Citations

Showing 10 of 108036 citations.

Effective use of panobinostat in combination with other active agents in myeloma in a novel five‐drug combination: Case report and interesting observations
Rajan, Archana , Buadi, Francis K. , Rajkumar, Vincent, Rajkumar, S. Vincent

Mayo Clinic

American Journal of Hematology | November 17, 2015 | Volume: 91 | Issue: 2 | Pages: No page available

10.1002/ajh.24244 | PMID 26572926 Get It

Gastrointestinal: Positron emission tomography/computed tomography imaging of peritoneal carcinomatosis secondary to prostate adenocarcinoma
Sridhar, S. , Sridhar, S, Nguyen, Ba D.

Mayo Clinic

Journal of Gastroenterology and Hepatology | November 17, 2015 | Volume: 31 | Issue: 4 | Pages: 704-704

10.1111/jgh.13227 | PMID 26574145 Get It

Simplified conversion method for unified Parkinson's disease rating scale motor examinations
Hentz, Joseph G. , Mehta, Shyamal H. , Shill, Holly A. , Driver‐Dunckley, Erika, Beach, Thomas G. , Driver‐Dunckley, Erika , Adler, Charles H.

Mayo Clinic

Movement Disorders | November 17, 2015 | Volume: 30 | Issue: 14 | Pages: 1967-1970

10.1002/mds.26435 | PMID 26779608 Get It

ABSTRACTBackgroundWe evaluated a simplified method for converting Unified Parkinson's Disease Rating Scale Part III Motor Examination total scores (UPDRS III) to the International Parkinson and Movement Disorder Society's (MDS) revised version of the scores.MethodsPD patients in the Arizona Study of Aging and Neurodegenerative Disorders were assessed with both scales. The accuracy of the predicted scores was assessed using regression modeling, classical intraclass correlation coefficients, and the Bland‐Altman method.ResultsThere was strong correlation between the two scores. Adding 7 points to a UPDRS III total score performed approximately as well as previously published conversion formulas (intraclass correlation: 0.96). The adjusted score is expected to be within 3 points of the MDS‐UPDRS III score 50% of the time and within 9 points 95% of the time.ConclusionsSimply adding 7 points to a UPDRS III total score provides a good approximation of the MDS‐UPDRS III total score. © 2015 International Parkinson and Movement Disorder Society
Subcutaneous infusion of kisspeptin‐54 stimulates gonadotrophin release in women and the response correlates with basal oestradiol levels
Narayanaswamy, Shakunthala, Jayasena, Channa , Ng, Noel , Ratnasabapathy, Risheka , Prague, Julia , Papadopoulou, Deborah , Abbara, Ali , Comninos, Alexander , Bassett, Paul , Bloom, Stephen R. , Veldhuis, Johannes D. , Dhillo, Waljit S. , Jayasena, Channa N

Mayo Clinic

Clinical Endocrinology | November 17, 2015 | Volume: 84 | Issue: 6 | Pages: 939-945

10.1111/cen.12977 | PMID 26572695 Get It

SummaryBackground and objectiveKisspeptin stimulates hypothalamic GnRH secretion resulting in gonadotrophin release and has potential as a future therapeutic. Chronic subcutaneous infusion of kisspeptin via a pump (similar to an insulin pump) may provide an alternative route of administration in the future. We investigated for the first time in humans, the gonadotrophin response to subcutaneous (SC) infusions of kisspeptin‐54 in healthy women. Women are markedly more responsive to exogenous kisspeptin in the late follicular phase preovulation when oestradiol levels are naturally high. Therefore, we further investigated whether there was a correlation between baseline oestradiol levels and LH response to kisspeptin.Design and patientsA prospective, single‐blinded placebo‐controlled study. Healthy women (n = 4) received an 8‐h SC infusion of kisspeptin‐54 0·1, 0·3 or 1·0 nmol/kg/h or saline in the early follicular phase of 4 separate menstrual cycles. Gonadotrophins and oestradiol were measured every 10 min during the infusions.ResultsSC infusion of kisspeptin‐54 increased LH and FSH. The LH response to SC infusion of kisspeptin‐54 (0·3 and 1·0 nmol/kg/h) positively correlated with baseline oestradiol levels (P < 0·001). Further statistical analyses showed that in the 1·0 nmol/kg/h group, a 100pmol/l rise in baseline oestradiol was associated with a 1·0 IU/l increase in LH.ConclusionsKisspeptin administered via a SC infusion could be a viable future therapeutic route of administration for patients with infertility. Baseline oestradiol levels may be an important determinant of the gonadotrophin response to kisspeptin treatment in women and should be taken into consideration when evaluating gonadotrophin response.
Impact of delay between imaging and treatment in patients with potentially curable pancreatic cancer
Sanjeevi, Srinivas , Lundell, Lars, Kartalis, Nikolaos , Andrén‐Sandberg, Åke, Blomberg, John, Chiaro, Marco Del , Ansorge, Christoph, Ivanics, Tommy

