Treatment options and patient perspectives in the management of fibromyalgia: future trends

per Lawson, Kim
Publicat 2008

A Brief Review of the Pharmacology of Amitriptyline and Clinical Outcomes in Treating Fibromyalgia

per Lawson, Kim
Publicat a Biomedicines (2017)

Comorbid Conditions, Mental Health and Cognitive Functions in Adults with Fibromyalgia

per Taylor, Sophie, Furness, Penny, Ashe, Simon, Haywood-Small, Sarah, Lawson, Kim
Publicat a West J Nurs Res (2020)

A qualitative exploration of the experiences of living with and being treated for fibromyalgia

per Ashe, Simon C, Furness, Penny J, Taylor, Sophie J, Haywood-Small, Sarah, Lawson, Kim
Publicat a Health Psychol Open (2017)

What causes fibromyalgia? An online survey of patient perspectives

per Furness, Penny J, Vogt, Katharina, Ashe, Simon, Taylor, Sophie, Haywood-Small, Sarah, Lawson, Kim
Publicat a Health Psychol Open (2018)

Association between hyperemesis gravidarum and psychological symptoms, psychosocial outcomes and infant bonding: a two-point prospective case–control multicentre survey study in an...

per Mitchell-Jones, Nicola, Lawson, Kim, Bobdiwala, Shabnam, Farren, Jessica Alice, Tobias, Aurelio, Bourne, Tom, Bottomley, Cecilia
Publicat a BMJ Open (2020)

Impact of adding a single allele in the 9p21 locus to traditional risk factors on reclassification of coronary heart disease risk and implications for lipid-modifying therapy in th...

per Brautbar, Ariel, Ballantyne, Christie M, Lawson, Kim, Nambi, Vijay, Chambless, Lloyd, Folsom, Aaron R, Willerson, James T., Boerwinkle, Eric
Publicat 2009

The 9p21 genetic variant is additive to carotid intima media thickness and plaque in improving coronary heart disease risk prediction in white participants of the Atherosclerosis R...

per Nambi, Vijay, Boerwinkle, Eric, Lawson, Kim, Brautbar, Ariel, Chambless, Lloyd, Franeschini, Nora, North, Kari E., Virani, Salim S, Folsom, Aaron R, Ballantyne, Christie M
Publicat 2012

Single-Nucleotide Polymorphisms in LPA Explain Most of the Ancestry-Specific Variation in Lp(a) Levels in African Americans

per Deo, Rahul C., Wilson, James G., Xing, Chao, Lawson, Kim, Kao, W. H. Linda, Reich, David, Tandon, Arti, Akylbekova, Ermeg, Patterson, Nick, Mosley, Thomas H., Boerwinkle, Eric, Taylor, Herman A.
Publicat 2011

Challenges in Image-Guided Therapy System Design

per DiMaio, Simon, Kapur, Tina, Cleary, Kevin, Aylward, Stephen, Kazanzides, Peter, Vosburgh, Kirby, Ellis, Randy, Duncan, Jim, Farahani, Keyvan, Lemke, Heinz, Peters, Terry, Lorensen, Bill, Gobbi, David, Haller, John, Clarke, Larry, Pizer, Steve, Galloway, Bob, Fichtinger, Gabor, Hata, Noby, Lawson, Kim, Tempany, Clare, Kikinis, Ron, Jolesz, Ferenc
Publicat 2007

Exome sequence analysis suggests genetic burden contributes to phenotypic variability and complex neuropathy

per Gonzaga-Jauregui, Claudia, Harel, Tamar, Gambin, Tomasz, Kousi, Maria, Griffin, Laurie B., Francescatto, Ludmila, Ozes, Burcak, Karaca, Ender, Jhangiani, Shalini, Bainbridge, Matthew N., Lawson, Kim S., Pehlivan, Davut, Okamoto, Yuji, Withers, Marjorie, Mancias, Pedro, Slavotinek, Anne, Reitnauer, Pamela J, Goksungur, Meryem T., Shy, Michael, Crawford, Thomas O., Koenig, Michel, Willer, Jason, Flores, Brittany N., Pediaditrakis, Igor, Us, Onder, Wiszniewski, Wojciech, Parman, Yesim, Antonellis, Anthony, Muzny, Donna M., Katsanis, Nicholas, Battaloglu, Esra, Boerwinkle, Eric, Gibbs, Richard A., Lupski, James R.
Publicat a Cell Rep (2015)

