Search Results - "Myrdal, U."

Oats to children with newly diagnosed coeliac disease: a randomised double blind study by Högberg, L, Laurin, P, Fälth-Magnusson, K, Grant, C, Grodzinsky, E, Jansson, G, Ascher, H, Browaldh, L, Hammersjö, J-Å, Lindberg, E, Myrdal, U, Stenhammar, L

“…Background: Treatment of coeliac disease (CD) requires lifelong adherence to a strict gluten free diet (GFD) which hitherto has consisted of a diet free of…”
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Approach to genetic analysis in the diagnosis of hereditary autoinflammatory syndromes by Simon, A., van der Meer, J. W. M., Veselý, R., Myrdal, U., Yoshimura, K., Duys, P., Drenth, J. P. H.

“…Objective. Hereditary autoinflammatory syndromes are characterized by recurrent episodes of fever and inflammation. Seven subtypes have been described, caused…”
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IA-2 autoantibodies in incident type I diabetes patients are associated with a polyadenylation signal polymorphism in GIMAP5 by Shin, J-H, Janer, M, McNeney, B, Blay, S, Deutsch, K, Sanjeevi, C B, Kockum, I, Lernmark, A, Graham, J, Arnqvist, Hans, Björck, Elizabeth, Eriksson, Jan, Nyström, Lennarth, Ohlson, Lars Olof, Scherstén, Bengt, Ostman, Jan, Aili, M, Bååth, L E, Carlsson, E, Edenwall, H, Forsander, G, Granström, B W, Gustavsson, I, Hanås, R, Hellenberg, L, Hellgren, H, Holmberg, E, Hörnell, H, Ivarsson, Sten-A, Johansson, C, Jonsell, G, Kockum, K, Lindblad, B, Lindh, A, Ludvigsson, J, Myrdal, U, Neiderud, J, Segnestam, K, Sjöblad, S, Skogsberg, L, Strömberg, L, Ståhle, U, Thalme, B, Tullus, K, Tuvemo, T, Wallensteen, M, Westphal, O, Aman, J

“…In a large case-control study of Swedish incident type I diabetes patients and controls, 0-34 years of age, we tested the hypothesis that the GIMAP5 gene, a…”
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Compliance in teenagers with coeliac disease--a Swedish follow-up study by Ljungman, G, Myrdal, U

“…A group of 47 children with coeliac disease, born between 1973 and 1978 in the Swedish county of Västmanland, participated in a controlled questionnaire study…”
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SUMO4 M55V polymorphism affects susceptibility to type I diabetes in HLA DR3- and DR4-positive Swedish patients by Sedimbi, S K, Luo, X R, Sanjeevi, C B, Lernmark, Ake, Landin-Olsson, Mona, Arnqvist, Hans, Björck, Elizabeth, Nyström, Lennarth, Ohlson, Lars Olof, Scherstén, Bengt, Ostman, Jan, Aili, M, Bååth, L E, Carlsson, E, Edenwall, H, Forsander, G, Granström, B W, Gustavsson, I, Hanås, R, Hellenberg, L, Hellgren, H, Holmberg, E, Hörnell, H, Ivarsson, Sten-A, Johansson, C, Jonsell, G, Kockum, K, Lindblad, B, Lindh, A, Ludvigsson, J, Myrdal, U, Neiderud, J, Segnestam, K, Sjöblad, S, Skogsberg, L, Strömberg, L, Ståhle, U, Thalme, B, Tullus, K, Tuvemo, T, Wallensteen, M, Westphal, O, Dahlquist, Gisela, Aman, J

“…SUMO4 M55V, located in IDDM5, has been a focus for debate because of its association to type I diabetes (TIDM) in Asians but not in Caucasians. The current…”
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Reversal of protein‐losing enteropathy in a child with Fontan circulation is correlated with central venous pressure after heart transplantation by Holmgren, D., Berggren, H., Wåhlander, H., Hallberg, M., Myrdal, U.

“…: We report on the reversal of protein‐losing enteropathy (PLE) after heart transplantation (HTx) in a 10‐yr‐old boy with Fontan circulation, previously…”
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Studies on lipoprotein metabolism in a family with jejunal chylomicron retention by Nemeth, A, Myrdal, U, Veress, B, Rudling, M, Berglund, L, Angelin, B

“…We describe two siblings with fat malabsorption and jejunal chylomicron retention. Plasma lipoproteins were studied in the patients and their first-degree…”
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Erythromycin in neonatal postoperative intestinal dysmotility by Simkiss, D E, Adams, I P, Myrdal, U, Booth, I W

“…The motilin agonist erythromycin was used successfully in four infants receiving prolonged parenteral nutrition for severe intestinal dysmotility after…”
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Colorectal Inflammation is Well Predicted by Fecal Calprotectin in Children with Gastrointestinal Symptoms by Fagerberg, Ulrika Lorentzon, Lööf, Lars, Myrdal, Urban, Hansson, Lars‐Olof, Finkel, Yigael

