335 results on '"Rossmann, Heidi"'
Search Results
2. A novel von Willebrand factor multimer ratio as marker of disease activity in thrombotic thrombocytopenic purpura
3. Severe high-molecular-weight kininogen deficiency: clinical characteristics, deficiency–causing KNG1 variants, and estimated prevalence
4. Protective behavior and SARS-CoV-2 infection risk in the population – Results from the Gutenberg COVID-19 study
5. CEP162 deficiency causes human retinal degeneration and reveals a dual role in ciliogenesis and neurogenesis
6. Anti-ADAMTS13 autoantibody profiling in patients with immune-mediated thrombotic thrombocytopenic purpura
7. Pathogenic lipid‐binding antiphospholipid antibodies are associated with severity of COVID‐19
8. Immunogenic hotspots in the spacer domain of ADAMTS13 in immune‐mediated thrombotic thrombocytopenic purpura
9. Open ADAMTS-13 conformation index predicts earlier relapse in immune-mediated thrombotic thrombocytopenic purpura
10. Evaluation of a laboratory-based high-throughput SARS-CoV-2 antigen assay for non-COVID-19 patient screening at hospital admission
11. Severe plasma prekallikrein deficiency: Clinical characteristics, novel KLKB1 mutations, and estimated prevalence
12. Distribution of estimated glomerular filtration rate and determinants of its age dependent loss in a German population-based study
13. Thrombotic thrombocytopenic purpura: 100 years of research on Moschcowitz syndrome
14. Biallelic MAD2L1BP (p31comet) mutation is associated with mosaic aneuploidy and juvenile granulosa cell tumors
15. Prevalence of overweight and obesity, its complicationscomplications and progression in a 10-year follow-up in the Gutenberg Health Study (GHS).
16. Open ADAMTS-13 conformation index predicts earlier relapse in immune-mediated thrombotic thrombocytopenic purpura
17. Thrombotic thrombocytopenic purpura: 100 years of research on Moschcowitz syndrome
18. Evidence for the utility of cfDNA plasma concentrations to predict disease severity in COVID-19: a retrospective pilot study
19. Head and Neck Paragangliomas
20. Prevalence of Overweight and Obesity, Its Complications, and Progression in a 10-Year Follow-Up in the Gutenberg Health Study (GHS).
21. Hypertension and multiple cardiovascular risk factors increase the risk for retinal vein occlusions: results from the Gutenberg Retinal Vein Occlusion Study
22. One fits all: a highly sensitive combined ddPCR/pyrosequencing system for the quantification of microchimerism after hematopoietic and solid organ transplantation
23. Hereditary Spherocytosis: Can Next-Generation Sequencing of the Five Most Frequently Affected Genes Replace Time-Consuming Functional Investigations?
24. Correction to: Molecular karyotyping and gene expression analysis in childhood cancer patients
25. Definite diagnosis of plasma prekallikrein deficiency should not be based exclusively on shortening of the aPTT upon prolonged pre-incubation
26. Novel GATA1 Variant Causing a Bleeding Phenotype Associated with Combined Platelet α-/δ-Storage Pool Deficiency and Mild Dyserythropoiesis Modified by a SLC4A1 Variant
27. Abstract 19896: Il-6 is Not Crucial for the Development of Deep Venous Thrombosis
28. Quantification of the Fabry marker lysoGb3 in human plasma by tandem mass spectrometry
29. Differential Inhibition of Platelet Reactivity by Dual Therapy With Aspirin and Low-Dose Rivaroxaban in Peripheral Arterial Disease: A Pilot Study
30. Definite diagnosis of plasma prekallikrein deficiency should not be based exclusively on shortening of the aPTT upon prolonged pre‐incubation
31. Second MAFA Variant Causing a Phosphorylation Defect in the Transactivation Domain and Familial Insulinomatosis
32. Hypermethylation of RAD9A intron 2 in childhood cancer patients, leukemia and tumor cell lines suggest a role for oncogenic transformation
33. Additional file 1 of Protective behavior and SARS-CoV-2 infection risk in the population – Results from the Gutenberg COVID-19 study
34. c.451dupT in KLKB1 is common in Nigerians, confirming a higher prevalence of severe prekallikrein deficiency in Africans compared to Europeans
35. Loss of CEP162 function at the primary cilium delays ciliogenesis and causes retinal ciliopathy in humans
36. Severe High Molecular Weight Kininogen (HK) Deficiency: Clinical Characteristics, Deficiency-Causing KNG1 Variants in Reported and New Cases, and Estimated Prevalence
37. Chronically Elevated Interleukin-6 Disturbs the Coagulation Cascade in Mice
38. Heme oxygenase-1 suppresses a pro-inflammatory phenotype in monocytes and determines endothelial function and arterial hypertension in mice and humans
39. High incidence of extraadrenal paraganglioma in families with SDHx syndromes detected by functional imaging with [18F]fluorodihydroxyphenylalanine PET
40. Dynamic changes of lipid profile in Romanian patients with Gaucher disease type 1 under enzyme replacement therapy: a prospective study
41. Distribution of HOMA-IR in a population-based cohort and proposal for reference intervals
42. Invited commentary to: ADAMTS13 deficiency is associated with abnormal distribution of von Willebrand factor multimers in patients with COVID-19 by Tiffany Pascreau et al. Letter to the Editors-in-Chief, Thrombosis Research
43. Comment on 'Worldwide Distribution of PK Deficiency: the Defect Seems Mainly Concentrated in West African Countries and the United States'
44. Phenotypic Variability and Risk of Malignancy in SDHC-Linked Paragangliomas: Lessons From Three Unrelated Cases With an Identical Germline Mutation (p.Arg133*)
45. Severe high-molecular-weight kininogen deficiency: clinical characteristics, deficiency–causing KNG1variants, and estimated prevalence
46. Evidence for the utility of cfDNA plasma concentrations to predict disease severity in COVID-19
47. Distribution of estimated glomerular filtration rate and determinants of its age dependent loss in a German population-based study
48. Molecular karyotyping and gene expression analysis in childhood cancer patients
49. Severe plasma prekallikrein deficiency: Clinical characteristics, novel KLKB1 mutations, and estimated prevalence
50. Diagnosis of Hereditary TTP Caused by Homozygosity for a Rare Complex ADAMTS13 Allele After Salmonella Infection in a 43-Year-Old Asylum Seeker
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