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You searched for: Author/Creator Martin, Martin G.

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1. Atypical Alexander disease with dystonia, retinopathy, and a brain mass mimicking astrocytoma. (August 2018)

3. EPCAM mutation update: Variants associated with congenital tufting enteropathy and Lynch syndrome. Issue 2 (29th November 2018)

4. Esophageal IgG4: Clinical, Endoscopic, and Histologic Correlations in Eosinophilic Esophagitis. Issue 5 (May 2019)

5. Expansion of NEUROD2 phenotypes to include developmental delay without seizures. Issue 4 (13th January 2021)