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Neuromuscular Disorders : NMD|July 22, 2017
Congenital myopathy due to myosin heavy chain 2 mutation presenting as chronic aspiration pneumonia in infancyR Tsabari, H Daum, E Kerem, et al.Thorax|November 23, 2006
Lymphocytic interstitial pneumonia associated with common variable immunodeficiency resolved with intravenous immunoglobulinsN Arish, R Eldor, Y Fellig, et al.Molecular Pathology : MP|July 31, 2001
Nitric oxide synthase immunoreactivity in human bladder carcinomaM Shochina, Y Fellig, M Sughayer, et al.Pediatric Neurosurgery|November 30, 2000
Rathke's cleft cyst abscessZ H Israel, M Yacoub, J M Gomori, et al.Clinical and Experimental Dermatology|December 2, 2015
Isotretinoin treatment of autosomal recessive congenital ichthyosis complicated by coexisting dysferlinopathyJ Mashiah, A Harel, O Bitterman, et al.Journal of Clinical Pathology|September 29, 2005
H19 expression in hepatic metastases from a range of human carcinomasY Fellig, I Ariel, P Ohana, et al.Molecular Psychiatry|September 18, 2013
Neural mechanisms underlying stress resilience in Ahi1 knockout mice: relevance to neuropsychiatric disordersA Lotan, T Lifschytz, A Slonimsky, et al.Journal of Oncology|November 6, 2010
Use of H19 Gene Regulatory Sequences in DNA-Based Therapy for Pancreatic CancerV Scaiewicz, V Sorin, Y Fellig, et al.Molecular Pathology : MP|February 24, 2001
The imprinted H19 gene is a marker of early recurrence in human bladder carcinomaI Ariel, M Sughayer, Y Fellig, et al.Acta Neuropathologica Communications|November 6, 2019
BRAF V600E mutation in Juvenile Xanthogranuloma family neoplasms of the central nervous system (CNS-JXG): a revised diagnostic algorithm to include pediatric Erdheim-Chester diseaseJ Picarsic, T Pysher, H Zhou, et al.Pageof 1