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Importance of Adequate Diagnostic Workup for Correct Diagnosis of Advanced Systemic Mastocytosis2020 The Journal of Allergy and Clinical Immunology In Practice article Immunology and Microbiology Mast cells and histamine Open access
Juliana Schwaab, Nicole Cabral do O Hartmann, Nicole Naumann, Mohamad Jawhar, Christel Weiß, Georgia Metzgeroth, +11 more
48citations -
Diagnostic Use of Genome Sequencing in Patients With 11p15.5 Imprinting Disorder Features: A Pilot Study2024 Clinical Genetics article Biochemistry, Genetics and Molecular Biology Genomic variations and chromosomal abnormalities Open access
Luise Kessler, Jeremias Krause, Florian Kraft, Asmaa K. Amin, György Fekete, Anna Lengyel, +7 more
3citations -
ABSTRACT NUMBER: ESOC2026A312 CARDIAC PHOTON-COUNTING DETECTOR COMPUTED TOMOGRAPHY IN ACUTE ISCHEMIC STROKE: DIAGNOSTIC ACCURACY FOR DETECTION OF LEFT ATRIAL APPENDAGE THROMBUS2026 European Stroke Journal conference-abstract Medicine Atrial Fibrillation Management and Outcomes Open access
Annemarie Kirschfink, Mohamed Elhalal, Stefanie Kammer, Dimah Hasan, Michael Frick, Nikolaus Marx, +6 more
0citations -
Cardiac photon-counting detector computed tomography in acute ischemic stroke: diagnostic accuracy for detection of left atrial appendage thrombus2026 Therapeutic Advances in Neurological Disorders article Medicine Atrial Fibrillation Management and Outcomes Open access
Annemarie Kirschfink, Mohamed Elhalal, Stefanie Kammer, Dimah Hasan, Michael Frick, Nikolaus Marx, +6 more
0citations -
Value of ultra‐high‐field MRI in patients with drug‐resistant focal epilepsy and negative 3T MRI ( EpiUltraStudy ): Diagnostic gain of 7T structural analysis
Rick H. G. J. van Lanen, Daniel Uher, M. Christianne Hoeberigs, Paul A.M. Hofman, Remco Santegoeds, Christopher J. Wiggins, +29 more
1citations -
Diagnosis and Treatment of Nonspecific Spondylodiscitis in Adults in Germany, Austria, and Switzerland (DACH): Analysis of an Online Survey2026 Zeitschrift für Orthopädie und Unfallchirurgie article Medicine Infectious Diseases and Tuberculosis
Nicolas Heinz von der Höh, Christian Herren, Max J. Scheyerer, Valentin Michael Quack, Steffen Drange
0citations -
Interdisziplinäre Diagnostik bei interstitiellen Lungenerkrankungen: Was wird empfohlen?2023 Zeitschrift für Pneumologie article Medicine Interstitial Lung Diseases and Idiopathic Pulmonary Fibrosis
Hans‐Joachim Kabitz, Okka Wilkea Hamer, Danny David Jonigk, Andreas Krause, Julia Wälscher, Juergen Hetzel, +1 more
0citations -
Patient with an autosomal‐recessive MBTPS1 ‐linked phenotype and clinical features of Silver–Russell syndrome2020 American Journal of Medical Genetics Part A article Biochemistry, Genetics and Molecular Biology Genetic Syndromes and Imprinting Open access
Robert Meyer, Miriam Elbracht, Thomas Opladen, Thomas Eggermann
17citations -
Open surgery appears to be the preferred treatment in patients with nutcracker syndrome: A vascular low frequency disease consortium analysis2026 Journal of Vascular Surgery Venous and Lymphatic Disorders article Medicine Vascular anomalies and interventions Open access
Bjoern Dominik Suckow, Aravind S. Ponukumati, Lily Hui-Ching Wang, Jesse A. Columbo, David H. Stone, Richard J. Powell, +31 more
0citations -
Cardiovascular Disease May Be Underestimated in Patients Considered Fit for Open Thoraco-abdominal Aortic Aneurysm Repair: A Retrospective Single Centre Study2025 European Journal of Vascular and Endovascular Surgery article Medicine Aortic aneurysm repair treatments Open access
Hanif Krabbe, Nico Geropp, Panagiotis Doukas, Jelle Frankort, Christian Uhl, Michael Johan Jacobs, +2 more
1citations -
False‐positive test results in diagnosing allergy to glatiramer acetate: Case report and a systematic literature review2020 Immunity Inflammation and Disease article Medicine Allergic Rhinitis and Sensitization Open access
Stefani Röseler, Friederike Leufgens, Hans Friedrich Merk, Jens Malte Baron, Silke Moll‐Slodowy, Gerda Wurpts, +1 more
2citations -
Genetic testing in inherited endocrine disorders: joint position paper of the European reference network on rare endocrine conditions (Endo-ERN)2020 Orphanet Journal of Rare Diseases article Biochemistry, Genetics and Molecular Biology Genomics and Rare Diseases Open access
Thomas Eggermann, Miriam Elbracht, Ingo Kurth, Anders Juul, Trine Holm Johannsen, Irène Netchine, +88 more
28citations -
Diagnosis, treatment and monitoring of chronic nonbacterial osteomyelitis (CNO) and chronic recurrent multifocal osteomyelitis (CRMO) – Evidence, practice and consensus-based recommendations from the German pediatric rheumatology society (GKJR)
Anja Schnabel, Christiane Reiser, M. BEER, Normi Brück, C. Förster, V. Grote, +13 more
2citations