听力与言语-语言病理学

行为科学

医学伦理学

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  • Expression of CD22 on peripheral B cells in patients with rheumatoid arthritis: relation to CD5-positive B cells.

    abstract::B cells in patients with rheumatoid arthritis (RA) are hyperactivated. Although B cell receptor signal transduction may be affected by various response regulators, CD22 plays an important role as a response regulator of B cells. Therefore, we investigated and examined CD22 expression on peripheral blood B cells of pat...

    journal_title:Clinical rheumatology

    pub_type: 杂志文章

    doi:10.1007/s10067-007-0665-3

    authors: Nakiri Y,Minowa K,Suzuki J,Mitsuo A,Amano H,Morimoto S,Tokano Y,Takasaki Y

    更新日期:2007-10-01 00:00:00

  • Specificity and sensitivity of anti-beta2-glycoprotein I as compared with anticardiolipin antibody and lupus anticoagulant in Thai systemic lupus erythematosus patients with clinical features of antiphospholipid syndrome.

    abstract::Antibodies to beta(2)-glycoprotein I (anti-beta(2)-GPI) have been reported to have stronger association with clinical antiphospholipid syndrome (APS) than anticardiolipin antibodies (aCL) and lupus anticoagulant (LAC). We investigated the sensitivity and specificity of ELISA for anti-beta(2)-GPI in Thai systemic lupus...

    journal_title:Clinical rheumatology

    pub_type: 杂志文章

    doi:10.1007/s10067-007-0566-5

    authors: Parkpian V,Verasertniyom O,Vanichapuntu M,Totemchokchyakarn K,Nantiruj K,Pisitkul P,Angchaisuksiri P,Archararit N,Rachakom B,Ayurachai K,Janwityanujit S

    更新日期:2007-10-01 00:00:00

  • Evaluation of pulmonary function and bicycle ergometry tests in patients with Behçet's disease.

    abstract::Behçet's disease (BD) has well-defined pulmonary complications, but cardiopulmonary exercise testing and the strength of the respiratory muscles have not been studied in detail. We aimed to investigate the pulmonary functions tests, inspiratory and expiratory muscle strength and endurance, cardiopulmonary exercise tes...

    journal_title:Clinical rheumatology

    pub_type: 杂志文章

    doi:10.1007/s10067-006-0508-7

    authors: Gökoğlu F,Yorgancioğlu ZR,Ustün N,Ardiç FA

    更新日期:2007-09-01 00:00:00

  • Lymphocytic interstitial pneumonitis (LIP) in Sjögren's syndrome: a case report and a review of the literature.

    abstract::Sjõgren's disease is one of the most common rheumatological diseases and can present with a variety of extra-glandular manifestations. Lymphocytic Interstitial Pneumonitis (LIP) is the most common lung pathology in these patients. It is important to know and recognize this condition because it is potentially treatable...

    journal_title:Clinical rheumatology

    pub_type: 杂志文章,评审

    doi:10.1007/s10067-006-0351-x

    authors: Dalvi V,Gonzalez EB,Lovett L

    更新日期:2007-08-01 00:00:00

  • Inflammatory myositis complicating hypocomplementemic urticarial vasculitis despite on-going immunosuppression.

    abstract::We present a patient with previously diagnosed hypocomplementemic urticarial vasculitis syndrome, with skin, lung, and renal involvement, who presented with congestive cardiac failure. During the course of her hospitalization, she was also found to have profound proximal muscle weakness in both upper and lower limbs a...

    journal_title:Clinical rheumatology

    pub_type: 杂志文章

    doi:10.1007/s10067-006-0397-9

    authors: Chew GY,Gatenby PA

    更新日期:2007-08-01 00:00:00

  • Atherosclerosis and inflammation: insights from rheumatoid arthritis.

    abstract::Cardiovascular disease is a major health care problem and the most common cause of death among individuals from developed nations. Our understanding of atherosclerosis has evolved from a passive process resulting in narrowing of the lumen and consequent myocardial ischemia to a dynamic process that involves inflammati...

