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2474 citation(s) found for "Ee, Miller".

Assessment of Chronic Hepatitis and Fibrosis: Comparison of MR Elastography and Diffusion-Weighted Imaging
Wang, Yi , Ganger, Daniel , Levitsky, Josh , Sternick, Laura A., McCarthy, Robert J. , Chen, Zongming E., Fasanati, Charles, Bolster, Bradley D. , Shah, Saurabh , Zuehlsdorff, Sven , Omary, Reed A. , Miller, Frank H. , Ehman, Richard L. , Miller, Frank H

American Journal of Roentgenology | February 22, 2011 | Volume: 196 | Issue: 3 | Pages: 553-561

10.2214/ajr.10.4580 | PMID 21343496 Get It

Comparison of Mass Spectrometry and Clinical Assay Measurements of Circulating Fragments of B-Type Natriuretic Peptide in Patients With Chronic Heart Failure
Phelps, Mary, Wood, Christina M., Schellenberger, Ute , Le, Anh Van , Périchon, Régis, Jaffe, Allan S. , Miller, Wayne L. , Jaffe, Allan S.

Circulation: Heart Failure | February 4, 2011 | Volume: 4 | Issue: 3 | Pages: 355-360

10.1161/circheartfailure.110.960260 | PMID 21292992 Get It

Background— Multiple B-type natriuretic peptide (BNP) fragments circulate in patients with heart failure (HF) but the types and relative quantities, particularly in relation to bioactive BNP 1-32, remain poorly defined. The purpose of the study was to relate clinically available BNP values with quantitative information on the concentration of pre-secretion and post-processed fragments of BNP detected by mass spectrometry. Methods and Results— Seventy Class I–IV patients were prospectively enrolled with blood drawn into tubes containing a preservative to protect against BNP degradation. Samples were analyzed by quantitative mass spectrometry (MS) immunoassay for intact BNP 1-32 and its fragments. Clinical BNP 1-2 was measured by standard clinical laboratory methods. ProBNP 1-108, corin, and clinically measured BNP levels were elevated, but MS BNP 1-32 levels were low and differed from clinical BNP ( P =0.01). Intact MS BNP 1-32 correlated modestly with clinical BNP ( r =0.46, P <0.001). MS BNP fragments 3-32, 4-32, and 5-32 demonstrated the best associations with clinical BNP; fragment 5-32 with a correlation coefficient of r =0.81 ( P <0.001). Conclusions— ProBNP 1-108 is measured by clinical BNP assays and contributes to the cumulative results of the BNP assay. However, the observation that clinically measured BNP correlates best with MS degradation fragments and relatively poorly with MS BNP 1-32 suggests that a significant component of circulating clinical BNP is composed of such fragments that are known to demonstrate little biological activity. There appear to be multiple pathways involved in the dysregulation of proBNP in HF, and both the processing of proBNP and the downstream degradation to BNP 1-32 appear to be critical.
Revision of the criteria for Alzheimer's disease: A symposium
DeKosky, Steven T. , Phelps, Creighton H., Petersen, Ronald C. , Frank, Richard , Schenk, Dale, Masterman, Donna, Siemers, Eric , Cedarbaum, Jesse M. , Morimoto, Bruce H., Khachaturian, Ara S. , Mohs, Richard C. , Carrillo, María C. , Knopman, David S. , Gold, Michael , Miller, David S.

Alzheimer's & Dementia | February 2, 2011 | Volume: 7 | Issue: 1 | Pages: No page available

