نتایج جستجو برای: canavan

تعداد نتایج: 211  

Journal: :Obstetrics and gynecology 2009

Certain autosomal recessive disease conditions are more prevalent in individuals of Eastern European Jewish (Ashkenazi) descent. Previously, the American College of Obstetricians and Gynecologists recommended that individuals of Eastern European Jewish ancestry be offered carrier screening for Tay-Sachs disease, Canavan disease, and cystic fibrosis as part of routine obstetric care. Based on th...

Journal: :Human gene therapy 2002
Christopher Janson Scott McPhee Larissa Bilaniuk John Haselgrove Mark Testaiuti Andrew Freese Dah-Jyuu Wang David Shera Peter Hurh Joan Rupin Elizabeth Saslow Olga Goldfarb Michael Goldberg Ghassem Larijani William Sharrar Larisa Liouterman Angelique Camp Edwin Kolodny Jude Samulski Paola Leone

This clinical protocol describes virus-based gene transfer for Canavan disease, a childhood leukodystrophy. Canavan disease, also known as Van Bogaert-Bertrand disease, is a monogeneic, autosomal recessive disease in which the gene coding for the enzyme aspartoacylase (ASPA) is defective. The lack of functional enzyme leads to an increase in the central nervous system of the substrate molecule,...

Journal: :Journal of Ultrasound 2014

Journal: :iranian journal of child neurology 0
bita shalbafan neurologist, specialist on neurometabolic disorders, social security organization, tehran, iran

how to cite this article: shalbafan b. alexander and canavan disease. iran j child neurol. autumn 2014;8;4(suppl.1):20-21.

Journal: :Journal of the Neurological Sciences 2016

Journal: :iranian journal of child neurology 0
mahmoodreza ashrafi 1. pediatric neurology division, growth and development research center, children’s medical center, pediatric center of excellence, tehran university of medical science, tehran, iran alireza tavasoli 1. pediatric neurology division, growth and development research center, children’s medical center, pediatric center of excellence, tehran university of medical science, tehran, iran pegah katibeh 1. pediatric neurology division, growth and development research center, children’s medical center, pediatric center of excellence, tehran university of medical science, tehran, iran omid aryani 2. department of medical genetic, national institute for genetic engineering and biotechnology, tehran, iran mohammad vafaee-shahi 1. pediatric neurology division, growth and development research center, children’s medical center, pediatric center of excellence, tehran university of medical science, tehran, iran

how to cite this article: ashrafi mr, tavasoli ar, katibeh p, aryani o, vafaee-shahi m. a novel mutation in aspartoacylase gene; canavan disease. iran j child neurol. autumn 2015; 9(4): 54-57. abstract objective canavan disease (cd) is a type of vacuolating leukodystrophy with autosomal recessive inheritance. aspartoacylase deficiency results in decrease of myelin biosynthesis, dysmyelination a...

Journal: :Journal of chemical theory and computation 2016
Daniel Reta Ibério de P R Moreira Francesc Illas

In the most general case of three electrons in three symmetry unrelated centers with Ŝ1 = Ŝ2 = Ŝ3 = 1/2 localized magnetic moments, the low energy spectrum consists of one quartet (Q) and two doublet (D1, D2) pure spin states. The energy splitting between these spin states can be described with the well-known Heisenberg-Dirac-Van Vleck (HDVV) model spin Hamiltonian, and their corresponding ener...

Journal: :Journal of colloid and interface science 2004
Jonas Ortegren Klaus-Dieter Wantke Hubert Motschmann Helmuth Möhwald

The dilatational properties of fluid surfaces and interfaces have been comprehensively investigated in recent years. For example, an improved oscillating bubble device provided experimental results that allow for critical testing of established surface models, such as the Lucassen/van den Tempel (LvdT) model. The comparison of the LvdT model with the oscillating bubble experiments demonstrates ...

Journal: :Journal of the neurological sciences 2016
Rebecca B Roscoe Christina Elliott Apostolos Zarros George S Baillie

Canavan disease (CD) is a rare leukodystrophy characterized by diffuse spongiform white matter degeneration, dysmyelination and intramyelinic oedema with consequent impairment of psychomotor development and early death. The molecular cause of CD has been identified as being mutations of the gene encoding the enzyme aspartoacylase (ASPA) leading to its functional deficiency. The physiological ro...

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