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Microscopic Cell Analysis

Our Work

Browse key publications that reflect the consortium’s commitment to accelerating research in X-linked neurodevelopmental disorders. This page includes foundational studies, cross-disciplinary collaborations, and emerging insights that shape the future of the field.

DNA Double Helix

Building a Natural History and Patient Registry Platform for Coffin-Lowry Syndrome (CLS): A Roadmap for Therapeutic Readiness

​Authors: Mary C Hames, PhD  (BioLogic Pharma Solutions), Jin Lee, PhD  (CURENDD), Theresa Moxley (Coffin Lowry Foundation), Tobin Chettiath (BioLogic Pharma Solutions), Amanda Singleton, PhD (Gene dx), Kasey Creel (BioLogic Pharma Solutions)

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Every day counts for children and families affected by X-linked neurodevelopmental disorders.

Cure NDD, a 501(c)(3) nonprofit, is working to fast-track research and therapies where options are limited or nonexistent.

Your tax-deductible donation directly supports the path to cures.

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EIN: 39-5006055

CureNDDs@gmail.com

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