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  1. Book: Mitificación y desmitificación del canon y literaturas en España y Hispanoamérica

    Chicharro Chamorro, Antonio / Kumor, Karolina / Moszczynska, Katarzyna

    2013  

    Author's details Antonio Chicharro; Karolina Kumor; Katarzyna Moszczyńska-Dürst (eds. y coords.)
    Keywords Canon (Literature) ; Spanish American literature/History and criticism ; Spanish literature/History and criticism
    Language Spanish
    Size 262 p, 22 cm
    Publisher Universidad de Granada
    Publishing place Granada
    Document type Book
    Note Collected essays
    ISBN 9788433855831 ; 8433855832
    Database Former special subject collection: coastal and deep sea fishing

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  2. Article: Chorioangioma--opis przypadku.

    Moszczyńska, Katarzyna / Szułczyński, Jarosław / Wasik, Damian / Tretyn, Andrzej / Breborowicz, Grzegorz H / Dubiel, Mariusz

    Ginekologia polska

    2014  Volume 85, Issue 3, Page(s) 230–233

    Abstract: Chorioangioma (chorionic angioma) is the most common non-malignant placental tumor Taking into account its morphological structure, it can have significant influence on fetal condition and pregnancy depending on its size. In the presented case a ... ...

    Title translation Chorioangioma--a case study.
    Abstract Chorioangioma (chorionic angioma) is the most common non-malignant placental tumor Taking into account its morphological structure, it can have significant influence on fetal condition and pregnancy depending on its size. In the presented case a substantial placental tumor was diagnosed and complications typical for chorioangioma, such as fetal hemodynamic disorders, polyhydramnios, gestational diabetes and premature labor were observed. The applied treatment led to normalization of the fetal and maternal condition and to prolongation of the pregnancy
    MeSH term(s) Adult ; Diabetes, Gestational/diagnosis ; Diabetes, Gestational/etiology ; Female ; Fetal Diseases/diagnosis ; Hemangioma/complications ; Hemangioma/diagnosis ; Hemangioma/pathology ; Hemangioma/therapy ; Humans ; Obstetric Labor, Premature/etiology ; Placenta Diseases/diagnosis ; Placenta Diseases/pathology ; Placenta Diseases/therapy ; Polyhydramnios/diagnosis ; Polyhydramnios/etiology ; Pregnancy ; Pregnancy Complications, Neoplastic/diagnosis ; Pregnancy Complications, Neoplastic/pathology ; Pregnancy Complications, Neoplastic/therapy ; Young Adult
    Language Polish
    Publishing date 2014-04-29
    Publishing country Poland
    Document type Case Reports ; English Abstract ; Journal Article
    ZDB-ID 130894-4
    ISSN 0017-0011
    ISSN 0017-0011
    DOI 10.17772/gp/1719
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article: Pekniety tetniak tetnicy śledzionowej w ciazy donoszonej--opis przypadku.

    Moszczyńska, Katarzyna / Latoch, Izabela / Makarewicz, Michał / Szułczyński, Jarosław / Porzych, Marcin / Ludwikowski, Grzegorz / Dubiel, Mariusz

    Ginekologia polska

    2011  Volume 82, Issue 12, Page(s) 940–942

    Abstract: A case of a primigravida with hypovolemic shock symptoms and acute intrauterine fetal hypoxia was described. Emergency caesarean section, during which a hemorrhage to the peritoneal cavity caused by an unrecognized splenic artery aneurysm rupture was ... ...

    Title translation Rupture of a splenic artery aneurysm in full term pregnancy--case report.
    Abstract A case of a primigravida with hypovolemic shock symptoms and acute intrauterine fetal hypoxia was described. Emergency caesarean section, during which a hemorrhage to the peritoneal cavity caused by an unrecognized splenic artery aneurysm rupture was diagnosed, was immediately performed.
    MeSH term(s) Adult ; Aneurysm, Ruptured/diagnosis ; Aneurysm, Ruptured/surgery ; Cesarean Section ; Female ; Humans ; Infant, Newborn ; Obstetric Labor Complications/diagnosis ; Obstetric Labor Complications/surgery ; Pregnancy ; Pregnancy Complications, Cardiovascular/diagnosis ; Pregnancy Complications, Cardiovascular/surgery ; Pregnancy Trimester, Third ; Rupture, Spontaneous/diagnosis ; Rupture, Spontaneous/surgery ; Splenectomy ; Splenic Artery/pathology ; Splenic Artery/surgery
    Language Polish
    Publishing date 2011-12
    Publishing country Poland
    Document type Case Reports ; English Abstract ; Journal Article
    ZDB-ID 130894-4
    ISSN 0017-0011
    ISSN 0017-0011
    Database MEDical Literature Analysis and Retrieval System OnLINE

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    In stock of ZB MED Cologne/Königswinter

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  4. Article: Rodzinnie uwarunkowana dysplazja tanatoforyczna.

    Lauda-Swieciak, Anna / Moszczyńska, Katarzyna / Skórczewski, Jacek / Ludwikowski, Grzegorz / Szułczyński, Jarosław / Tretyn, Andrzej / Dubiel, Mariusz

    Ginekologia polska

    2010  Volume 81, Issue 8, Page(s) 629–632

    Abstract: Thanatophoric dysplasia was first described in 1967 by Maroteaux. It is one of the most common lethal neonatal dwarfisms. Estimated incidence of thanatophoric dysplasia is 0.2-0.5 per 10,000 births. In the following report we have described a prenatally ... ...

