Search Results - "Nordenskjöld, M"

Cell‐free tumour DNA testing for early detection of cancer – a potential future tool by Barbany, G., Arthur, C., Liedén, A., Nordenskjöld, M., Rosenquist, R., Tesi, B., Wallander, K., Tham, E.

“…In recent years, detection of cell‐free tumour DNA (ctDNA) or liquid biopsy has emerged as an attractive noninvasive methodology to detect cancer‐specific…”
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Predictors of adverse outcome in patients with myocardial infarction with non-obstructive coronary artery (MINOCA) disease by Nordenskjöld, A.M., Baron, T., Eggers, K.M., Jernberg, T., Lindahl, B.

“…Myocardial infarction (MI) with non-obstructive coronary arteries (MINOCAs) is an increasingly recognized entity. No previous study has evaluated predictors…”
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Impact of IKZF1 deletions and PAX5 amplifications in pediatric B-cell precursor ALL treated according to NOPHO protocols by Öfverholm, I, Tran, A N, Heyman, M, Zachariadis, V, Nordenskjöld, M, Nordgren, A, Barbany, G

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Morbidity and cause‐specific mortality in first‐time myocardial infarction with nonobstructive coronary arteries by Eggers, K. M., Hjort, M., Baron, T., Jernberg, T., Nordenskjöld, A. M., Tornvall, P., Lindahl, B.

“…Background Myocardial infarction (MI) with nonobstructive coronary arteries (MINOCA) is receiving increasing interest as a prognostically adverse entity…”
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Risk factors for mortality of medical causes within 30 days of electroconvulsive therapy by Lindblad, L., Nordenskjöld, A., Otterbeck, A., Nordenskjöld, A.M.

“…Electroconvulsive therapy (ECT) is used to treat severe psychiatric disorders and is associated with reduced risk of suicide and all-cause mortality in…”
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Major adverse cardiovascular events following electroconvulsive therapy in depression: A register-based nationwide Swedish cohort study with 1-year follow-up by Nordenskjöld, Axel, Güney, Pelin, Nordenskjöld, Anna M.

“…•Electroconvulsive therapy (ECT) is associated with reduced risk of cardiovascular events.•This association may be explained by:(1)reduced depressive symptoms…”
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Circadian onset and prognosis of myocardial infarction with non-obstructive coronary arteries (MINOCA) by Nordenskjöld, Anna M, Eggers, Kai M, Jernberg, Tomas, Mohammad, Moman A, Erlinge, David, Lindahl, Bertil

“…Many acute cardiovascular events such as myocardial infarction (MI) follow circadian rhythms. Myocardial infarction with non-obstructive coronary arteries…”
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Survival in Patients With Suspected Myocardial Infarction With Nonobstructive Coronary Arteries: A Comprehensive Systematic Review and Meta-Analysis From the MINOCA Global Collaboration by Pasupathy, Sivabaskari, Lindahl, Bertil, Litwin, Peter, Tavella, Rosanna, Williams, Michael J.A., Air, Tracy, Zeitz, Christopher, Smilowitz, Nathaniel R., Reynolds, Harmony R., Eggers, Kai M., Nordenskjöld, Anna M., Barr, Peter, Jernberg, Tomas, Marfella, Raffaele, Bainey, Kevin, Sodoon Alzuhairi, Karam, Johnston, Nina, Kerr, Andrew, Beltrame, John F.

“…Background: Suspected myocardial infarction (MI) with nonobstructive coronary arteries (MINOCA) occurs in ≈5% to 10% of patients with MI referred for coronary…”
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Randomized evaluation of beta blocker and ACE-inhibitor/angiotensin receptor blocker treatment in patients with myocardial infarction with non-obstructive coronary arteries (MINOCA-BAT): Rationale and design by Nordenskjöld, Anna M, Agewall, Stefan, Atar, Dan, Baron, Tomasz, Beltrame, John, Bergström, Olle, Erlinge, David, Gale, Chris P, López-Pais, Javier, Jernberg, Tomas, Johansson, Pelle, Ravn-Fisher, Annica, Reynolds, Harmony R., Somaratne, Jithendra B., Tornvall, Per, Lindahl, Bertil

“…Myocardial infarction with non-obstructive coronary arteries (MINOCA) is common and occurs in 6–8% of all patients fulfilling the diagnostic criteria for acute…”
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The tight junction gene Claudin-1 is associated with atopic dermatitis among Ethiopians by Asad, S., Winge, M.C.G., Wahlgren, C.-F., Bilcha, K.D., Nordenskjöld, M., Taylan, F., Bradley, M.

“…Background The strong association between epidermal barrier gene variants and Atopic Dermatitis (AD) highlights that impaired skin barrier is a key feature in…”
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Novel filaggrin mutation but no other loss-of-function variants found in Ethiopian patients with atopic dermatitis by Winge, M.C.G., Bilcha, K.D., Liedén, A., Shibeshi, D., Sandilands, A., Wahlgren, C.-F., McLean, W.H.I., Nordenskjöld, M., Bradley, M.

