Challenges of Phenotype-Genotype Correlations in Rare Diseases von Masten, Margaux C, Augustine, Erika F, Mink, Jonathan W

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The CLN3 Disease Staging System: A new tool for clinical research in Batten disease von Masten, Margaux C., Williams, Justin D., Vermilion, Jennifer, Adams, Heather R., Vierhile, Amy, Collins, Alyssa, Marshall, Frederick J., Augustine, Erika F., Mink, Jonathan W.

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A diagnostic confidence scheme for CLN3 disease von Masten, Margaux C., Corre, Camille, Paciorkowski, Alex R., Vierhile, Amy, Adams, Heather R., Vermilion, Jennifer, Zimmerman, Grace A., Augustine, Erika F., Mink, Jonathan W.

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Epidemiology and Access to Expert Care for the Neuronal Ceroid Lipofuscinoses (NCL) (1878) von Masten, Margaux C., van wijngaarden, Edwin, Augustine, Erika F., Mink, Jonathan W.

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Diagnostic Confidence for CLN3 Disease (Juvenile Batten Disease) (1863) von Masten, Margaux C., Vierhile, Amy, Vermilion, Jennifer, Adams, Heather R., Zimmerman, Grace A., Corre, Camille, Augustine, Erika F., Mink, Jonathan W.

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Genotype-phenotype associations in CLN3 disease von Masten, Margaux C., Vierhile, Amy, Vermilion, Jennifer, Adams, Heather R., Augustine, Erika F., Mink, Jonathan W.

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Epidemiology and access to expert care for the neuronal ceroid lipofuscinoses (NCLs) von Masten, Margaux C., van Wijngaarden, Edwin, Augustine, Erika F., Mink, Jonathan W.

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CLN1 disease natural history data: Prospective and retrospective analysis von Masten, Margaux C., Thatcher, Alyssa, Bonifacio, Kristen, Vierhile, Amy, Adams, Heather R., Mink, Jonathan W., Augustine, Erika F.

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Cross-sectional and longitudinal quantification of CLN3 disease progression von Mink, Jonathan W., Masten, Margaux C., Vermilion, Jennifer, Adams, Heather R., Vierhile, Amy, Marshall, Frederick J., Beck, Christopher A., Augustine, Erika F.

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Hamburg Late Infantile neuronal ceroid lipofucinosis scale (H-LINCLS) vs. the Unified Batten Disease Rating Scale (UBDRS): Comparison and cross-validation von Masten, Margaux C., Adams, Heather R., Vierhile, Amy, Augustine, Erika F., Mink, Jonathan W.

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The CLN3 Disease Staging System (CLN3SS): A tool for stratification based on disease severity von Masten, Margaux C., Williams, Justin D., Augustine, Erika F., Vermilion, Jennifer, Adams, Heather R., Vierhile, Amy, Thatcher, Alyssa, Marshall, Frederick J., Mink, Jonathan W.

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Age-at-onset of core features of CLN3 disease: A cross-sectional and longitudinal natural history study von Masten, Margaux C., Vermilion, Jennifer, Adams, Heather R., Vierhile, Amy, Marshall, Frederick J., Beck, Christopher A., Augustine, Erika F., Mink, Jonathan W.

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Diagnostic confidence for CLN3 disease von Masten, Margaux C., Vierhile, Amy, Vermilion, Jennifer, Adams, Heather, Zimmerman, Grace A., Corre, Camille, Mink, Jonathan W., Augustine, Erika F.

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Challenges of Phenotype-Genotype Correlations in Rare Diseases\Challenges of Phenotype-Genotype Correlations in Rare Diseases-Reply von Masten, Margaux C, Augustine, Erika F, Mink, Jonathan W, Smirnov, Vasily M, Zeitz, Christina, Audo, Isabelle

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Toward meaningful networks: How qualitative research can inform idiographic assessment and personalized care von De Smet, Melissa Miléna, Schoofs, Margaux, Peeters, Hanne, Van Nieuwenhove, Kimberly, Meganck, Reitske

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145th Annual Meeting American Neurological Association

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Inter‐rater Agreement for Movement Disorder Classification in Children with Hyperkinetic Movement Disorders von Yilmaz, Sanem, Vermilion, Jennifer, Dean, Shannon, Pourdeyhimi, Roxanna, Mink, Jonathan W.

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London Calling? Preferred Emigration Destinations among Icelandic Youth von Bjarnason, Thoroddur

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AUT DIABOLUS AUT NIHIL von X L

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AUT DIABOLUS AUT NIHIL von X L

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