Suchergebnisse

PubPharm (15.044)

51

Public preferences for pharmacogenetic testing in the NHS : Embedding a discrete choice experiment within service design to better meet user needs

enthalten in: British journal of clinical pharmacology | 2024

von McDermott, J. | Sharma, V. | Newman, W. | +3

52

Neurological, cardiac, musculoskeletal, and renal manifestations of scleroderma along with insights into its genetics, pathophysiology, diagnostic, and therapeutic updates

enthalten in: Health science reports | 2024

von Prajjwal, P. | Marsool, M. | Yadav, V. | +12

53

Familial Chiari malformation : a systematic review and illustrative cases

enthalten in: Journal of neurosurgery. Spine | 2024

von Dhawan, A. | Dhawan, J. | Sharma, A. | +3

54

Genetics may affect the risk of undergoing surgery for rhizarthrosis

enthalten in: Journal of orthopaedic research : official publication of the Orthopaedic Research Society | 2024

von Henkel, C. | DBDS Genomic Consortium | Erikstrup, C. | +3

55

Genetic backgrounds and clinical characteristics of congenital neutropenias in Israel

enthalten in: European journal of haematology | 2024

von Yeshareem, L. | Yacobovich, J. | Lebel, A. | +26

56

Genetic factors acting prior to dormancy in sour cherry influence bloom time the following spring

enthalten in: Journal of experimental botany | 2024

von Goeckeritz, C. | Grabb, C. | Grumet, R. | +2

57

SCN5A gene variants and arrhythmic risk in Brugada Syndrome : an updated systematic review and meta-analysis

enthalten in: Heart rhythm | 2024

von Doundoulakis, I. | Pannone, L. | Chiotis, S. | +17

58

Factors associated with genetic markers for rotator cuff disease in patients with atraumatic rotator cuff tears

enthalten in: Journal of orthopaedic research : official publication of the Orthopaedic Research Society | 2024

von Yanik, E. | Saccone, N. | Aleem, A. | +4

59

Genetic variation drives differences in obesity-related gene regulation

enthalten in: Trends in genetics : TIG | 2024

von Kaikkonen, M.

60

Letter to the Editor from Janot et al : « Single-Exon Deletions of ZNRF3 Exon 2 cause Congenital Adrenal Hypoplasia »

enthalten in: The Journal of clinical endocrinology and metabolism | 2024

von Janot, C. | Bachelot, A. | Mallet, D. | +3