Providing education, support, advocacy, and promoting research
for CTX patients, their families, and medical professionals
who treat and study this rare disease.
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michael2025-03-17 15:11:012025-03-17 15:11:01Allelic prevalence and geographic distribution of cerebrotendinous xanthomatosis
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michael2025-03-17 15:07:522025-03-17 15:08:03Chenodeoxycholic acid (CDCA) treatment during pregnancy in women with cerebrotendinous xanthomatosis (CTX): Lessons learned from 19 pregnancies
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michael2025-03-17 15:03:282025-03-17 15:12:34Cerebrotendinous Xanthomatosis occurs at high frequency in Ashkenazi Jews
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michael2021-11-18 00:20:182021-12-01 03:05:57Apparent underdiagnosis of Cerebrotendinous Xanthomatosis revealed by analysis of ~60,000 human exomes
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michael2021-09-13 00:17:012021-12-01 03:05:55Cerebrotendinous Xanthomatosis
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michael2021-08-27 00:14:152021-11-30 20:51:06Epidemiology, diagnosis, and treatment of cerebrotendinous xanthomatosis (CTX)
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michael2021-07-05 00:09:012021-12-01 03:06:35Expert opinion on diagnosing, treating and managing patients with cerebrotendinous xanthomatosis (CTX): a modified Delphi study
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michael2021-06-22 00:02:542021-12-01 03:06:33Newborn screening for cerebrotendinous xanthomatosis is the solution for early identification and treatment