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Artykuły w czasopismach na temat „Montefiore family”

Autor: Grafiati

Data publikacji: 27 lipca 2024

Data aktualizacji: 31 lipca 2025

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1

Belmar, Roberto. "The Department of Social Medicine at Montefiore and Vic Sidel." Social Medicine 7, no. 3 (2013): 142–43. https://doi.org/10.71164/socialmedicine.v7i3.2013.732.

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Montefiore’s Division of Social Medicine (DSM) (later a Department) was conceived and created by Martin Cherkasky, MD, in 1950 shortly before Cherkasky became the Director of Montefiore Hospital. As DSM’s first Chairman, Cherkasky understood health care as a social endeavor. The Department not only delivered first-class medical and health care, but understood the individual, the family, and the community as social entities involved in the creation of a more just and egalitarian society.

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Jose, Anita, and Scott Wetzler. "Implementing a Provider Partnership to Improve Substance Abuse and Child Welfare Outcomes in Urban High-Needs Parents." Families in Society: The Journal of Contemporary Social Services 100, no. 3 (2019): 328–35. http://dx.doi.org/10.1177/1044389419836612.

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This Practice Note describes the implementation of a partnership between child welfare and substance use providers in New York City, with the aim of supporting cross-systems collaboration and improving outcomes for dually involved families. Specifically, this report focuses on improving both coordination and communication between a preventive child welfare service provider (Montefiore Family Treatment & Rehabilitation Program), an outpatient substance abuse treatment provider (Montefiore Division of Substance Abuse), and the local department of social services (New York City Administration

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Gold, Marji. "From Reproductive Rights to Reproductive Justice." Social Medicine 12, no. 2 (2019): 84–92. https://doi.org/10.71164/socialmedicine.v12i2.2019.1069.

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This month the Social Medicine Journal of-fers readers the text of the Annual Harold Wise Memorial Lecture held on June 13, 2017 at the Department of Family and Social Medicine at Montefiore Medical Center. Harold Wise was the founder of the Residency Program in Social Medicine and the award recognizes a faculty member who best represents the values of the Residency Program.

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Capps, Linnea, and Clyde Lanford (Lanny) Smith. "Honoring Vic Sidel." Social Medicine 11, no. 3 (2018): 90–97. https://doi.org/10.71164/socialmedicine.v11i3.2018.995.

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Victor W. Sidel, MD, a long-time member of the faculty of the Albert Einstein College of Medicine and Montefiore Medical Center passed away on January 30, 2018. He was 86 years old. Dr, Sidel had dual appointments in Family and Social Medicine and Epidemiology and Population Health. He was pre-deceased by his wife, Ruth. This interview was published in October of 2013 as part of a Festschrift devoted to Vic’s life and work. It explores several aspects of his long career, concentrating on activism and social justice issues. The transcript is based on two interviews. One was conducted by Lanny S

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5

Hudson, Hugh. "Amateur Photography in the Nineteenth-Century Jewish Diaspora: The Colonial, National, and Transnational Aspects of a Montefiore Family Album." History of Photography 43, no. 3 (2019): 266–83. http://dx.doi.org/10.1080/03087298.2020.1732074.

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Beider, Alexander. "Surnames of Jewish People in the Land of Israel from the Sixteenth Century to the Beginning of the Twentieth Century." Genealogy 7, no. 3 (2023): 49. http://dx.doi.org/10.3390/genealogy7030049.

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This paper outlines a study of surnames used by various Jewish groups in the Land of Israel for Ashkenazic Jews, prior to the First Aliyah (1881), and for Sephardic and Oriental Jews up to the end of the 1930s. For the 16th–18th centuries, the surnames of Jews who lived in Jerusalem, Safed, Tiberias, and Hebron can be mainly extracted from the rabbinic literature. For the 19th century, by far the richest collection is provided by the materials of the censuses organized by Moses Montefiore (1839–1875). For the turn of the 20th century, data for several additional censuses are available, while f

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Saleem, Aushna, Janice N. Simpson, Della Makower, and Susan D. Klugman. "Uptake of Hereditary Cancer Screening in a Breast Cancer Survivorship Clinic in the Bronx, New York: A Pilot Study [ID 830]." Obstetrics & Gynecology 145, no. 6S (2025): 12S—13S. https://doi.org/10.1097/aog.0000000000005916.040.

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INTRODUCTION: Breast cancer is the most commonly diagnosed cancer in women worldwide, and survivors account for 40% of female cancer survivors. Genetic testing can influence care of both breast cancer patients and their family members. Although changes in guidelines have led to an increase in newly diagnosed breast cancer patients who are eligible for testing, many survivors have not had testing. This retrospective review was conducted to evaluate rates of and barriers to genetic testing in patients at an urban breast cancer survivorship center. As obstetrician–gynecologists are often the prim

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Karnik, Arati, Asiya Tscahnnerl, and Matthew Anderson. "What is a social medicine doctor?" Social Medicine 9, no. 2 (2016): 56–62. https://doi.org/10.71164/socialmedicine.v9i2.2015.837.

