Detail page

Knowledge Web

Person

Barbara Zieger

Ärztin

Name	Barbara Zieger
Place	Freiburg im Breisgau (Wirkungsort) Deutschland
Academic degree	Prof. Dr.
Profession	Ärztin (characteristic profession)
Related	Universitätsklinikum Freiburg. Zentrum für Kinder- und Jugendmedizin
Further information	Oberärztin am Zentrum für Kinder- und Jugendmedizin, Kinderklinik, Universitätsklinikum Freiburg
Record type	Person
GND-Identifier	1077058551
Record ID	1077058551
Involved in show all Catheter intervention in a patient with intracranial aneurysms and Glanzmann Thrombasthenia caused by a novel homozygous likely pathogenic variant in the ITGA2B gene Diskrepanz zwischen Laborparameter und MRT-Informationen bei chronisch rezidivierender multifokaler Osteomyelitis (CRMO) bei Kindern und Jugendlichen Genetic landscape of factor VII deficiency: insights from a comprehensive analysis of pathogenic variants and their impact on coagulation activity Suppressed ORAI1-STIM1-dependent Ca2+ entry by protein kinase C isoforms regulating platelet procoagulant activity Development of an in-vitro model for extracorporeal blood pumps to study the effects of artificial pulsatility on human blood Editorial: Hemostasis in ECMO and VAD, volume II Glanzmann thrombasthenia in pakistani patients: identification of 7 novel pathogenic variants in the fibrinogen receptor [alpha]iib[beta]3 High-throughput microfluidic blood testing to phenotype genetically linked platelet disorders: an aid to diagnosis Hochdurchsatzsequenzierung bei Patienten mit von Willebrand Erkrankung oder Hämophilie A mittels Multigenanalyse Mild acquired von willebrand syndrome and cholestasis in pediatric and adult patients with fontan circulation Pervasive platelet secretion defects in patients with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) The effect of recombinant versus plasma-derived von Willebrand factor on prolonged PFA closure times in ECMO patients with acquired von Willebrand syndrome – an observational study The endogenous thrombin potential in patients with left ventricular assist device or heart transplant Novel GNE Gene Variants Associated with Severe Congenital Thrombocytopenia and Platelet Sialylation Defect A cross-sectional analysis of treatment in PUPs in 2021 in Germany – first data from the GEPHARD Study Group A novel GATA1 variant in the C-terminal zinc finger compared with the platelet phenotype of patients with a likely pathogenic variant in the N-terminal zinc finger A Novel GATA1 Variant in the C-Terminal Zinc Finger Compared with the Platelet Phenotype of Patients with A Likely Pathogenic Variant in the N-Terminal Zinc Finger Acquired bleeding disorders Acquired von Willebrand syndrome and desmopressin resistance during venovenous extracorporeal membrane oxygenation in patients with COVID-19 : : a prospective observational study Bleeding during veno-venous ECMO: prevention and treatment Comprehensive analyses of coagulation parameters in patients with vascular anomalies Emicizumab in children: bleeding episodes and outcome before and after transition to Emicizumab Endothelial cells and coagulation Erratum: A cross-sectional analysis of treatment in PUPs in 2021 in Germany – first data from the GEPHARD Study Group Fibrinogen regulates lesion border‐forming reactive astrocyte properties after vascular damage Hermansky-Pudlak Syndrome: identification of novel variants in the genes HPS3, HPS5, and DTNBP1 (HPS-7) Neonatal platelets: lower G12/13 expression contributes to reduced secretion of dense granules Endothelial cells and coagulation Type 2B von Willebrand Disease: Early Manifestation as Neonatal Thrombocytopenia A novel likely pathogenic variant in the BLOC1S5 gene associated with Hermansky-Pudlak syndrome Type 11 and an overview of human BLOC-1 deficiencies Age-dependent control of collagen-dependent platelet responses by Thrombospondin-1 - comparative analysis of platelets from neonates, children, adolescents, and adults Familial multiple coagulation factor deficiencies (FMCFDs) in a large cohort of patients - a single-center experience in genetic diagnosis Hypercoagulopathy, acquired coagulation disorders and anticoagulation before, during and after extracorporeal membrane oxygenation in COVID-19: a case series Role of septins in endothelial cells and platelets The role of von Willebrand factor in microvascular surgery in severely injured patients The septin complex links the catenin complex to the actin cytoskeleton for establishing epithelial cell polarity Impaired Platelet Function in Sept8-Deficient Mice In Vitro Acquired von Willebrand Syndrome and Platelet Function Defects during Extracorporeal Life Support (Mechanical Circulatory Support) Acquired bleeding disorders Antithrombotic prophylaxis for surgery-associated venous thromboembolism risk in patients with inherited platelet disorders : : the SPATA-DVT Study Coagulation disorders in Duchenne muscular dystrophy? Results of a registry-based online survey Impaired iloprost-induced platelet inhibition and phosphoproteome changes in patients with confirmed pseudohypoparathyroidism type Ia, linked to genetic mutations in GNAS Panel sequencing identified a novel splice site mutation in Hermansky-Pudlak syndrome type 1 patients Severe plasma prekallikrein deficiency : clinical characteristics, novel KLKB1 mutations, and estimated prevalence Severe plasma prekallikrein deficiency: clinical characteristics, novel KLKB1 mutations, and estimated prevalence Acquired von Willebrand syndrome in patients with ventricular assist device Editorial: Hemostasis in ECMO and VAD Hereditary neuralgic amyotrophy in childhood caused by duplication within the SEPT9 gene: a family study Impaired human hematopoiesis due to a cryptic intronic GATA1 splicing mutation Increased von Willebrand factor parameters in children with febrile seizures Alteration of von Willebrand Factor after Transcatheter Aortic Valve Replacement in the Absence of Paravalvular Regurgitation Platelet secretion defects and acquired von Willebrand syndrome in patients with ventricular assist devices Variable impairment of platelet functions in patients with severe, genetically linked immune deficiencies Deletion of human GP1BB and SEPT5 is associated with Bernard-Soulier syndrome, platelet secretion defect, polymicrogyria, and developmental delay Bleeding risk of surgery and its prevention in patients with inherited platelet disorders The mammalian septin interactome Inherited dysfunctional platelet P2Y12 receptor mutations associated with bleeding disorders Erworbenes von-Willebrand-Syndrom bei Patienten mit Ventricular Assist Device Identifizierung neuer Interaktionsproteine des humanen Septins SEPT4 (hCDCrel-2) in fetalem Gehirn Highlight: The 5th International Workshop on Septin Biology

