Katalog der Deutschen Nationalbibliothek

Expertensuche ?

Servicezeiten in Frankfurt am Main ab 1. Dezember 2025: Montag bis Freitag 9–18 Uhr und Samstag 10–16 Uhr
Service hours in Frankfurt am Main from 1 December 2025: Monday to Friday 9:00-18:00 and Saturday 10:00-16:00

Leichte Bedienung, intuitive Suche: Die Betaversion unseres neuen Katalogs ist online! → Zur Betaversion des neuen DNB-Katalogs

Ergebnis der Suche nach: "Closing"
im Bestand: Gesamter Bestand

4571 - 4580 von 4601

	4571	Through the looking glass : part 2. Scene with Humpty Dumpty and Finale. Song: "Humpty Dumpty" (traditional); Closing chorus / Lewis Carroll, S. Clark & W. Slaughter His Master's Voice C 3245 [Seite 2 von 2]
	4572	Tibial Tuberosity Transposition Tool Technique in Combination with Distal Femoral Lateral Closing Wedge Osteotomy for Patellar Luxation Treatment in Five Dogs Enthalten in VCOT open Bd. 06, 2023, Nr. 01: e52-e55
	4573	Tissue Staplers in Transcervical Diverticulectomy - A Novel Approach to Closing Zenker’s Diverticulum Enthalten in Indian journal of otolaryngology and head and neck surgery Bd. 77, 4.6.2025, Nr. 8, date:8.2025: 3164-3168
	4574	Total knee arthroplasty after high tibial osteotomy: a comparison of opening and closing wedge osteotomy Enthalten in International orthopaedics Bd. 37, 4.1.2013, Nr. 3, date:3.2013: 427-431
	4575	Total knee arthroplasty following lateral closing-wedge high tibial osteotomy versus primary total knee arthroplasty: a propensity score matching study Enthalten in Journal of orthopaedic surgery and research Bd. 19, 7.5.2024, Nr. 1, date:12.2024: 1-9
	4576	Total Synthesis and Cytotoxicity of (+)‐ and (‐)‐Goniodiol and 6‐epi‐Goniodiol. Construction of α,β‐Unsaturated Lactones by Ring‐Closing Metathesis. Enthalten in ChemInform Bd. 38, 2007, Nr. 24: no-no. 1 S.
	4577	Total Synthesis of Amphidinolide Y by Formation of Trisubstituted (E)‐Double Bond via Ring‐Closing Metathesis of Densely Functionalized Alkenes. Enthalten in ChemInform Bd. 38, 2007, Nr. 44: no-no. 1 S.
	4578	Total Synthesis of Cyclic Diterpene Tonantzitlolone Based on a Highly Stereoselective Substrate‐Controlled Aldol Reaction and Ring‐Closing Metathesis. Enthalten in ChemInform Bd. 38, 2007, Nr. 12: no-no. 1 S.
	4579	Total Synthesis of (‐)‐Kendomycin (I) Exploiting a Petasis—Ferrier Rearrangement/Ring‐Closing Olefin Metathesis Synthetic Strategy. Enthalten in ChemInform Bd. 36, 2005, Nr. 39: no-no. 1 S.
	4580	Total Synthesis of (+)‐Phomopsolide C (VIIb) by Ring‐Size Selective Ring‐Closing Metathesis/Cross‐Metathesis. Enthalten in ChemInform Bd. 37, 2006, Nr. 14: no-no. 1 S.