Search Results - "Zenker M"

Argon plasma coagulation for open surgical and endoscopic applications: state of the art.

Authors: Raiser, J. Zenker, M.

Source: Journal of Physics: D Applied Physics; August 21 2006, Vol. 39 Issue 16, p3520-3523, 4p

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Reducing the incidence of acute puerperal metritis in primiparous cows by application of pegbovigrastim in a Holstein dairy herd.

Authors: FREICK, M. ZENKER, M. PASSARGE, O. et al.

Source: Veterinární Medicína. 2018, Vol. 63 Issue 4, p151-160. 10p.

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A macrosomic newborn with a cystic adrenal mass.

Authors: Zenker, M. Schindler, C. Kändler, C. et al.

Source: European Journal of Pediatrics. 1999, Vol. 158 Issue 3, p261-263. 3p.

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A new Ultra Precision Interferometer for absolute length measurements down to cryogenic temperatures.

Authors: Schödel, R. Walkov, A. Zenker, M. et al.

Source: Measurement Science & Technology; Sep2012, Vol. 23 Issue 9, p1-19, 19p

Percutaneous endovascular catheter aspiration thrombectomy of severe superior vena cava syndrome.

Authors: Ries, M. Zenker, M. Girisch, M. et al.

Source: Archives of Disease in Childhood -- Fetal & Neonatal Edition. Jul2002, Vol. 87 Issue 1, pF64. 4p. 1 Black and White Photograph.

Non-catheter-related aortic thrombosis and resistance to activated protein C in a premature newborn.

Authors: Zenker, M Ries, M Vetter, V et al.

Source: Acta Paediatrica. 9/8/1999, Vol. 88 Issue 9, p1035-1038. 4p. 2 Diagrams.

Le syndrome de Pierson, Michel Pierson

Alternate Title: Michel Pierson's syndrome

Authors: Cochat, P. Zenker, M.

Source: Archives de Pédiatrie. Nov2011, Vol. 18 Issue 11, p1127-1129. 3p.

The mosaic hedgehog spectrum: another lesson on the polymorphy of mosaicism.

Authors: Zenker, M.¹ (AUTHOR) martin.zenker@med.ovgu.de

Source: British Journal of Dermatology. Jan2020, Vol. 182 Issue 1, p22-23. 2p.

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A case associated with Walker Warburg syndrome phenotype and homozygous pericentric inversion 9: coincidental finding or aetiological factor?

Authors: Zenker, M. Dörr, H. G. Dörr, H G

Source: Acta Paediatrica. Jun2000, Vol. 89 Issue 6, p750-751. 2p.

Nephrotic syndrome in the first year of life: two thirds of cases are caused by mutations in 4 genes (NPHS1, NPHS2, WT1, and LAMB2)

Authors: Hinkes BG Mucha B Vlangos CN et al.

Source: Pediatrics. Apr2007, Vol. 119 Issue 4, pe907-19. 1p.

Facets of shame are differently expressed in dermatological disease: a prospective observational study.

Authors: Aberer, E. Hiebler‐Ragger, M. Zenker, M. et al.

Source: British Journal of Dermatology. Jul2020, Vol. 183 Issue 1, p169-171. 3p.