10.1016/j.jalz.2010.12.007 | PMID 21322828 Get It

The current criteria for classification of Alzheimer's disease (AD) have deficiencies that limit drug development, research, and practice. The current standard for the clinical diagnosis of AD, the National Institute of Neurological and Communicative Disorders and Stroke (now known as the National Institute of Neurological Disorders and Stroke), and the Alzheimer's Disease and Related Disorders Association (now known as the Alzheimer's Association) criteria, are nearly 25 years old and have not been revised to incorporate advances in the epidemiology and genetics of AD, studies of clinicopathologic correlations and recent studies of potential diagnostic biomarkers. In a very real sense our ability to diagnose AD with a very high level of certainty has outpaced our current diagnostic criteria. The Alzheimer's Association Research Roundtable convened a meeting in April 2009 to discuss new data and technologies that could, with further development, enable improvements in the clinical diagnosis of AD, especially in its earliest and mildest stages. This meeting reviewed the current standards for detecting and defining the clinical presentation of AD and discussed areas that could contribute to earlier and more accurate definitive clinical diagnosis. These included clinical, neuropsychological, and other performance‐based assessments, genetic contributions, and biochemical and neuroimaging biomarkers that could reflect AD pathology and lead to better ascertainment of AD, mild cognitive impairment, and presymptomatic AD.
An algorithm for genetic testing of frontotemporal lobar degeneration
Goldman, Jill , Rademakers, Rosa , Huey, Edward D. , Boxer, Adam L. , Mayeux, Richard , Miller, Bruce L. , Boeve, Bradley F. , Goldman, Jill S

Neurology | January 31, 2011 | Volume: 76 | Issue: 5 | Pages: 475-483

10.1212/wnl.0b013e31820a0d13 | PMID 21282594 Get It

Resectable pancreatic small cell carcinoma
Narang, Amol , Mansfield, Aaron S. , Herman, Joseph M. , Cameron, John L., Laheru, Dan, Eckhauser, Fred E., Olson, Mathew T., Hruban, Ralph H. , Miller, Robert C. , Andersen, Dana K. , Winter, Jordan Michael , Mansfield, Aaron S

Rare Tumors | January 28, 2011 | Volume: 3 | Issue: 1 | Pages: 13-17

10.4081/rt.2011.e5 | PMID 21464878 Get It

Primary pancreatic small cell carcinoma (SCC) is rare, with just over 30 cases reported in the literature. Only 7 of these patients underwent surgical resection with a median survival of 6 months. Prognosis of SCC is therefore considered to be poor, and the role of adjuvant therapy is uncertain. Here we report two institutions’ experience with resectable pancreatic SCC. Six patients with pancreatic SCC treated at the Johns Hopkins Hospital (4 patients) and the Mayo Clinic (2 patients) were identified from prospectively collected pancreatic cancer databases and re-reviewed by pathology. All six patients underwent a pancreaticoduodenectomy. Clinicopathologic data were analyzed, and the literature on pancreatic SCC was reviewed. Median age at diagnosis was 50 years (range 27–60). All six tumors arose in the head of the pancreas. Median tumor size was 3 cm, and all cases had positive lymph nodes except for one patient who only had five nodes sampled. There were no perioperative deaths and three patients had at least one postoperative complication. All six patients received adjuvant therapy, five of whom were given combined modality treatment with radiation, cisplatin, and etoposide. Median survival was 20 months with a range of 9–173 months. The patient who lived for 9 months received chemotherapy only, while the patient who lived for 173 months was given chemoradiation with cisplatin and etoposide and represents the longest reported survival time from pancreatic SCC to date. Pancreatic SCC is an extremely rare form of cancer with a poor prognosis. Patients in this surgical series showed favorable survival rates when compared to prior reports of both resected and unresectable SCC. Cisplatin and etoposide appears to be the preferred chemotherapy regimen, although its efficacy remains uncertain, as does the role of combined modality treatment with radiation.
New Toys for Nuclear Cardiologists
Miller, Todd D., Askew, J. Wells , O’Connor, Michael K.