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Background: In 1970 Montefiore Medical Center created the Residency Program in Social Medicine (RPSM) to train physicians to provide care for the underserved. We investigated the characteristics identified by RPSM residents, faculty, and alumni to be those of a “social medicine doctor.” Methods: Current residents, faculty, and alumni of the RPSM were eligible to participate in the survey, which was sent via email. The survey had seven items: status (resident, faculty, or alumni); specialty (Family Medicine, Internal Medicine, Pediatrics); the role of social medicine in their clinical practice,

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Risinger, Mary A., Edyta Glogowska, Amber Hogart Begtrup, et al. "The Novel PIEZO1 Mutation p.L2023V Is Causal for Hereditary Xerocytosis Resulting in Delayed Channel Inactivation and a Dehydrated Red Blood Cell Phenotype." Blood 124, no. 21 (2014): 741. http://dx.doi.org/10.1182/blood.v124.21.741.741.

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Abstract The regulation of cell volume is important for the maintenance of integrity in all cells and is especially critical for the highly specialized red blood cell (RBC) which must withstand pressure changes within the vasculature and remain deformable to traverse small vessels. Disorders that interfere with volume homeostasis result in the premature destruction of RBCs. One protein that appears to play a prominent role in RBC hydration is the recently described nonselective cation channel PIEZO1 which is involved in mechanotransduction. Mutations of PIEZO1 have been associated with an auto

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10

Sheni, Risha, Danielle Tomer, Dana Watnick, Della F. Makower, Anjuli M. Gupta, and Vikas Mehta. "Further assessment of structural and social determinant of health effects on breast cancer care timelines: A qualitative study." JCO Oncology Practice 20, no. 10_suppl (2024): 121. http://dx.doi.org/10.1200/op.2024.20.10_suppl.121.

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121 Background: Time to treatment (TTI) delays result in increased morbidity and mortality for cancer patients. These treatment delays disproportionately occur within marginalized communities due to structural challenges with social determinants of health (SDoH), disengagement with the healthcare system and limited or low health literacy that impacts their ability to obtain timely, appropriate care. We conducted semi-structured interviews with patients treated for breast cancer about their care treatment trajectories to further understand barriers and facilitators for timely treatment from the

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Lederman, Michael M. "Charlie van der Horst (1952-2019)." Pathogens and Immunity 4, no. 1 (2019): 161. http://dx.doi.org/10.20411/pai.v4i1.305.

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Charlie van der Horst, an emeritus professor at the University of North Carolina and a friend of Pathogens and Immunity, disappeared from sight on Friday, June 14 during a marathon swim in the Hudson River. His death was confirmed. Few who knew him would call him Charles as formality was not his strong-suit. Charlie was born in Holland to a Dutch father and a Polish Holocaust survivor mother. His family moved to the Buffalo, New York area and sent Charlie to school at Andover. He attended Duke University where he captained the varsity swim team in 1973-74. He remained a powerful swimmer, compe

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O'Mahony, Sean, Patricia Marthone, Gabriella Santoro, et al. "Preliminary Report of a Pilot Tele-Health Palliative Care and Bioethics Program for Residents in Skilled Nursing Facilities." Palliative Care: Research and Treatment 3 (January 2009): PCRT.S3296. http://dx.doi.org/10.4137/pcrt.s3296.

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Currently about 25% of Americans die in nursing homes, many with poorly controlled pain and other symptoms, with minimal provisions for psychosocial support. New models are necessary to lessen structural and process barriers to give effective end-of-life care in nursing homes. Objectives 1) To extend hospital-based Bioethics Consultation Services (BCS) and Palliative Care Services (PCS) at Montefiore Medical Center (MMC) in the Bronx to two local Skilled Nursing Facilities (SNFs), Morningside House Aging in America (MSH) using direct face-to-face consultations and Beth Abraham Health Systems (

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13

Campbell, Andrew, Biree Andemariam, Fredericka Sey, et al. "Sickle Cell Disease Proteinuria Is Not Associated With Systolic Blood Pressure, CSSCD-Defined Hypertension, or Family History Of Hypertension In An International Cohort Of SCD Patients." Blood 122, no. 21 (2013): 981. http://dx.doi.org/10.1182/blood.v122.21.981.981.

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Abstract Background The prevalence of renal disease in sickle cell disease (SCD) is strikingly high and is associated with morbidity and mortality (Becker et al 2010, Powars et al 2005). In SCD children there is initially hyperfiltration with high GFRs followed by increasing proteinuria in the adolescent and adult SCD pts. (Becker at al 2010). Historically, hypertension (HTN) has been associated with Renal Disease in the general population and a few adult sickle cell nephropathy studies. HTN has been associated with Stroke in SCD. In an ongoing multicenter, international Renal SCD Cohort Study

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14

Manwani, Deepa, Veronica Carullo, Michael Rinke, Steven Choi, and Catherine Driscoll. "Reducing Health Care Utilization in Sickle Cell Disease Patients By Implementation of an Individualized, Multimodal Care Plan during Hospital Admission and at Inpatient to Outpatient Discharge." Blood 124, no. 21 (2014): 444. http://dx.doi.org/10.1182/blood.v124.21.444.444.

