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Diabetes Antibody Standardization Program: evaluation of assays for autoantibodies to glutamic acid decarboxylase and islet antigen-2

program evaluation

Bonifacio E.
GSID: 48igUZnRAzAJ
C Törn, PW Mueller, M Schlosser, E Bonifacio… - Diabetologia, 2008 - Springer

… The aims of the first DASP evaluation were to assess and improve comparability of islet autoantibody measurements among laboratories and to undertake extended evaluation of the new WHO international reference reagent for antibodies to GAD and IA-2 [8,...

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Törn, C., Mueller, P. W., Schlosser, M., Bonifacio, E., & Bingley, P. J. (2008). Diabetes Antibody Standardization Program: evaluation of assays for autoantibodies to glutamic acid decarboxylase and islet antigen-2. Diabetologia, 51(5), 846-852.
Törn, Carina, et al. "Diabetes Antibody Standardization Program: evaluation of assays for autoantibodies to glutamic acid decarboxylase and islet antigen-2." Diabetologia 51.5 (2008): 846-852.
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The ITP syndrome: pathogenic and clinical diversity

diversity

Liebman HA.
GSID: Y0cjQnKIvsoJ
DB Cines, JB Bussel, HA Liebman… - Blood, The Journal of …, 2009 - ashpublications.org

Immune thrombocytopenia (ITP) is mediated by platelet autoantibodies that accelerate platelet destruction and inhibit their production. Most cases are considered idiopathic, whereas others are secondary to coexisting conditions. Insights from secondary forms suggest that the …

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Cines, D. B., Bussel, J. B., Liebman, H. A., & Luning Prak, E. T. (2009). The ITP syndrome: pathogenic and clinical diversity. Blood, The Journal of the American Society of Hematology, 113(26), 6511-6521.
Cines, Douglas B., et al. "The ITP syndrome: pathogenic and clinical diversity." Blood, The Journal of the American Society of Hematology 113.26 (2009): 6511-6521.
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Diabetes Antibody Standardization Program: evaluation of assays for insulin autoantibodies

program evaluation

Bonifacio E.
GSID: JSvQx-iCH2YJ
M Schlosser, PW Mueller, C Törn, E Bonifacio… - Diabetologia, 2010 - Springer

Aims/hypothesis Insulin autoantibodies (IAA) are important in type 1 diabetes risk assessment. However, their determination varies more between laboratories than other diabetes autoantibodies. The Diabetes Antibody Standardization Program (DASP) aims to improve and …

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Schlosser, M., et al. "Diabetes Antibody Standardization Program: evaluation of assays for insulin autoantibodies." Diabetologia 53.12 (2010): 2611-2620.
Schlosser M. et al. Diabetes Antibody Standardization Program: evaluation of assays for insulin autoantibodies //Diabetologia. – 2010. – Т. 53. – №. 12. – С. 2611-2620.
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Moxifloxacin-Induced Immune-Mediated Thrombocytopenia in a Chronic Kidney Disease Patient Receiving Hemodialysis.

The Annals of pharmacotherapy

Mailman JF, Stigant C, Martinusen D.
PMID: 24687544
Ann Pharmacother. 2014 Jul;48(7):919-922. doi: 10.1177/1060028014529929. Epub 2014 Mar 31.

OBJECTIVE: To alert clinicians to a serious complication from a commonly prescribed medication, moxifloxacin.CASE SUMMARY: A 65-year-old male, septic, hemodialysis patient developed thrombocytopenia following exposure to vancomycin, ceftazidime, and moxifloxacin. Drug-specific immunoglobulin testing showed positive autoantibodies against only moxifloxacin,...

