Publications by authors named "Warrick A"

Authors of previous studies of patients with acute hamstring strains have reported injury to the biceps femoris and semitendinosus (ST) in 50% to 100% and 0% to 30%, respectively. This retrospective case series of hamstring injuries in National Collegiate Athletic Association Division I collegiate athletes exhibited an injury pattern on ultrasound imaging that differed from what would be expected based on prior literature. We examined ultrasound images of 38 athletes with acute hamstring strains for injury location (proximal muscle, proximal myotendinous junction, midportion of muscle, distal muscle) and affected muscles (biceps femoris, ST, or semimembranosus).

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Background: Short and long-term health consequences surrounding Low Energy Availability can be mitigated by recognizing the risk factors and making early diagnosis of the Female Athlete Triad (Triad) and Relative Energy Deficiency in Sport (RED-S). While awareness of the Triad among physicians and allied health professionals has been studied, there are very few studies that assess physician awareness of both the Triad and RED-S.

Methods: Our study assesses Low Energy Availability, the Triad, and RED-S knowledge with an electronic survey, educational handout, and follow up survey among physicians across multiple specialties at a single academic institution.

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Neurogenic thoracic outlet syndrome (NTOS) is an etiologically and clinically diverse disorder caused by compression of the brachial plexus traversing the thoracic outlet. Athletes who perform repetitive overhead activities are at risk of developing NTOS with sport-specific symptoms. This article reviews the controversial NTOS nomenclature, common sites of anatomic compression, and red flag symptoms that require immediate intervention.

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Ventricular septal defects (VSDs) are the most common congenital cardiac abnormalities occurring in five out of every 1000 births. Supracristal VSDs (located above the crista supraventicularis) are very rare and comprise only 2%-3% of all VSDs. Many VSDs close spontaneously during childhood; however, a substantial portion may not and are present in adulthood with a myriad of symptoms.

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The purpose of this study was to identify plasma metabolites associated with superior endurance running performance. In 2016, participants at the Western States Endurance Run (WSER), a 100-mile (161-km) foot race, underwent non-targeted metabolomic testing of their post-race plasma. Metabolites associated with faster finish times were identified.

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Objective: The inflammatory response elicited by robotically enhanced coronary artery bypass grafting (r-CABG) has not been well described. When r-CABG is performed as part of hybrid coronary revascularization, the inflammatory milieu and the timing of percutaneous coronary intervention may affect the stent patency negatively in the short and long term. The goal of this study was to describe the extent and time course of cytokine release after r-CABG compared with conventional CABG (c-CABG) and to elucidate the optimal timing for r-CABG in the setting of hybrid coronary revascularization for a future study.

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Background: Smokers are a stigmatized population, but an important population to reach for the purpose of research. Therefore, innovative recruitment methods are needed that are both cost-effective and efficacious in recruiting this population.

Objective: The aim of the present article was to evaluate the feasibility of Facebook-targeted advertisement to recruit long-term smokers eligible for lung cancer screening for a descriptive, cross-sectional survey.

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Article Synopsis
  • * A next-generation sequencing method using a multiplex PCR-based panel effectively identifies fusion transcripts from 19 driver genes and 94 partner genes associated with solid tumors, including control assays for detecting unidentified fusions.
  • * The new panel showed strong agreement with traditional methods in correctly identifying fusion genes in cancer specimens and provided insights through 3'/5' expression ratios; however, further validation was needed for some predicted fusions.
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  • Primary neuroendocrine carcinoma of the breast is a rare and aggressive form of breast cancer, comprising only 2% to 5% of cases.
  • A study identified genetic mutations in neuroendocrine breast tumors, revealing that PIK3CA mutations are prevalent, while mutations in FGFR and RAS family members are rare.
  • This research highlights the importance of comprehensive genetic analysis in understanding and potentially treating uncommon tumors like neuroendocrine breast carcinoma.
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  • A basket clinical trial was conducted to evaluate the effectiveness of various targeted therapies on different cancer types with specific genetic mutations, focusing on patients with advanced lung cancer and thymic malignancies.
  • Six hundred forty-seven patients were enrolled, with genomic testing revealing significant mutation frequencies for EGFR (22.1%) and KRAS (24.9%), leading to variable response rates to treatments like erlotinib and selumetinib.
  • Although the trial design faced challenges with feasibility for arms targeting rare mutations, it provided valuable insights into the genetic profiles and survival outcomes of the studied malignancies.
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Coronary artery disease (CAD) is characterised by progressive atherosclerotic plaque leading to flow-limiting stenosis, while myocardial infarction (MI) occurs due to plaque rupture or erosion with abrupt coronary artery occlusion. Multiple inflammatory pathways influence plaque stability, but direct assessment of endothelial inflammation at the site of coronary artery stenosis has largely been limited to pathology samples or animal models of atherosclerosis. We describe a technique for isolating and characterising endothelial cells (ECs) and EC microparticles (EMPs) derived directly from the site of coronary artery plaque during balloon angioplasty and percutaneous coronary intervention.