    journal_title:Clinical rheumatology

    pub_type: 杂志文章,评审

    doi:10.1007/s10067-007-0548-7

    authors: Chung CP,Avalos I,Raggi P,Stein CM

    更新日期:2007-08-01 00:00:00

  • Thoracic outlet syndrome: another cause for unilateral palmar hyperhidrosis.

    abstract::One of the most important therapeutic goal in hyperhidrosis treatment is to seek for the underlying cause and to tailor the treatment accordingly. A detailed history and prompt physical examination are needed to clarify the etiological factor. In this study, we report a 34-year-old woman with a diagnosis of thoracic o...

    journal_title:Clinical rheumatology

    pub_type: 杂志文章

    doi:10.1007/s10067-006-0400-5

    authors: Ozdemir O,Ozçakar L

    更新日期:2007-08-01 00:00:00

  • Visceral leishmaniasis infection in a patient with rheumatoid arthritis treated with etanercept.

    abstract::Visceral leishmaniasis (VL) is a severe disease that can develop in immunocompromised patients. Antitumor necrosis factor-alpha (TNF-alpha) treatment of rheumatoid arthritis can result in clinical benefits, but with an increased risk of opportunistic infections. Leishmania infection in patients treated with TNF-alpha ...

    journal_title:Clinical rheumatology

    pub_type: 杂志文章

    doi:10.1007/s10067-006-0356-5

    authors: Bagalas V,Kioumis I,Argyropoulou P,Patakas D

    更新日期:2007-08-01 00:00:00

  • Unusual long bone and metacarpo-carpal abnormalities in a case of pseudo-pseudohypoparathyroidism.

    abstract::A case of pseudo-pseudohypoparathyroidism (PPH) with shortening of the left femur and tibia and coalition of the base of the fourth metacarpals with capitatum and hamatum in bilateral wrist joints was presented. Involvement of the fourth digits both in hands and feet were more prominent on the left side, with shorteni...

    journal_title:Clinical rheumatology

    pub_type: 杂志文章

    doi:10.1007/s10067-006-0279-1

    authors: Unlu Z,Orguc S,Yilmaz Ovali G,Bayindir P

    更新日期:2007-07-01 00:00:00

  • Combination therapy with cyclosporine A and anti-TNF-alpha agents in the treatment of rheumatoid arthritis and concomitant hepatitis C virus infection.

    abstract::We describe two cases of rheumatoid arthritis (RA) patients and concomitant hepatitis C virus infection (HCV), treated with cyclosporine A (CsA) and anti-TNF-alpha agents. SGOT/SGPT and HCV-RNA serum levels remained unchanged longer than 1 year of treatment. No side effects were registered. We suggest that combination...

    journal_title:Clinical rheumatology

    pub_type: 杂志文章

    doi:10.1007/s10067-006-0412-1

    authors: Bellisai F,Giannitti C,Donvito A,Galeazzi M

    更新日期:2007-07-01 00:00:00

  • A follow-up study of minimally invasive lip biopsy in the diagnosis of Sjögren's syndrome.

    abstract::The aims of this study were to characterize a minimally invasive technique of minor salivary gland biopsy of the lower lip and to present a large patient material undergoing this procedure because of a suspicion of Sjögren's syndrome (SS), as well as to assess the procedure's short-term and long-term value as a diagno...

    journal_title:Clinical rheumatology

    pub_type: 杂志文章

    doi:10.1007/s10067-006-0457-1

    authors: Teppo H,Revonta M

    更新日期:2007-07-01 00:00:00

  • Improving management of musculoskeletal disorders in primary care: the Joint Adventures Program.

    abstract::Musculoskeletal disorders represent a large and growing clinical challenge to primary care clinicians. Unfortunately, there appears to be a gap in current training and continuing education to meet this challenge. We used script concordance within a continuing medical education program entitled "Joint Adventures" to as...

