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SLC7A3 : in silico prediction of a potential new cause of childhood epilepsy
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Tone reduction and physical therapy : strengthening partners in treatment of children with spastic cerebral palsy
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Neurocysticercosis in Europe : need for a One Health approach
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Gastric dysmotility following orthopaedic scoliosis surgery in patients with cerebral palsy: a case series
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Aicardi syndrome in a male patient
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Ethylmalonic encephalopathy: Clinical and biochemical observations
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Delayed neuromotor development combined with albinism and increased very long chain fatty acids.
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Diagnostics in mitochondrial diseases: the need of collaboration between clinician and research laboratories.
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Nijmegen breakage syndrome: A neuropathological study
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Mental retardation in amaurosis congenita of Leber.