Clinical profile of patients with ATP1A3 mutations in Alternating Hemiplegia of Childhood—a study of 155 patients

Overview of attention for article published in Orphanet Journal of Rare Diseases, September 2015

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Perfil clínico de pacientes con mutaciones ATP1A3 en…

I risultati di un altro importante studio internazionale delle correlazioni genotipo-fenotipo nell'Emiplegia Alternante, sono…

Od dawna oczekiwana puplikacja ukazała się wczoraj. Przedstawia wyniki badań nad 155 osobami chorymi na AHC. Wersja "Full text…

Seit Langem erwartete Publikation ist gestern…

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