Citations

Showing 10 of 108015 citations.

Commentary
Frazee, Erin N, Frazee, Erin N, Kashani, Kianoush

Mayo Clinic

Clinical Chemistry | May 29, 2015 | Volume: 61 | Issue: 6 | Pages: 808-808

10.1373/clinchem.2014.231829 Get It

Transcatheter closure of postmyocardial infarction, iatrogenic, and postoperative ventricular septal defects: The Mayo Clinic experience
Egbe, Alexander C. , Poterucha, Joseph T., Rihal, Charanjit S. , Taggart, Nathaniel W. , Cetta, Frank , Pollak, Peter , Reeder, Guy S., Hagler, Donald J. , Cabalka, Allison K. , Pollak, Peter M, Rihal, Charanjit S. , Taggart, Nathaniel W

Mayo Clinic

Catheterization and Cardiovascular Interventions | May 29, 2015 | Volume: 86 | Issue: 7 | Pages: 1264-1270

10.1002/ccd.25989 | PMID 26033272 Get It

Objectives To determine event‐free survival after transcatheter closure of ventricular septal defect (VSD), and to identify predictors of adverse events (AE) in post myocardial infarction VSD (post‐MI VSD) subgroup. Background There are limited data on mid‐term follow‐up after transcatheter VSD closure. Methods Retrospective review of 27 cases of transcatheter VSD closure (post‐MI = 18 and non‐ischemic = 9) performed from 1999 to 2013. We defined AE as death, device embolization, hemolysis requiring blood transfusion, heart block and reintervention. Results In the post‐MI VSD subgroup, mean age and follow‐up was 69 ± 11 and 7.3 ± 7 years, respectively. AE occurred in 8 (44%) patients (death‐3, device embolization‐1, hemolysis‐1, surgical VSD closure‐2, reintervention‐1). Event‐free survival was 56% at 1 month and 5 years, and all AE occurred in the periprocedural period. Cardiogenic shock (HR: 3.21, CI: 1.82–5.41, P = 0.002), and VSD closure in acute phase (HR: 2.14, CI: 1.12–4.31, P = 0.004) were independent predictors of AE. In the non‐ischemic VSD subgroup, mean age and follow‐up was 49 ± 15 and 8.7 ± 8 years, respectively. AE occurred in 3 (33%) patients (late death‐1, surgical VSD closure‐2). For the entire cohort, freedom from death was 89% and 85% at 1 month and 5 years, and event‐free survival was 70% and 61% at 1 month and 5 years. Conclusions Transcatheter closure of post‐MI VSD carries a moderate risk of periprocedural complications but low event rates afterwards. By comparison, device closure of non‐ischemic VSD has lower periprocedural morbidity but some patients continued to experience AE during follow‐up. © 2015 Wiley Periodicals, Inc.
Aqueous Humor Outflow: Dynamics and Disease
Chowdhury, Uttio Roy, Hann, Cheryl R., Fautsch, Michael P. , Roy Chowdhury, Uttio, Stamer, William Daniel

Mayo Clinic

Investigative Opthalmology & Visual Science | May 29, 2015 | Volume: 56 | Issue: 5 | Pages: 2993

10.1167/iovs.15-16744 | PMID 26024085 Get It

Traumatic anterior cervical pseudomeningocele causing intracranial hypotension successfully treated with blood patch: case report
Takahashi, Edwin A. , Eckel, Laurence J. , Schwartz, Kara M., Diehn, Felix E. , Hunt, Christopher H. , Daniels, David J. , Takahashi, Edwin A

Mayo Clinic

Journal of Neurosurgery: Spine | May 29, 2015 | Volume: 23 | Issue: 3 | Pages: 303-305

10.3171/2014.12.spine14735 | PMID 26023899 Get It

Cervical pseudomeningocele is a rare complication of trauma. It develops when an extradural collection of cerebrospinal fluid (CSF) develops after a dural breach. The authors present the unusual case of a 33-year-old man with progressive headache, neck pain, mental status changes, and cardiopulmonary instability after polytrauma sustained from a motorcycle-versus-deer collision, without improvement during a 5-day hospitalization. Magnetic resonance imaging revealed a collection of CSF anterior to the cervical thecal sac compatible with an anterior cervical pseudomeningocele. A nontargeted epidural blood patch was performed with subsequent resolution of the patient's symptoms. Anterior cervical pseudomeningoceles are usually asymptomatic; however, these lesions can cause orthostatic headaches, neck pain, and cardiopulmonary compromise, as it did in the featured patient. Pseudomeningoceles should be included in the differential diagnosis for posttrauma patients with progressive neurological decline or postural headache, and blood patch may be an effective minimally invasive treatment.
Electronic Cigarettes and Cardiovascular Risk: Hype Or Up in smoke?
Nelluri, B.K., Murphy, Katie , Mookadam, Farouk, Nelluri, Bhargava Krishna, Mookadam, Farouk