Please note

The beta version does not yet contain all functions and information of the DNB portal catalogue. If you are missing information or want to order a medium, please visit the page in the DNB portal catalogue via the following link:

Katalog der Deutschen Nationalbibliothek

Barbara Zieger

Catheter intervention in a patient with intracranial aneurysms and Glanzmann Thrombasthenia caused by a novel homozygous likely pathogenic variant in the ITGA2B gene

Diskrepanz zwischen Laborparameter und MRT-Informationen bei chronisch rezidivierender multifokaler Osteomyelitis (CRMO) bei Kindern und Jugendlichen

Genetic landscape of factor VII deficiency: insights from a comprehensive analysis of pathogenic variants and their impact on coagulation activity

Suppressed ORAI1-STIM1-dependent Ca2+ entry by protein kinase C isoforms regulating platelet procoagulant activity

Development of an in-vitro model for extracorporeal blood pumps to study the effects of artificial pulsatility on human blood

Editorial: Hemostasis in ECMO and VAD, volume II

Glanzmann thrombasthenia in pakistani patients: identification of 7 novel pathogenic variants in the fibrinogen receptor [alpha]iib[beta]3

High-throughput microfluidic blood testing to phenotype genetically linked platelet disorders: an aid to diagnosis

Hochdurchsatzsequenzierung bei Patienten mit von Willebrand Erkrankung oder Hämophilie A mittels Multigenanalyse

Mild acquired von willebrand syndrome and cholestasis in pediatric and adult patients with fontan circulation

Pervasive platelet secretion defects in patients with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2)

The effect of recombinant versus plasma-derived von Willebrand factor on prolonged PFA closure times in ECMO patients with acquired von Willebrand syndrome – an observational study

The endogenous thrombin potential in patients with left ventricular assist device or heart transplant

Novel GNE Gene Variants Associated with Severe Congenital Thrombocytopenia and Platelet Sialylation Defect

A cross-sectional analysis of treatment in PUPs in 2021 in Germany – first data from the GEPHARD Study Group

