Ilse Wieland

Medizinische Hochschule Hannover — Germany

Medicine · Health Sciences

27h-index2.6kcitations146works0.72yr avg
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Research Topics

Hemophilia Treatment and Research(18), Platelet Disorders and Treatments(16), Genomic variations and chromosomal abnormalities(10), Cancer Genomics and Diagnostics(9), Cancer-related gene regulation(9)

Publications145 total

Functional Assessment in Haemophilia Care: Insights from an Expert Panel on the Use and Applicability of Functional Tests in Clinical Practice
Hämostaseologie·2026
Antiboby mediated Acquired Glanzmann Thrombasthenia – a diagnostic and therapeutic challenge – with Concizumab as Promising Therapeutic Approach: A Case Report
Hämostaseologie·2026
Novel ITI concept using Efasenoctocog alfa in a modified Atlanta Protocol – the Gephard protocol
Hämostaseologie·2026
Immune-mediated platelet dysfunction with spontaneous formation of aggregates in pediatric end-stage liver disease: A case report
Hämostaseologie·2026
Emicizumab levels in patients with acquired and congenital Hemophilia A
Blood·2025
Tiny clots, big choices: intervening on neonatal aortic thrombosis—a novel framework for clinical decision-making
Cardiology in the Young·2025Open Access
Effectiveness of emicizumab under real-world conditions in patients of all ages with hemophilia A with and without FVIII inhibitors: Third interim analysis of the non-interventional study EMIIL
Hämostaseologie·2025
Real-World Effectiveness and Usage of Recombinant Factor IX Fc: Interim Analysis in Paediatric Patients from the 24-Month, Prospective, Non-Interventional B-MORE Study
Hämostaseologie·2025
Efficacy of Rivaroxaban in Children with Short Bowel Syndrome
Hämostaseologie·2025
Heavy menstrual bleeding in female haemophilia carriers in 2024
Hämostaseologie·2025
Pregnancy complications in female haemophilia patients and carriers of haemophilia A and B- a nationwide survey
Hämostaseologie·2025
Correction to: Assessment of gene–disease associations and recommendations for genetic testing for somatic variants in vascular anomalies by VASCERN-VASCA
Orphanet Journal of Rare Diseases·2024Open Access
Assessment of gene–disease associations and recommendations for genetic testing for somatic variants in vascular anomalies by VASCERN-VASCA
Orphanet Journal of Rare Diseases·2024· 10 citedOpen Access
Development of a low-titer inhibitor in a boy with congenital mild hemophilia A: clinical and immunological follow up of 1 year
Hämostaseologie·2024
Biallelic inactivation of the <scp><i>NF1</i></scp> tumour suppressor gene in juvenile myelomonocytic leukaemia: Genetic evidence of driver function and implications for diagnostic workup
British Journal of Haematology·2023· 5 citedOpen Access
Achromatopsia—Visual Cortex Stability and Plasticity in the Absence of Functional Cones
Investigative Ophthalmology & Visual Science·2023· 10 citedOpen Access
PB1301 Low-Titer Inhibitor and Decreased FVIII Activity to 1.1% with Increased Bleeding in a 4 Year Old Patient with Congenital Mild Hemophilia A
Research and Practice in Thrombosis and Haemostasis·2023Open Access
PB0260 Immune Complex-Mediated Acquired von Willebrand Syndrome in a 5-year-old Boy after Allogeneic Hematopoietic Stem Cell Transplantation
Research and Practice in Thrombosis and Haemostasis·2023Open Access
Bilateral lung transplantation for pediatric pulmonary arterial hypertension: perioperative management and one-year follow-up
Frontiers in Cardiovascular Medicine·2023· 5 citedOpen Access
Anterior Spinal Artery Syndrome Due to Fibrocartilaginous Embolism—Case Report and Treatment Options
Neuropediatrics·2023
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Frequent Co-authors

Malte Böhm(13), Peter Wieacker(11), Martin Zenker(10), Sibylle Jakubiczka(5), Petra Muschke(3), H. Rübben(3), B. Totzeck(3), Walter Birchmeier(3), Ulrich H. Weidle(3), Denny Schanze(3), Sigrid Tinschert(3), Albrecht Röpke(3), Klaus Mohnike(3), Winfried Barthlen(3), Christian Sell(3), Graeme B. Bolger(2), Michael Wigler(2), Sangamitra Boppudi(2), Elaine H. Zackai(2), William Reardon(2)