Search Results - Strazisar, B. Gnidovec

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  1. 1
    On the rise and fall of the apnea−hypopnea index: A historical review and critical appraisal

    On the rise and fall of the apnea−hypopnea index: A historical review and critical appraisal by Pevernagie, Dirk A., Gnidovec‐Strazisar, Barbara, Grote, Ludger, Heinzer, Raphael, McNicholas, Walter T., Penzel, Thomas, Randerath, Winfried, Schiza, Sophia, Verbraecken, Johan, Arnardottir, Erna S.

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  2. 2
    Serum ferritin and vitamin D levels in sleep disordered children with attention-deficit/hyperactivity disorder and/or autism

    Serum ferritin and vitamin D levels in sleep disordered children with attention-deficit/hyperactivity disorder and/or autism by Korosec, D., Knez, M., Strazisar, B. Gnidovec

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  3. 3
    P187 – 2088 A case of debilitating fluctuating myotonia due to autosomal dominant mutation in SCN4A gene

    P187 – 2088 A case of debilitating fluctuating myotonia due to autosomal dominant mutation in SCN4A gene by Gnidovec Strazisar, B, Writzl, K, Leonardis, L

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  4. 4
    P57 – 1731 A case of early onset epilepsy due to duplication of the sodium gene cluster on 2q24 with early seizure remission

    P57 – 1731 A case of early onset epilepsy due to duplication of the sodium gene cluster on 2q24 with early seizure remission by Gnidovec Strazisar, B, Rener Primec, Z, Writzl, K

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  5. 5
    Content validation of a test battery for assessing sleep quality in adolescents in Slovenia

    Content validation of a test battery for assessing sleep quality in adolescents in Slovenia by Mlakar, A, Kukec, A, Rejc, T, Šmigoc, M, Gril Rogina, K, Gnidovec Stražišar, B

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  6. 6
    Childhood narcolepsy in Slovenia

    Childhood narcolepsy in Slovenia by Gnidovec Stražišar, B., Dolenc Grošelj, L.

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  7. 7
    P15 – 1733 A novel SCN2A missense mutation in a Slovenian girl with early-onset epileptic encephalopathy

    P15 – 1733 A novel SCN2A missense mutation in a Slovenian girl with early-onset epileptic encephalopathy by Gnidovec Strazisar, B, Writzl, K, Paro Panjan, D, Neubauer, D, Nakamura, K, Matsumoto, N, Saitsu, H

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  8. 8
    Novel oligophrenin 1 mutation in a neonate evaluated for possible congenital toxoplasmosis

    Novel oligophrenin 1 mutation in a neonate evaluated for possible congenital toxoplasmosis by Stražišar, B. Gnidovec, Writzl, K

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  9. 9
    Pediatric sleep medicine organisation in Europe

    Pediatric sleep medicine organisation in Europe by Stražišar, B. Gnidovec, Deleanu, O.C., Korostovtseva, L., Khachatryan, S., Van der Werf, Y., Parrino, L., Verbraecken, J., Arnardottir, E.S.

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  10. 10
    CBO05 Sleep disturbances in Smith-Magenis syndrome: a report on the first Slovenian case

    CBO05 Sleep disturbances in Smith-Magenis syndrome: a report on the first Slovenian case by Strazisar, B. Gnidovec, Grošelj, L. Dolenc, Claustrat, B, Brun, J

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  11. 11
    PP04.2 – 2598: The varicella-zoster virus vasculopathy: Case report

    PP04.2 – 2598: The varicella-zoster virus vasculopathy: Case report by Hostnik, T, Stražišar, B. Gnidovec, Vipotnik Vesnaver, T, Benedik, M. Perkovič

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