Search Results - "Orlova, K A"

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  1. 1

    Difficulties in the differential diagnosis of epileptic and hypocalcemic seizures in children and adolescents by Shchederkina, I. O., Orlova, K. A., Koltunov, I. E., Orlova, E. M., Korneev, D. Yu, Vykhristyuk, O. F.

    “…Epileptic seizures require differential diagnosis with other paroxysmal conditions, including metabolic seizures. A variety of electrolyte changes can result…”
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    Journal Article
  2. 2

    EFFICACY OF RUFINAMIDE IN THE TREATMENT OF DRUG-RESISTANT FOCAL EPILEPSIES IN PAEDIATRIC PRACTICE by Shchederkina, I. O., Orlova, K. A., Koltunov, I. E., Dorofeeva, M. Yu

    Published in Russkiĭ zhurnal detskoĭ nevrologii (01-02-2017)
    “…Among drug-resistant epilepsies, epileptic syndromes, characterized by combination of several types of seizures, are considered to be the most difficult in…”
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    Journal Article
  3. 3

    SPEECH DELAY IN THE PRACTICE OF A PAEDIATRICIAN AND CHILD’S NEUROLOGIST by Zavadenko, N. N., Shchederkina, I. O., Zavadenko, A. N., Kozlova, E. V., Orlova, K. A., Davydova, L. A., Doronicheva, M. M., Shadrova, A. A.

    Published in Voprosy sovremennoĭ pediatrii (01-02-2015)
    “…The article describes the main clinical forms and causes of speech delay in children. It presents modern data on the role of neurobiological factors in the…”
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    Journal Article
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    Neurodevelopmental disorders in children with epilepsy by Zavadenko, N N, Kholin, A A, Zavadenko, A N, Shadrova, A A, Orlova, K A

    “…Neurodevelopmental disorders, including intellectual disability, autistic-spectrum disorders, speech disorders, attention deficit hyperactivity disorder…”
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  7. 7

    Rapamycin prevents seizures after depletion of STRADA in a rare neurodevelopmental disorder by Parker, Whitney E, Orlova, Ksenia A, Parker, William H, Birnbaum, Jacqueline F, Krymskaya, Vera P, Goncharov, Dmitry A, Baybis, Marianna, Helfferich, Jelte, Okochi, Kei, Strauss, Kevin A, Crino, Peter B

    Published in Science translational medicine (24-04-2013)
    “…A rare neurodevelopmental disorder in the Old Order Mennonite population called PMSE (polyhydramnios, megalencephaly, and symptomatic epilepsy syndrome; also…”
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    Journal Article
  8. 8

    Early Progenitor Cell Marker Expression Distinguishes Type II From Type I Focal Cortical Dysplasias by Orlova, Ksenia A, Tsai, Victoria, Baybis, Marianna, Heuer, Gregory G, Sisodiya, Sanjay, Thom, Maria, Strauss, Kevin, Aronica, Eleonora, Storm, Phillip B, Crino, Peter B

    “…Type I and type II focal cortical dysplasias (FCDs) exhibit distinct histopathologic features that suggest different pathogenic mechanisms. Type I FCDs are…”
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    STRADa deficiency results in aberrant mTORCI signaling during corticogenesis in humans and mice by Orlova, KA, Parker, W E, Heuer, G G, Tsai, V, Yoon, J, Baybis, M, Fenning, R S, Strauss, K, Crino, P B

    Published in The Journal of clinical investigation (01-05-2010)
    “…Polyhydramnios, megalencephaly, and symptomatic epilepsy syndrome (PMSE) is a rare human autosomal-recessive disorder characterized by abnormal brain…”
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    Journal Article
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