Mayo Clinic

Future Cardiology | May 29, 2015 | Volume: 11 | Issue: 3 | Pages: 271-273

10.2217/fca.15.13 | PMID 26021631 Get It

Common Pesticide, Dichlorodiphenyltrichloroethane (DDT), Increases Amyloid-β Levels by Impairing the Function of ABCA1 and IDE: Implication for Alzheimer’s Disease
Li, Gongbo , Kim, Chaeyoung, Kim, Jaekwang , Yoon, Hyejin , Zhou, Huadong , Kim, Jungsu, Kim, Jungsu, Kim, Jungsu , Kim, Jungsu, Kim, Jungsu, Kim, Jungsu

Mayo Clinic

Journal of Alzheimer's Disease | May 29, 2015 | Volume: 46 | Issue: 1 | Pages: 109-122

10.3233/jad-150024 | PMID 25720399 Get It

Therapeutic Effect on Bladder Cancer with a Conditionally Replicating Oncolytic Virus Derived from Type II Herpes Simplex Virus
Joo, Kwan Joong , Zhang, Xiaoliu , Li, Hongtao , Lerner, Seth P.

Mayo Clinic

Bladder Cancer | May 29, 2015 | Volume: 1 | Issue: 1 | Pages: 81-90

10.3233/blc-150013 | PMID 30561438 Get It

Purpose: Despite recent improvements, resistance to traditional immunotherapy or chemotherapy is still common in patients with bladder cancer. We constructed an oncolytic virus from herpes simplex virus type II (HSV-2), which selectively targets tumor cells with an activated Ras signaling pathway. We evaluated the antitumor effect of this oncolytic HSV-2 (FusOn-H2) against bladder cancer, and compared with that of a first generation oncolytic virus derived from HSV-1 (Baco-1). Materials and methods: We established bladder tumor at the orthotopic site in C3H/He mice using the MBT-2 cells. Baco-1 or FusOn-H2 was instilled into the bladder through the urethra respectively. Tumor volume and weight were recorded by the end of the experiment. Animal spleens were also collected to determine if any anti-tumor immunity was elicited during virotherapy in this syngeneic bladder cancer model. Results: Two instillations of the oncolytic HSVs into bladder of tumor-bearing mice almost completely eradicated the tumor in majority of tumor bearing mice. The results of tumor-specific cytotoxic T lymphocyte activity assay showed that tumor destruction by oncolytic viruses in vivo, especially by the FusOn-H2, induced potent anti-tumor immune responses. Conclusion: Oncolytic virus derived from HSV-2 has potent anti-tumor activity against bladder cancer. Oncolytic effect of this virus in vivo induces tumor specific cellular immunity that further enhances the overall anti-tumor activity. Translating this novel virotherapy into the clinic could present an alternative intravesical therapy strategy for patients with bladder cancer.
Linear synthesis and immunological properties of a fully synthetic vaccine candidate containing a sialylated MUC1 glycopeptide
Thompson, Pamela, Lakshminarayanan, Vani , Supekar, Nitin T. , Cohen, Peter A. , Wolfert, Margreet A. , Gendler, Sandra , Boons, Geert‐Jan , Bradley, Judy Martina

Mayo Clinic

Chemical Communications | May 29, 2015 | Volume: 51 | Issue: 50 | Pages: 10214-10217

10.1039/c5cc02199e | PMID 26022217 Get It

A strategically designed sialyl-Tn building block was synthesized in a stereospecific manner for the rapid linear construction of a glycolipopeptide cancer vaccine.
Atrial Fibrillation Pathophysiology and Prognosis
Siontis, Konstantinos C. , Geske, Jeffrey B. , Gersh, Bernard J. , Geske, Jeffrey B

Mayo Clinic

Circulation: Cardiovascular Imaging | May 29, 2015 | Volume: 8 | Issue: 6 | Pages: No page available

10.1161/circimaging.115.003020 | PMID 26022381 Get It

Draft Genome Sequences of 24 Microbial Strains Assembled from Direct Sequencing from 4 Stool Samples
Jeraldo, Patricio , Hernandez, Alvaro G. , White, Bryan A. , O’Brien, Daniel R. , Ahlquist, David A. , Boardman, Lisa, Ahlquist, David, Boardman, Lisa, Chia, Nicholas , Jeraldo, Patricio R

Mayo Clinic

Genome Announcements | May 29, 2015 | Volume: 3 | Issue: 3 | Pages: No page available

10.1128/genomea.00526-15 | PMID 26021920 Get It

ABSTRACT The ability to assemble genomes from metagenomic sequencing avoids the need for culture and any associated culture biases. We assembled 24 essentially complete draft genomes from metagenomic pair-end and size-selected mate pair sequencing from 4 stool samples, 2 from subjects diagnosed with colorectal cancer and 2 from healthy controls.