    journal_title:Clinical rheumatology

    pub_type: 杂志文章

    doi:10.1007/s10067-006-0446-4

    authors: Petrella RJ,Davis P

    更新日期:2007-07-01 00:00:00

  • Prognostic factors of radiographic progression in early rheumatoid arthritis: a two year prospective study after a structured therapeutic strategy using DMARDs and very low doses of glucocorticoids.

    abstract::The objective of the study was to analyze the prognostic factors of radiographic progression in a series of patients with early rheumatoid arthritis (RA) after 2 years of therapy with a structured algorithm using disease-modifying antirheumatic drugs (DMARDs) and very low doses of oral glucocorticoids. One hundred and...

    journal_title:Clinical rheumatology

    pub_type: 临床试验,杂志文章

    doi:10.1007/s10067-006-0462-4

    authors: Sanmartí R,Gómez-Centeno A,Ercilla G,Larrosa M,Viñas O,Vazquez I,Gómez-Puerta JA,Gratacós J,Salvador G,Cañete JD

    更新日期:2007-07-01 00:00:00

  • Polymyositis complicating donor lymphocyte infusion after stem cell transplantation for relapsed chronic myeloid leukemia: report of a case and review of literature.

    abstract::Polymyositis may occur along with other manifestations of chronic graft vs host disease after allogeneic bone marrow transplantation (BMT). Donor lymphocyte infusion (DLI) could produce durable remissions in relapsed patients with chronic myelogenous leukemia (CML) but it may contribute to the development of polymyosi...

    journal_title:Clinical rheumatology

    pub_type: 杂志文章

    doi:10.1007/s10067-006-0346-7

    authors: Liu FC,Chen CH,Chao TY

    更新日期:2007-07-01 00:00:00

  • Tacrolimus as a reinforcement therapy for a patient with MPO-ANCA-associated diffuse alveolar hemorrhage.

    abstract::A 67-year-old woman, suffering from continuous hemoptysis, was admitted to our hospital where she was managed with mechanical ventilation. Computed tomography of the chest demonstrated bilateral massive alveolar hemorrhage without evidence of infectious disease. She was diagnosed with anti-myeloperoxidase antineutroph...

    journal_title:Clinical rheumatology

    pub_type: 杂志文章

    doi:10.1007/s10067-006-0355-6

    authors: Kawasaki S,Nakamura H,Honda E,Iwanaga N,Kawakami A,Ida H,Origuchi T,Honda S,Tsuchihashi Y,Yoshimine H,Eguchi K

    更新日期:2007-07-01 00:00:00

  • Infliximab in Takayasu arteritis: a safe alternative?

    abstract:OBJECTIVE:To test the efficacy of Infliximab, a chimeric monoclonal antibody against TNF-alpha, in the treatment of Takayasu arteritis. MATERIALS AND METHODS:We used infliximab at an initial dose of 3 mg/kg i.v. at weeks 0, 2, 6, and 8 thereafter in combination with methotrexate or azathioprine, to treat four patients...

    journal_title:Clinical rheumatology

    pub_type: 临床试验,杂志文章

    doi:10.1007/s10067-006-0227-0

    authors: Karageorgaki ZT,Mavragani CP,Papathanasiou MA,Skopouli FN

    更新日期:2007-06-01 00:00:00

  • Severe gastrointestinal involvement in systemic sclerosis.

    abstract::Gastrointestinal tract (GIT) is the most common organ system involved in systemic sclerosis (SSc). GIT involvement is mainly attributed to GIT dismobility and wide mouth diverticular. GIT involvement in SSc can be also severely debilitating and even life threatening. To our knowledge, the presence of gastrointestinal ...

    journal_title:Clinical rheumatology

    pub_type: 杂志文章

    doi:10.1007/s10067-006-0264-8

    authors: Plastiras SC,Tzivras M,Vlachoyiannopoulos PG

    更新日期:2007-06-01 00:00:00

  • SAA1 alpha/alpha alleles in Behçet's disease related amyloidosis.

