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TUBA1A mutations: from isolated lissencephaly to familial polymicrogyria
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Facial nerve palsy as the presenting manifestation of a cerebellopontine angle meningeal melanocytoma
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Bilateral striatal necrosis with a novel point mutation in the mitochondrial ATPase 6 gene
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Retroperitoneal teratoma as first sign of klinefelters-syndrome
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A functioning double aortic arch in an infant : a case report
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Diagnosis and management of catheter-related infected intracardiac thrombosis in premature infants
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Neonatal tuberous sclerosis : US, CT, and MR diagnosis of brain and cardiac lesions