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Prenatal Diagnosis|August 20, 2010
Sixteen years of prenatal consultations for the N370S/N370S Gaucher disease genotype: what have we learned?Yael Eitan, Ayala Abrahamov, Mici Phillips, et al.Hematology (Amsterdam, Netherlands)|July 16, 2005
Survey of hematological aspects of Gaucher diseaseAri Zimran, Gheona Altarescu, Bernard Rudensky, et al.Blood Cells, Molecules & Diseases|May 12, 2005
C-reactive protein and NT-proBNP as surrogate markers for pulmonary hypertension in Gaucher diseaseDeborah Elstein, Amiram Nir, Marc Klutstein, et al.Blood Cells, Molecules & Diseases|February 6, 2004
Effect of enzyme replacement therapy on gammopathies in Gaucher diseaseAriel Brautbar, Deborah Elstein, Guy Pines, et al.Blood Cells, Molecules & Diseases|May 12, 2005
Incidence of malignancies among patients with type I Gaucher disease from a single referral clinicAri Zimran, Irena Liphshitz, Micha Barchana, et al.American Journal of Ophthalmology|July 26, 2005
Uveitis in Gaucher diseaseAltoon Dweck, Jaacov Rozenman, Suzy Ronen, et al.Clinica Chimica Acta; International Journal of Clinical Chemistry|August 2, 2015
Rapid, single-phase extraction of glucosylsphingosine from plasma: A universal screening and monitoring toolMaria Fuller, Jeff Szer, Samantha Stark, et al.Blood Cells, Molecules & Diseases|April 25, 2017
Clinical course and disease burden in patients with paroxysmal nocturnal hemoglobinuria by hemolytic statusMustafa N Yenerel, Petra Muus, Amanda Wilson, et al.Journal of Ultrasound in Medicine : Official Journal of the American Institute of Ultrasound in Medicine|September 10, 2002
Multiple hypoechoic hepatic lesions in a patient with Gaucher diseaseMichael Patlas, Irith Hadas-Halpern, Constantin Reinus, et al.Genetic Testing|April 29, 2005
Phenotypic heterogeneity in patients with Gaucher disease and the N370S/V394L genotypeDeborah Elstein, C Ronald Scott, Marsha Zeigler, et al.Pageof 35