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Temperature compensated planar narrow-band notch filter with fully automated laser-trimming

2001 IEEE MTT-S International Microwave Sympsoium Digest (Cat. No.01CH37157), 2001, Vol.3, p.1919-1922 vol.3

Schallner, M.

2001

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Adjustment of a temperature compensated Ka-band ring resonator VCO using fully automated laser-trimming

2001 IEEE MTT-S International Microwave Sympsoium Digest (Cat. No.01CH37157), 2001, Vol.3, p.2179-2182 vol.3

2001

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Alternating Hemiplegia of Childhood as a New Presentation of Adenylate Cyclase 5 -Mutation-Associated Disease: A Report of Two Cases

The Journal of pediatrics, 2017-02, Vol.181, p.306-308.e1

2017

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Intraoperative Pulmonary Tumor Embolism from Renal Cell Carcinoma and a Patent Foramen Ovale Detected by Transesophageal Echocardiography

Journal of cardiothoracic and vascular anesthesia, 2011-02, Vol.25 (1), p.145-147

2011

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Dielectric properties of Fe-doped Ba Sr1−TiO3 thin films on polycrystalline substrates at temperatures between −35 and +85 °C

Solid-state electronics, 2003-12, Vol.47 (12), p.2199-2203

2003

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Dielectric properties of Fe-doped Ba xSr 1− xTiO 3 thin films on polycrystalline substrates at temperatures between −35 and +85 °C

Solid-state electronics, 2003, Vol.47 (12), p.2199-2203

2003

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Millimetre wave VCOs with wide electronic tuning range for synthesised radios

33rd European Microwave Conference Proceedings (IEEE Cat. No.03EX723C), 2003, Vol.3, p.1187-1190 Vol.3

2003

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The Influence of the Human Body on Electric and Magnetic Field Components in the Immediate Vicinity of the Body

Frequenz, 1998-09, Vol.52 (9-10), p.170-174

1998

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Fully Automated Laser-Adjustable Compact Microwave Transceivers with Integrated Local Oscillator

2006 European Microwave Conference, 2006, p.228-231

2006

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T-cell dysfunction in the glioblastoma microenvironment is mediated by myeloid cells releasing interleukin-10

Nature communications, 2022-02, Vol.13 (1), p.925-16, Article 925

2022

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Handgrip and finger flexion strength in children: A cross-sectional assessment of age-related normative data and application as a clinical functional marker in paediatric neuromuscular disorders

Brain & development (Tokyo. 1979), 2023-01, Vol.45 (1), p.26-38

2023

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The clinical-phenotype continuum in DYNC1H1-related disorders—genomic profiling and proposal for a novel classification

Journal of human genetics, 2020-11, Vol.65 (11), p.1003-1017

2020

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Carbon Monoxide Preserves Circadian Rhythm to Reduce the Severity of Subarachnoid Hemorrhage in Mice

Stroke (1970), 2017-09, Vol.48 (9), p.2565-2573

2017

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Psychometrische Eigenschaften des KoCoN-V: Ein Fragebogen zur Versorgungsqualität von Kindern und Jugendlichen mit komplex-chronisch neurologischen Erkrankungen

Monatsschrift Kinderheilkunde, 2023-10

2023

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Can biological soil crusts be prominent landscape components in rangelands? A case study from New Mexico, USA

Geoderma, 2022-03, Vol.410, p.115658, Article 115658

2022

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Acquired sensorimotor polyneuropathy in an adolescent boy with primary intracranial sarcoma

European journal of paediatric neurology, 2019-07, Vol.23 (4), p.662-667

2019

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Heterozygous truncation mutations of the SMC1A gene cause a severe early onset epilepsy with cluster seizures in females: Detailed phenotyping of 10 new cases

Epilepsia (Copenhagen), 2017-04, Vol.58 (4), p.565-575

2017

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A phase 3 randomized placebo-controlled trial of tadalafil for Duchenne muscular dystrophy

Neurology, 2017-10, Vol.89 (17), p.1811-1820

2017

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Early and Rapid Identification of COVID-19 Patients with Neutralizing Type I Interferon Auto-antibodies