Circulation: Cardiovascular Imaging | January 18, 2011 | Volume: 4 | Issue: 1 | Pages: 5-7

10.1161/circimaging.110.961987 | PMID 21245363 Get It

Skin thickness as a measure of breast lymphedema.
Degnim, AC, Hoskin, TL, Cheville, AL, Gl, Gamble, Baddour, L.M., Donohue, JH, Thomsen, KM, Maloney, SD, Boughey, JC , Miller, J. Philip

Cancer Research | December 30, 2010 | Volume: 69 | Issue: 2_Supplement | Pages: 3103

10.1158/0008-5472.sabcs-3103 Get It

Abstract Abstract #3103 Introduction: Lymphedema is well-known in the arm but can also occur in the breast. Diagnosis is currently non-standardized and based on clinical impression. We sought to determine if skin thickness could serve as a useful measure in the diagnosis of breast lymphedema (BLE).&#x2028; Methods: Patients undergoing unilateral non-mastectomy procedures were enrolled on this prospective clinical study preoperatively and evaluated for signs and symptoms of lymphedema in the operated breast in the postoperative period. Patients with established BLE were also studied. BLE diagnosis was independent of ultrasound findings and was based on a graded physical exam targeting clinical signs of edema and erythema. Skin thickness was measured with ultrasound at the 6 o'clock position of both breasts. Differences in skin thickness were assessed by the ratio of skin thickness in the operated and contralateral breasts, with comparison of means by two-sample t-test. Receiver operating characteristic curves were constructed to estimate the area under the curve (AUC) and to determine optimal cutpoints.&#x2028; Results: Ninety-seven women were studied; 85 were enrolled preoperatively and 12 postoperatively after a diagnosis of BLE. Median length of follow-up overall was 8 months. Of the 97 women, 46 had BLE at one or more follow-up visit with median time to first diagnosis of 3 months. Mean measured skin thickness was 2.3 ± 0.5mm in unaffected breasts and 3.2 ± 1.0 mm in operated breasts. Women with BLE had significantly greater skin thickness in the operated breast compared to the contralateral breast, with a mean skin thickness ratio of 1.83 ± 0.57 in patients with BLE compared to 1.18 ± 0.40 among those without BLE (p&lt;0.0001). Skin thickness ratio provided excellent discrimination for BLE, with an area under the curve (AUC) of 0.86. At a ratio of 1.32 or greater (32% greater skin thickness in operated versus contralateral breast), sensitivity and specificity for diagnosing BLE were 81% and 82% respectively. A single measure of skin thickness in the operated breast also correlated well with diagnosis of BLE, with skin thickness of 3.2 mm or greater demonstrating sensitivity of 78% and specificity of 82%, AUC 0.82.&#x2028; Conclusions: Breast lymphedema results in skin edema and increased skin thickness that can be quantified with ultrasound. Measuring breast skin thickness- either as a single reading or as a ratio to the unaffected breast- may be useful in the diagnosis of breast lymphedema. Citation Information: Cancer Res 2009;69(2 Suppl):Abstract nr 3103.
PGC-1 α, A Potential Therapeutic Target for Early Intervention in Parkinson’s Disease
Liao, Zhixiang , Locascio, Joseph J. , Lesniak, Kristen A., Roderick, Sarah S., Watt, Marla L., Eklund, Aron C. , Zhang‐James, Yanli , Kim, Peter D., Hauser, Michael A. , Grünblatt, Edna , Moran, Linda, Mandel, Silvia, Riederer, Peter , Miller, Renee M. , Federoff, Howard J. , Papapetropoulos, Spyridon , Youdim, Moussa B. H. , Cantuti‐Castelvetri, Ippolita, Young, Anne B., Vance, Jeffery M. , Hedreen, John C. , Beach, Thomas G. , Graeber, Manuel B., Middleton, Frank A. , Rochet, Jean‐Christophe , Scherzer, Clemens R. , Papapetropoulos, Spyros , Zheng, Bin , Wüllner, Ullrich , Davis, Richard L. , Adler, Charles H.

Science Translational Medicine | October 6, 2010 | Volume: 2 | Issue: 52 | Pages: No page available

10.1126/scitranslmed.3001059 | PMID 20926834 Get It

Abnormal expression of genes for energy regulation in Parkinson’s disease patients identifies a master regulator as a possible therapeutic target for early intervention.
Estrogen Metabolomics
Miller, Virginia M.

Hypertension | October 5, 2010 | Volume: 56 | Issue: 5 | Pages: 816-818

10.1161/hypertensionaha.110.154385 | PMID 20921431 Get It