Search Results - "Presutti, Richard J"

Perspectives of primary care providers regarding multicancer early detection panels by Ueberroth, Benjamin E, Presutti, Richard J, McGary, Alyssa, Borad, Mitesh J, Agrwal, Neera

“…Multicancer early detection panels have recently become available to patients with healthcare provider prescriptions and available funds. These tests utilize…”
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Identification of individuals at high-risk for pancreatic cancer using a digital patient-input tool combining family cancer history screening and new-onset diabetes by Klatte, Derk C.F., Clift, Kristin E., Mantia, Sarah K., Millares, Lindsey, Hoogenboom, Sanne A.M., Presutti, Richard J., Wallace, Michael B.

“…Capturing family history might be a valuable tool for identification of individuals at increased risk of pancreatic cancer, which would allow enrollment into…”
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Patient-Centered Medical Home With Colocation: Observations and Insights From an Academic Family Medicine Clinic by Pujalte, George G. A., Pantin, Sally Ann, Waller, Thomas A., Maruoka Nishi, Livia Y., Willis, Floyd B., Jethwa, Tarang P., Presutti, Richard J.

“…There is a movement in the United States to transform family medicine practices from single physician–based patient care to team-based care. These teams are…”
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Nurse practitioner and physician assistant onboarding in a family medicine practice by Chaney, Amanda, Martin, Angela, Cardona, Kathy, Presutti, Richard J.

“…The nurse practitioner (NP) and physician assistant (PA) professions are rapidly growing. Historically, these professions have filled a health care delivery…”
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Delayed Presentation of Basal Cell Carcinoma: A Case Report by Abadin, Andre A, Fosko, Scott, Boniface, Michael, Presutti, Richard J

“…Basal cell carcinoma (BCC) is the most common skin cancer in the United States. Although BCC has a low metastatic potential, it can be locally invasive and…”
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Connecting the Dots of a Rare Connective Tissue Disease: Pseudoxanthoma Elasticum by Yenior, Ashley L, Pujalte, George, Nadwodny, Jeff, Costa, Lorena C, Presutti, Richard J

“…Pseudoxanthoma elasticum (PXE) is a rare, autosomal recessive connective tissue disease that manifests primarily in the skin, eyes, vasculature, and…”
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Exome Sequencing Identifies Carriers of the Autosomal Dominant Cancer Predisposition Disorders Beyond Current Practice Guideline Recommendations by Samadder, N Jewel, Gay, Emily, Lindpere, Vanda, Bublitz, Michelle L, Bandel, Lorelei A, Armasu, Sebastian M, Vierkant, Robert A, Ferber, Matthew J, Klee, Eric W, Larson, Nicholas B, Kruisselbrink, Teresa M, Egan, Jan B, Kemppainen, Jennifer L, Bidwell, Jessa S, Anderson, Jennifer L, McAllister, Tammy M, Walker, T'Nita S, Kunze, Katie L, Golafshar, Michael A, Klint, Margaret A, Presutti, Richard J, Bobo, William V, Sekulic, Aleksander, Summer-Bolster, Jolene M, Willman, Cheryl L, Lazaridis, Konstantinos N

“…The autosomal dominant cancer predisposition disorders hereditary breast and ovarian cancer (HBOC) and Lynch syndrome (LS) are genetic conditions for which…”
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Sharing is Caring: Minimizing the Disruption with Palliative Care by Abu Dabrh, Abd Moain, Shannon, Robert P, Presutti, Richard J

“…There is an upward trend incidence of multiple chronic life-limiting conditions with a well-documented associated impact on patients and their caregivers. When…”
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"No Waiting" in the "Waiting Room": The Self-rooming Patient Pilot Study by Presutti, Richard J, Willis, Floyd B, Scott, Ruel, Greig, Hope E, Abu Dabrh, Abd Moain

“…Although patient timeliness and appointment flow are highly important for patients and practices, the impact of technology on improving these aspects of…”
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Mo1162 GUIDELINE COMPLIANCE AND OUTCOMES OF GENETIC TESTING IN PANCREATIC CANCER PATIENTS by Klatte, Derk C., Hardway, Heather, Starr, Jason, Riegert-Johnson, Douglas L., Clift, Kristin, Potjer, Thomas, Van Hooft, Jeanin E., Van Leerdam, Monique, Presutti, Richard J., Wallace, Michael B., Bi, Yan

