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Personality functioning in anxiety disorders

BMC psychiatry, 2018-09, Vol.18 (1), p.294-294, Article 294

2018

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Personality functioning and self-disorders in individuals at ultra-high risk for psychosis, with first-episode psychosis and with borderline personality disorder

BJPsych open, 2023-08, Vol.9 (5), p.e150-e150, Article e150

2023

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Men don't cry: The supporting role as necessary for women's well‐being after termination of pregnancy

International journal of gynecology and obstetrics, 2024-03, Vol.164 (3), p.1205-1211

2024

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Termination of pregnancy for fetal malformation: A traumatic event? A qualitative analysis of women’s perception

Zeitschrift für Psychosomatische Medizin und Psychotherapie, 2023-02, Vol.69 (1), p.36-55

2023

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A spoonful of L‐fucose—an efficient therapy for GFUS‐CDG, a new glycosylation disorder

EMBO molecular medicine, 2021-09, Vol.13 (9), p.e14332-n/a

2021

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Bildspuren - Sprachspuren : Postkarten als Quellen zur Mehrsprachigkeit in der späten Habsburger Monarchie (Edition 1)

1, 2020

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Case Report-An Inherited Loss-of-Function NRXN3 Variant Potentially Causes a Neurodevelopmental Disorder with Autism Consistent with Previously Described 14q24.3-31.1 Deletions

Genes, 2023-06, Vol.14 (6), p.1217

2023

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A TSHZ3 Frame-Shift Variant Causes Neurodevelopmental and Renal Disorder Consistent with Previously Described Proximal Chromosome 19q13.11 Deletion Syndrome

Genes, 2022-11, Vol.13 (12), p.2191

2022

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De novo variants in TCF7L2 are associated with a syndromic neurodevelopmental disorder

American journal of medical genetics. Part A, 2021-08, Vol.185 (8), p.2384-2390

2021

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PPA1 Deficiency Causes a Deranged Galactose Metabolism Recognizable in Neonatal Screening

Metabolites, 2023-11, Vol.13 (11), p.1141

2023

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Bi-allelic LETM1 variants perturb mitochondrial ion homeostasis leading to a clinical spectrum with predominant nervous system involvement

American journal of human genetics, 2022-09, Vol.109 (9), p.1692-1712

2022

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Durvalumab impacts progression-free survival while high-dose radiation >66 Gy improves local control without excess toxicity in unresectable NSCLC stage III: Real-world data from the Austrian radio-oncological lung cancer study association registry (ALLSTAR)

Radiotherapy and oncology, 2024-07, Vol.196, p.110294, Article 110294

2024

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Case Report—An Inherited Loss-of-Function INRXN3/I Variant Potentially Causes a Neurodevelopmental Disorder with Autism Consistent with Previously Described 14q24.3-31.1 Deletions

Genes, 2023-06, Vol.14 (6)

2023

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Resolving tumor heterogeneity: genes involved in chordoma cell development identified by low-template analysis of morphologically distinct cells

PloS one, 2014-02, Vol.9 (2), p.e87663

2014

Volltextzugriff (PDF)

A ITSHZ3/I Frame-Shift Variant Causes Neurodevelopmental and Renal Disorder Consistent with Previously Described Proximal Chromosome 19q13.11 Deletion Syndrome

Genes, 2022-11, Vol.13 (12)

2022

Volltextzugriff (PDF)

Lernen ohne Grenzen: das Modell "European primary school": Kinder auf dem Weg nach Europa - Lernen und Leben in der Europäischen Volksschule Wien 15

Erziehung & Unterricht, 2007, Vol.157 (3-4), p.233-4<233-238

2007

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Polyglottes Habsburg: Mehrsprachigkeit im politischen, staatsrechtlichen und gesellschaftlichen Kontext

Bildspuren - Sprachspuren, 2020, Vol.165, p.23-44

2020

Volltextzugriff (PDF)

Polyglottes Habsburg: Mehrsprachigkeit im politischen, staatsrechtlichen und gesellschaftlichen Kontext

Bildspuren - Sprachspuren, 2020, Vol.165, p.23-44

2020

Volltextzugriff (PDF)