    Title translation Genetically-determined familial recurrent thanatophoric dysplasia.
    Abstract Thanatophoric dysplasia was first described in 1967 by Maroteaux. It is one of the most common lethal neonatal dwarfisms. Estimated incidence of thanatophoric dysplasia is 0.2-0.5 per 10,000 births. In the following report we have described a prenatally diagnosed case of recurrent thanatophoric dysplasia in the same patient.
    MeSH term(s) Fatal Outcome ; Female ; Humans ; Pedigree ; Pregnancy ; Pregnancy Trimester, Second/genetics ; Thanatophoric Dysplasia/diagnostic imaging ; Thanatophoric Dysplasia/genetics ; Ultrasonography, Prenatal
    Language Polish
    Publishing date 2010-08
    Publishing country Poland
    Document type Case Reports ; Journal Article
    ZDB-ID 130894-4
    ISSN 0017-0011
    ISSN 0017-0011
    Database MEDical Literature Analysis and Retrieval System OnLINE

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    In stock of ZB MED Cologne/Königswinter

    Zs.B 118: Show issues Location:
    Je nach Verfügbarkeit (siehe Angabe bei Bestand)
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  5. Article: Holoprosencefalia--przodomózgowie jednokomorowe--opis przypadku.

    Lauda-Swieciak, Anna / Szułczyński, Jarosław / Moszczyńska, Katarzyna / Przybył, Barbara / Skórczewski, Jacek / Ludwikowski, Grzegorz / Tretyn, Andrzej / Dubiel, Mariusz

    Ginekologia polska

    2010  Volume 81, Issue 12, Page(s) 940–943

    Abstract: Holoprosencephaly is a brain malformation caused by abnormal division of the forebrain into two separate hemispheres. Abnormal structures of the central nervous system often occur with other midline forebrain and face failures. In this report we present ... ...

    Title translation Holoprosencephaly--a case report.
    Abstract Holoprosencephaly is a brain malformation caused by abnormal division of the forebrain into two separate hemispheres. Abnormal structures of the central nervous system often occur with other midline forebrain and face failures. In this report we present a case of a prenatal diagnosis of holoprosencephaly.
    MeSH term(s) Adult ; Fatal Outcome ; Female ; Holoprosencephaly/diagnostic imaging ; Holoprosencephaly/embryology ; Humans ; Infant, Newborn ; Pregnancy ; Pregnancy Trimester, Third ; Ultrasonography, Prenatal
    Language Polish
    Publishing date 2010-12
    Publishing country Poland
    Document type Case Reports ; Journal Article
    ZDB-ID 130894-4
    ISSN 0017-0011
    ISSN 0017-0011
    Database MEDical Literature Analysis and Retrieval System OnLINE

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    In stock of ZB MED Cologne/Königswinter

    Zs.B 118: Show issues Location:
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  6. Article: Prenatalne rozpoznanie Zespołu Smitha, Lemlego i Opitza--opis przypadku.

    Lauda-Swieciak, Anna / Przybył, Barbara / Moszczyńska, Katarzyna / Skórczewski, Jacek / Lach, Jarosław / Szułczyński, Jarosław / Ludwikowski, Grzegorz / Dubiel, Mariusz

    Ginekologia polska

    2009  Volume 80, Issue 10, Page(s) 778–781

    Abstract: Smith-Lemli-Opitz syndrome (SLOS) is a hereditary, autosomal recessive abnormality of cholesterol metabolism, leading to malformations of multiple organs. It is probably one of the most frequent metabolic disorders but variable clinical presentation ... ...

    Title translation Prenatal diagnosis of Smith-Lemli-Opitz syndrome--case report.
    Abstract Smith-Lemli-Opitz syndrome (SLOS) is a hereditary, autosomal recessive abnormality of cholesterol metabolism, leading to malformations of multiple organs. It is probably one of the most frequent metabolic disorders but variable clinical presentation makes the diagnosis of the syndrome difficult. The authors of the following work present a case report of prenatal diagnosis of SLOS in fetus with malformations of multiple organs and negative family history.
    MeSH term(s) Fatal Outcome ; Female ; Fetal Diseases/diagnosis ; Fetal Diseases/genetics ; Humans ; Infant, Newborn ; Pregnancy ; Prenatal Diagnosis/methods ; Smith-Lemli-Opitz Syndrome/diagnosis ; Smith-Lemli-Opitz Syndrome/genetics
    Language Polish
    Publishing date 2009-10
    Publishing country Poland
    Document type Case Reports ; English Abstract ; Journal Article
    ZDB-ID 130894-4
    ISSN 0017-0011
    ISSN 0017-0011
    Database MEDical Literature Analysis and Retrieval System OnLINE

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    In stock of ZB MED Cologne/Königswinter

    Zs.B 118: Show issues Location:
    Je nach Verfügbarkeit (siehe Angabe bei Bestand)
    bis Jg. 2021: Bestellungen von Artikeln über das Online-Bestellformular
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