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Developmental Neuroscience|January 1, 1991
Molecular and clinical heterogeneity of adult GM2 gangliosidosisR NavonHuman Heredity|January 1, 1990
Thermolabile hexosaminidase (Hex) B: diverse frequencies among Jewish communities and implication for screening of sera for Hex A deficienciesR Navon, A AdamAnnals of Neurology|July 1, 1984
Clinical and genetic variations in the syndrome of adult GM2 gangliosidosis resulting from hexosaminidase A deficiencyZ Argov, R NavonBiochemical and Biophysical Research Communications|November 13, 1987
Depletion of cellular beta-hexosaminidase by imipramine is prevented by dexamethasone; implications for treating psychotic hexosaminidase-A deficient patientsR Navon, D BaramMolecular Genetics and Metabolism|December 16, 1998
At least six different mutations in HEXA gene cause Tay-Sachs disease among the Turkish populationH A Ozkara, R NavonAmerican Journal of Human Genetics|February 1, 1991
Tay-Sachs disease in Moroccan Jews: deletion of a phenylalanine in the alpha-subunit of beta-hexosaminidaseR Navon, R L ProiaScience (New York, N.Y.)|March 17, 1989
The mutations in Ashkenazi Jews with adult GM2 gangliosidosis, the adult form of Tay-Sachs diseaseR Navon, R L ProiaAnnals of Neurology|September 1, 1988
Hexosaminidase A deficiency manifesting as spinal muscular atrophy of late onsetA Karni, R Navon, M SadehAmerican Journal of Medical Genetics|May 1, 1986
Hexosaminidase A deficiency in adultsR Navon, Z Argov, A FrischPageof 5