    abstract::Behçet's disease (BD) related amyloidosis is relatively rare. Serum amyloid A protein (SAA) protein gene polymorphism is one of the factors implicated in the pathogenesis of AA type amyloidosis. The aim of this study is to investigate SAA1 gene polymorphism in different patient groups: (1) BD related amyloidosis, (2) ...

    journal_title:Clinical rheumatology

    pub_type: 杂志文章

    doi:10.1007/s10067-006-0435-7

    authors: Utku U,Dilek M,Akpolat I,Bedir A,Akpolat T

    更新日期:2007-06-01 00:00:00

  • A case report of tumor necrosis factor-alpha antibody-induced thrombocytopenia associated with emerging IgM anticardiolipin antibody in patients with scleroderma overlap/rheumatoid arthritis.

    abstract::It is commonly believed that infliximab-induced anticardiolipin antibody belongs to the IgM subclass but not the IgG subclass and that the IgM subclass could not produce clinical symptoms. However, we had a patient with scleroderma overlap/rheumatoid arthritis who developed thrombocytopenia associated with the appeara...

    journal_title:Clinical rheumatology

    pub_type: 杂志文章

    doi:10.1007/s10067-006-0229-y

    authors: Hamaguchi M,Kawahito Y,Ishino H,Yoshida M,Yoshikawa T

    更新日期:2007-06-01 00:00:00

  • Increased seropositivity of Helicobacter pylori cytotoxin-associated gene-A in Behçet's disease.

    abstract::Behçet's disease is a systemic vasculitic syndrome with unknown etiology. The aim of the present study was to compare the Helicobacter pylori seropositivity and cytotoxin associated gene-A status in patients with Behçet's disease. Ninety-one patients with Behçet's disease and 83 age- and sex-matched persons with or wi...

    journal_title:Clinical rheumatology

    pub_type: 杂志文章

    doi:10.1007/s10067-006-0416-x

    authors: Apan TZ,Gürsel R,Dolgun A

    更新日期:2007-06-01 00:00:00

  • The levels of sCD30 and of sCD40L in a group of patients with systemic lupus erythematodes and their diagnostic value.

    abstract::CD30/CD30L and CD40/CD40L are molecules from the tumor necrosis factor (TNF) superfamily. They have a major effect on communications between the B and T cells, which leads to control of maturation, proliferation, and apoptosis of those cells. The aim of this study was to compare the levels of a soluble form of CD30 (s...

    journal_title:Clinical rheumatology

    pub_type: 杂志文章

    doi:10.1007/s10067-006-0389-9

    authors: Ciferská H,Horák P,Hermanová Z,Ordeltová M,Zadrazil J,Tichý T,Scudla V

    更新日期:2007-05-01 00:00:00

  • Central sensitization: a biopsychosocial explanation for chronic widespread pain in patients with fibromyalgia and chronic fatigue syndrome.

    abstract::In addition to the debilitating fatigue, the majority of patients with chronic fatigue syndrome (CFS) experience chronic widespread pain. These pain complaints show the greatest overlap between CFS and fibromyalgia (FM). Although the literature provides evidence for central sensitization as cause for the musculoskelet...

    journal_title:Clinical rheumatology

    pub_type: 杂志文章,评审

    doi:10.1007/s10067-006-0433-9

    authors: Meeus M,Nijs J

    更新日期:2007-04-01 00:00:00

  • Primary biliary cirrhosis (PBC)-CREST overlap syndrome with coexistence of Sjögren's syndrome and thyroid dysfunction.

    abstract::Calcinosis, Raynaud's phenomenon, oesophageal dysmotility, sclerodactyly, telangiectasia (CREST) syndrome, a limited form of systemic sclerosis, is sometimes complicated by primary biliary cirrhosis (PBC). A 52- and 61-year-old Japanese woman with PBC-CREST overlap syndrome accompanied by Sjögren's syndrome, and Hashi...

