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Technique for Concurrent Internal Calibration during Data Acquisition for SAR Systems

Remote sensing (Basel, Switzerland), 2020-06, Vol.12 (11), p.1773

2020

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Expertenempfehlung zur Magnetresonanztomographie bei Muskelerkrankungen

Die Radiologie, 2024, Vol.64 (8), p.653-662

2024

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Radiometric Comparison within the Sentinel-1 SAR Constellation over a Wide Backscatter Range

Remote sensing (Basel, Switzerland), 2020-03, Vol.12 (5), p.854

2020

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The genomic and clinical landscape of fetal akinesia

Genetics in medicine, 2020-03, Vol.22 (3), p.511-523

2020

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Protein signature of human skin fibroblasts allows the study of the molecular etiology of rare neurological diseases

Orphanet journal of rare diseases, 2021-02, Vol.16 (1), p.73-73, Article 73

2021

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Sporadic late-onset nemaline myopathy: clinico-pathological characteristics and review of 76 cases

Orphanet journal of rare diseases, 2017-05, Vol.12 (1), p.86-86, Article 86

2017

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The missense mutation C667F in murine β-dystroglycan causes embryonic lethality, myopathy and blood-brain barrier destabilization

Disease models & mechanisms, 2024-06, Vol.17 (6)

2024

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Making sense of missense variants in TTN-related congenital myopathies

Acta neuropathologica, 2021-03, Vol.141 (3), p.431-453

2021

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Loss of the smallest subunit of cytochrome c oxidase, COX8A, causes Leigh-like syndrome and epilepsy

Brain (London, England : 1878), 2016-02, Vol.139 (Pt 2), p.338-345

2016

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Characterization of the Amazon Rainforest Backscatter At X-Band Using TanDEM-X Data

IEEE journal of selected topics in applied earth observations and remote sensing, 2024-01, Vol.17, p.1-19

2024

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Highly Accurate Radar Cross-Section and Transfer Function Measurement of a Digital Calibration Transponder without Known Reference—Part I: Measurement and Results

Remote sensing (Basel, Switzerland), 2023-02, Vol.15 (4), p.1153

2023

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Highly Accurate Radar Cross-Section and Transfer Function Measurement of a Digital Calibration Transponder without Known Reference—Part II: Uncertainty Estimation and Validation

Remote sensing (Basel, Switzerland), 2023-04, Vol.15 (8), p.2148

2023

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Missense mutations in small muscle protein X-linked (SMPX) cause distal myopathy with protein inclusions

Acta neuropathologica, 2021-08, Vol.142 (2), p.375-393

2021

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Screening for lipoprotein receptor-related protein 4-, agrin-, and titin-antibodies and exploring the autoimmune spectrum in myasthenia gravis

Journal of neurology, 2017-06, Vol.264 (6), p.1193-1203

2017

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Geometric Accuracy of Sentinel-1A and 1B Derived from SAR Raw Data with GPS Surveyed Corner Reflector Positions

Remote sensing (Basel, Switzerland), 2018-04, Vol.10 (4), p.523

2018

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Mass Spectrometric Profiling of Extraocular Muscle and Proteomic Adaptations in the mdx-4cv Model of Duchenne Muscular Dystrophy

Life (Basel, Switzerland), 2021-06, Vol.11 (7), p.595

2021

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The Oral Antidiabetic Pioglitazone Protects from Neurodegeneration and Amyotrophic Lateral Sclerosis-Like Symptoms in Superoxide Dismutase-G93A Transgenic Mice

The Journal of neuroscience, 2005-08, Vol.25 (34), p.7805-7812

2005

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Computed tomography derived cervical fat-free muscle fraction as an imaging-based outcome marker in patients with acute ischemic stroke: a pilot study

BMC neurology, 2023-02, Vol.23 (1), p.86-86, Article 86

2023

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The phenotypic spectrum of neutral lipid storage myopathy due to mutations in the PNPLA2 gene