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Mailman JF, Stigant C, Martinusen D. Moxifloxacin-Induced Immune-Mediated Thrombocytopenia in a Chronic Kidney Disease Patient Receiving Hemodialysis. Ann Pharmacother. 2014;48(7):919-922doi: 10.1177/1060028014529929.
Mailman, J. F., Stigant, C., & Martinusen, D. (2014). Moxifloxacin-Induced Immune-Mediated Thrombocytopenia in a Chronic Kidney Disease Patient Receiving Hemodialysis. The Annals of pharmacotherapy, 48(7), 919-922. https://doi.org/10.1177/1060028014529929
Mailman, Jonathan F, et al. "Moxifloxacin-Induced Immune-Mediated Thrombocytopenia in a Chronic Kidney Disease Patient Receiving Hemodialysis." The Annals of pharmacotherapy vol. 48,7 (2014): 919-922. doi: https://doi.org/10.1177/1060028014529929
Mailman JF, Stigant C, Martinusen D. Moxifloxacin-Induced Immune-Mediated Thrombocytopenia in a Chronic Kidney Disease Patient Receiving Hemodialysis. Ann Pharmacother. 2014 Jul;48(7):919-922. doi: 10.1177/1060028014529929. Epub 2014 Mar 31. PMID: 24687544.
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Clinicopathological analysis of mechanic's hand associated with dermatomyositis.

The Australasian journal of dermatology

Mori T, Ohashi T, Kato Y, Ohtsuka M, Yamamoto T.
PMID: 26299387
Australas J Dermatol. 2016 Nov;57(4):e123-e126. doi: 10.1111/ajd.12381. Epub 2015 Aug 23.

Mechanic's hand is often seen in the fingers of patients with dermatomyositis and is frequently associated with anti-aminoacyl-transfer RNA synthetase autoantibodies and interstitial lung disease. We analysed the clinical symptoms of 50 patients with dermatomyositis who had visited our...

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Mori T, Ohashi T, Kato Y, et al. Clinicopathological analysis of mechanic's hand associated with dermatomyositis. Australas J Dermatol. 2015;57(4):e123-e126doi: 10.1111/ajd.12381.
Mori, T., Ohashi, T., Kato, Y., Ohtsuka, M., & Yamamoto, T. (2016). Clinicopathological analysis of mechanic's hand associated with dermatomyositis. The Australasian journal of dermatology, 57(4), e123-e126. https://doi.org/10.1111/ajd.12381
Mori, Tatsuhiko, et al. "Clinicopathological analysis of mechanic's hand associated with dermatomyositis." The Australasian journal of dermatology vol. 57,4 (2016): e123-e126. doi: https://doi.org/10.1111/ajd.12381
Mori T, Ohashi T, Kato Y, Ohtsuka M, Yamamoto T. Clinicopathological analysis of mechanic's hand associated with dermatomyositis. Australas J Dermatol. 2016 Nov;57(4):e123-e126. doi: 10.1111/ajd.12381. Epub 2015 Aug 23. PMID: 26299387.
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Experimental lupus is aggravated in mouse strains with impaired induction of neutrophil extracellular traps.

JCI insight

Kienhöfer D, Hahn J, Stoof J, Csepregi JZ, Reinwald C, Urbonaviciute V, Johnsson C, Maueröder C, Podolska MJ, Biermann MH, Leppkes M, Harrer T, Hultqvist M, Olofsson P, Munoz LE, Mocsai A, Herrmann M, Schett G, Holmdahl R, Hoffmann MH.
PMID: 28515366
JCI Insight. 2017 May 18;2(10). doi: 10.1172/jci.insight.92920. eCollection 2017 May 18.

Many effector mechanisms of neutrophils have been implicated in the pathogenesis of systemic lupus erythematosus (SLE). Neutrophil extracellular traps (NETs) have been assigned a particularly detrimental role. Here we investigated the functional impact of neutrophils and NETs on a...

