Suchergebnisse - "Humans"

PubPharm (26)

1

Feasibility of cardiovascular magnetic resonance to detect oxygenation deficits in patients with multi-vessel coronary artery disease triggered by breathing maneuvers

enthalten in: Journal of cardiovascular magnetic resonance | 7 May 2018

von Fischer, K. | Yamaji, K. | Luescher, S. | +7

2

Sample heterogeneity in unipolar depression as assessed by functional connectivity analyses is dominated by general disease effects

enthalten in: Journal of affective disorders | November 2017

von Feder, S.

3

Spatial variations in ambient ultrafine particle concentrations and the risk of incident prostate cancer: A case-control study

enthalten in: Environmental research | 2017

von Weichenthal, S. | Lavigne, E. | Valois, M. | +6

4

A variant of the CXCL11 gene may influence susceptibility to contact allergy, particularly in polysensitized patients

enthalten in: Contact dermatitis | 28 April 2016

von Westphal, G. | Schäkel, K.

5

CYP24A1 variant modifies the association between use of oestrogen plus progestogen therapy and colorectal cancer risk

enthalten in: British journal of cancer | 14 January 2016

von Garcia-Albeniz, X. | Brenner, H. | Hoffmeister, M. | +2

6

Reduced glyoxalase 1 activity in carotid artery plaques of nondiabetic patients with increased hemoglobin A1c level

enthalten in: Journal of vascular surgery | October 2016

von Peters, A. | Lercher, M. | Fleming, T. | +5

7

T-786C single nucleotide polymorphism of the endothelial nitric oxide synthase gene as a risk factor for endothelial dysfunction in polymyalgia rheumatica

enthalten in: Clinical and experimental rheumatology | 27 August 2015

von Löffers, C. | Heilig, B. | Hecker, M.

8

Sleep-associated aspects of myofascial pain in the orofacial area among Temporomandibular Disorder patients and controls

enthalten in: Sleep medicine | 11 May 2015

von Schmitter, M. | Kares-Vrincianu, A. | Kares, H. | +2

9

High levels of brain-type creatine kinase activity in human platelets and leukocytes : a genetic anomaly with autosomal dominant inheritance

enthalten in: Blood cells, molecules & diseases | 2012

von Arnold, H. | Kemp, K. | Bugert, P.

10

Hemodynamic and clinical onset in patients with hereditary pulmonary arterial hypertension and BMPR2 mutations

enthalten in: Respiratory research | 29 July 2011

von Pfarr, N. | Szamalek-Hoegel, J. | Fischer, C. | +9