    journal_title:Clinical rheumatology

    pub_type: 杂志文章

    doi:10.1007/s10067-005-0178-x

    authors: Nakamura T,Higashi S,Tomoda K,Tsukano M,Sugi K

    更新日期:2007-04-01 00:00:00

  • From molecular mimicry to cross-reactivity or pathogen expansion? A hypothesis.

    abstract::Very recently, several studies have convincingly demonstrated the role of infection in the development of the antiphospholipid syndrome. Cross antibody-mediated reactivity due to molecular mimicry between endothelial glycoproteins and microbial products was considered as an important pathogenic mechanism. However, ano...

    journal_title:Clinical rheumatology

    pub_type: 杂志文章,评审

    doi:10.1007/s10067-006-0352-9

    authors: Rozin AP

    更新日期:2007-03-01 00:00:00

  • Action potential simulation (APS) in patients with fibromyalgia syndrome (FMS): a controlled single subject experimental design.

    abstract:OBJECTIVES:Action potential simulation (APS) is becoming a popular method of pain reduction. Nevertheless, little is known about the efficacy of this relatively new treatment. The aim of this study was to investigate whether APS helps to reduce pain, improves patients' perception of daily functioning and social partici...

    journal_title:Clinical rheumatology

    pub_type: 杂志文章,随机对照试验

    doi:10.1007/s10067-006-0297-z

    authors: Fengler RK,Jacobs JW,Bac M,van Wijck AJ,van Meeteren NL

    更新日期:2007-03-01 00:00:00

  • A case of myeloperoxidase-antineutrophil cytoplasmic antibody positive-polyarteritis nodosa complicated by interstitial pneumonia and rapidly progressive renal failure.

    abstract::A 73-year-old woman was admitted to our hospital because of persistent high fever and cough, generalized myalgia, and renal dysfunction. Laboratory examination revealed severe inflammatory signs, pulmonary fibrosis, progression of renal impairment with active nephritic urinary sediments, and a high titer of myeloperox...

    journal_title:Clinical rheumatology

    pub_type: 杂志文章

    doi:10.1007/s10067-005-0142-9

    authors: Sugimoto T,Kanasaki K,Koyama T,Yokomaku Y,Yasuda H,Kashiwagi A,Koya D

    更新日期:2007-03-01 00:00:00

  • Rheumatologic aspects of lysosomal storage diseases.

    abstract::Lysosomal storage diseases are rare metabolic disorders, some of which can now be treated using enzyme replacement therapies. Because the time point of treatment initiation significantly influences the outcome in Gaucher disease, Fabry disease, and mucopolysaccharidosis type I, early diagnosis is of utmost importance....

    journal_title:Clinical rheumatology

    pub_type: 杂志文章

    doi:10.1007/s10067-006-0299-x

    authors: Manger B,Mengel E,Schaefer RM

    更新日期:2007-03-01 00:00:00

  • Sjögren's syndrome in patients with ankylosing spondylitis.

    abstract::There are few reports about the coexistence of Sjögren's syndrome (SS) and ankylosing spondylitis (AS). To evaluate the frequency of SS in patients with AS. We studied 70 patients with AS presenting to the university outpatient clinic between January 2002 and November 2003. All the patients were asked about sicca symp...

    journal_title:Clinical rheumatology

    pub_type: 杂志文章

    doi:10.1007/s10067-006-0255-9

    authors: Kobak S,Kobak AC,Kabasakal Y,Doganavsargil E

    更新日期:2007-02-01 00:00:00

  • Could 2'5'-oligoadenylate synthetase isoforms be biomarkers to differentiate between disease flare and infection in lupus patients? A pilot study.

    abstract::2'5'-Oligoadenylate synthetase (OAS) was shown to be related to systemic lupus erythematosus (SLE) 20 years ago, and was rediscovered to be involved in type I interferon pathway in SLE by several microarray gene expression studies recently. The goal of this study was to investigate OAS isoform expressions in lupus pat...

