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113 Possible Causes for Ab, Serum, Sulfate 3 Glucuronyl, [Presence], IN, paragloboside

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  • Idiopathic Neutropenia

    […] of PBMCs and granulocytes of CIN patients and healthy controls was determined using the highly sensitive TeloTAGGG Telomerase PCR ELISA kit (Roche Diagnostics Scandinavia AB[haematologica.org] : Patients with NI-CINA have significant changes in serum immunoglobulins and some inflammation-related cytokines.[ncbi.nlm.nih.gov] The Severe Chronic Neutropenia International Registry Idiopathic Neutropenia The term ‘idiopathic neutropenia’ describes various types of neutropenia that may occur at any[depts.washington.edu] Abstract Chronic idiopathic neutropenia (CIN) is a bone marrow (BM) disorder characterized by presence of activated T-lymphocytes in peripheral blood (PB) and BM.[ncbi.nlm.nih.gov] PubMed Central View Article PubMed Google Scholar Liu H, Ozaki K, Matsuzaki Y, Abe M, Kosaka M, Saito S: Suppression of haematopoiesis by IgG autoantibodies from patients[arthritis-research.biomedcentral.com] […] showed poor colony forming activity, but a normal differentiating capacity to the stimulation with rhG-CSF, although they displayed a normal colony forming capacity in the presence[ncbi.nlm.nih.gov]

    Missing: Sulfate 3 Glucuronyl paragloboside
  • Adult Idiopathic Neutropenia

    Kojima H, Hasegawa Y, Shibuya K, Nakazawa M, Yoda Y, Abe T. Chronic idiopathic neutropenia improved by recombinant granulocyte colony stimulating factor.[link.springer.com] Serum levels of inflammatory cytokines and chemokines were measured in 132 patients with chronic idiopathic neutropenia of adults (CINA) and 34 healthy volunteers (controls[ncbi.nlm.nih.gov] Risk idiopathic neutropenia adults of serious infections. Rheumatoid arthritis. By ukneutropeniasupportgroup. Indications and usage. Idiopathic neutropenia.[friends-acronym.ga] Abstract Our study describes the presence of antineutrophil cytoplasmic antibodies (ANCA) in a group of different pathologies comprising 101 patients.[ncbi.nlm.nih.gov] […] defined by an absolute neutrophil count (ANCs) lower than 1.8 x10 3 /µL in white and 1.5 x10 3 /µL in black people for more than 3 months, either in the absence or in the presence[bloodjournal.org] This study describes the frequency of serum organ-specific and organ-nonspecific autoantibodies in 157 patients with nonimmune chronic idiopathic neutropenia of adults (NI-CINA[ncbi.nlm.nih.gov]

    Missing: Sulfate 3 Glucuronyl paragloboside
  • Monoclonal Gammopathy of Undetermined Significance

    Eriko Sugawara, Motoi Kuwahara, Susumu Kusunoki, Fumiaki Tanaka and Tatsuya Takahashi , A case of IgM paraproteinemic neuropathy associated with anti-sulfated glucuronic paragloboside[doi.org] Yoshiko Matsuhashi, Taizo Tasaka, Naoki Kakazu, Masami Nagai, Ken Sadahira, Kazuhiro Nishida, Masafumi Taniwaki, Tatsuo Abe and Toshihiko Ishida , Establishment and characterization[doi.org] Serum samples, named as non-MGUS, were also collected from patients with subjacent immunological pathologies who were discarded of having MGUS through serum immunofixation[ncbi.nlm.nih.gov] We present a case in which the nerve biopsy revealed the presence of crystalline inclusions in the endoneurium, a very unusual finding.[ncbi.nlm.nih.gov] Similarly, very recent results reported by Abe et al 59 showed an increase of Mip-1α secretion in highly purified MM plasma cells compared with normal PCs.[bloodjournal.org] Repeated magnetic resonance imaging (MRI) of the brain and spinal cord documented the presence of demyelinating plaques spread in the white matter of the periventricular region[ncbi.nlm.nih.gov]