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Kienhöfer D, Hahn J, Stoof J, et al. Experimental lupus is aggravated in mouse strains with impaired induction of neutrophil extracellular traps. JCI Insight. 2017;2(10)doi: 10.1172/jci.insight.92920.
Kienhöfer, D., Hahn, J., Stoof, J., Csepregi, J. Z., Reinwald, C., Urbonaviciute, V., Johnsson, C., Maueröder, C., Podolska, M. J., Biermann, M. H., Leppkes, M., Harrer, T., Hultqvist, M., Olofsson, P., Munoz, L. E., Mocsai, A., Herrmann, M., Schett, G., Holmdahl, R., & Hoffmann, M. H. (2017). Experimental lupus is aggravated in mouse strains with impaired induction of neutrophil extracellular traps. JCI insight, 2(10), . https://doi.org/10.1172/jci.insight.92920
Kienhöfer, Deborah, et al. "Experimental lupus is aggravated in mouse strains with impaired induction of neutrophil extracellular traps." JCI insight vol. 2,10 (2017). doi: https://doi.org/10.1172/jci.insight.92920
Kienhöfer D, Hahn J, Stoof J, Csepregi JZ, Reinwald C, Urbonaviciute V, Johnsson C, Maueröder C, Podolska MJ, Biermann MH, Leppkes M, Harrer T, Hultqvist M, Olofsson P, Munoz LE, Mocsai A, Herrmann M, Schett G, Holmdahl R, Hoffmann MH. Experimental lupus is aggravated in mouse strains with impaired induction of neutrophil extracellular traps. JCI Insight. 2017 May 18;2(10). doi: 10.1172/jci.insight.92920. eCollection 2017 May 18. PMID: 28515366; PMCID: PMC5436535.
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Aptamers in Therapeutics.

Journal of clinical and diagnostic research : JCDR

Parashar A.
PMID: 27504277
J Clin Diagn Res. 2016 Jun;10(6):BE01-6. doi: 10.7860/JCDR/2016/18712.7922. Epub 2016 Jun 01.

Aptamers are single strand DNA or RNA molecules, selected by an iterative process known as Systematic Evolution of Ligands by Exponential Enrichment (SELEX). Due to various advantages of aptamers such as high temperature stability, animal free, cost effective production...

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Parashar A. Aptamers in Therapeutics. J Clin Diagn Res. 2016;10(6):BE01-6doi: 10.7860/JCDR/2016/18712.7922.
Parashar, A. (2016). Aptamers in Therapeutics. Journal of clinical and diagnostic research : JCDR, 10(6), BE01-6. https://doi.org/10.7860/JCDR/2016/18712.7922
Parashar, Abhishek. "Aptamers in Therapeutics." Journal of clinical and diagnostic research : JCDR vol. 10,6 (2016): BE01-6. doi: https://doi.org/10.7860/JCDR/2016/18712.7922
Parashar A. Aptamers in Therapeutics. J Clin Diagn Res. 2016 Jun;10(6):BE01-6. doi: 10.7860/JCDR/2016/18712.7922. Epub 2016 Jun 01. PMID: 27504277; PMCID: PMC4963637.
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Anti-HMGCR Autoantibodies in Juvenile Idiopathic Inflammatory Myopathies Identify a Rare but Clinically Important Subset of Patients.

The Journal of rheumatology

[No authors listed]
PMID: 28864670
J Rheumatol. 2017 Sep;44(9):1417. doi: 10.3899/jrheum.160871.C1.

No abstract available.

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Anti-HMGCR Autoantibodies in Juvenile Idiopathic Inflammatory Myopathies Identify a Rare but Clinically Important Subset of Patients. J Rheumatol. 2017;44(9):1417doi: 10.3899/jrheum.160871.C1.
(2017). Anti-HMGCR Autoantibodies in Juvenile Idiopathic Inflammatory Myopathies Identify a Rare but Clinically Important Subset of Patients. The Journal of rheumatology, 44(9), 1417. https://doi.org/10.3899/jrheum.160871.C1
"Anti-HMGCR Autoantibodies in Juvenile Idiopathic Inflammatory Myopathies Identify a Rare but Clinically Important Subset of Patients." The Journal of rheumatology vol. 44,9 (2017): 1417. doi: https://doi.org/10.3899/jrheum.160871.C1
Anti-HMGCR Autoantibodies in Juvenile Idiopathic Inflammatory Myopathies Identify a Rare but Clinically Important Subset of Patients. J Rheumatol. 2017 Sep;44(9):1417. doi: 10.3899/jrheum.160871.C1. PMID: 28864670.
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New-Onset Refractory Status Epilepticus with Claustrum Damage: Definition of the Clinical and Neuroimaging Features.