    journal_title:Clinical rheumatology

    pub_type: 杂志文章

    doi:10.1007/s10067-006-0260-z

    authors: Ye S,Guo Q,Tang JP,Yang CD,Shen N,Chen SL

    更新日期:2007-02-01 00:00:00

  • Functional disability and health-related quality of life in South Africans with rheumatoid arthritis and systemic lupus erythematosus.

    abstract:UNLABELLED:There is a paucity of data on the impact of chronic rheumatic diseases on functional disability and overall health-related quality of life (HRQOL) in Africans. MATERIALS AND METHODS:We compared Black South Africans (BSA) with rheumatoid arthritis (RA) (n=50) and systemic lupus erythematosus (SLE) (n=50) to ...

    journal_title:Clinical rheumatology

    pub_type: 杂志文章

    doi:10.1007/s10067-006-0215-4

    authors: Benitha R,Tikly M

    更新日期:2007-01-01 00:00:00

  • Morbidity and mortality of patients diagnosed with systemic sclerosis after the age of 75: a nested case-control study.

    abstract::This study aims to characterize the clinical features of a cohort of patients diagnosed with systemic sclerosis (SSc) after the age of 75 and compare them to a group diagnosed at a younger age. We record the review of 769 patients diagnosed with SSc over the past 16 years. Utilizing a nested case-control model, we com...

    journal_title:Clinical rheumatology

    pub_type: 杂志文章

    doi:10.1007/s10067-005-0177-y

    authors: Derk CT,Artlett CM,Jimenez SA

    更新日期:2006-11-01 00:00:00

  • Evaluation of left ventricular diastolic dysfunction with conventional and current Doppler techniques in Behcet's disease.

    abstract::Behcet's disease (BD) is a systemic vasculitis characterized by genital and oral ulcers, uveitis, and other organs' involvement. Left ventricular (LV) diastolic dysfunction has been documented in BD. However, conventional echocardiographic techniques have serious limitations like its dependence on preload, afterload a...

    journal_title:Clinical rheumatology

    pub_type: 杂志文章

    doi:10.1007/s10067-006-0208-3

    authors: Baris N,Okan T,Gurler O,Akdeniz B,Turker S,Ilknur T,Akkoc N,Goldeli O

    更新日期:2006-11-01 00:00:00

  • An adolescent girl with Meyer-Betz syndrome.

    abstract::Idiopathic paroxysmal rhabdomyolysis indicating a classical triad of symptoms consisting of muscle pain, weakness, and discolored urine is known as "Meyer-Betz syndrome". It may result in acute renal failure due to precipitation of the myoglobin casts in the tubuli or to the direct toxic effects of myoglobin to the tu...

    journal_title:Clinical rheumatology

    pub_type: 杂志文章

    doi:10.1007/s10067-005-0091-3

    authors: Kasap B,Soylu A,Türkmen M,Kavukcu S

    更新日期:2006-11-01 00:00:00

  • Headache may be a risk factor for complex regional pain syndrome.

    abstract::We investigated whether headache and family history of headache are risk factors for complex regional pain syndrome (CRPS) or not. Twenty-three CRPS patients and 69 healthy persons were interviewed whether or not they suffered from headache and had first-degree family history of headache. A headache sufferer was defin...

    journal_title:Clinical rheumatology

    pub_type: 杂志文章

    doi:10.1007/s10067-005-0161-6

    authors: Toda K,Muneshige H,Maruishi M,Kimura H,Asou T

    更新日期:2006-09-01 00:00:00

  • Partial construction of apoptotic pathway in PBMC obtained from active SLE patients and the significance of plasma TNF-alpha on this pathway.

    abstract::Systemic lupus erythematosus (SLE) is a complex autoimmune disorder that affects various organs and systems. Increased apoptosis, together with defects in the uptake of apoptotic bodies, are thought to have a pathogenic role in SLE. By detection of chromatin condensation, 30% of apoptosis was detected in peripheral bl...

