نتائج البحث - Gropman, Andrea L.
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Response to Finsterer’s “Exclude hereditary and acquired differential disorders before attributing retinoschisis to Kears-Sayre syndrome” حسب Chertkof, Julia, Hufnagel, Robert B., Blain, Delphine, Gropman, Andrea L., Brooks, Brian P.
منشور في 2020نص -
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(1)H MRS allows brain phenotype differentiation in sisters with late onset ornithine transcarbamylase deficiency (OTCD) and discordant clinical presentations حسب Gropman, Andrea L, Seltzer, Rebecca R., Yudkoff, Marc, Sawyer, Alice, vanMeter, John, Fricke, Stanley T.
منشور في 2008نص -
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