Search Results - Wolanska, Ewelina

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  1. 1
    Case Report: Further Delineation of Neurological Symptoms in Young Children Caused by Compound Heterozygous Mutation in the PIEZO2 Gene

    Case Report: Further Delineation of Neurological Symptoms in Young Children Caused by Compound Heterozygous Mutation in the PIEZO2 Gene by Klaniewska, Magdalena, Jedrzejowska, Maria, Rydzanicz, Malgorzata, Paprocka, Justyna, Biela, Mateusz, Wolanska, Ewelina, Pollak, Agnieszka, Debek, Emilia, Sasiadek, Maria, Ploski, Rafal, Gos, Monika, Smigiel, Robert

    Published in Frontiers in genetics
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  2. 2
    The Role of the Reanalysis of Genetic Test Results in the Diagnosis of Dysmorphic Syndrome Caused by Inherited xq24 Deletion including the UBE2A and CXorf56 Genes

    The Role of the Reanalysis of Genetic Test Results in the Diagnosis of Dysmorphic Syndrome Caused by Inherited xq24 Deletion including the UBE2A and CXorf56 Genes by Wolańska, Ewelina, Pollak, Agnieszka, Rydzanicz, Małgorzata, Pesz, Karolina, Kłaniewska, Magdalena, Rozensztrauch, Anna, Skiba, Paweł, Stawiński, Piotr, Płoski, Rafał, Śmigiel, Robert

    Published in Genes
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  3. 3
    Primitive Reflex Activity in Relation to the Sensory Profile in Healthy Preschool Children

    Primitive Reflex Activity in Relation to the Sensory Profile in Healthy Preschool Children by Pecuch, Anna, Gieysztor, Ewa, Telenga, Marlena, Wolańska, Ewelina, Kowal, Mateusz, Paprocka-Borowicz, Małgorzata

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  4. 4
    Primitive Reflex Activity in Relation to Motor Skills in Healthy Preschool Children

    Primitive Reflex Activity in Relation to Motor Skills in Healthy Preschool Children by Pecuch, Anna, Gieysztor, Ewa, Wolańska, Ewelina, Telenga, Marlena, Paprocka-Borowicz, Małgorzata

    Published in Brain sciences
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  5. 5
    Case Report: Expanded delineation of phenotype of TRPM3-related neurodevelopmental disorders

    Case Report: Expanded delineation of phenotype of TRPM3-related neurodevelopmental disorders by Pawelak, Agnieszka, Polczyk, Artur, Wolańska, Ewelina, Kłaniewska, Magdalena, Biela, Mateusz, Basiak, Aleksander, Franaszczyk, Maria, Rydzanicz, Małgorzata, Płoski, Rafał, Śmigiel, Robert

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  6. 6
    A Child’s Perception of Their Developmental Difficulties in Relation to Their Adult Assessment. Analysis of the INPP Questionnaire

    A Child’s Perception of Their Developmental Difficulties in Relation to Their Adult Assessment. Analysis of the INPP Questionnaire by Demiy, Alina, Kalemba, Agata, Lorent, Maria, Pecuch, Anna, Wolańska, Ewelina, Telenga, Marlena, Gieysztor, Ewa Z.

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  7. 7
    FINCA syndrome—Defining neurobehavioral phenotype in survivors into late childhood

    FINCA syndrome—Defining neurobehavioral phenotype in survivors into late childhood by Badura‐Stronka, Magdalena, Śmigiel, Robert, Rutkowska, Karolina, Szymańska, Krystyna, Hirschfeld, Adam Sebastian, Monkiewicz, Michał, Kosińska, Joanna, Wolańska, Ewelina, Rydzanicz, Małgorzata, Latos‐Bieleńska, Anna, Płoski, Rafał

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  8. 8
    Case Report: Further Delineation of Neurological Symptoms in Young Children Caused by Compound Heterozygous Mutation in the PIEZO2 Gene

    Case Report: Further Delineation of Neurological Symptoms in Young Children Caused by Compound Heterozygous Mutation in the PIEZO2 Gene by Klaniewska, Magdalena, Jedrzejowska, Maria, Rydzanicz, Malgorzata, Paprocka, Justyna, Biela, Mateusz, Wolanska, Ewelina, Pollak, Agnieszka, Debek, Emilia, Sasiadek, Maria, Ploski, Rafal, Gos, Monika, Smigiel, Robert

    Published in Frontiers in genetics
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  9. 9
    The Role of the Reanalysis of Genetic Test Results in the Diagnosis of Dysmorphic Syndrome Caused by Inherited xq24 Deletion including the UBE2A and CXorf56 Genes

    The Role of the Reanalysis of Genetic Test Results in the Diagnosis of Dysmorphic Syndrome Caused by Inherited xq24 Deletion including the UBE2A and CXorf56 Genes by Wolańska, Ewelina, Pollak, Agnieszka, Rydzanicz, Małgorzata, Pesz, Karolina, Kłaniewska, Magdalena, Rozensztrauch, Anna, Skiba, Paweł, Stawiński, Piotr, Płoski, Rafał, Śmigiel, Robert

    Published in Genes
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  10. 10
    High Molecular Complexes of Insulin-Like Growth Factor-I in Human Saliva

    High Molecular Complexes of Insulin-Like Growth Factor-I in Human Saliva by Dargiewicz, Ewelina, Wolańska, Małgorzata, Sobolewski, Krzysztof

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  11. 11
    Tumor necrosis factor in uterine leiomyomas at various stages of tumor growth

    Tumor necrosis factor in uterine leiomyomas at various stages of tumor growth by Wolańska, Małgorzata, Taudul, Ewelina, Bańkowska-Guszczyn, Emilia, Kinalski, Maciej

    Published in Ginekologia polska
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