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  • The study investigates the genetic mutations associated with melanomas and melanocytic nevi in the female genital tract, focusing on specific genes: BRAF, NRAS, KIT, GNA11, and GNAQ.
  • Researchers screened 25 melanoma samples, 7 benign melanocytic nevi, and 4 atypical melanocytic nevi to identify mutation frequencies.
  • Findings revealed that KIT, NRAS, and BRAF mutations occur in some female genital tract melanomas, while BRAF mutations were common in benign nevi, highlighting the need for further genetic screening for effective treatments.
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  • Gallbladder cancer is a serious disease that's often found late, and its genetic makeup is not well understood, prompting this study to identify mutations that could aid in early diagnosis and treatment.
  • The researchers analyzed 49 gallbladder cancer cases using specialized technology to check for mutations in 30 genes, finding notable mutations in four specific genes in a small number of cases.
  • The results align with existing literature and suggest that discovering mutations like PIK3CA and KRAS could lead to better-targeted therapies, highlighting the need for more extensive research to uncover additional genetic targets.
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Pharmacogenomic testing is viewed as an integral part of precision medicine. To achieve this, we originated The 1,200 Patients Project which offers broad, preemptive pharmacogenomic testing to patients at our institution. We analyzed enrollment, genotype, and encounter-level data from the first year of implementation to assess utility of providing pharmacogenomic results.

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The neutron imaging system at the National Ignition Facility (NIF) is an important diagnostic tool for measuring the two-dimensional size and shape of the neutrons produced in the burning deuterium-tritium plasma during the ignition stage of inertial confinement fusion (ICF) implosions at NIF. Since the neutron source is small (∼100 μm) and neutrons are deeply penetrating (>3 cm) in all materials, the apertures used to achieve the desired 10-μm resolution are 20-cm long, single-sided tapers in gold. These apertures, which have triangular cross sections, produce distortions in the image, and the extended nature of the pinhole results in a non-stationary or spatially varying point spread function across the pinhole field of view.

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  • The study aimed to identify actionable mutations in patients with high-risk localized prostate cancer to aid in developing targeted therapies.
  • Researchers analyzed tumor samples for common mutations and specific protein markers using sequencing and immunohistochemistry.
  • Results revealed that while point mutations in cancer genes were rare (10%), PTEN loss was associated with shorter relapse-free survival, highlighting its potential importance in treatment outcomes.
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  • * In a study of 22 radial scars, 63.6% were found to have activating mutations in the PIK3CA gene, which is commonly seen in invasive breast cancers, with a notably higher mutation rate compared to typical invasive cases.
  • * The presence of PIK3CA mutations in radial scars raises new questions about their role in the development of breast cancer, indicating a need for larger studies to explore the relationship between these lesions and cancer risk further.
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  • The phosphatidylinositol-3-kinase (PIK3CA) pathway is commonly mutated in invasive breast cancer, with about 25% of cases showing PIK3CA mutations.
  • A study screened 192 breast lesions for genetic mutations, finding that PIK3CA mutations were present in various types of breast tissue, including proliferative lesions and atypical hyperplasia.
  • The research indicates significant genetic differences between benign proliferative lesions and concurrent invasive cancer, suggesting that while proliferative lesions may carry mutations, they do not necessarily lead to cancer, highlighting their complex role in breast cancer development.
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A rare sclerosing variant of rhabdomyosarcoma characterized by prominent hyalinization and pseudovascular pattern has recently been described as a subtype biologically distinct from embryonal, alveolar, and pleomorphic forms. We present cytogenetic and molecular findings as well as experimental studies of an unusual case of sclerosing rhabdomyosarcoma. The primary lesion arose within the plantar subcutaneous tissue of the left foot of an otherwise healthy 23-year-old male who eventually developed pulmonary nodules despite systemic chemotherapy.

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Somatic mutations in PIK3CA are commonly seen in invasive breast cancer and several other carcinomas, occurring in three hotspots: codons 542 and 545 of exon 9 and in codon 1047 of exon 20. We designed a locked nucleic acid (LNA)-PCR sequencing assay to detect low levels of mutant PIK3CA DNA with attention to avoiding amplification of a pseudogene on chromosome 22 that has >95% homology to exon 9 of PIK3CA. We tested 60 FFPE breast DNA samples with known PIK3CA mutation status (48 cases had one or more PIK3CA mutations, and 12 were wild type) as identified by PCR-mass spectrometry.

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Micropapillary carcinoma of the breast is associated with increased rates of lymph node metastasis and lymphovascular invasion. While activating point mutations in PIK3CA (encoding phosphatidylinositol-3-kinase catalytic subunit) or AKT1 are found in 25% to 30% of invasive ductal carcinomas, the mutational profile of invasive micropapillary carcinomas has not been characterized in detail. Micropapillary carcinomas, concurrent metastatic and precursor breast lesions from 19 patients were identified.

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