Frontiers in neurology

Meletti S, Giovannini G, d'Orsi G, Toran L, Monti G, Guha R, Kiryttopoulos A, Pascarella MG, Martino T, Alexopoulos H, Spilioti M, Slonkova J.
PMID: 28396650
Front Neurol. 2017 Mar 27;8:111. doi: 10.3389/fneur.2017.00111. eCollection 2017.

New-onset refractory status epilepticus (NORSE) is a rare but challenging condition occurring in a previously healthy patient, often with no identifiable cause. We describe the electro-clinical features and outcomes in a group of patients with NORSE who all demonstrated...

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Meletti S, Giovannini G, d'Orsi G, et al. New-Onset Refractory Status Epilepticus with Claustrum Damage: Definition of the Clinical and Neuroimaging Features. Front Neurol. 2017;8:111doi: 10.3389/fneur.2017.00111.
Meletti, S., Giovannini, G., d'Orsi, G., Toran, L., Monti, G., Guha, R., Kiryttopoulos, A., Pascarella, M. G., Martino, T., Alexopoulos, H., Spilioti, M., & Slonkova, J. (2017). New-Onset Refractory Status Epilepticus with Claustrum Damage: Definition of the Clinical and Neuroimaging Features. Frontiers in neurology, 8111. https://doi.org/10.3389/fneur.2017.00111
Meletti, Stefano, et al. "New-Onset Refractory Status Epilepticus with Claustrum Damage: Definition of the Clinical and Neuroimaging Features." Frontiers in neurology vol. 8 (2017): 111. doi: https://doi.org/10.3389/fneur.2017.00111
Meletti S, Giovannini G, d'Orsi G, Toran L, Monti G, Guha R, Kiryttopoulos A, Pascarella MG, Martino T, Alexopoulos H, Spilioti M, Slonkova J. New-Onset Refractory Status Epilepticus with Claustrum Damage: Definition of the Clinical and Neuroimaging Features. Front Neurol. 2017 Mar 27;8:111. doi: 10.3389/fneur.2017.00111. eCollection 2017. PMID: 28396650; PMCID: PMC5366956.
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Serum Protein Profile in Women With Pregnancy Morbidity Associated With Antiphospholipid Syndrome.

Journal of human reproductive sciences

Alvarez AM, Neubeck S, Parra S, Markert UR, Cadavid AP.
PMID: 28479750
J Hum Reprod Sci. 2017 Jan-Mar;10(1):10-17. doi: 10.4103/0974-1208.204018.

CONTEXT: Antiphospholipid antibodies (aPL) are related with a high risk of pregnancy morbidity (PM) and also of vascular thrombosis. On the basis of recent studies, we expect that in women with PM associated with antiphospholipid syndrome (APS), further factors...

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Alvarez AM, Neubeck S, Parra S, et al. Serum Protein Profile in Women With Pregnancy Morbidity Associated With Antiphospholipid Syndrome. J Hum Reprod Sci. 2017;10(1):10-17doi: 10.4103/0974-1208.204018.
Alvarez, A. M., Neubeck, S., Parra, S., Markert, U. R., & Cadavid, A. P. (2017). Serum Protein Profile in Women With Pregnancy Morbidity Associated With Antiphospholipid Syndrome. Journal of human reproductive sciences, 10(1), 10-17. https://doi.org/10.4103/0974-1208.204018
Alvarez, Angela M, et al. "Serum Protein Profile in Women With Pregnancy Morbidity Associated With Antiphospholipid Syndrome." Journal of human reproductive sciences vol. 10,1 (2017): 10-17. doi: https://doi.org/10.4103/0974-1208.204018
Alvarez AM, Neubeck S, Parra S, Markert UR, Cadavid AP. Serum Protein Profile in Women With Pregnancy Morbidity Associated With Antiphospholipid Syndrome. J Hum Reprod Sci. 2017 Jan-Mar;10(1):10-17. doi: 10.4103/0974-1208.204018. PMID: 28479750; PMCID: PMC5405641.
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Clinical and histopathological features of myopathies in Japanese patients with anti-SRP autoantibodies.

