Search Results - Konuskan, B

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  1. 1
    Synthetic MRI in Neurofibromatosis Type 1

    Synthetic MRI in Neurofibromatosis Type 1 by Coban, G., Parlak, S., Gumeler, E., Altunbuker, H., Konuşkan, B., Karakaya, J., Anlar, B., Oguz, K.K.

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  2. 2
    Pediatric headache and neuroimaging: experience of two tertiary centers

    Pediatric headache and neuroimaging: experience of two tertiary centers by Pektezel, M. Y., Konuskan, B., Sonmez, F. M., Oguz, K. K., Anlar, B.

    Published in Child's nervous system
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  3. 3
    Nonsense mutation dystrophinopathy: How mutation-specific treatments changed our clinical practice?

    Nonsense mutation dystrophinopathy: How mutation-specific treatments changed our clinical practice? by Ardicli, D, Konuskan, B, Haliloglu, G, Alikasifoglu, M, Topaloğlu, H

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  4. 4
    P134 – 2952: Magnetic resonance imaging findings in pediatric tuberous sclerosis patients

    P134 – 2952: Magnetic resonance imaging findings in pediatric tuberous sclerosis patients by Anlar, B, Gocmen, R, Serdaroglu, E, Konuskan, B, Yalnizoglu, D

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  5. 5
    G.P.222 - Nonsense mutation dystrophinopathy: How mutation-specific treatments changed our clinical practice?

    G.P.222 - Nonsense mutation dystrophinopathy: How mutation-specific treatments changed our clinical practice? by Ardicli, D., Konuskan, B., Haliloglu, G., Alikasifoglu, M., Topaloğlu, H.

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  6. 6
    G.P.141

    G.P.141 by Öncel, İ, Töpf, A, Evangelista, T, Konuşkan, B, Talim, B, Abicht, A, Lochmüller, H, Topaloglu, H

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  7. 7
    P.366 - Riboflavin transporter deficiency

    P.366 - Riboflavin transporter deficiency by Serdaroğlu, E., Konuşkan, B., Haliloğlu, G., Alikaşifoğlu, M., Topaloğlu, H.

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  8. 8
    Riboflavin transporter deficiency

    Riboflavin transporter deficiency by Serdaroğlu, E., Konuşkan, B., Haliloğlu, G., Alikaşifoğlu, M., Topaloğlu, H.

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  9. 9
    G.P.141: Dpagt1 mutation: Limb-girdle congenital myasthenic syndrome due to glycosylation defect

    G.P.141: Dpagt1 mutation: Limb-girdle congenital myasthenic syndrome due to glycosylation defect by Öncel, İ., Töpf, A., Evangelista, T., Konuşkan, B., Talim, B., Abicht, A., Lochmüller, H., Topaloglu, H.

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  10. 10
    P18 – 2040 A series of epileptic encephalopathies: an array-based genotype-phenotype correlation in a Turkish cohort of children

    P18 – 2040 A series of epileptic encephalopathies: an array-based genotype-phenotype correlation in a Turkish cohort of children by Topcu, M, Konuşkan, B, Alikasifoglu, M, Aktas, D

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  11. 11
    Cadaveric observation of an aberrant left subclavian artery: A possible cause of thoracic outlet syndrome

    Cadaveric observation of an aberrant left subclavian artery: A possible cause of thoracic outlet syndrome by Konuşkan, Bahadır, Bozkurt, M. Cem, Tağıl, Süleyman Murat, Özçakar, Levent

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  12. 12
    P108 – 1741 Anti-N-methyl-D-aspartate receptor encephalitis in a child

    P108 – 1741 Anti-N-methyl-D-aspartate receptor encephalitis in a child by Aksoy, A, Konuşkan, B, Saygi, S, Ozkan, M, Çenesiz, F, Yüksel, D

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  13. 13
    Maintenance of phosphorus fertilizer and residual phosphorus effect on corn production

    Maintenance of phosphorus fertilizer and residual phosphorus effect on corn production by Ibrikci, H, Ryan, J, Ulger, A.C, Buyuk, G, Cakir, B, Korkmaz, K, Karnez, E, Ozgenturk, G, Konuskan, O

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  14. 14
    Genotypic Responses of Corn to Phosphorus Fertilizer Rates in Calcareous Soils

    Genotypic Responses of Corn to Phosphorus Fertilizer Rates in Calcareous Soils by Ibrikci, H, Ulger, A.C, Korkmaz, K, Oktem, A, Buyuk, G, Ryan, J, Amar, B, Konuskan, O, Karnez, E, Ozgenturk, G, Cakir, B, Oguz, H

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