Journal of clinical immunology, 2022-08, Vol.42 (6), p.1111-1129

2022

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Mutations in EXOSC2 are associated with a novel syndrome characterised by retinitis pigmentosa, progressive hearing loss, premature ageing, short stature, mild intellectual disability and distinctive gestalt

Journal of medical genetics, 2016-06, Vol.53 (6), p.419-425

2016

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Homozygous loss of CHRNA7 on chromosome 15q13.3 causes severe encephalopathy with seizures and hypotonia

American journal of medical genetics. Part A, 2010-11, Vol.152A (11), p.2908-2911

2010

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Assessment of Anthropometric Measures and Hand Muscle Strength in Children to Establish Standardized Parameters for Pediatric Neurorehabilitation

Neuropediatrics, 2017, Vol.48 (S 01), p.S1-S45

2017

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Proximal variants in CCND2 associated with microcephaly, short stature, and developmental delay: A case series and review of inverse brain growth phenotypes

American journal of medical genetics. Part A, 2021-09, Vol.185 (9), p.2719-2738

2021

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Rhombencephalosynapsis Leading to an Easily Missed, Underdiagnosed Neurocutaneous Syndrome

Neuropediatrics, 2016, Vol.47 (S 01)

2016

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Temperature compensated planar narrow-band notch filter with fully automated laser-trimming

Adjustment of a temperature compensated Ka-band ring resonator VCO using fully automated laser-trimming

Alternating Hemiplegia of Childhood as a New Presentation of Adenylate Cyclase 5 -Mutation-Associated Disease: A Report of Two Cases

Intraoperative Pulmonary Tumor Embolism from Renal Cell Carcinoma and a Patent Foramen Ovale Detected by Transesophageal Echocardiography

Dielectric properties of Fe-doped Ba Sr1−TiO3 thin films on polycrystalline substrates at temperatures between −35 and +85 °C

Dielectric properties of Fe-doped Ba xSr 1− xTiO 3 thin films on polycrystalline substrates at temperatures between −35 and +85 °C

Millimetre wave VCOs with wide electronic tuning range for synthesised radios

The Influence of the Human Body on Electric and Magnetic Field Components in the Immediate Vicinity of the Body

Fully Automated Laser-Adjustable Compact Microwave Transceivers with Integrated Local Oscillator

T-cell dysfunction in the glioblastoma microenvironment is mediated by myeloid cells releasing interleukin-10

Handgrip and finger flexion strength in children: A cross-sectional assessment of age-related normative data and application as a clinical functional marker in paediatric neuromuscular disorders

The clinical-phenotype continuum in DYNC1H1-related disorders—genomic profiling and proposal for a novel classification

Carbon Monoxide Preserves Circadian Rhythm to Reduce the Severity of Subarachnoid Hemorrhage in Mice

Psychometrische Eigenschaften des KoCoN-V: Ein Fragebogen zur Versorgungsqualität von Kindern und Jugendlichen mit komplex-chronisch neurologischen Erkrankungen

Can biological soil crusts be prominent landscape components in rangelands? A case study from New Mexico, USA

Recurrent de novo missense variants in GNB2 can cause syndromic intellectual disability

Acquired sensorimotor polyneuropathy in an adolescent boy with primary intracranial sarcoma

Heterozygous truncation mutations of the SMC1A gene cause a severe early onset epilepsy with cluster seizures in females: Detailed phenotyping of 10 new cases

A phase 3 randomized placebo-controlled trial of tadalafil for Duchenne muscular dystrophy

Early and Rapid Identification of COVID-19 Patients with Neutralizing Type I Interferon Auto-antibodies

Mutations in EXOSC2 are associated with a novel syndrome characterised by retinitis pigmentosa, progressive hearing loss, premature ageing, short stature, mild intellectual disability and distinctive gestalt

Homozygous loss of CHRNA7 on chromosome 15q13.3 causes severe encephalopathy with seizures and hypotonia

Assessment of Anthropometric Measures and Hand Muscle Strength in Children to Establish Standardized Parameters for Pediatric Neurorehabilitation

Proximal variants in CCND2 associated with microcephaly, short stature, and developmental delay: A case series and review of inverse brain growth phenotypes

Rhombencephalosynapsis Leading to an Easily Missed, Underdiagnosed Neurocutaneous Syndrome

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