Mayo Clinic

Journal of British Surgery | November 17, 2015 | Volume: 103 | Issue: 3 | Pages: 267-275

10.1002/bjs.10046 | PMID 26572509 Get It

Abstract Background Locoregional pancreatic ductal adenocarcinoma (PDAC) may progress rapidly and/or disseminate despite having an early stage at diagnostic imaging. A prolonged interval from imaging to resection might represent a risk factor for encountering tumour progression at laparotomy. The aim of this study was to determine the therapeutic window for timely surgical intervention. Methods This observational cohort study included patients with histologically confirmed PDAC scheduled for resection with curative intent from 2008 to 2014. The impact of imaging-to-resection/reassessment (IR) interval, vascular involvement and tumour size on local tumour progression or presence of metastases at reimaging or laparotomy was evaluated using univariable and multivariable regression. Risk estimates were approximated using hazard ratios (HRs). Results Median IR interval was 42 days. Of 349 patients scheduled for resection, 82 had unresectable disease (resectability rate 76·5 per cent). The unresectability rate was zero when the IR interval was 22 days or shorter, and was lower for an IR interval of 32 days or less compared with longer waiting times (13 versus 26·2 per cent; HR 0·42, P = 0·021). It was also lower for tumours smaller than 30 mm than for larger tumours (13·9 versus 32·5 per cent; HR 0·34, P &lt; 0·001). Tumours with no or minor vascular involvement showed decreased rates of unresectable disease (20·6 per cent versus 38 per cent when there was major or combined vascular involvement; HR 0·43, P = 0·007). However, this failed to reach statistical significance on multivariable analysis (P = 0·411), in contrast to IR interval (P = 0·028) and tumour size (P &lt; 0·001). Conclusion Operation within 32 days of diagnostic imaging reduced the risk of tumour progression to unresectable disease by half compared with a longer waiting time. The results of this study highlight the importance of efficient clinical PDAC management.
Bone Marrow Concentrate Improves Early Cartilage Phase Maturation of a Scaffold Plug in the Knee
Krych, Aaron J. , Nawabi, Danyal H. , Farshad‐Amacker, Nadja A. , Jones, Kristofer J. , Maak, Travis G. , Potter, Hollis G. , Williams, Riley J. , Krych, Aaron J

Mayo Clinic

The American Journal of Sports Medicine | November 16, 2015 | Volume: 44 | Issue: 1 | Pages: 91-98

10.1177/0363546515609597 | PMID 26574602 Get It

Background: Limited information exists on the clinical use of a synthetic osteochondral scaffold plug for cartilage restoration in the knee. Purpose/Hypothesis: The purpose of this study was to compare the early magnetic resonance imaging (MRI) appearance, including quantitative T2 values, between cartilage defects treated with a scaffold versus a scaffold with platelet-rich plasma (PRP) or bone marrow aspirate concentrate (BMAC). The hypothesis was that the addition of PRP or BMAC would result in an improved cartilage appearance. Study Design: Cohort study; Level of evidence, 3. Methods: Forty-six patients with full-thickness cartilage defects of the femur were surgically treated with a control scaffold (n = 11), scaffold with PRP (n = 23), or scaffold with BMAC (n = 12) and were followed prospectively. Patients underwent MRI with a qualitative assessment and quantitative T2 mapping at 12 months after surgery. An image assessment was performed retrospectively by a blinded musculoskeletal radiologist. The cartilage phase was measured by cartilage fill and quantitative T2 values on MRI. A comparison between groups after cartilage repair was performed. Results: The control scaffold group consisted of 8 male and 3 female patients (mean age, 38 years; mean body mass index [BMI], 25 kg/m 2 ), the PRP group had 15 male and 8 female patients (mean age, 39 years; mean BMI, 26 kg/m 2 ), and the BMAC group consisted of 8 male and 4 female patients (mean age, 36 years; mean BMI, 26 kg/m 2 ). The PRP-treated ( P = .002) and BMAC-treated ( P = .03) scaffolds had superior cartilage fill compared with the control group. With quantitative methods, the PRP group demonstrated a mean T2 value (49.1 ms) that was similar to that of the control scaffold group (42.7 ms; P = .07), but the BMAC group demonstrated a mean T2 value (60.5 ms) closer to that of superficial hyaline cartilage ( P = .01). The stratification of T2 values between the deep and superficial zones was not observed in any of the groups. Conclusion: In this comparative study, patients treated with scaffold implantation augmented with BMAC had improved cartilage maturation with greater fill and mean T2 values closer to that of superficial native hyaline cartilage at 12 months. Further work will determine if this translates into improved clinical outcomes.
Globular Glial Tauopathy Presenting as Semantic Variant Primary Progressive Aphasia
Graff‐Radford, Jonathan , Josephs, Keith A. , Parisi, Joseph E. , Dickson, Dennis W. , Giannini, Caterina , Boeve, Bradley F.

