Search Results - "Haack T"

U.S. West Coast Surface Heat Fluxes, Wind Stress, and Wind Stress Curl from a Mesoscale Model.

Authors: Haack, T. Burk, S. D. Hodur, R. M.

Source: Monthly Weather Review; November 2005, Vol. 133 Issue 11, p3202-3216, 15p

Island Wake Dynamics and Wake Influence on the Evaporation Duct and Radar Propagation.

Authors: Burk, S. D. Haack, T. Rogers, L. T.

Source: Journal of Applied Meteorology; March 2003, Vol. 42 Issue 3, p349-367, 19p

THE TROPICAL AIR-SEA PROPAGATION STUDY (TAPS).

Authors: KULESSA, A. S. BARRIOS, A. CLAVERIE, J. et al.

Source: Bulletin of the American Meteorological Society; Mar2017, Vol. 98 Issue 3, p517-537, 21p

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An Empirical Evaluation of Turbulence Closure Models in the Coastal Ocean.

Authors: Savelyev, I. B. Martin, P. J. Fan, Y. et al.

Source: Journal of Geophysical Research. Oceans. Apr2022, Vol. 127 Issue 4, p1-21. 21p.

Subject Terms: *Ocean waves, *Ocean circulation, *Circulation models, *Ocean, Ocean turbulence, Turbulence, Speed of sound

Geographic Terms: North Carolina

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Ketaminrazemat bei "Fast-track"-Anästhesie. Einfluss auf Aufwachzeiten und postoperativen Opioidbedarf.

Alternate Title: [Ketamine racemate and fast track anaesthesia. Influence on recovery times and postoperative opioid needs].

Authors: Lux EA Haack T Hinrichs K et al.

Source: Der Anaesthesist. Oct2009, Vol. 58 Issue 10, p1027-1034. 8p.

Hereditary spastic paraplegia caused by compound heterozygous mutations outside the motor domain of the KIF1A gene.

Authors: Krenn, M. Zulehner, G. Hotzy, C. et al.

Source: European Journal of Neurology. May2017, Vol. 24 Issue 5, p741-747. 7p.

Subjects: Paraplegia, Leg diseases, Motor neurons, Neurological disorders, Spasticity

Leukoencephalopathy with thalamus and brainstem involvement and high lactate 'LTBL' caused by EARS2 mutations.

Authors: Steenweg ME Ghezzi D Haack T et al.

Source: Brain: A Journal of Neurology; May2012, Vol. 135 Issue 5, p1387-1394, 8p

Diagnostic Evaluation of Mitochondrial DNA Disease Across Diverse Sequencing Approaches.

Authors: Amaya, A. B. Hinojosa Bader, I. Pogoda, M. et al.

Source: Neuropediatrics. 2026 Supplement 1, Vol. 57, pS1-S24. 24p.

Clinical, Biochemical and Neuroradiological Features in a Boy with Pyruvate Dehydrogenase Deficiency and a De Novo Missense-Variant in X-Linked PDHA1 (p.Ala349Thr).

Authors: Hinojosa-Amaya, A. B. Doebler-Neumann, M. Dufke, A. et al.

Source: Neuropediatrics. 2026 Supplement 1, Vol. 57, pS1-S24. 24p.

Exome sequencing as an approach to identify disease causing mutations in pediatric patients with mitochondrial diseases.

Authors: Haack, T. Strom, T. Freisinger, P. et al.

Source: Mitochondrion. Nov2013, Vol. 13 Issue 6, p920-920. 1p.

Phenotypic spectrum of 7 patients and 4 novel MTFMT mutations.

Authors: Freisinger, P. Haack, T. Mayr, J. et al.

Source: Mitochondrion. Nov2013, Vol. 13 Issue 6, p920-920. 1p.

Large-scale mutation screening in combination with lentiviral complementation of rare variants aid gene identification in mitochondrial disorders

Authors: Prokisch⁎, H. Haack, T. Madignier, F. et al.

Source: Mitochondrion. Jul2011, Vol. 11 Issue 4, p660-660. 1p.

Homozygous Frameshift Mutation in the ATP1A2 Gene Leading to Severe Pseudo-TORCH Syndrome.

Authors: Alber, M. Quante, M. Wiechers, C. et al.

Source: Neuropediatrics. 2023 Supplement 1, Vol. 54, pS1-S32. 32p.

A New Mixing-Length Formulation for the Parameterization of Dry Convection: Implementation and Evaluation in a Mesoscale Model.

Authors: Teixeira, J. Ferreira, J. P. Miranda, P. M. A. et al.

Source: Monthly Weather Review. Nov2004, Vol. 132 Issue 11, p2698-2707. 10p.

Extension of the phenotype of biallelic loss‐of‐function mutations in SLC25A46 to the severe form of pontocerebellar hypoplasia type I.

Authors: Braunisch, M. C. Gallwitz, H. Abicht, A. et al.

Source: Clinical Genetics. Feb2018, Vol. 93 Issue 2, p255-265. 12p. 1 Color Photograph, 1 Black and White Photograph, 1 Diagram, 3 Charts.

Aerial Observations of Symmetric Instability at the North Wall of the Gulf Stream.

Authors: Savelyev, I. Thomas, L. N. Smith, G. B. et al.

Source: Geophysical Research Letters. 1/16/2018, Vol. 45 Issue 1, p236-244. 9p.

Cofactor defects as a cause of mitochondrial encephalomyopathies.

Authors: Mayr, J.A. Freisinger, P. Haack, T. et al.

Source: Mitochondrion. Nov2013, Vol. 13 Issue 6, p908-908. 1p.

C19orf12 mutations in neurodegeneration with brain iron accumulation mimicking juvenile amyotrophic lateral sclerosis.

Authors: Deschauer, M. Gaul, C. Behrmann, C. et al.

Source: Journal of Neurology. Nov2012, Vol. 259 Issue 11, p2434-2439. 6p. 1 Color Photograph, 2 Black and White Photographs.