about
POMGnT1 mutation and phenotypic spectrum in muscle-eye-brain diseaseDysfunctional ADAM22 implicated in progressive encephalopathy with cortical atrophy and epilepsy[Imaging of acute brain infarction]Neuroimaging of pediatric diseases.Fetal hypoxia and structural brain abnormalities in schizophrenic patients, their siblings, and controls.Effect of Inhaled Xenon on Cerebral White Matter Damage in Comatose Survivors of Out-of-Hospital Cardiac Arrest: A Randomized Clinical Trial.Cerebroretinal microangiopathy with calcifications and cysts.Incidence, phenotypic features and molecular genetics of Kallmann syndrome in Finland.Selenoprotein biosynthesis defect causes progressive encephalopathy with elevated lactate.Genetic Overlap between Holoprosencephaly and Kallmann Syndrome.Neuroimaging supports the clinical diagnosis of methanol poisoning.Radiation therapy and concurrent topotecan followed by maintenance triple anti-angiogenic therapy with thalidomide, etoposide, and celecoxib for pediatric diffuse intrinsic pontine glioma.Atypical craniosynostosis with torticollis and neurological symptoms: a rhombencephalosynapsis sequence.Brain magnetic resonance imaging of infants exposed prenatally to buprenorphine.Bilateral hippocampal infarction as etiology of sudden and prolonged memory lossCerebral infarction in a child with sickle cell trait.Progressive Stroke-Like Symptoms in a Patient with Sporadic Creutzfeldt-Jakob Disease.Mitochondrial phenylalanyl-tRNA synthetase mutations underlie fatal infantile Alpers encephalopathy.Cortical somatosensory processing measured by magnetoencephalography predicts neurodevelopment in extremely low-gestational-age infants.MRI findings in children with school problems who had been exposed prenatally to alcohol.Proton spectroscopic imaging shows abnormalities in glial and neuronal cell pools in frontal lobe epilepsy.Brain anomalies in 121 children with non-syndromic single suture craniosynostosis by MR imaging.Focal and global cortical hypometabolism in patients with newly diagnosed infantile spasms.Herpes simplex myelitis simulating neoplasm on magnetic resonance imaging.Mild brain atrophy in early HIV infection: the lack of association with cognitive deficits and HIV-specific intrathecal immune response.Radiological signs in newborns exposed to primary Toxoplasma infection in utero.Low-grade gliomas and focal cortical developmental malformations: differentiation with proton MR spectroscopy.Functional plasticity of the motor cortical structures demonstrated by navigated TMS in two patients with epilepsy.Five new cases of a recently described leukoencephalopathy with high brain lactate.Acute and delayed cerebral infarction after wasp sting anaphylaxis.POLG1 manifestations in childhood.Neurodevelopmental burden at age 5 years in patients with univentricular heart.Radiological study of the brain at various stages of human immunodeficiency virus infection: early development of brain atrophy.Dravet syndrome: new potential genetic modifiers, imaging abnormalities, and ictal findings.DARS2 mutations in mitochondrial leucoencephalopathy and multiple sclerosis.Recessive twinkle mutations cause severe epileptic encephalopathy.The effect of surgery in encephalopathy with electrical status epilepticus during sleep.Hippocampal volumes in schizophrenic twins.[Tuberous sclerosis].A juvenile case of MELAS with T3271C mitochondrial DNA mutation.
P50
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P50
description
hulumtuese
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հետազոտող
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name
Leena Valanne
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Leena Valanne
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Leena Valanne
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Leena Valanne
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Leena Valanne
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type
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Leena Valanne
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Leena Valanne
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Leena Valanne
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Leena Valanne
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Leena Valanne
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Leena Valanne
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Leena Valanne
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Leena Valanne
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Leena Valanne
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Leena Valanne
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P106
P21
P31
P496
0000-0002-8572-829X