Suchergebnisse - "Eggermann, Thomas"

PubPharm (206)

1

Complement and inflammasome overactivation mediates paroxysmal nocturnal hemoglobinuria with autoinflammation

enthalten in: The Journal of clinical investigation | 2019

von Höchsmann, B. | Murakami, Y. | Osato, M. | +18

CommentIn: J Clin Invest. 2019 Dec 2;129(12):5074-5076. - PMID 31638602

2

Male infant with paternal uniparental diploidy mosaicism and a 46,XX/46,XY karyotype

enthalten in: American journal of medical genetics. Part A | 2019

von Spier, I. | Engels, H. | Stutte, S. | +6

3

Molecular and Clinical Opposite Findings in 11p15.5 Associated Imprinting Disorders : Characterization of Basic Mechanisms to Improve Clinical Management

enthalten in: International journal of molecular sciences | 2019

von Wesseler, K. | Kraft, F. | Eggermann, T.

4

Genetic Variants in the Promoter Region of the Macrophage Migration Inhibitory Factor are Associated with the Severity of Hepatitis C Virus-Induced Liver Fibrosis

enthalten in: International journal of molecular sciences | 2019

von Wirtz, T. | Fischer, P. | Backhaus, C. | +14

5

Contribution of GRB10 to the prenatal phenotype in Silver-Russell syndrome? Lessons from 7p12 copy number variations

enthalten in: European journal of medical genetics | 2019

von Eggermann, T. | Begemann, M. | Kurth, I. | +1

6

Next generation sequencing and imprinting disorders : Current applications and future perspectives: Lessons from Silver-Russell syndrome

enthalten in: Molecular and cellular probes | 2019

von Neuheuser, L. | Meyer, R. | Begemann, M. | +2

7

Genomic imprinting disorders : lessons on how genome, epigenome and environment interact

enthalten in: Nature reviews. Genetics | 2019

von Monk, D. | Mackay, D. | Eggermann, T. | +2

8

Discrepant molecular and clinical diagnoses in Beckwith-Wiedemann and Silver-Russell syndromes

enthalten in: Genetics research | 2019

von Mackay, D. | Bliek, J. | Lombardi, M. | +11

9

Novel familial distal imprinting centre 1 (11p15.5) deletion provides further insights in imprinting regulation

enthalten in: Clinical epigenetics | 2019

von Kraft, F. | Wesseler, K. | Begemann, M. | +3

10

Novel familial distal imprinting centre 1 (11p15.5) deletion provides further insights in imprinting regulation

enthalten in: Clinical epigenetics | 2019

von Kraft, F. | Wesseler, K. | Begemann, M. | +3

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