    Missing: Sulfate 3 Glucuronyl IN
  • GM2 Gangliosidosis Variant AB

    In addition, a glycolipid with a mobility, by thin-layer chromatography, similar to that of paragloboside was observed in the CSF of the patient with the variant AB of GM2[wwww.unboundmedicine.com] Homepage Rare diseases Search Search for a rare disease GM2 gangliosidosis, AB variant Disease definition GM2 gangliosidosis, AB variant is an extremely rare, severe genetic[orpha.net] Abstract A fluorometric method showed the activity of hexosaminidase A in human serum to be markedly deficient in serum specimens from nine patients with Tay–Sachs disease[nejm.org] The minor acitivity of the extracts from variants B and 0 in the presence of detergent is probably due to the presence of hexosaminidase B and S, respectively, in these ex[zdoc.site] In addition, a glycolipid with a mobility, by thin-layer chromatography, similar to that of paragloboside was observed in the CSF of the patient with the variant AB of G M2[pediatrics.aappublications.org] Signs and symptoms of the AB variant become apparent in infancy.[ghr.nlm.nih.gov]

    Missing: Sulfate 3 Glucuronyl IN
  • Anemia of Chronic Disease

    Pathogenesis of ACD is built on three prin ci pal ab nor mal i ties: short ened erythrocyte survival, impaired bone marrow response and disturbance in iron metabolism.[zurnalas.llmd.lt] We conclude that unlike serum ferritin levels, which are disproportionately elevated in relation to iron stores in patients with inflammation or liver disease, the serum transferrin[ncbi.nlm.nih.gov] Abstract This study describes the frequency and the type of anemia seen in patients with nonimmune chronic idiopathic neutropenia of adults (NI-CINA).[ncbi.nlm.nih.gov] The results of these three key laboratory tests may help to identify functional iron deficiency in the presence of chronic inflammation.[ncbi.nlm.nih.gov] Hepcidin was detected on the blots using rabbit anti-human hepcidin Ab’s ( 12 ) with goat anti-rabbit HRP as a secondary Ab.[doi.org] In patients with a low total iron binding capacity, iron therapy should not be instituted without clearly establishing the presence of iron deficiency irrespective of the[ncbi.nlm.nih.gov]

    Missing: Sulfate 3 Glucuronyl paragloboside
  • Gamma Globulin

    F(ab)(2), but not Fc fragments, led to suppressed MMP-9 activity.[ncbi.nlm.nih.gov] Serum IgG, IgG2 and IgG4 were also significantly raised.[ncbi.nlm.nih.gov] neutropenia and aplastic anemia; (3) atopic allergy with IgG subclass deficiency including bronchial asthma; (4) in severe infections in combination therapy with antibiotics[ncbi.nlm.nih.gov] Microbiology, Russian Academy of Medical Sciences, Moscow, Russia. [email protected] Abstract Interferon-alpha was detected in IFN pool produced by human leukocytes in the presence[ncbi.nlm.nih.gov] However, the presence of highly abundant proteins often masks those of lower abundance and thus generally prevents their detection and identification in proteomic studies.[ncbi.nlm.nih.gov] ) 1, F(ab) 2 and Fc.[google.com]

    Missing: Sulfate 3 Glucuronyl paragloboside
  • Peripheral Motor Neuropathy - Dysautonomia Syndrome

    Guillain-Barre syndrome; MAG, myelin-associated glycoprotein; MFS, Miller-Fisher syndrome; MMN, multifocal motor neuropathy; MND, motor neuron disease; SGPG, sulfate-3-glucuronyl paragloboside[arupconsult.com] […] glucocorticoids and immunosuppresives Myasthenia Gravis Characteristics Autoimmune disease with variable course characterized by weakness and skeletal muscle fatigability - Ab[quizlet.com] Results: Serum levels of HBV DNA decreased in all patients and fell to undetectable levels during treatment in four of five patients.[annals.org] The presence of anti-synthetase antibodies is a negative predictor for the presence of cancer.[bloodjournal.org] AB - Guillain-Barré syndrome includes acute inflammatory demyelinating polyradiculoneuropathy, acute motor axonal neuropathy, acute motor and sensory axonal neuropathy, Miller[uthealth.influuent.utsystem.edu] By: Granero R; Fernández-Aranda F; Aymamí N; Gómez-Peña M; Fagundo AB; Sauchelli S; Del Pino-Gutiérrez A; Moragas L; Savvidou LG; Islam MA; Tàrrega S; Menchón JM; Jiménez-Murcia[tikpdf.tips]

