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Online Ressourcen 341 Generation of multiple human iPSC lines from peripheral blood mononuclear cells of two SLC2A3 deletion and two SLC2A3 duplication carriers
Ziegler, Georg C.. - Würzburg : Universität Würzburg, 2022
Online Ressource
Online Ressourcen 342 Long-term methylphenidate exposure and 24-hours blood pressure and left ventricular mass in adolescents and young adults with attention deficit hyperactivity disorder
Buitelaar, J. K.. - Aachen : Universitätsbibliothek der RWTH Aachen, 2022
Online Ressource
Online Ressourcen 343 Long-term outcome after allogeneic hematopoietic cell transplantation for myelofibrosis
Robin, Marie. - Würzburg : Universität Würzburg, 2022
Online Ressource
Online Ressourcen 344 Patterns of peripheral blood B-cell subtypes are associated with treatment response in patients treated with immune checkpoint inhibitors: a prospective longitudinal pan-cancer study
Barth, Dominik A.. - Augsburg : Universität Augsburg, 2022
Online Ressource
Online Ressourcen 345 Vorhersage von schweren Blutungsereignissen bei Patienten mit peripherer arterieller Verschlusskrankheit: Der OAC3-PAD-Risikoscore
Behrendt, Christian-Alexander. - Aachen : Universitätsbibliothek der RWTH Aachen, 2022
Online Ressource
Artikel 346 Accuracy of a Novel Transcutaneous PCO 2 and PO 2 Sensor with Optical PO 2 Measurement in Neonatal Intensive Care: A Single-Centre Prospective Clinical Trial
Enthalten in Neonatology Bd. 119, 2022, Nr. 2: 230-237. 8 S.
Online Ressource
Artikel 347 Oxygen Saturation Index in Neonates with a Congenital Diaphragmatic Hernia: A Retrospective Cohort Study
Enthalten in Neonatology Bd. 119, 2022, Nr. 1: 111-118. 8 S.
Online Ressource
Artikel 348 Risk Factors for Prolonged Mechanical Ventilation and Weaning Failure: A Systematic Review
Enthalten in Respiration Bd. 101, 2022, Nr. 10: 959-969. 11 S.
Online Ressource
Artikel 349 Mosaic GLUD1 Mutations Associated with Hyperinsulinism Hyperammonemia Syndrome
Enthalten in Hormone research in paediatrics Bd. 95, 2022, Nr. 5: 492-498. 7 S.
Online Ressource
Artikel 350 The Prevalence of JAK2 Exon 12 Mutations in Vietnamese Patients with JAK2 V617F-Negative Polycythemia Vera: Frequent or Rare?
Enthalten in Human heredity Bd. 87, 2022, Nr. 3-4: 102-106. 5 S.
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