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Correction: Implementation of genomic medicine for rare disease in a tertiary healthcare system: Mayo Clinic Program for Rare and Undiagnosed Diseases (PRaUD) by Pinto E Vairo, Filippo, Kemppainen, Jennifer L, Vitek, Carolyn R Rohrer, Whalen, Denise A, Kolbert, Kayla J, Sikkink, Kaitlin J, Kroc, Sarah A, Kruisselbrink, Teresa, Shupe, Gabrielle F, Knudson, Alyssa K, Burke, Elizabeth M, Loftus, Elle C, Bandel, Lorelei A, Prochnow, Carri A, Mulvihill, Lindsay A, Thomas, Brittany, Gable, Dale M, Graddy, Courtney B, Garzon, Giovanna G Moreno, Ekpoh, Idara U, Porquera, Eva M Carmona, Fervenza, Fernando C, Hogan, Marie C, El Ters, Mireille, Warrington, Kenneth J, Davis, 3rd, John M, Koster, Matthew J, Orandi, Amir B, Basiaga, Matthew L, Vella, Adrian, Kumar, Seema, Creo, Ana L, Lteif, Aida N, Pittock, Siobhan T, Tebben, Peter J, Abate, Ejigayehu G, Joshi, Avni Y, Ristagno, Elizabeth H, Patnaik, Mrinal S, Schimmenti, Lisa A, Dhamija, Radhika, Sabrowsky, Sonia M, Wierenga, Klaas J, Keddis, Mira T, Samadder, Niloy Jewel J, Presutti, Richard J, Robinson, Steven I, Stephens, Michael C, Roberts, Lewis R, Faubion, Jr, William A, Driscoll, Sherilyn W, Wong-Kisiel, Lily C, Selcen, Duygu, Flanagan, Eoin P, Ramanan, Vijay K, Jackson, Lauren M, Mauermann, Michelle L, Ortega, Victor E, Anderson, Sarah A, Aoudia, Stacy L, Klee, Eric W, McAllister, Tammy M, Lazaridis, Konstantinos N

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Implementation of genomic medicine for rare disease in a tertiary healthcare system: Mayo Clinic Program for Rare and Undiagnosed Diseases (PRaUD) by Pinto E Vairo, Filippo, Kemppainen, Jennifer L, Vitek, Carolyn R Rohrer, Whalen, Denise A, Kolbert, Kayla J, Sikkink, Kaitlin J, Kroc, Sarah A, Kruisselbrink, Teresa, Shupe, Gabrielle F, Knudson, Alyssa K, Burke, Elizabeth M, Loftus, Elle C, Bandel, Lorelei A, Prochnow, Carri A, Mulvihill, Lindsay A, Thomas, Brittany, Gable, Dale M, Graddy, Courtney B, Garzon, Giovanna G Moreno, Ekpoh, Idara U, Porquera, Eva M Carmona, Fervenza, Fernando C, Hogan, Marie C, El Ters, Mireille, Warrington, Kenneth J, Davis, 3rd, John M, Koster, Matthew J, Orandi, Amir B, Basiaga, Matthew L, Vella, Adrian, Kumar, Seema, Creo, Ana L, Lteif, Aida N, Pittock, Siobhan T, Tebben, Peter J, Abate, Ejigayehu G, Joshi, Avni Y, Ristagno, Elizabeth H, Patnaik, Mrinal S, Schimmenti, Lisa A, Dhamija, Radhika, Sabrowsky, Sonia M, Wierenga, Klaas J, Keddis, Mira T, Samadder, Niloy Jewel J, Presutti, Richard J, Robinson, Steven I, Stephens, Michael C, Roberts, Lewis R, Faubion, Jr, William A, Driscoll, Sherilyn W, Wong-Kisiel, Lily C, Selcen, Duygu, Flanagan, Eoin P, Ramanan, Vijay K, Jackson, Lauren M, Mauermann, Michelle L, Ortega, Victor E, Anderson, Sarah A, Aoudia, Stacy L, Klee, Eric W, McAllister, Tammy M, Lazaridis, Konstantinos N

“…In the United States, rare disease (RD) is defined as a condition that affects fewer than 200,000 individuals. Collectively, RD affects an estimated 30 million…”
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Abstract 5768: Genetic screening in a tertiary medical center identifies carriers of cancer predisposition diseases that would be missed by clinical guidelines by Gay, Emily, Samadder, Niloy Jewel, Bublitz, Michelle L., Peterson, Melanie M., Wilson, Tammy A., Bandel, Lorelei A., Armasu, Sebastian M., Vierkant, Robert A., Ferber, Matthew J., Klee, Eric W., Larson, Nicholas B., Kruisselbrink, Teresa M., Curry, Timothy B., Egan, Jan B., Kemppainen, Jennifer L., Bidwell, Jessa S., Anderson, Jennifer L., McAllister, Tammy M., Walker, T'Nita S., Kunze, Katie L., Lindpere, Vanda, Golafshar, Michael A., Klint, Margaret, Presutti, Richard J., Bobo, William V., Sekulic, Aleksander, Bolster, Jolene M. Summer, Willman, Cheryl L., Lazaridis, Konstantinos N.

“…Abstract Two inherited autosomal dominant cancer predisposition conditions - BRCA related hereditary breast and ovarian cancer (HBOC) and Lynch syndrome (LS) -…”
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Patients with Celiac Disease Should Not Consume Beer/IN REPLY by Grossman, Nancy Beth, Presutti, Richard J

“…An internet search for "gluten-free beer" also yields many listings of beers advertising to be free of gluten; however, patients should be cautioned to read…”
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Patients with Celiac Disease Should Not Consume Beer by Presutti, Richard J., DO

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Delayed Presentation of Basal Cell Carcinoma: A Case Report by Abadin, Andre A, Fosko, Scott, Boniface, Michael, Presutti, Richard J

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Connecting the Dots of a Rare Connective Tissue Disease: Pseudoxanthoma Elasticum by Yenior, Ashley L, Pujalte, George, Nadwodny, Jeff, Costa, Lorena C, Presutti, Richard J

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