Suchergebnisse - "Holz, Anja"

PubPharm (32)

1

Childhood and adolescence factors and multiple sclerosis : results from the German National Cohort (NAKO)

enthalten in: BMC neurology | 2024

von Holz, A. | Obi, N. | Ahrens, W. | +31

2

Childhood and adolescence factors and multiple sclerosis: results from the German National Cohort (NAKO)

enthalten in: BMC neurology | 2024

von Holz, A. | Obi, N. | Ahrens, W. | +31

3

Breastfeeding and Risk of Multiple Sclerosis : A Systematic Review and Meta-Analysis of Observational Studies

enthalten in: Neuroepidemiology | 2022

von Holz, A. | Riefflin, M. | Heesen, C. | +3

4

Pitfalls and solutions in case fatality risk estimation – A multi-country analysis on the effects of demographics, surveillance, time lags between case reports and deaths and healthcare system capacity on COVID-19 CFR estimates

Erschienen: 2022

von Vanella, P. | Wiessner, C. | Holz, A. | +5

5

A human multisystem disorder with autoinflammation, leukoencephalopathy and hepatopathy is caused by mutations in C2orf69

enthalten in: bioRxiv.org | 2021

von Lausberg, E. | Gießelmann, S. | Dewulf, J. | +29

6

C2orf69 mutations disrupt mitochondrial function and cause a multisystem human disorder with recurring autoinflammation

enthalten in: The Journal of clinical investigation | 2021

von Lausberg, E. | Gießelmann, S. | Dewulf, J. | +31

7

Pitfalls and solutions in case fatality risk estimation – A multi-country analysis on the role of demographics, surveillance, time lags between reporting and death and healthcare system capacity on COVID-19

enthalten in: bioRxiv.org | 2021

von Vanella, P. | Wiessner, C. | Holz, A. | +5

8

Identification of a New Genetic Mutation Associated With Peters Anomaly

enthalten in: Cornea | 2021

von Faber, H. | Puk, O. | Holz, A. | +2

9

The Role of Age Distribution, Time Lag Between Reporting and Death and Healthcare System Capacity in Case Fatality Estimates of COVID-19

enthalten in: ResearchSquare.com | 2020

von Vanella, P. | Wiessner, C. | Holz, A. | +5

10

NUP188 Biallelic Loss of Function May Underlie a New Syndrome : Nucleoporin 188 Insufficiency Syndrome?

enthalten in: Molecular syndromology | 2020

von Sandestig, A. | Engström, K. | Pepler, A. | +5