    Missing: IN
  • Multifocal Motor Neuropathy

    Yu , Sensitization of Lewis rats with sulfoglucuronosyl paragloboside: Electrophysiological and immunological studies of an animal model of peripheral neuropathy , Journal[doi.org] Although the etiology of this condition is not known, high titers of IgM Ab to GM1 may serve as a biomarker for this disease.[ncbi.nlm.nih.gov] Abstract Various data support the pathogenetic significance of serum IgM autoantibodies against glycolipid GM1 in patients with multifocal motor neuropathy.[ncbi.nlm.nih.gov] The most typical laboratory finding is the presence of high levels of serum IgM antibodies to the ganglioside GM1, and less frequently to asialo-GM1, GD1a or GM2.[ncbi.nlm.nih.gov] MMN ALS Distribution of weakness Asymmetric,Arms Ultimately generalized Upper motor neuron findings Absent Usually present EMG Conduction block Motor axonal loss Anti GM1 Ab[mmcneuro.wordpress.com] AB - The multifocal motor neuropathy (MMN) is a rare peripheral disorder characterized by persistent conduction blocks confined to motor axons at sites not prone to compression[moh-it.pure.elsevier.com]

    Missing: Sulfate 3 Glucuronyl IN
  • Paroxysmal Cold Hemoglobinuria

    Basic structure is the precursor substance, but is called globoside (P) or paragloboside (p) in the P system as the diagram below shows: from the AABB Technical Manual, 13th[faculty.madisoncollege.edu] Alberta, Canada PACD - Cold Bay Airport, Cold Bay, Alaska, United States hpn - Hemoglobinuria paroxística nocturna PNH - Paroxysmal Nocturnal Hemoglobinuria YOD - Cold Lake, AB[acronymsandslang.com] The serum-mediated hemagglutination and the serum and complement-mediated immunohemolysis were inhibited by globoside (P antigen GalNAc beta 1-3Gal alpha 1-4Gal beta 1-4Glc-ceramide[ncbi.nlm.nih.gov] Hemolysis is severe to the extent that urine may appear brown-colored, with no or, rarely, minimal presence of blood.[symptoma.com] Whipple, Dawn AB. Moreau, JoAnn M. Moulds, Jane S. Hankins, Winfred C. Wang and Kerri A.[doi.org] AIHA, but more common in cold ab AIHA).[errolozdalga.com]

    Missing: Sulfate 3 Glucuronyl IN
  • Acute Tubular Necrosis

    Nephrol Dial Transplant 11 : 293 -299, 1996 Groeneveld AB: Pathogenesis of acute renal failure during sepsis.[jasn.asnjournals.org] Evidence is presented that the low serum EPO level is due to defective synthesis and not to increased catabolism.[ncbi.nlm.nih.gov] Abstract The HNK-1 carbohydrate epitope is a 3-sulfo-glucuronyl residue attached to lactosamine structures on glycoproteins, proteoglycans, or glycolipids mostly expressed[ncbi.nlm.nih.gov] While most nephrologists use urine microscopy to assess for the presence of glomerular diseases, they are less apt to use this diagnostic test when pre-renal acute kidney[ncbi.nlm.nih.gov] Renal tubular dysfunction presents within the first year of life, followed by a serum creatinine level that increases with age.[ncbi.nlm.nih.gov] The renal biopsy confirmed the presence of acute tubular necrosis. The reversibility of captopril-induced ARF is confirmed and the patient made an uneventful recovery.[ncbi.nlm.nih.gov]

    Missing: IN paragloboside