Chordoma Low-Template Microarray Analysis

Biomedizinische Technik, 2013-08, Vol.58 Suppl 1

2013

Volltextzugriff (PDF)

Resolving Tumor Heterogeneity: Genes Involved in Chordoma Cell Development Identified by Low-Template Analysis of Morphologically Distinct Cells: e87663

PloS one, 2014-02, Vol.9 (2)

2014

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Case Report-An Inherited Loss-of-Function NRXN3 Variant Potentially Causes a Neurodevelopmental Disorder with Autism Consistent with Previously Described 14q24.3-31.1 Deletions

Genes, 2023, Vol.14 (6)

2023

Volltextzugriff (PDF)

A TSHZ3 Frame-Shift Variant Causes Neurodevelopmental and Renal Disorder Consistent with Previously Described Proximal Chromosome 19q13.11 Deletion Syndrome

Genes, 2022, Vol.13 (12)

2022

Volltextzugriff (PDF)

Book reviews

Zeitschrift für Operations Research, 1986, Vol.30 (5), p.A243-A251

1986

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Personality functioning in anxiety disorders

Personality functioning and self-disorders in individuals at ultra-high risk for psychosis, with first-episode psychosis and with borderline personality disorder

Men don't cry: The supporting role as necessary for women's well‐being after termination of pregnancy

Termination of pregnancy for fetal malformation: A traumatic event? A qualitative analysis of women’s perception

A spoonful of L‐fucose—an efficient therapy for GFUS‐CDG, a new glycosylation disorder

Bildspuren - Sprachspuren : Postkarten als Quellen zur Mehrsprachigkeit in der späten Habsburger Monarchie (Edition 1)

Case Report-An Inherited Loss-of-Function NRXN3 Variant Potentially Causes a Neurodevelopmental Disorder with Autism Consistent with Previously Described 14q24.3-31.1 Deletions

A TSHZ3 Frame-Shift Variant Causes Neurodevelopmental and Renal Disorder Consistent with Previously Described Proximal Chromosome 19q13.11 Deletion Syndrome

De novo variants in TCF7L2 are associated with a syndromic neurodevelopmental disorder

PPA1 Deficiency Causes a Deranged Galactose Metabolism Recognizable in Neonatal Screening

Bi-allelic LETM1 variants perturb mitochondrial ion homeostasis leading to a clinical spectrum with predominant nervous system involvement

Durvalumab impacts progression-free survival while high-dose radiation >66 Gy improves local control without excess toxicity in unresectable NSCLC stage III: Real-world data from the Austrian radio-oncological lung cancer study association registry (ALLSTAR)

Case Report—An Inherited Loss-of-Function INRXN3/I Variant Potentially Causes a Neurodevelopmental Disorder with Autism Consistent with Previously Described 14q24.3-31.1 Deletions

Resolving tumor heterogeneity: genes involved in chordoma cell development identified by low-template analysis of morphologically distinct cells

A ITSHZ3/I Frame-Shift Variant Causes Neurodevelopmental and Renal Disorder Consistent with Previously Described Proximal Chromosome 19q13.11 Deletion Syndrome

Lernen ohne Grenzen: das Modell "European primary school": Kinder auf dem Weg nach Europa - Lernen und Leben in der Europäischen Volksschule Wien 15

Polyglottes Habsburg: Mehrsprachigkeit im politischen, staatsrechtlichen und gesellschaftlichen Kontext

Polyglottes Habsburg: Mehrsprachigkeit im politischen, staatsrechtlichen und gesellschaftlichen Kontext

Chordoma Low-Template Microarray Analysis

Resolving Tumor Heterogeneity: Genes Involved in Chordoma Cell Development Identified by Low-Template Analysis of Morphologically Distinct Cells: e87663

Case Report-An Inherited Loss-of-Function NRXN3 Variant Potentially Causes a Neurodevelopmental Disorder with Autism Consistent with Previously Described 14q24.3-31.1 Deletions

A TSHZ3 Frame-Shift Variant Causes Neurodevelopmental and Renal Disorder Consistent with Previously Described Proximal Chromosome 19q13.11 Deletion Syndrome

Book reviews

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