“…ABSTRACT Objectives: The protein calprotectin is mainly derived from neutrophils. Increased fecal excretion of calprotectin has been reported in inflammatory…”
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Mutations in a Sar1 GTPase of COPII vesicles are associated with lipid absorption disorders by Naik, Sandhia, Jones, Emma L, Annesi, Grazia, Levy, Emile, Patel, Hetal N, Islam, Suhail A, Bonney, Stephanie A, Jones, Bethan, Myrdal, Urban, Infante, Recaredo, Naoumova, Rossitza P, Quattrone, Aldo, Roy, Claude C, Mensenkamp, Arjen R, Eichenbaum-Voline, Sophie, Shoulders, Carol C, Rudling, Mats, Angelin, Bo, Freemont, Paul S, Meadows, Nigel, Scott, James

“…Dietary fat is an important source of nutrition. Here we identify eight mutations in SARA2 that are associated with three severe disorders of fat…”
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Cold exposure increases cyclic guanosine monophosphate in healthy women but not in women with Raynaud's phenomenon by Leppert, J, Ringqvist, A, Ahlner, J, Myrdal, U, Sørensen, S, Ringqvist, I

“…To investigate influence of whole-body cooling on cyclic GMP (cGMP) in women with Raynaud's phenomenon and in healthy women. The study was performed as an…”
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Non-HLA type 1 diabetes genes modulate disease risk together with HLA-DQ and islet autoantibodies by Maziarz, M, Hagopian, W, Palmer, J P, Sanjeevi, C B, Kockum, I, Breslow, N, Lernmark, Å

“…The possible interrelations between human leukocyte antigen (HLA)-DQ, non-HLA single-nucleotide polymorphisms (SNPs) and islet autoantibodies were investigated…”
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Plasma nitric oxide metabolite in women with primary Raynaud's phenomenon and in healthy subjects by Ringqvist, Å., Leppert, J., Myrdal, U., Ahlner, J., Ringqvist, I., Wennmalm, Å.

“…Primary Raynaud's phenomenon (PRP) is characterized by cold‐ or stressinduced transient attacks of impaired skin circulation in fingers and/or toes. PRP…”
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Sympathetic activation after two weeks of nifedipine treatment in primary Raynaud's patients and controls by LEPPERT, J, NILSSON, H, MYRDAL, U, EDVINSSON, L, HEDNER, T, RINGQVIST, I

“…The effect of a standardized cold pressor test on circulating noradrenaline and neuropeptide-Y-like immunoreactivity was investigated in 12 women with primary…”
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Variability in the CIITA gene interacts with HLA in multiple sclerosis by Gyllenberg, A, Piehl, F, Alfredsson, L, Hillert, J, Bomfim, I L, Padyukov, L, Orho-Melander, M, Lindholm, E, Landin-Olsson, M, Lernmark, Å, Olsson, T, Kockum, I

“…The human leukocyte antigen (HLA) is the main genetic determinant of multiple sclerosis (MS) risk. Within the HLA, the class II HLA-DRB1*15:01 allele exerts a…”
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Magnesium sulphate infusion decreases circulating calcitonin gene-related peptide (CGRP) in women with primary Raynaud's phenomenon by Myrdal, U, Leppert, J, Edvinsson, L, Ekman, R, Hedner, T, Nilsson, H, Ringqvist, I

“…The effects of two different vasodilating agents (MgSO4 infusion and the calcium antagonist nifedipine) on circulating levels of calcitonin gene-related…”
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A boy with complete triploidy and unusually long survival by Arvidsson, C G, Hamberg, H, Johnsson, H, Myrdal, U, Annerén, G, Brun, A

“…A boy with complete triploidy and extensive external and internal congenital malformations who survived for almost seven months is presented. He was born after…”
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CRYAB -650 C>G (rs2234702) affects susceptibility to Type 1 diabetes and IAA-positivity in Swedish population by Sun, Chengjun, Sedimbi, Saikiran K, Ashok, Ayyappa K, Sanjeevi, Carani B

“…Abstract Background Single nucleotide polymorphisms (SNPs) in the promoter region of CRYAB gene have been associated with in multiple sclerosis. CRYAB gene,…”
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The risk conferred by HLA-DR and DQ for type 1 diabetes in 0-35-year age group are different in different regions of Sweden by Sanjeevi, Carani B., Sedimbi, Saikiran K., Landin-Olsson, Mona, Kockum, Ingrid, Lernmark, Åke, Aili, M., Bååth, L.E., Carlsson, E., Edenwall, H., Forsander, G., Granström, B.W., Gustavsson, I., Hanås, R., Hellenberg, L., Hellgren, H., Holmberg, E., Hörnell, H., Ivarsson, Sten-A., Johansson, C., Jonsell, G., Kockum, K., Lindblad, B., Lindh, A., Ludvigsson, J., Myrdal, U., Neiderud, J., Segnestam, K., Sjöblad, S., Skogsberg, L., Strömberg, L., Ståhle, U., Thalme, B., Tullus, K., Tuvemo, Torsten, Wallensteen, M., Westphal, O., Dahlquist, G., Åman, J.

“…HLA DR4-DQ8 and DR3-DQ2 haplotypes account for 89% of newly diagnosed cases of type 1 diabetes (T1D) in Sweden. The presence of a single copy of DQ6 confers…”
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P0584 FOCAL LOSS OF DUODENAL ENTEROCYTE HEPARAN SULPHATE PROTEOGLYCANS MAY CONTRIBUTE TO PROTEIN‐LOSING ENTEROPATHY AFTER FONTAN SURGERY by Murch, S. H., Salvestrini, C., Myrdal, U., Holmgren, D., Spray, C., Bode, L., Freeze, H.

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