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The Journal of Hand Surgery|March 18, 2025
Intraoperative Pain During Carpal Tunnel Release Performed by Experienced Surgeons: A Prospective Randomized Trial Comparing WALANT with Local Anesthesia and TourniquetIgnacio Rellán, Nicolas Martin Molho, Agustín Guillermo Donndorff, et al.Plos One|December 28, 2020
The prevalence of dyads in social lifeLeonard S Peperkoorn, D Vaughn Becker, Daniel Balliet, et al.The Oncologist|June 11, 2026
Women's Health Across the Reproductive Lifespan in Women with Germline TP53 Pathogenic Variants: A Clinical PerspectiveNaama Halpern, Rinat Bernstein-Molho, Yehudit Peerless, et al.Israel Journal of Health Policy Research|September 10, 2024
Adverse health effects of exposure to plastic, microplastics and their additives: environmental, legal and policy implications for IsraelIlana Belmaker, Evelyn D Anca, Lisa P Rubin, et al.Haemophilia : the Official Journal of the World Federation of Hemophilia|January 13, 2000
Epidemiological survey of the orthopaedic status of severe haemophilia A and B patients in France. The French Study Group. secretariat.haemophiles@cch.ap-hop-paris.frP Molho, N Rolland, T Lebrun, et al.Haemophilia : the Official Journal of the World Federation of Hemophilia|April 24, 1999
A retrospective study on chemical and radioactive synovectomy in severe haemophilia patients with recurrent haemarthrosisP Molho, P Verrier, N Stieltjes, et al.The Journal of Clinical Investigation|October 1, 1989
Molecular characterization of antithrombin III (ATIII) variants using polymerase chain reaction. Identification of the ATIII Charleville as an Ala 384 Pro mutationP Molho-Sabatier, M Aiach, I Gaillard, et al.Thrombosis Research|May 23, 2001
Embolized ischemic lesions of toes in an afibrinogenemic patient: possible relevance to in vivo circulating thrombinE Dupuy, C Soria, P Molho, et al.Journal of the American Academy of Dermatology|July 31, 2007
Evidence for clinical and genetic heterogeneity in hereditary benign telangiectasiaVered Molho-Pessach, Ziad Agha, Diana Libster, et al.Journal of Medical Genetics|March 28, 2014
Mutation in KANK2, encoding a sequestering protein for steroid receptor coactivators, causes keratoderma and woolly hairYuval Ramot, Vered Molho-Pessach, Tomer Meir, et al.Pageof 37