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Abstract Background: SickleCell Disease (SCD) is a chronic illness characterized by vaso-occlusive complications leading to unpredictable episodes of pain, cumulative organ damage and high health care utilization rates. National estimates of total hospital costs for sickle cell related hospitalizations are approximately $488 billion (Steiner 2006). 30 day readmission rates are used as a quality metric for a variety of chronic diseases: 33% of patients with SCD are readmitted within 30 days, compared to 3.4% for asthma, 12% for pneumonia, 16% for heart failure and 20% for diabetes (Brousseau 20

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15

Shastri, Aditi, Mendel Goldfinger, Ioannis Mantzaris, et al. "A Phase 1 Study Investigating the Safety and Efficacy of Danvatirsen As Monotherapy Followed By Combination with Venetoclax in Patients with Relapsed/Refractory MDS and AML." Blood 144, Supplement 1 (2024): 4265.5. https://doi.org/10.1182/blood-2024-208998.

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Background: In spite of the emergence of targeted & novel therapies, only 30% of patients with newly diagnosed acute myeloid leukemia (AML) enjoy long-term survival, while the majority still succumb to their illness. Even patients with MRD negative complete remissions may relapse due to chemotherapy-resistant leukemic stem cells (LSCs). Eradication of residual disease at the LSC level is the ultimate goal of anti-leukemia therapy. STAT3 belongs to the STAT family of seven transcription factors. STAT3 is activated in the cytoplasm when growth factors & cytokines bind to the upstream Jan

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16

Nandan Seelaboyina, Kranthi, Jennifer Alison Busse, Sandeep Malik та Thomas Moulton. "A Novel β Globin Gene Mutation, Reported As An α Chain Hemoglobin Variant By High Performance Liquid Chromatography (HPLC) & As Sickle Cell Trait On New Born Screening: A case Report". Blood 122, № 21 (2013): 954. http://dx.doi.org/10.1182/blood.v122.21.954.954.

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Abstract Introduction There are 827 variants of β thalassemia reported to the registry of human hemoglobin variants and thalassemias registry 1. Genetic mutations of β thalassemia are very diverse but can be broadly divided in to non deletion forms and deletion forms. The new mutation is a frame shift insertion in exon 2 of the β globin gene. To the best of our knowledge this mutation has never been described before and presents as a mild form β thalassemia intermedia. Objective To describe the phenotypic presentation of the new β globin variant, due to insertion of 9 nucleotides (AAAGTGCTC) b

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17

Ramachandran, Sujatha, Kateryna Slinchenkova, Jonathan Leff, et al. "The Impact of the COVID-19 Surge Response on Motivation Among Anesthesiology Residents and Fellows: A discussion of findings from semi-structured interviews at Montefiore Medical Center and educational takeaways." Health Psychology Research 11 (May 13, 2023). http://dx.doi.org/10.52965/001c.74137.

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Background The American Board of Medical Specialties definition of medical professionalism cites the need to acquire, maintain, and advance a value system serving the patients’ and public’s interests above self-interests.4 Medical professionalism is a one of the core physician competencies assessed by both the ACGME training program evaluation and the ABA certification process. However, a growing concern for the decline of professionalism and altruism in medicine resulted in increased publications on the matter, citing various potential sources for the issue. Methods All residents and fellows

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18

Lorenzatti, Daniel, Pamela Piña, Dou Huang, et al. "Interaction Between Risk Factors, Coronary Calcium, and CCTA Plaque Characteristics in Patients Age 18-45." European Heart Journal - Cardiovascular Imaging, April 5, 2024. http://dx.doi.org/10.1093/ehjci/jeae094.

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Abstract Aims The atherosclerotic profile and advanced plaque subtype burden in symptomatic patients ≤45 years old have not been established. This study aimed to assess the prevalence and predictors of coronary artery calcium (CAC), plaque subtypes, and plaque burden by coronary computed tomography angiography (CCTA) in symptomatic young patients. Methods and Results We included 907 symptomatic young patients (18-45 years) from Montefiore undergoing CCTA for chest pain evaluation. Prevalence and predictors of CAC, plaque subtypes, and burden were evaluated using semi-automated software. In the

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Azevedo, Pedro Correia. "O Desafio da Hospitalização Domiciliária." Gazeta Médica, December 30, 2020. http://dx.doi.org/10.29315/gm.v7i4.408.

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Após a II Grande Guerra, em 1945, a lotação dos hospitais americanos tornou necessário criar uma alternativa que permitisse o tratamento dos doentes, o início da sua reabilitação e a criação de um ambiente psicológico mais favorável. É assim que, no Hospital Montefiore em Nova Iorque, nasce a Hospitalização Domiciliária aliando os benefícios para o doente e as necessidades do sistema – hospital at home. Na Europa, esta realidade surge em França, em 1957, no Assistance Publique – Hôpitaux de Paris, seguindo-se a Suíça, a Alemanha, o Reino Unido, Espanha, entre outros.1 Em Portugal, o Serviço de

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