Mayo Clinic

JAMA Neurology | November 16, 2015 | Volume: 73 | Issue: 1 | Pages: 123

10.1001/jamaneurol.2015.2711 | PMID 26571405 Get It

Clinical-Genetic Associations in the Prospective Huntington at Risk Observational Study (PHAROS)
Investigators, The Huntington Study Group PHAROS, Biglan, Kevin , Shoulson, Ira , Kieburtz, Karl , Oakes, David , Kayson, Elise, Shinaman, M. Aileen, Zhao, Hongwei , Romer, Megan, Young, Anne B., Hersch, Steven M. , Penney, Jack, Marder, Karen, Paulsen, Jane S. , Quaid, Kimberly A., Siemers, Eric , Mallonee, William, Suter, Greg, Dubinsky, Richard , Nance, Martha , Bundlie, Scott R., Radtke, Dawn, Kostyk, Sandra K. , Baic, Corrine, Walker, Francis O. , Hunt, Victoria, Chouinard, Sylvain, Wood‐Siverio, Cathy, Corey‐Bloom, Jody , Peavy, Guerry M. , Moskowitz, Carol, Wesson, Melissa, Samii, Ali, Bird, Thomas D. , Lipe, Hillary, Blindauer, Karen, Marshall, Frederick J., Zimmerman, Carol, Goldstein, Jody, Rosas, Diana, Novák, Péter , Caviness, John N., Duffy, Amy, Wheelock, Vicki, Tempkin, Teresa, Seeberger, Lauren , Albin, Roger L. , Racette, Brad A. , Perlman, Susan , Bordelon, Yvette , Martin, W. R. Wayne , Wieler, Marguerite , Raymond, Lynn A. , Decolongon, Joji, Hunter, Christine , Hauser, Robert A. , Furtado, Sarah , Suchowersky, Oksana , Klimek, Mary Lou, Guttman, Mark, Sethna, Rustom, Feigin, Andrew, Cox, Marie, Shannon, Barbara , Percy, Alan K. , Dure, Leon , Harrison, Madaline B. , Higgins, Donald S. , Molho, Eric , Nickerson, Constance, Evans, Sharon, Hobson, Douglas, Singer, Carlos , Gálvez-Jiménez, Néstor, Shannon, Kathleen M. , Comella, Cynthia , Ross, Christopher A. , Hogarth, Penelope , Weiner, William J., Como, Peter G., Kumar, Rajeev , Cotto, Candace, Stout, Julie C. , Brocht, Alicia, Watts, Arthur, Eberly, Shirley , Weaver, Christine , Gusella, James F. , MacDonald, Marcy E., Fahn, Stanley, Shults, Clifford W., Caviness, John, Investigators, The Huntington Study Group PHAROS, Tanner, Caroline M. , Gray, Carolyn Steele , Baic, Corrine L., Caress, James B. , O’Neill, Christine J. , Factor, Stewart Alan , Greenamyre, J. Timothy , Song, David , Adler, Charles H. , Richman, David P. , Chou, Kelvin L. , Perlmutter, Joel S. , Leavitt, Blair R. , Clarke, Lorne A. , Jankovic, Joseph J. , Sanchez‐Ramos, Juan , Johnson, William , Saint‐Hilaire, Marie , Testa, Claudia M. , Rosenblatt, Adam E , Foroud, Tatiana , Myers, Richard H. , Ross, Christopher A , Hauser, Robert A

Mayo Clinic

JAMA Neurology | November 16, 2015 | Volume: 73 | Issue: 1 | Pages: 102

10.1001/jamaneurol.2015.2736 | PMID 26569098 Get It

Association Between Olfactory Dysfunction and Amnestic Mild Cognitive Impairment and Alzheimer Disease Dementia
Roberts, Rosebud O., Christianson, Teresa J., Kremers, Walter K. , Mielke, Michelle M. , Vassilaki, Maria , Alhurani, Rabe E., Geda, Yonas E. , Petersen, Ronald C. , Christianson, Teresa J H, Machulda, Mary M. , Knopman, David S. , Mielke, Michelle M , Geda, Yonas E , Kremers, Walter K

Mayo Clinic

JAMA Neurology | November 16, 2015 | Volume: 73 | Issue: 1 | Pages: 93

10.1001/jamaneurol.2015.2952 | PMID 26569387 Get It

Letter from the Editor-in-Chief
Dodick, David W.

Mayo Clinic

Cephalalgia | November 16, 2015 | Volume: 35 | Issue: 14 | Pages: 1239-1239

10.1177/0333102415616976 | PMID 26574595 Get It