Search Results - "Rautenberg M"

Mechanochemical Synthesis as a Greener Way to Produce Iron‐based Oxygen Reduction Catalysts.

Authors: Gernhard, M. Rautenberg, M. Hörner, G. et al.

Source: Zeitschrift für Anorganische und Allgemeine Chemie. 11/25/2021, Vol. 647 Issue 22, p2080-2087. 8p.

A distinction between different types of stall in a centrifugal compressor stage.

Authors: Kämmer, N. Rautenberg, M.

Source: Journal of Engineering for Gas Turbines & Power; January 1986, Vol. 108, p83-92, 10p

Blade vibration measurements on centrifugal compressors by means of telemetry and holographic interferometry.

Authors: Haupt, U. Rautenberg, M.

Source: Journal of Engineering for Gas Turbines & Power; January 1984, Vol. 106, p70-78, 9p

Investigation of blade vibration of radial impellers by means of telemetry and holographic interferometry.

Authors: Haupt, U. Rautenberg, M.

Source: Journal of Engineering for Power; October 1982, Vol. 104, p838-843, 6p

Daily rat tibial growth in vivo following hypothalamic sex reversal with neonatal and pubertal treatments with gonadal steroids.

Authors: Rol De Lama, M. A. Roest, C. Rolf, K. et al.

Source: Annals of Human Biology. Jan2001, Vol. 28 Issue 1, p38-50.

Thermal isocreep curves obtained during multi-axial creep tests on recrystallized Zircaloy-4 and M5™ alloy.

Authors: Rautenberg, M. Poquillon, D. Pilvin, P. et al.

Source: Nuclear Engineering & Design. Apr2014, Vol. 269, p33-37. 5p.

Subjects: Zirconium alloys, Thermal analysis, Creep (Materials), Testing-machines, Nuclear industry, Anisotropy, Strains & stresses (Mechanics)

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The vibration behavior of impeller blades in the five-axis CNC flank milling process.

Authors: Sonthipermpoon, Kawin Bohez, E. Hasemann, H. et al.

Source: International Journal of Advanced Manufacturing Technology. May2010, Vol. 46 Issue 9-12, p1171-1177. 7p. 2 Black and White Photographs, 6 Diagrams, 3 Graphs.

Insulin-like growth factors and insulin-like growth factor-binding proteins in relation to disease status and incidence of hypoglycaemia in patients with a gastrointestinal stromal tumour.

Authors: Rikhof, B. Van Doorn, J. Suurmeijer, A. J. H. et al.

Source: Annals of Oncology. Sep2009, Vol. 20 Issue 9, p1582-1588. 7p. 5 Charts.

A new PNPLA6 mutation presenting as Oliver McFarlane syndrome.

Authors: Patsi, O. De Beaufort, C. Kerschen, P. et al.

Source: Journal of the Neurological Sciences. Sep2018, Vol. 392, p1-2. 2p.

eNanoMapper – A database and ontology framework for design and safety assessment of nanomaterials.

Authors: Kilic, G. Fadeel, B. Farcal, L. et al.

Source: Toxicology Letters. Sep2016 Supplement, Vol. 258, pS118-S119. 1p.

Loss-of-function variants in the CAPN1 activator CD99L2 cause X-linked spastic ataxia.

Authors: Menden B Incebacak Eltemur RD Demidov G et al.

Corporate Authors: Menden B Incebacak Eltemur RD Demidov G et al.

Source: Nature communications [Nat Commun] 2026 Feb 14; Vol. 17 (1), pp. 1698. Date of Electronic Publication: 2026 Feb 14.

Publication Type: Journal Article

Journal Info: Publisher: Nature Pub. Group Country of Publication: England NLM ID: 101528555 Publication Model: Electronic Cited Medium: Internet ISSN: 2041-1723 (Electronic) Linking ISSN: 20411723 NLM ISO Abbreviation: Nat Commun Subsets: MEDLINE

Information Mode-Dependent Success Rates of Obtaining German Medical Informatics Initiative-Compliant Broad Consent in the Emergency Department: Single-Center Prospective Observational Study.

Authors: Hans FP Kleinekort J Boerries M et al.

Source: JMIR medical informatics [JMIR Med Inform] 2024 Dec 17; Vol. 12, pp. e65646. Date of Electronic Publication: 2024 Dec 17.

Publication Type: Journal Article; Observational Study

Journal Info: Publisher: JMIR Publications Country of Publication: Canada NLM ID: 101645109 Publication Model: Electronic Cited Medium: Internet ISSN: 2291-9694 (Electronic) Linking ISSN: 22919694 NLM ISO Abbreviation: JMIR Med Inform Subsets: MEDLINE

Integrating row level security in i2b2: segregation of medical records into data marts without data replication and synchronization.

Authors: Scheible R Thomczyk F Blum M et al.

