Institution
Rambam Health Care Campus
Healthcare•Haifa, Israel•
About: Rambam Health Care Campus is a healthcare organization based out in Haifa, Israel. It is known for research contribution in the topics: Population & Transplantation. The organization has 2498 authors who have published 3715 publications receiving 104362 citations. The organization is also known as: Rambam Hospital & Bet ha-ḥolim ha-memshalti Rambam.
Topics: Population, Transplantation, Cancer, Heparanase, Breast cancer
Papers published on a yearly basis
Papers
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University of Texas MD Anderson Cancer Center1, Peter MacCallum Cancer Centre2, The Royal Marsden NHS Foundation Trust3, Emory University4, Sarah Cannon Research Institute5, University of California, Los Angeles6, Harvard University7, Anschutz Medical Campus8, Vanderbilt University9, Duke University10, Rambam Health Care Campus11, University of Hamburg12, BOTAŞ13, Université catholique de Louvain14, Edinburgh Cancer Research Centre15, University of North Carolina at Chapel Hill16, University of Nebraska Medical Center17, Stanford University18, Seattle Genetics19
TL;DR: In heavily pretreated patients with HER2-positive metastatic breast cancer, including those with brain metastases, adding tucatinib to trastuzumab and capecitabine resulted in better progression-free survival and overall survival outcomes than adding placebo.
Abstract: Background Patients with human epidermal growth factor receptor 2 (HER2)–positive metastatic breast cancer who have disease progression after therapy with multiple HER2-targeted agents hav...
676 citations
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TL;DR: It is demonstrated that low SMI at cancer diagnosis is associated with worse survival in patients with solid tumours and further research into understanding and mitigating the negative effects of sarcopenia in adults with cancer is needed.
674 citations
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TL;DR: The results showed that the nanosensor array could differentiate between ‘healthy’ and ‘cancerous’ breath, and between the breath of patients having different cancer types, and could lead to the development of an inexpensive, easy-to-use, portable, non-invasive tool that overcomes many of the deficiencies associated with the currently available diagnostic methods for cancer.
Abstract: Tumour growth is accompanied by gene and/or protein changes that may lead to peroxidation of the cell membrane species and, hence, to the emission of volatile organic compounds (VOCs). In this study, we investigated the ability of a nanosensor array to discriminate between breath VOCs that characterise healthy states and the most widespread cancer states in the developed world: lung, breast, colorectal, and prostate cancers. Exhaled alveolar breath was collected from 177 volunteers aged 20–75 years (patients with lung, colon, breast, and prostate cancers and healthy controls). Breath from cancerous subjects was collected before any treatment. The healthy population was healthy according to subjective patient's data. The breath of volunteers was examined by a tailor-made array of cross-reactive nanosensors based on organically functionalised gold nanoparticles and gas chromatography linked to the mass spectrometry technique (GC-MS). The results showed that the nanosensor array could differentiate between ‘healthy’ and ‘cancerous’ breath, and, furthermore, between the breath of patients having different cancer types. Moreover, the nanosensor array could distinguish between the breath patterns of different cancers in the same statistical analysis, irrespective of age, gender, lifestyle, and other confounding factors. The GC-MS results showed that each cancer could have a unique pattern of VOCs, when compared with healthy states, but not when compared with other cancer types. The reported results could lead to the development of an inexpensive, easy-to-use, portable, non-invasive tool that overcomes many of the deficiencies associated with the currently available diagnostic methods for cancer.
666 citations
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TL;DR: The observation that Ho-Tr and, for the first time, karyotype complexity confer an increased risk of treatment failure demonstrates that cytogenetic subgroups other than the Ph chromosome can and should be used to risk stratify adults with ALL in future trials.
660 citations
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TL;DR: It is shown that co-activation of clustered neighbouring basal inputs initiated local dendritic spikes, which resulted in a 5.9 ± 1.5 mV change at the soma that amplified the somatic voltage response by 226 ± 46%.
Abstract: Basal dendrites are a major target for synaptic inputs innervating cortical pyramidal neurons At present little is known about signal processing in these fine dendrites Here we show that coactivation of clustered neighbouring basal inputs initiated local dendritic spikes, which resulted in a 59 +/- 15 mV (peak) and 644 +/- 198 ms (half-width) cable-filtered voltage change at the soma that amplified the somatic voltage response by 226 +/- 46% These spikes were accompanied by large calcium transients restricted to the activated dendritic segment In contrast to conventional sodium or calcium spikes, these spikes were mediated mostly by NMDA (N-methyl-D-aspartate) receptor channels, which contributed at least 80% of the total charge The ionic mechanism of these NMDA spikes may allow 'dynamic spike-initiation zones', set by the spatial distribution of glutamate pre-bound to NMDA receptors, which in turn would depend on recent and ongoing activity in the cortical network In addition, NMDA spikes may serve as a powerful mechanism for modification of the cortical network by inducing long-term strengthening of co-activated neighbouring inputs
654 citations
Authors
Showing all 2516 results
Name | H-index | Papers | Citations |
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Jorge E. Cortes | 163 | 2784 | 124154 |
James A. Russell | 124 | 1024 | 87929 |
Barry M. Brenner | 121 | 540 | 65006 |
Razelle Kurzrock | 118 | 1121 | 56594 |
Alan R. Saltiel | 99 | 336 | 49325 |
Michael Aviram | 94 | 479 | 31141 |
Jacob M. Rowe | 75 | 328 | 20043 |
Richard G. Wunderink | 72 | 368 | 26892 |
Doron Aronson | 64 | 261 | 13357 |
Nathan McDannold | 64 | 208 | 16293 |
Jacob I. Sznajder | 61 | 273 | 12201 |
Joseph Itskovitz-Eldor | 60 | 212 | 38298 |
Yehuda Chowers | 60 | 211 | 14526 |
Raanan Shamir | 60 | 379 | 19927 |
David Tanne | 60 | 264 | 41513 |