Journal of neurology, 2011-11, Vol.258 (11), p.1987-1997

2011

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Correction: The genomic and clinical landscape of fetal akinesia

Genetics in medicine, 2020-08, Vol.22 (8), p.1426-1428

2020

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Precise Antenna Pointing Determination in Elevation for Spaceborne SAR Systems Using Coherent Pattern Differences

Remote sensing (Basel, Switzerland), 2019-02, Vol.11 (3), p.320

2019

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Radiometric Performance of the TerraSAR-X Mission over More Than Ten Years of Operation

Remote sensing (Basel, Switzerland), 2018-05, Vol.10 (5), p.754

2018

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Synaptopodin-2 Isoforms Have Specific Binding Partners and Display Distinct, Muscle Cell Type-Specific Expression Patterns

Cells (Basel, Switzerland), 2023-12, Vol.13 (1), p.85

2023

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Strumpellin is a novel valosin-containing protein binding partner linking hereditary spastic paraplegia to protein aggregation diseases

Brain (London, England : 1878), 2010-10, Vol.133 (10), p.2920-2941

2010

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Diagnostic challenge and therapeutic dilemma in necrotizing myopathy

Neurology, 2013-09, Vol.81 (10), p.932-935

2013

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Technique for Concurrent Internal Calibration during Data Acquisition for SAR Systems

Expertenempfehlung zur Magnetresonanztomographie bei Muskelerkrankungen

Radiometric Comparison within the Sentinel-1 SAR Constellation over a Wide Backscatter Range

The genomic and clinical landscape of fetal akinesia

Protein signature of human skin fibroblasts allows the study of the molecular etiology of rare neurological diseases

Sporadic late-onset nemaline myopathy: clinico-pathological characteristics and review of 76 cases

The missense mutation C667F in murine β-dystroglycan causes embryonic lethality, myopathy and blood-brain barrier destabilization

Making sense of missense variants in TTN-related congenital myopathies

Loss of the smallest subunit of cytochrome c oxidase, COX8A, causes Leigh-like syndrome and epilepsy

Characterization of the Amazon Rainforest Backscatter At X-Band Using TanDEM-X Data

Highly Accurate Radar Cross-Section and Transfer Function Measurement of a Digital Calibration Transponder without Known Reference—Part I: Measurement and Results

Highly Accurate Radar Cross-Section and Transfer Function Measurement of a Digital Calibration Transponder without Known Reference—Part II: Uncertainty Estimation and Validation

Missense mutations in small muscle protein X-linked (SMPX) cause distal myopathy with protein inclusions

Screening for lipoprotein receptor-related protein 4-, agrin-, and titin-antibodies and exploring the autoimmune spectrum in myasthenia gravis

Geometric Accuracy of Sentinel-1A and 1B Derived from SAR Raw Data with GPS Surveyed Corner Reflector Positions

Mass Spectrometric Profiling of Extraocular Muscle and Proteomic Adaptations in the mdx-4cv Model of Duchenne Muscular Dystrophy

The Oral Antidiabetic Pioglitazone Protects from Neurodegeneration and Amyotrophic Lateral Sclerosis-Like Symptoms in Superoxide Dismutase-G93A Transgenic Mice

Computed tomography derived cervical fat-free muscle fraction as an imaging-based outcome marker in patients with acute ischemic stroke: a pilot study

The phenotypic spectrum of neutral lipid storage myopathy due to mutations in the PNPLA2 gene

Correction: The genomic and clinical landscape of fetal akinesia

Precise Antenna Pointing Determination in Elevation for Spaceborne SAR Systems Using Coherent Pattern Differences

Radiometric Performance of the TerraSAR-X Mission over More Than Ten Years of Operation

Synaptopodin-2 Isoforms Have Specific Binding Partners and Display Distinct, Muscle Cell Type-Specific Expression Patterns

Strumpellin is a novel valosin-containing protein binding partner linking hereditary spastic paraplegia to protein aggregation diseases

Diagnostic challenge and therapeutic dilemma in necrotizing myopathy

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