Source: JAMIA open [JAMIA Open] 2023 Aug 14; Vol. 6 (3), pp. ooad068. Date of Electronic Publication: 2023 Aug 14 (Print Publication: 2023).

Publication Type: Journal Article

Journal Info: Publisher: Oxford University Press on behalf of the American Medical Informatics Association Country of Publication: United States NLM ID: 101730643 Publication Model: eCollection Cited Medium: Internet ISSN: 2574-2531 (Electronic) Linking ISSN: 25742531 NLM ISO Abbreviation: JAMIA Open Subsets: PubMed not MEDLINE

The prodromal phase of hereditary spastic paraplegia type 4: the preSPG4 cohort study.

Authors: Rattay TW Völker M Rautenberg M et al.

Source: Brain : a journal of neurology [Brain] 2023 Mar 01; Vol. 146 (3), pp. 1093-1102.

Publication Type: Journal Article; Research Support, Non-U.S. Gov't

Journal Info: Publisher: Oxford University Press Country of Publication: England NLM ID: 0372537 Publication Model: Print Cited Medium: Internet ISSN: 1460-2156 (Electronic) Linking ISSN: 00068950 NLM ISO Abbreviation: Brain Subsets: MEDLINE

Adult-Onset Neurodegeneration in Nucleotide Excision Repair Disorders (NERDND ): Time to Move Beyond the Skin.

Authors: Cordts I Önder D Traschütz A et al.

Source: Movement disorders : official journal of the Movement Disorder Society [Mov Disord] 2022 Aug; Vol. 37 (8), pp. 1707-1718. Date of Electronic Publication: 2022 Jun 14.

Publication Type: Journal Article; Multicenter Study; Research Support, Non-U.S. Gov't

Journal Info: Publisher: Wiley-Liss Country of Publication: United States NLM ID: 8610688 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1531-8257 (Electronic) Linking ISSN: 08853185 NLM ISO Abbreviation: Mov Disord Subsets: MEDLINE

De Novo and Dominantly Inherited SPTAN1 Mutations Cause Spastic Paraplegia and Cerebellar Ataxia.

Authors: Van de Vondel L De Winter J Beijer D et al.

Corporate Authors: Van de Vondel L De Winter J Beijer D et al.

Source: Movement disorders : official journal of the Movement Disorder Society [Mov Disord] 2022 Jun; Vol. 37 (6), pp. 1175-1186. Date of Electronic Publication: 2022 Feb 12.

Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, N.I.H., Extramural

Journal Info: Publisher: Wiley-Liss Country of Publication: United States NLM ID: 8610688 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1531-8257 (Electronic) Linking ISSN: 08853185 NLM ISO Abbreviation: Mov Disord Subsets: MEDLINE

Heterozygous UCHL1 loss-of-function variants cause a neurodegenerative disorder with spasticity, ataxia, neuropathy, and optic atrophy.

Authors: Park J Tucci A Cipriani V et al.

Corporate Authors: Park J Tucci A Cipriani V et al.

Source: Genetics in medicine : official journal of the American College of Medical Genetics [Genet Med] 2023 Oct; Vol. 25 (10), pp. 100961. Date of Electronic Publication: 2023 Aug 31.

Publication Type: Published Erratum

Journal Info: Publisher: Elsevier Country of Publication: United States NLM ID: 9815831 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1530-0366 (Electronic) Linking ISSN: 10983600 NLM ISO Abbreviation: Genet Med Subsets: MEDLINE; PubMed not MEDLINE

Synthesis and In Situ Monitoring of Mechanochemical Preparation of Highly Proton Conductive Hydrogen-Bonded Metal Phosphonates.

Authors: Akhmetova I Rautenberg M Das C et al.

Source: ACS omega [ACS Omega] 2023 May 04; Vol. 8 (19), pp. 16687-16693. Date of Electronic Publication: 2023 May 04 (Print Publication: 2023).

Publication Type: Journal Article

Journal Info: Publisher: American Chemical Society Country of Publication: United States NLM ID: 101691658 Publication Model: eCollection Cited Medium: Internet ISSN: 2470-1343 (Electronic) Linking ISSN: 24701343 NLM ISO Abbreviation: ACS Omega Subsets: PubMed not MEDLINE

Heterozygous UCHL1 loss-of-function variants cause a neurodegenerative disorder with spasticity, ataxia, neuropathy, and optic atrophy.

Authors: Park J Tucci A Cipriani V et al.

Corporate Authors: Park J Tucci A Cipriani V et al.

Source: Genetics in medicine : official journal of the American College of Medical Genetics [Genet Med] 2022 Oct; Vol. 24 (10), pp. 2079-2090. Date of Electronic Publication: 2022 Aug 20.

Publication Type: Journal Article; Research Support, Non-U.S. Gov't

Journal Info: Publisher: Elsevier Country of Publication: United States NLM ID: 9815831 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1530-0366 (Electronic) Linking ISSN: 10983600 NLM ISO Abbreviation: Genet Med Subsets: MEDLINE