نتایج جستجو برای: gad antibodies

تعداد نتایج: 163897  

فیروزرای, محسن, قرانلر, جمیله, نخجوانی, منوچهر, کیهانی, مهین‌دخت ,

Glutamic Acid Decarboxylase(GAD) catalyses the conversion of glutamic acid to Gama amino Butyric Acid(GABA) which is one of the major inhibitory neurotransmitters in central nervous system. GAD has two isoforms with molecular weights of 65 Kda(GAD 65) and 67 Kda (GAD 67). GAD 65 gene is located on chromosome 10 and expressed in β-cells of pancrease. The presence of high concentrations o...

Journal: :Diabetes 1993
W Richter J Seissler W Northemann S Wolfahrt H M Meinck W A Scherbaum

Cytoplasmic islet cell antibodies are well-established predictive markers of IDDM. Although target molecules of ICA have been suggested to be gangliosides, human monoclonal ICA of the immunoglobulin G class (MICA 1-6) produced from a patient with newly diagnosed IDDM recognized glutamate decarboxylase as a target antigen. Here we analyzed the possible heterogeneity of target antigens of ICA by ...

2015
Mario Manto Jérôme Honnorat Christiane S. Hampe Rafael Guerra-Narbona Juan Carlos López-Ramos José María Delgado-García Fumihito Saitow Hidenori Suzuki Yuchio Yanagawa Hidehiro Mizusawa Hiroshi Mitoma

Autoantibodies to the smaller isoform of glutamate decarboxylase (GAD) can be found in patients with type 1 diabetes and a number of neurological disorders, including stiff-person syndrome, cerebellar ataxia and limbic encephalitis. The detection of disease-specific autoantibody epitopes led to the hypothesis that distinct GAD autoantibodies may elicit specific neurological phenotypes. We explo...

Journal: :Journal of neurology, neurosurgery, and psychiatry 1998
M Hummel I Durinovic-Bello E Bonifacio V Lampasona J Endl S Fessele F Then Bergh C Trenkwalder E Standl A G Ziegler

OBJECTIVES Humoral and cellular immune reactivity are reported for two neuroendocrine autoantigens-glutamic acid decarboxylase (GAD) and the protein tyrosine phosphatase IA-2-in a patient with the autoimmune type of stiff-man syndrome and insulin dependent diabetes (IDDM). METHODS Antibodies and T cell proliferation against GAD and IA-2 and cytokine release of antigen stimulated T cells (IFN-...

2016
Ioannis E Dagklis Sotirios Papagiannopoulos Varvara Theodoridou Dimitrios Kazis Ourania Argyropoulou Sevasti Bostantjopoulou

Miller-Fisher syndrome (MFS) is considered as a variant of the Guillain-Barre syndrome (GBS) and its characteristic clinical features are ophthalmoplegia, ataxia, and areflexia. Typically, it is associated with anti-GQ1b antibodies; however, a significant percentage (>10%) of these patients are seronegative. Here, we report a 67-year-old female patient who presented with the typical clinical fe...

1998
M Hummel

Objectives—Humoral and cellular immune reactivity are reported for two neuroendocrine autoantigens—glutamic acid decarboxylase (GAD) and the protein tyrosine phosphatase IA-2—in a patient with the autoimmune type of stiV-man syndrome and insulin dependent diabetes (IDDM). Methods—Antibodies and T cell proliferation against GAD and IA-2 and cytokine release of antigen stimulated T cells (IFN-ã) ...

Journal: :Diabetes 2001
E Bosi S Braghi P Maffi M Scirpoli F Bertuzzi G Pozza A Secchi E Bonifacio

Islet allotransplantation into patients with autoimmune type 1 diabetes represents a reexposure to autoantigen. Here, measurement of antibodies to GAD and IA-2 autoantigens before and after islet transplantation in 36 patients (33 receiving islet plus kidney grafts with cyclosporin and steroid-based immunosuppression, and 3 receiving solitary islet transplants with mycophenolate but cyclosporin...

2015
Susanne Fauser Ingo Uttner Helena Ariño Werner A. Scherbaum Albert Saiz Jan Lewerenz

BACKGROUND In the pathogenesis of limbic encephalitis other promoting factors besides the pure existence of autoantibodies are increasingly discussed to play a significant role. This is to our knowledge the first described patient in whom the presence of autoantibodies precedes the manifestation of limbic encephalitis for many years. CASE PRESENTATION At the age of 38 years, in the serum of a...

Journal: :Journal of neurology, neurosurgery, and psychiatry 1997
A Vincent L M Grimaldi G Martino C Davenport I Todd

Antibodies to glutamic acid decarboxylase (GAD) are found in about 40% of patients with stiff man syndrome. A new assay involving immunoprecipitation of (125)I-glutamic acid decarboxylase was used to measure anti-GAD antibodies in 18 patients with stiff man syndrome. Of the eight serum samples from patients with stiff man syndrome, that had previously been found positive by immunoprecipitation ...

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