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Euvgeni Vlodavsky

Splenic littoral cell haemangioendothelioma: a new low‐grade variant of malignant littoral cell tumour
2001 · O Ben‐Izhak, J Bejar, et al. · Histopathology · 95
Autosomal recessive lissencephaly with cerebellar hypoplasia is associated with a loss-of-function mutation in CDK5
2015 · Daniella Magen, Ayala Ofir, et al. · Human Genetics · 72
Rheumatoid lung nodulosis and osteopathy associated with leflunomide therapy
2005 · Alexander Rozin, Mordechai Yigla, et al. · Clinical Rheumatology · 70
Gliosarcoma Arising in Oligodendroglial Tumors (“Oligosarcoma”)
2007 · Fausto J. Rodriguez, Bernd W. Scheithauer, et al. · The American Journal of Surgical Pathology · 68
Ovarian Adrenal Rest Tumor in a Congenital Adrenal Hyperplasia Patient with Adrenocorticotropin Hypersecretion following Adrenalectomy
2010 · Dov Tiosano, Euvgeni Vlodavsky, et al. · Hormone Research in Paediatrics · 65
Heparanase promotes glioma progression via enhancing CD24 expression
2019 · Uri Barash, Argyris Spyrou, et al. · International Journal of Cancer · 56
Deficiency of HTRA2/Omi is associated with infantile neurodegeneration and 3-methylglutaconic aciduria
2016 · Hanna Mandel, Shotaro Saita, et al. · Journal of Medical Genetics · 35
PRIMARY INTRASPINAL PRIMITIVE NEUROECTODERMAL TUMOR TREATED WITH AUTOLOGOUS STEM CELL TRANSPLANTATION: Case Report and Review of the Literature
2006 · Amir Nutman, Sergey Postovsky, et al. · Pediatric Hematology and Oncology · 22
KRAS mutation positive mucinous adenocarcinoma originating in mature ovarian teratoma: Case report and review of literature
2013 · Dov Hershkovitz, Euvgeni Vlodavsky, et al. · Pathology International · 17
The role of advanced MR methods in the diagnosis of cerebral amyloidoma
2009 · Erez Nossek, Dafna Ben Bashat, et al. · Amyloid · 13
Prostatic tissue in a benign cystic teratoma of the ovary. Report of two cases.
2000 · E Vlodavsky, H Kerner · PubMed · 11
A novel loss-of-function mutation in LACC1 underlies hereditary juvenile arthritis with extended intra-familial phenotypic heterogeneity
2021 · Yonatan Butbul Aviel, Ayala Ofir, et al. · Lara D. Veeken · 8
Sengers syndrome caused by biallelic TIMM29 variants and RNAi silencing in Drosophila orthologue recapitulates the human phenotype
2025 · Adel Shalata, Ann Saada, et al. · Human Genomics · 4
The Natural History and Treatment Guidelines of Cerebellar Liponeurocytoma—A Case Report
2011 · Or Cohen-Inbar, Euvgeni Vlodavsky, et al. · Open Journal of Modern Neurosurgery · 2
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Solitary Fibrous Tumor/Hemangiopericytoma of the Cervical Spine – A Case Report
2021 · haggai suisa, Galia Ronen, et al. · Research Square · 1
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Erratum to: Autosomal recessive lissencephaly with cerebellar hypoplasia is associated with a loss-of-function mutation in CDK5
2015 · Daniella Magen, Ayala Ofir, et al. · Human Genetics · 1
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[Rapidly vanishing hip--a mystery].
2013 · Yaniv Keren, Amit Sigal, et al. · PubMed · 1
Diagnostic Performance of Ultrasound-guided Percutaneous Biopsy Versus Open Surgical Biopsy In Inflammatory Myopathies
2026 · Lutof Zreik, Yonit Tavor, et al. · Academic Radiology
Primary ectopic meningioma of the brachial plexus: A case report and literature review
2025 · Segev Gabay, Marga Serafimova, et al. · Surgical Neurology International
Silent Persistence: Late Pulmonary Recurrence of Metastatic Osteosarcoma
2025 · Oz Mordechai, Anat Ilivitzki, et al.
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The heparanase-CD24-L1CAM axis promotes glioma tumorigenesis
2018 · Uri Barash, Argyris Spyrou, et al.
Unusual Origin of Anemia With Gluteus Red Spots
2014 · Alexander Rozin, Euvgeni Vlodavsky, et al. · Journal of Hematology
Pigmented Villonodular Synovitis for Combined Therapy
2014 · Alexander Rozin, Gabriel Nierenberg, et al. · Journal of Medical Cases
Works count: 23
Citation count: 541
H-index: 11
I10-index: 11
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