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Artikel 551 Molecular mechanisms underlying osteoarthritis development: Notch and NF-κB
Enthalten in Arthritis Research & Therapy Bd. 19, 15.5.2017, Nr. 1, date:12.2017: 1-7
Online Ressource
Artikel 552 Molekulare Pathogenese der Fibrose bei Muskeldystrophie vom Typ Duchenne
Enthalten in Der Pathologe Bd. 38, 17.1.2017, Nr. 1, date:2.2017: 21-29
Online Ressource
Artikel 553 More preoperative flexibility implies adequate neural pliability for curve correction without prophylactic untethering in scoliosis patients with asymptomatic tethered spinal cord, a retrospective study
Enthalten in BMC musculoskeletal disorders Bd. 18, 15.6.2017, Nr. 1, date:12.2017: 1-11
Online Ressource
Artikel 554 Morphological evidence of telocytes in human synovium
Enthalten in Scientific reports Bd. 8, 26.2.2018, Nr. 1, date:12.2018: 1-10
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Artikel 555 Motivational counselling and SMS-reminders for reduction of daily sitting time in patients with rheumatoid arthritis: a descriptive randomised controlled feasibility study
Enthalten in BMC musculoskeletal disorders Bd. 17, 18.10.2016, Nr. 1, date:12.2016: 1-13
Online Ressource
Artikel 556 Multisite peripheral joint pain: a cross-sectional study of prevalence and impact on general health, quality of life, pain intensity and consultation behaviour
Enthalten in BMC musculoskeletal disorders Bd. 18, 16.12.2017, Nr. 1, date:12.2017: 1-8
Online Ressource
Artikel 557 Muscle MRI and functional outcome measures in Becker muscular dystrophy
Enthalten in Scientific reports Bd. 7, 22.11.2017, Nr. 1, date:12.2017: 1-11
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Artikel 558 Musculo-skeletal pain among 40- and 45-year olds in Oslo: differences between two socioeconomically contrasting areas, and their possible explanations
Enthalten in International journal for equity in health Bd. 3, 19.10.2004, Nr. 1, date:12.2004: 1-5
Online Ressource
Artikel 559 Musculoskeletal disorders as underlying cause of death in 58 countries, 1986–2011: trend analysis of WHO mortality database
Enthalten in BMC musculoskeletal disorders Bd. 18, 2.2.2017, Nr. 1, date:12.2017: 1-12
Online Ressource
Artikel 560 Mutations outside the N-terminal part of RBCK1 may cause polyglucosan body myopathy with immunological dysfunction: expanding the genotype–phenotype spectrum
Enthalten in Journal of neurology Bd. 265, 19.12.2017, Nr. 2, date:2.2018: 394-401
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