Treffer 1 - 7 von 7 für Suche 'Katerelos, Adamantios', Suchdauer: 0,43s Treffer weiter einschränken
  1. 1
    Cognitive function in amyotrophic lateral sclerosis: a cross-sectional and prospective pragmatic clinical study with review of the literature

    Cognitive function in amyotrophic lateral sclerosis: a cross-sectional and prospective pragmatic clinical study with review of the literature von Katerelos, Adamantios, Alexopoulos, Panagiotis, Economou, Polychronis, Polychronopoulos, Panagiotis, Chroni, Elisabeth

    Veröffentlicht in Neurological sciences

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  2. 2
    Correction to: Cognitive function in amyotrophic lateral sclerosis: a cross‑sectional and prospective pragmatic clinical study with review of the literature

    Correction to: Cognitive function in amyotrophic lateral sclerosis: a cross‑sectional and prospective pragmatic clinical study with review of the literature von Katerelos, Adamantios, Alexopoulos, Panagiotis, Economou, Polychronis, Polychronopoulos, ·Panagiotis, Chroni, Elisabeth

    Veröffentlicht in Neurological sciences

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  3. 3
    Growth Hormone Deficiency due to p.(Gln467Argfs64) Mutation in the ARID1B Gene in a Girl with Coffin-Siris Syndrome

    Growth Hormone Deficiency due to p.(Gln467Argfs64) Mutation in the ARID1B Gene in a Girl with Coffin-Siris Syndrome von Mouskou, Stella, Leka-Emiri, Sofia, Korona, Anastasia, Mastroyanni, Sotiria, Manolakos, Emmanouil, Papoulidis, Ioannis, Sekouris, Nick, Katerelos, Adamantios, Katsarou-Pectasides, Efstathia, Voudris, Konstantinos

    Veröffentlicht in Molecular syndromology

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  4. 4
    Novel Hemizygous Missense Variant of Spermine Synthase (SMS) Gene Causes Snyder-Robinson Syndrome in a Four-Year-Old Boy

    Novel Hemizygous Missense Variant of Spermine Synthase (SMS) Gene Causes Snyder-Robinson Syndrome in a Four-Year-Old Boy von Mouskou, Stella, Katerelos, Adamantios, Doulgeraki, Artemis, Leka-Emiri, Sofia, Manolakos, Emmanouil, Papoulidis, Ioannis, Ververi, Athina, Vartzelis, Georgios, Korona, Anastasia, Mastroyanni, Sotiria, Voudris, Konstantinos

    Veröffentlicht in Molecular syndromology

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  5. 5
    Pharmacoresistant epilepsy associated with mutations in the KCNB1 and RELN genes. A case report

    Pharmacoresistant epilepsy associated with mutations in the KCNB1 and RELN genes. A case report von Katerelos, Adamantios, Zagkos, Nikolaos, Alexopoulou, Dimitra, Mouskou, Stella, Korona, Anastasia, Manolakos, Emmanouil

    Veröffentlicht in Journal of epileptology

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  6. 6
    Growth Hormone Deficiency due to p.(Gln467Argfs64) Mutation in the ARID1B Gene in a Girl with Coffin-Siris Syndrome

    Growth Hormone Deficiency due to p.(Gln467Argfs64) Mutation in the ARID1B Gene in a Girl with Coffin-Siris Syndrome von Mouskou, Stella, Leka-Emiri, Sofia, Korona, Anastasia, Mastroyanni, Sotiria, Manolakos, Emmanouil, Papoulidis, Ioannis, Sekouris, Nick, Katerelos, Adamantios, Katsarou-Pectasides, Efstathia, Voudris, Konstantinos

    Veröffentlicht in Molecular syndromology

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  7. 7
    Novel Hemizygous Missense Variant of Spermine Synthase (SMS) Gene Causes Snyder-Robinson Syndrome in a Four-Year-Old Boy

    Novel Hemizygous Missense Variant of Spermine Synthase (SMS) Gene Causes Snyder-Robinson Syndrome in a Four-Year-Old Boy von Mouskou, Stella, Katerelos, Adamantios, Doulgeraki, Artemis, Leka-Emiri, Sofia, Manolakos, Emmanouil, Papoulidis, Ioannis, Ververi, Athina, Vartzelis, Georgios, Korona, Anastasia, Mastroyanni, Sotiria, Voudris, Konstantinos

    Veröffentlicht in Molecular syndromology

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