Diagnostic Yield of Sequencing Familial Hypercholesterolemia Genes in Severe Hypercholesterolemia

per Khera, Amit V., Won, Hong-Hee, Peloso, Gina M., Lawson, Kim S., Bartz, Traci M., Deng, Xuan, van Leeuwen, Elisabeth M., Natarajan, Pradeep, Emdin, Connor A., Bick, Alexander G., Morrison, Alanna C., Brody, Jennifer A., Gupta, Namrata, Nomura, Akihiro, Kessler, Thorsten, Duga, Stefano, Bis, Joshua C., van Duijn, Cornelia M., Cupples, L. Adrienne, Psaty, Bruce, Rader, Daniel J., Danesh, John, Schunkert, Heribert, McPherson, Ruth, Farrall, Martin, Watkins, Hugh, Lander, Eric, Wilson, James G., Correa, Adolfo, Boerwinkle, Eric, Merlini, Piera Angelica, Ardissino, Diego, Saleheen, Danish, Gabriel, Stacey, Kathiresan, Sekar
Publicat a J Am Coll Cardiol (2016)

Association of Low-Frequency and Rare Coding-Sequence Variants with Blood Lipids and Coronary Heart Disease in 56,000 Whites and Blacks

per Peloso, Gina M., Auer, Paul L., Bis, Joshua C., Voorman, Arend, Morrison, Alanna C., Stitziel, Nathan O., Brody, Jennifer A., Khetarpal, Sumeet A., Crosby, Jacy R., Fornage, Myriam, Isaacs, Aaron, Jakobsdottir, Johanna, Feitosa, Mary F., Davies, Gail, Huffman, Jennifer E., Manichaikul, Ani, Davis, Brian, Lohman, Kurt, Joon, Aron Y., Smith, Albert V., Grove, Megan L., Zanoni, Paolo, Redon, Valeska, Demissie, Serkalem, Lawson, Kim, Peters, Ulrike, Carlson, Christopher, Jackson, Rebecca D., Ryckman, Kelli K., Mackey, Rachel H., Robinson, Jennifer G., Siscovick, David S., Schreiner, Pamela J., Mychaleckyj, Josyf C., Pankow, James S., Hofman, Albert, Uitterlinden, Andre G., Harris, Tamara B., Taylor, Kent D., Stafford, Jeanette M., Reynolds, Lindsay M., Marioni, Riccardo E., Dehghan, Abbas, Franco, Oscar H., Patel, Aniruddh P., Lu, Yingchang, Hindy, George, Gottesman, Omri, Bottinger, Erwin P., Melander, Olle, Orho-Melander, Marju, Loos, Ruth J.F., Duga, Stefano, Merlini, Piera Angelica, Farrall, Martin, Goel, Anuj, Asselta, Rosanna, Girelli, Domenico, Martinelli, Nicola, Shah, Svati H., Kraus, William E., Li, Mingyao, Rader, Daniel J., Reilly, Muredach P., McPherson, Ruth, Watkins, Hugh, Ardissino, Diego, Zhang, Qunyuan, Wang, Judy, Tsai, Michael Y., Taylor, Herman A., Correa, Adolfo, Griswold, Michael E., Lange, Leslie A., Starr, John M., Rudan, Igor, Eiriksdottir, Gudny, Launer, Lenore J., Ordovas, Jose M., Levy, Daniel, Chen, Y.-D. Ida, Reiner, Alexander P., Hayward, Caroline, Polasek, Ozren, Deary, Ian J., Borecki, Ingrid B., Liu, Yongmei, Gudnason, Vilmundur, Wilson, James G., van Duijn, Cornelia M., Kooperberg, Charles, Rich, Stephen S., Psaty, Bruce M., Rotter, Jerome I., O’Donnell, Christopher J., Rice, Kenneth, Boerwinkle, Eric, Kathiresan, Sekar, Cupples, L. Adrienne
Publicat 2014