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Christiane Stieber

Observed names: Dr. Christiane Stieber, Stieber, Christiane
OpenAlex ID: A5113298564
A systematic review on the role of vitamins, minerals, proteins, and other supplements for the treatment of cachexia in cancer: a European Palliative Care Research Centre cachexia project
2016 · Mochamat, Henning Cuhls, et al. · Journal of Cachexia Sarcopenia and Muscle · 138
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Diagnostic needs for rare diseases and shared prediagnostic phenomena: Results of a German-wide expert Delphi survey
2017 · Susanne Blöß, Christian Klemann, et al. · PLoS ONE · 121
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Hereditary Angioedema with Normal C1 Inhibitor and F12 Mutations in 42 Brazilian Families
2017 · Camila Lopes Veronez, Adriana S. Moreno, et al. · The Journal of Allergy and Clinical Immunology In Practice · 70
Next-generation phenotyping integrated in a national framework for patients with ultrarare disorders improves genetic diagnostics and yields new molecular findings
2024 · Axel Schmidt, Magdalena Danyel, et al. · Nature Genetics · 59
Measurement of Quality of Life in Palliative Care: Evidence for Criterion-Oriented Validity of a Single-Item Approach
2017 · Rupert Conrad, Martin Mücke, et al. · Journal of Palliative Medicine · 17
So behandeln Sie das schmerzende Knie
2018 · Dorian Emmert, Tim Rasche, et al. · MMW - Fortschritte der Medizin · 15
Next-generation phenotyping integrated in a national framework for patients with ultra-rare disorders improves genetic diagnostics and yields new molecular findings
2023 · Axel Schmidt, Magdalena Danyel, et al. · medRxiv · 12
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Kurze Wege zur Diagnose
2017 · Christiane Stieber, Martin Mücke, et al. · Bundesgesundheitsblatt - Gesundheitsforschung - Gesundheitsschutz · 10
The combined prevalence of classified rare rheumatic diseases is almost double that of ankylosing spondylitis
2021 · Judith Leyens, Tim Th. A. Bender, et al. · Orphanet Journal of Rare Diseases · 4
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Clinical Utility Gene Card for hereditary angioedema with normal C1 inhibitor (HAEnC1)
2017 · Christiane Stieber, Sven Cichon, et al. · European Journal of Human Genetics · 4
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Variable acceleration influences cyclic AMP levels in Paramecium biaurelia.
2002 · Ruth Hemmersbach, Manuela Wilczek, et al. · PubMed · 4
Hypergravity modulates cyclic GMP efflux in nitric oxide-stimulated human melanocytic cells
2005 · Christiane Stieber, Krassimira Ivannova, et al. · ESASP · 3
Impfstoffmanagement in der ambulanten Versorgung: ein systematischer Review internationaler Empfehlungen und Implikationen für das deutsche Gesundheitswesen.
2023 · Laura Knepper, Christiane Stieber, et al. · Das Gesundheitswesen · 2
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Analysis of genetic impact on smell impairment in patients with hereditary angioedema type 1 and 2
2021 · Ulrike Förster‐Ruhrmann, Greta Pierchalla, et al. · JDDG Journal der Deutschen Dermatologischen Gesellschaft · 1
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Seltene Erkrankungen in der Neurologie Diagnosestellung, Lebensqualität und Kosten
2015 · Richard Dodel, Christiane Stieber, et al. · Der Klinikarzt · 1
Author Correction: Next-generation phenotyping integrated in a national framework for patients with ultrarare disorders improves genetic diagnostics and yields new molecular findings
2025 · Axel Schmidt, Magdalena Danyel, et al. · Nature Genetics
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Author Correction: Next-generation phenotyping integrated in a national framework for patients with ultrarare disorders improves genetic diagnostics and yields new molecular findings
2025 · Schmidt, Axel, Danyel, Magdalena, et al. · RWTH Publications (RWTH Aachen)
Clinical Practice Guidelines for Vaccine Management in Ambulatory Care - A Systematic Review following the AGREE II Approach
2022 · Nur Ikar, Dr. Christiane Stieber, et al. · OSF Preprints (OSF Preprints)
Untersuchung genetischer Einflüsse auf Riechstörungen bei Patienten mit hereditärem Angioödem Typ 1 und 2
2021 · Ulrike Förster‐Ruhrmann, Greta Pierchalla, et al. · JDDG Journal der Deutschen Dermatologischen Gesellschaft
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Geleitwort
2018 · Christiane Stieber · Elsevier eBooks
Adressen
2018 · Tim Theodor, Albert Bender, et al. · Elsevier eBooks
„Selten“ geschwollen
2018 · Dorian Emmert, Martin Mücke, et al. · Elsevier eBooks
Patients without diagnosis: A profile
2017 · Isabelle C Windheuser Martin Muecke Frank Klawonn, Christiane Stieber · Journal of Genetic Syndromes & Gene Therapy
Hereditary Angioedema Without C1 Inhibitor Deficiency: Observation Of Patients Homozygous For FXII GENE Mutation
2014 · Christiane Stieber, Camila Veronez, et al. · Journal of Allergy and Clinical Immunology
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Hereditary Angioedema Without C1 Inhibitor Deficiency: Clinical Evaluation Of 67 Brazilian Patients
2014 · Elisabete Cordeiro, Camila Veronez, et al. · Journal of Allergy and Clinical Immunology
Works count: 37
Citation count: 461
H-index: 8
I10-index: 8
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