Found: 30
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Magnetic and Thermal Behavior of a Planar Toroidal Transformer.
- Published in:
- Energies (19961073), 2024, v. 17, n. 11, p. 2454, doi. 10.3390/en17112454
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- Publication type:
- Article
Eddy Current Microsensor Dedicated to the Nondestructive Testing of Conductive Plates.
- Published in:
- Applied Computational Electromagnetics Society Journal, 2022, v. 37, n. 1, p. 117, doi. 10.13052/2022.ACES.J.370114
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- Publication type:
- Article
Integrated square shape inductor with magnetic core in a buck converter DC-DC.
- Published in:
- Przeglad Elektrotechniczny, 2019, v. 95, n. 9, p. 57, doi. 10.15199/48.2019.09.11
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- Publication type:
- Article
Design of micro-transformer in monolithic technology for high-frequency flyback-type converters.
- Published in:
- Electrical Engineering, 2018, v. 100, n. 4, p. 2589, doi. 10.1007/s00202-018-0730-8
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- Publication type:
- Article
Design of Micro-Transformer in Monolithic Technology for High Frequencies Fly-back Type Converters.
- Published in:
- Przeglad Elektrotechniczny, 2018, v. 94, n. 8, p. 85, doi. 10.15199/48.2018.08.22
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- Publication type:
- Article
Simulation of the operation of a DC-DC converter containing an inductor of planar type.
- Published in:
- Electrical Engineering, 2018, v. 100, n. 2, p. 953, doi. 10.1007/s00202-017-0558-7
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- Publication type:
- Article
A recessive ataxia diagnosis algorithm for the next generation sequencing era.
- Published in:
- 2017
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- Publication type:
- journal article
Using the variable width in a planar inductor on Kapton for optimizing its performance.
- Published in:
- Turkish Journal of Electrical Engineering & Computer Sciences, 2017, v. 25, n. 5, p. 3798, doi. 10.3906/elk-1606-343
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- Publication type:
- Article
The Performance of an Integrated Transformer in a DC/DC Converter.
- Published in:
- Telkomnika, 2017, v. 15, n. 3, p. 1031, doi. 10.12928/TELKOMNIKA.v15i3.4251
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- Publication type:
- Article
Towards a functional pathology of hereditary neuropathies.
- Published in:
- Acta Neuropathologica, 2017, v. 133, n. 4, p. 493, doi. 10.1007/s00401-016-1645-y
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- Publication type:
- Article
Modeling and Structure Optimization of Tapped Transformer.
- Published in:
- International Journal of Electrical & Computer Engineering (2088-8708), 2017, v. 7, n. 1, p. 41, doi. 10.11591/ijece.v7i1.pp41-49
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- Publication type:
- Article
Simulation Analysis of Geometrical Parameters of Monolithic On-Chip Transformers on Silicon Substrates.
- Published in:
- Przeglad Elektrotechniczny, 2017, v. 93, n. 1, p. 253, doi. 10.15199/48.2017.01.62
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- Publication type:
- Article
Underestimated associated features in CMT neuropathies: clinical indicators for the causative gene?
- Published in:
- Brain & Behavior, 2016, v. 6, n. 4, p. n/a, doi. 10.1002/brb3.451
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- Publication type:
- Article
Reply: Is SIGMAR1 a confirmed FTD/MND gene?
- Published in:
- 2015
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- Publication type:
- commentary
Is SIGMAR1 a confirmed FTD/MND gene?
- Published in:
- 2015
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- Publication type:
- commentary
Dysfunction in endoplasmic reticulummitochondria crosstalk underlies SIGMAR1 loss of function mediated motor neuron degeneration.
- Published in:
- Brain: A Journal of Neurology, 2015, v. 138, n. 4, p. 875, doi. 10.1093/brain/awv008
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- Publication type:
- Article
PLEKHG5 deficiency leads to an intermediate form of autosomal-recessive Charcot–Marie–Tooth disease.
- Published in:
- Human Molecular Genetics, 2013, v. 22, n. 20, p. 4224, doi. 10.1093/hmg/ddt274
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- Publication type:
- Article
New Findings in a Global Approach to Dissect the Whole Phenotype of <i>PLA2G6</i> Gene Mutations.
- Published in:
- PLoS ONE, 2013, v. 8, n. 10, p. 1, doi. 10.1371/journal.pone.0076831
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- Publication type:
- Article
KIF1A missense mutations in SPG30, an autosomal recessive spastic paraplegia: distinct phenotypes according to the nature of the mutations.
- Published in:
- European Journal of Human Genetics, 2012, v. 20, n. 6, p. 645, doi. 10.1038/ejhg.2011.261
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- Publication type:
- Article
Pantothenate kinase-associated neurodegeneration: Clinical description of 10 patients and identification of new mutations.
- Published in:
- Movement Disorders, 2011, v. 26, n. 9, p. 1777, doi. 10.1002/mds.23648
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- Publication type:
- Article
Screening of ARHSP-TCC patients expands the spectrum of SPG11 mutations and includes a large scale gene deletion.
- Published in:
- Human Mutation, 2009, v. 30, n. 3, p. E500, doi. 10.1002/humu.20945
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- Publication type:
- Article
Mutations in SPG11 are frequent in autosomal recessive spastic paraplegia with thin corpus callosum, cognitive decline and lower motor neuron degeneration.
- Published in:
- Brain: A Journal of Neurology, 2008, v. 131, n. 3, p. 772, doi. 10.1093/brain/awm293
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- Publication type:
- Article
Autosomal recessive axonal Charcot-Marie-Tooth disease (ARCMT2): phenotype-genotype correlations in 13 Moroccan families.
- Published in:
- Brain: A Journal of Neurology, 2007, v. 130, n. 4, p. 1062
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- Publication type:
- Article
A novel locus for autosomal recessive spastic ataxia on chromosome 17p.
- Published in:
- Human Genetics, 2007, v. 121, n. 3/4, p. 413, doi. 10.1007/s00439-007-0328-0
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- Publication type:
- Article
Mutations in SPG11, encoding spatacsin, are a major cause of spastic paraplegia with thin corpus callosum.
- Published in:
- Nature Genetics, 2007, v. 39, n. 3, p. 366, doi. 10.1038/ng1980
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- Publication type:
- Article
Spastic paraplegia with thin corpus callosum: description of 20 new families, refinement of the SPG11 locus, candidate gene analysis and evidence of genetic heterogeneity.
- Published in:
- Neurogenetics, 2006, v. 7, n. 3, p. 149, doi. 10.1007/s10048-006-0044-2
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- Publication type:
- Article
Autosomal recessive spastic paraplegia (SPG30) with mild ataxia and sensory neuropathy maps to chromosome 2q37.3.
- Published in:
- Brain: A Journal of Neurology, 2006, v. 129, n. 6, p. 1456, doi. 10.1093/brain/awl012
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- Publication type:
- Article
Mapping of a new form of pure autosomal recessive spastic paraplegia (SPG28).
- Published in:
- Annals of Neurology, 2005, v. 57, n. 4, p. 567
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- Publication type:
- Article
Spinocerebellar ataxia with sensory neuropathy (SCA25) maps to chromosome 2p.
- Published in:
- Annals of Neurology, 2004, v. 55, n. 1, p. 97
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- Publication type:
- Article
Phenotypic and genetic study of a family with hereditary sensory neuropathy and prominent weakness.
- Published in:
- 2000
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- Publication type:
- journal article