Syndrome and IgG4-Related Disease." In Sjögren’s Syndrome. Springer London, 2011. http://dx.doi.org/10.1007/978-0-85729-947-5_18.

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Kassan, S. S., and N. Talal. "Renal Disease with Sjögren’s Syndrome." In Sjögren’s Syndrome. Springer Berlin Heidelberg, 1987. http://dx.doi.org/10.1007/978-3-642-50118-0_11.

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Alexander, E. L. "Inflammatory Vascular Disease in Sjögren’s Syndrome." In Sjögren’s Syndrome. Springer Berlin Heidelberg, 1987. http://dx.doi.org/10.1007/978-3-642-50118-0_12.

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Kassan, S. S., and N. Talal. "Sjögren’s Syndrome with Systemic Lupus Erythematosus/Mixed Connective Tissue Disease." In Sjögren’s Syndrome. Springer Berlin Heidelberg, 1987. http://dx.doi.org/10.1007/978-3-642-50118-0_17.

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Tzioufas, Athanasios G., and Haralampos M. Moutsopoulos. "Current Treatment of Extraglandular Manifestations with Disease-Modifying and Immunosuppressive Agents." In Sjögren’s Syndrome. Springer New York, 2011. http://dx.doi.org/10.1007/978-1-60327-957-4_19.

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Vitali, Claudio, Chiara Baldini, and Stefano Bombardieri. "Current Concepts on Classification Criteria and Disease Status Indexes in Sjögren’s Syndrome." In Sjögren’s Syndrome. Springer New York, 2011. http://dx.doi.org/10.1007/978-1-60327-957-4_5.

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Baldini, Chiara, and Stefano Bombardieri. "Classification Criteria of Sjögren’s Syndrome." In Connective Tissue Disease. Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-24535-5_19.

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Priori, Roberta, Antonina Minniti, Giovanna Picarelli, and Guido Valesini. "Extraglandular Involvement in Sjögren’s Syndrome." In Connective Tissue Disease. Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-24535-5_23.

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Cavallo, Roberto, Maria Roberta Bongioanni, and Paola Richiardi. "Neurological Involvement in Sjögren’s Syndrome." In Connective Tissue Disease. Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-24535-5_25.

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Conference papers on the topic "Sjögren’s disease"

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Snéne, Houda, senda derouiche, Amal Harzali, et al. "Interstitial lung disease in Sjögren’s syndrome." In ERS Congress 2024 abstracts. European Respiratory Society, 2024. http://dx.doi.org/10.1183/13993003.congress-2024.pa4279.

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Bandeira, M., M. Silvério-António, R. Pereira Da Costa, et al. "POS1267 COMMON SYSTEMIC INVOLVEMENT AND WORSENING DISEASE BURDEN IN PATIENTS WITH SJÖGREN’S DISEASE: DATA FROM PORTRESS, THE PORTUGUESE REGISTRY OF SJÖGREN’S DISEASE." In EULAR 2024 European Congress of Rheumatology, 12-15 June. Vienna, Austria. BMJ Publishing Group Ltd and European League Against Rheumatism, 2024. http://dx.doi.org/10.1136/annrheumdis-2024-eular.214.

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Marino, A., O. Berardicurti, I. Genovali, et al. "POS1248 DAMAGE IN SJÖGREN’S DISEASE: INSIGHTS FROM THE GIRRCS SJOGREN’S DISEASE COHORT." In EULAR 2024 European Congress of Rheumatology, 12-15 June. Vienna, Austria. BMJ Publishing Group Ltd and European League Against Rheumatism, 2024. http://dx.doi.org/10.1136/annrheumdis-2024-eular.4270.

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Perdan-Pirkmajer, K., S. Praprotnik, Z. Rotar, and A. Hocevar. "POS0358 SALIVARY GLAND ULTRASOUND FOLLOW-UP IN SJÖGREN’S DISEASE." In EULAR 2024 European Congress of Rheumatology, 12-15 June. Vienna, Austria. BMJ Publishing Group Ltd and European League Against Rheumatism, 2024. http://dx.doi.org/10.1136/annrheumdis-2024-eular.3339.

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Meudec, L., N. Goudarzi, J. Pascaud, et al. "OP0329 DEVELOPMENT OF SALIVARY GLAND ORGANOIDS TO STUDY SJÖGREN’S DISEASE." In EULAR 2024 European Congress of Rheumatology, 12-15 June. Vienna, Austria. BMJ Publishing Group Ltd and European League Against Rheumatism, 2024. http://dx.doi.org/10.1136/annrheumdis-2024-eular.1959.

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Panagopoulos, P., L. Chatzis, E. Chatzinikita, et al. "AB0851 CLINICAL AND RESPIRATORY FEATURES OF PRIMARY SJÖGREN’S DISEASE PATIENTS WITH INTERSTITIAL LUNG DISEASE." In EULAR 2024 European Congress of Rheumatology, 12-15 June. Vienna, Austria. BMJ Publishing Group Ltd and European League Against Rheumatism, 2024. http://dx.doi.org/10.1136/annrheumdis-2024-eular.4051.

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Xavier, C., D. Calderaro, S. Araújo, et al. "POS1241 RELIABILITY OF HISTOPATHOLOGICAL SALIVARY GLAND BIOPSY ASSESSMENT IN SJÖGREN’S DISEASE." In EULAR 2024 European Congress of Rheumatology, 12-15 June. Vienna, Austria. BMJ Publishing Group Ltd and European League Against Rheumatism, 2024. http://dx.doi.org/10.1136/annrheumdis-2024-eular.1882.

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Flurie, M., Z. Cline, C. Baldini, et al. "AB0793 THE USE OF NATURAL LANGUAGE PROCESSING TO CHARACTERIZE DISEASE BURDEN: SEXUAL DISTRESS IN SJÖGREN’S DISEASE." In EULAR 2024 European Congress of Rheumatology, 12-15 June. Vienna, Austria. BMJ Publishing Group Ltd and European League Against Rheumatism, 2024. http://dx.doi.org/10.1136/annrheumdis-2024-eular.181.

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Yao, S., R. Wilbrink, P. Czarnota, et al. "OP0128 SPATIAL TRANSCRIPTOMICS IMPLICATES GLANDULAR CELL INVOLVEMENT IN PATHOPHYSIOLOGY OF SJÖGREN’S DISEASE." In EULAR 2024 European Congress of Rheumatology, 12-15 June. Vienna, Austria. BMJ Publishing Group Ltd and European League Against Rheumatism, 2024. http://dx.doi.org/10.1136/annrheumdis-2024-eular.1518.

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Perdan-Pirkmajer, K., L. Furjanič, M. Tomšič, A. Hocevar, S. Praprotnik, and S. Pirkmajer. "AB0859 A SINGLE-CENTRE EXPERIENCE WITH SJÖGREN’S DISEASE AND SARS-CoV-2." In EULAR 2024 European Congress of Rheumatology, 12-15 June. Vienna, Austria. BMJ Publishing Group Ltd and European League Against Rheumatism, 2024. http://dx.doi.org/10.1136/annrheumdis-2024-eular.1069.

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