Tel Aviv University

University / College


Location: Tel Aviv, Israel (IL) IL

ISNI: 0000000419370546

ROR: https://ror.org/04mhzgx49

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Types of publications

Journal article
Book chapter / Article in edited volumes
Authored book
Translation
Thesis
Edited Volume
Conference contribution
Other publication type
Unpublished / Preprint

Publication year

From
To

Abstract

Journal

International consensus statement on microbiome testing in clinical practice (2025) Porcari S, Mullish BH, Asnicar F, Ng SC, Zhao L, Hansen R, O'Toole PW, et al. Journal article, Review article Optimization of Pulsed Saturation Transfer MR Fingerprinting (ST MRF) Acquisition Using the Cramér–Rao Bound and Sequential Quadratic Programming (2025) Vladimirov N, Zaiß M, Perlman O Journal article Consensus on acromegaly therapeutic outcomes: an update (2025) Melmed S, di Filippo L, Fleseriu M, Mercado M, Karavitaki N, Gurnell M, Salvatori R, et al. Journal article Diagnosis and Management of Upper Gastrointestinal Involvement in Adult Patients With Crohn's Disease: A Systematic Review (2025) Cohen NA, Sror N, Naseer M, Bettenworth D, Lu C, Khedraki R, Abreu MT, et al. Journal article Cocreating the Visualization of Digital Mobility Outcomes: Delphi-Type Process With Patients (2025) Lumsdon J, Wilson C, Alcock L, Becker C, Benvenuti F, Bonci T, van den Brande K, et al. Journal article Quantitative molecular imaging using deep magnetic resonance fingerprinting (2025) Vladimirov N, Cohen O, Heo HY, Zaiß M, Farrar CT, Perlman O Journal article Automated Multicohort Mobility Assessment with an Instrumented L-test (iL-test) (2025) Albites-Sanabria J, Palumbo P, D'ascanio I, Bonci T, Caruso M, Salis F, Cereatti A, et al. Journal article In vivo mapping of the chemical exchange relayed nuclear Overhauser effect using deep magnetic resonance fingerprinting (2024) Power I, Rivlin M, Shmuely H, Zaiß M, Navon G, Perlman O Journal article TFE3-rearranged nonmelanotic renal PEComa: a case series expanding their phenotypic and fusion landscape (2024) Agaimy A, Acosta AM, Cheng L, Collins K, Fridman E, Schubart C, Williamson SR, et al. Journal article MSL2 variants lead to a neurodevelopmental syndrome with lack of coordination, epilepsy, specific dysmorphisms, and a distinct episignature (2024) Karayol R, Borroto MC, Haghshenas S, Namasivayam A, Reilly J, Levy MA, Relator R, et al. Journal article