Modern rheumatology

Takada T, Hirakata M, Suwa A, Kaneko Y, Kuwana M, Ishihara T, Ikeda Y.
PMID: 28925310
Mod Rheumatol. 2009 Apr;19(2):165. doi: 10.3109/s10165-009-0165-1.

No abstract available.

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Takada T, Hirakata M, Suwa A, et al. Clinical and histopathological features of myopathies in Japanese patients with anti-SRP autoantibodies. Mod Rheumatol. 2009;19(2):165doi: 10.3109/s10165-009-0165-1.
Takada, T., Hirakata, M., Suwa, A., Kaneko, Y., Kuwana, M., Ishihara, T., & Ikeda, Y. (2009). Clinical and histopathological features of myopathies in Japanese patients with anti-SRP autoantibodies. Modern rheumatology, 19(2), 165. https://doi.org/10.3109/s10165-009-0165-1
Takada, Tetsuya, et al. "Clinical and histopathological features of myopathies in Japanese patients with anti-SRP autoantibodies." Modern rheumatology vol. 19,2 (2009): 165. doi: https://doi.org/10.3109/s10165-009-0165-1
Takada T, Hirakata M, Suwa A, Kaneko Y, Kuwana M, Ishihara T, Ikeda Y. Clinical and histopathological features of myopathies in Japanese patients with anti-SRP autoantibodies. Mod Rheumatol. 2009 Apr;19(2):165. doi: 10.3109/s10165-009-0165-1. PMID: 28925310.
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In vivo imaging reveals rapid astrocyte depletion and axon damage in a model of neuromyelitis optica-related pathology.

Annals of neurology

Herwerth M, Kalluri SR, Srivastava R, Kleele T, Kenet S, Illes Z, Merkler D, Bennett JL, Misgeld T, Hemmer B.
PMID: 26946517
Ann Neurol. 2016 May;79(5):794-805. doi: 10.1002/ana.24630. Epub 2016 Apr 18.

OBJECTIVE: Neuromyelitis optica (NMO) is an autoimmune disease of the central nervous system, which resembles multiple sclerosis (MS). NMO differs from MS, however, in the distribution and histology of neuroinflammatory lesions and shows a more aggressive clinical course. Moreover,...

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Herwerth M, Kalluri SR, Srivastava R, et al. In vivo imaging reveals rapid astrocyte depletion and axon damage in a model of neuromyelitis optica-related pathology. Ann Neurol. 2016;79(5):794-805doi: 10.1002/ana.24630.
Herwerth, M., Kalluri, S. R., Srivastava, R., Kleele, T., Kenet, S., Illes, Z., Merkler, D., Bennett, J. L., Misgeld, T., & Hemmer, B. (2016). In vivo imaging reveals rapid astrocyte depletion and axon damage in a model of neuromyelitis optica-related pathology. Annals of neurology, 79(5), 794-805. https://doi.org/10.1002/ana.24630
Herwerth, Marina, et al. "In vivo imaging reveals rapid astrocyte depletion and axon damage in a model of neuromyelitis optica-related pathology." Annals of neurology vol. 79,5 (2016): 794-805. doi: https://doi.org/10.1002/ana.24630
Herwerth M, Kalluri SR, Srivastava R, Kleele T, Kenet S, Illes Z, Merkler D, Bennett JL, Misgeld T, Hemmer B. In vivo imaging reveals rapid astrocyte depletion and axon damage in a model of neuromyelitis optica-related pathology. Ann Neurol. 2016 May;79(5):794-805. doi: 10.1002/ana.24630. Epub 2016 Apr 18. PMID: 26946517; PMCID: PMC5021140.
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Showing 1 to 12 of 4386 entries