“…Summary Background  Filaggrin is a key protein involved in maintaining skin barrier function and hydration. Mutations in the filaggrin gene (FLG) cause…”
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Unrecognized Myocardial Infarction Assessed by Cardiac Magnetic Resonance Imaging--Prognostic Implications by Nordenskjöld, Anna M, Hammar, Per, Ahlström, Håkan, Bjerner, Tomas, Duvernoy, Olov, Eggers, Kai M, Fröbert, Ole, Hadziosmanovic, Nermin, Lindahl, Bertil

“…Clinically unrecognized myocardial infarctions (UMI) are not uncommon and may be associated with adverse outcome. The aims of this study were to determine the…”
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Unrecognized myocardial infarction assessed by cardiac magnetic resonance imaging is associated with adverse long-term prognosis by Nordenskjöld, Anna M, Hammar, Per, Ahlström, Håkan, Bjerner, Tomas, Duvernoy, Olov, Lindahl, Bertil

“…Unrecognized myocardial infarctions (UMIs) are common. The study is an extension of a previous study, aiming to investigate the long-term (>5 year) prognostic…”
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Cell-free human papillomavirus (HPV) DNA is a sensitive biomarker for prognosis and for early detection of relapse in locally advanced cervical cancer by Sivars, Lars, Jylhä, Cecilia, Crona Guterstam, Ylva, Zupancic, Mark, Lindqvist, Britta, Nordenskjöld, Magnus, Tham, Emma, Hellman, Kristina

“…Human papillomavirus (HPV) is the cause of the majority of cervical cancers and has been showed to be released as cell-free tumour DNA (ctHPV DNA) into the…”
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Mutations in FLVCR2 associated with Fowler syndrome and survival beyond infancy by Kvarnung, M., Taylan, F., Nilsson, D., Albåge, M., Nordenskjöld, M., Anderlid, B.M., Nordgren, A., Syk Lundberg, E.

“…Proliferative vasculopathy and hydranencephaly‐hydrocephaly syndrome (PVHH, OMIM 225790), also known as Fowler syndrome, is a rare autosomal recessive…”
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Chromatin interactions in differentiating keratinocytes reveal novel atopic dermatitis– and psoriasis-associated genes by Sahlén, Pelin, Spalinskas, Rapolas, Asad, Samina, Mahapatra, Kunal Das, Höjer, Pontus, Anil, Anandashankar, Eisfeldt, Jesper, Srivastava, Ankit, Nikamo, Pernilla, Mukherjee, Anaya, Kim, Kyu-Han, Bergman, Otto, Ståhle, Mona, Sonkoly, Enikö, Pivarcsi, Andor, Wahlgren, Carl-Fredrik, Nordenskjöld, Magnus, Taylan, Fulya, Bradley, Maria, Tapia-Páez, Isabel

“…Hundreds of variants associated with atopic dermatitis (AD) and psoriasis, 2 common inflammatory skin disorders, have previously been discovered through…”
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One-cell biopsy significantly improves the outcome of preimplantation genetic diagnosis (PGD) treatment: retrospective analysis of 569 PGD cycles at the Stockholm PGD centre by Haapaniemi Kouru, K., Malmgren, H., Nordenskjöld, M., Fridström, M., Csemiczky, G., Blennow, E.

“…STUDY QUESTION What are the significant factors that influence the outcome of a PGD treatment? SUMMARY ANSWER The age of the woman and the number of biopsied…”
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Moisturizing treatment of patients with atopic dermatitis and ichthyosis vulgaris improves dry skin, but has a modest effect on gene expression regardless of FLG genotype by Hoppe, T., Winge, M.C.G., Bradley, M., Nordenskjöld, M., Vahlquist, A., Törmä, H., Berne, B.

“…Background Loss‐of‐function mutations in FLG (encoding filaggrin) are a predisposing factor for atopic dermatitis (AD) and cause ichthyosis vulgaris (IV)…”
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A retrospective two centre study of Birt-Hogg-Dubé syndrome reveals a pathogenic founder mutation in FLCN in the Swedish population by Lagerstedt-Robinson, Kristina, Baranowska Körberg, Izabella, Tsiaprazis, Stefanos, Björck, Erik, Tham, Emma, Poluha, Anna, Hellström Pigg, Maritta, Paulsson-Karlsson, Ylva, Nordenskjöld, Magnus, Johansson-Soller, Maria, Aravidis, Christos

“…Birt-Hogg-Dube syndrome (BHDS) (MIM: 135150) is a rare autosomal dominant disorder with variable penetrance, caused by pathogenic variants in the FLCN gene…”
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Detection of chromosomal imbalances in children with idiopathic mental retardation by array based comparative genomic hybridisation (array-CGH) by Schoumans, J, Ruivenkamp, C, Holmberg, E, Kyllerman, M, Anderlid, B-M, Nordenskjöld, M

“…Chromosomal aberrations are a common cause of multiple anomaly syndromes that include growth and developmental delay and dysmorphism. Novel high resolution,…”
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