    journal_title:Clinical rheumatology

    pub_type: 杂志文章

    doi:10.1007/s10067-005-0162-5

    authors: Pitidhammabhorn D,Kantachuvesiri S,Totemchokchyakarn K,Kitiyanant Y,Ubol S

    更新日期:2006-09-01 00:00:00

  • A multicenter study of patients with adult-onset Still's disease compared with systemic juvenile idiopathic arthritis.

    abstract::Adult-onset Still's disease (AOSD) has often been regarded as the adult spectrum of systemic juvenile idiopathic arthritis (sJIA). The present study aims to compare the clinical and laboratory features, the disease course and the response to treatment in patients having AOSD with those having sJIA. Retrospective revie...

    journal_title:Clinical rheumatology

    pub_type: 杂志文章,多中心研究

    doi:10.1007/s10067-005-0138-5

    authors: Pay S,Türkçapar N,Kalyoncu M,Simşek I,Beyan E,Ertenli I,Oztürk MA,Düzgün N,Erdem H,Ozbalkan Z,Kiraz S,Kinikli G,Besbas N,Dinç A,Ateş A,Olmez U,Calgüneri M,Aydintuğ OT,Bakkaloğlu A,Turan M,Turgay M,Karaaslan Y,

    更新日期:2006-09-01 00:00:00

  • Infective endocarditis complicating rituximab (anti-CD20 monoclonal antibody) treatment in an SLE patient with a past history of Libman-Sacks endocarditis: a case for antibiotic prophylaxis?

    abstract::We report a 54 year old female whose successful treatment of cerebral lupus with rituximab was complicated by the development of streptococcus intermedius, on valves damaged by Libman-Sacks endocarditis more than 20 years previously. ...

    journal_title:Clinical rheumatology

    pub_type: 杂志文章

    doi:10.1007/s10067-005-0031-2

    authors: Armstrong D,Wright S,McVeigh C,Finch M

    更新日期:2006-07-01 00:00:00

  • Prolactinoma and systemic lupus erythematosus: do serum prolactin levels matter?

    abstract::The lactogenic hormone prolactin is produced in part by cells of the immune system and serves as an upregulator of immune function. Hyperprolactinemia is common in patients with systemic lupus erythematosus (SLE), raising the possibility that the hormone contributes to the excessive immune response in the disease. The...

    journal_title:Clinical rheumatology

    pub_type: 杂志文章

    doi:10.1007/s10067-005-0117-x

    authors: Li M,Keiser HD,Peeva E

    更新日期:2006-07-01 00:00:00

  • Ochronotic spondyloarthropathy: spinal involvement resembling ankylosing spondylitis.

    abstract::Ochronotic spondyloarthropathy is a rare metabolic disease with the musculoskeletal manifestations of alkaptonuria. Ochronotic arthropathy patients may have spinal abnormalities similar to ankylosing spondylitis (AS). The proof of sacroiliac involvement or bamboo spine appearance is not sufficient either for diagnosis...

    journal_title:Clinical rheumatology

    pub_type: 杂志文章

    doi:10.1007/s10067-005-0038-8

    authors: Balaban B,Taskaynatan M,Yasar E,Tan K,Kalyon T

    更新日期:2006-07-01 00:00:00

  • Adrenal axis functions in patients with familial Mediterranean fever.

    abstract:OBJECTIVE:Familial Mediterranean fever (FMF) is a hereditary disease characterized by recurrent attacks of fever with peritonitis, arthritis, pleuritis or erysipelas-like rash. It is unclear what effects of FMF itself on endocrine system and hormones are. None of the FMF patients without amyloidosis have been reported ...

    journal_title:Clinical rheumatology

    pub_type: 杂志文章

    doi:10.1007/s10067-005-0083-3

    authors: Sav T,Ozbakir O,Kelestimur F,Gursoy S,Baskol M,Kula M,Dundar M

    更新日期:2006-07-01 00:00:00

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