A novel GATA1 variant in the C-terminal zinc finger compared with the platelet phenotype of patients with a likely pathogenic variant in the N-terminal zinc finger

A Novel GATA1 Variant in the C-Terminal Zinc Finger Compared with the Platelet Phenotype of Patients with A Likely Pathogenic Variant in the N-Terminal Zinc Finger

Acquired bleeding disorders

Acquired von Willebrand syndrome and desmopressin resistance during venovenous extracorporeal membrane oxygenation in patients with COVID-19 : : a prospective observational study

Bleeding during veno-venous ECMO: prevention and treatment

Comprehensive analyses of coagulation parameters in patients with vascular anomalies

Emicizumab in children: bleeding episodes and outcome before and after transition to Emicizumab

Endothelial cells and coagulation

Erratum: A cross-sectional analysis of treatment in PUPs in 2021 in Germany – first data from the GEPHARD Study Group

Fibrinogen regulates lesion border‐forming reactive astrocyte properties after vascular damage

Hermansky-Pudlak Syndrome: identification of novel variants in the genes HPS3, HPS5, and DTNBP1 (HPS-7)

Neonatal platelets: lower G12/13 expression contributes to reduced secretion of dense granules

Endothelial cells and coagulation

Type 2B von Willebrand Disease: Early Manifestation as Neonatal Thrombocytopenia

A novel likely pathogenic variant in the BLOC1S5 gene associated with Hermansky-Pudlak syndrome Type 11 and an overview of human BLOC-1 deficiencies

Age-dependent control of collagen-dependent platelet responses by Thrombospondin-1 - comparative analysis of platelets from neonates, children, adolescents, and adults

Familial multiple coagulation factor deficiencies (FMCFDs) in a large cohort of patients - a single-center experience in genetic diagnosis

Hypercoagulopathy, acquired coagulation disorders and anticoagulation before, during and after extracorporeal membrane oxygenation in COVID-19: a case series

Role of septins in endothelial cells and platelets

The role of von Willebrand factor in microvascular surgery in severely injured patients

The septin complex links the catenin complex to the actin cytoskeleton for establishing epithelial cell polarity

Impaired Platelet Function in Sept8-Deficient Mice In Vitro

Acquired von Willebrand Syndrome and Platelet Function Defects during Extracorporeal Life Support (Mechanical Circulatory Support)

Acquired bleeding disorders

Antithrombotic prophylaxis for surgery-associated venous thromboembolism risk in patients with inherited platelet disorders : : the SPATA-DVT Study

Coagulation disorders in Duchenne muscular dystrophy? Results of a registry-based online survey

Impaired iloprost-induced platelet inhibition and phosphoproteome changes in patients with confirmed pseudohypoparathyroidism type Ia, linked to genetic mutations in GNAS

Panel sequencing identified a novel splice site mutation in Hermansky-Pudlak syndrome type 1 patients

Severe plasma prekallikrein deficiency : clinical characteristics, novel KLKB1 mutations, and estimated prevalence

Severe plasma prekallikrein deficiency: clinical characteristics, novel KLKB1 mutations, and estimated prevalence

Acquired von Willebrand syndrome in patients with ventricular assist device

Editorial: Hemostasis in ECMO and VAD

Hereditary neuralgic amyotrophy in childhood caused by duplication within the SEPT9 gene: a family study

Impaired human hematopoiesis due to a cryptic intronic GATA1 splicing mutation

Increased von Willebrand factor parameters in children with febrile seizures

Alteration of von Willebrand Factor after Transcatheter Aortic Valve Replacement in the Absence of Paravalvular Regurgitation

Platelet secretion defects and acquired von Willebrand syndrome in patients with ventricular assist devices

Variable impairment of platelet functions in patients with severe, genetically linked immune deficiencies

Deletion of human GP1BB and SEPT5 is associated with Bernard-Soulier syndrome, platelet secretion defect, polymicrogyria, and developmental delay

Bleeding risk of surgery and its prevention in patients with inherited platelet disorders

The mammalian septin interactome

Inherited dysfunctional platelet P2Y12 receptor mutations associated with bleeding disorders

Erworbenes von-Willebrand-Syndrom bei Patienten mit Ventricular Assist Device

Identifizierung neuer Interaktionsproteine des humanen Septins SEPT4 (hCDCrel-2) in fetalem Gehirn

Highlight: The 5th International Workshop on Septin Biology