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Population pharmacokinetics of sevoflurane in conjunction with the AnaConDa®: toward target-controlled infusion of volatiles into the breathing system

Acta anaesthesiologica Scandinavica, 2008-04, Vol.52 (4), p.553-560

2008

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Influence of intrinsic noise generated by a thermotesting device on thermal sensory detection and thermal pain detection thresholds

Muscle & nerve, 2009-08, Vol.40 (2), p.257-263

2009

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Prevention of patient bacterial contamination of anaesthesia-circle-systems: A clinical study of the contamination risk and performance of different heat and moisture exchangers with electret filter (HMEF)

European journal of anaesthesiology, 1997-07, Vol.14 (4), p.368-373

1997

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Measurement of water vapour pressure in the airways of mechanically ventilated patient using different types of humidifiers

Anästhesiologie, Intensivmedizin, Notfallmedizin, Schmerztherapie : AINS, 2001-09, Vol.36 (9), p.560

2001

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Evaluation of the new supraglottic airway devices Ambu AuraOnce and Intersurgical i-gel. Positioning, sealing, patient comfort and airway morbidity

Der Anaesthesist, 2009-08, Vol.58 (8), p.813-820

2009

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Heat and moisture exchangers for conditioning of inspired air of intubated patients in intensive care. The humidification properties of passive air exchangers under clinical conditions

Der Anaesthesist, 1995-04, Vol.44 (4), p.274

1995

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Is the lithium chloride-coated heat and moisture exchanger a danger for patients?

Der Anaesthesist, 1992-04, Vol.41 (4), p.204

1992

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Exome sequencing allows for rapid gene identification in a Charcot-Marie-Tooth family

Annals of neurology, 2011-03, Vol.69 (3), p.464-470

2011

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Mutations in a Gene Encoding a Novel SH3/TPR Domain Protein Cause Autosomal Recessive Charcot-Marie-Tooth Type 4C Neuropathy

American journal of human genetics, 2003-11, Vol.73 (5), p.1106-1119

2003

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Whole exome sequencing of rare variants in EIF4G1 and VPS35 in Parkinson disease

Neurology, 2013-03, Vol.80 (11), p.982-989

2013

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Early-onset stroke associated with a mutation in mitofusin 2

Neurology, 2008-05, Vol.70 (21), p.2010-2011

2008

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Axonal neuropathy with optic atrophy is caused by mutations in mitofusin 2

Annals of neurology, 2006-02, Vol.59 (2), p.276-281

2006

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Pure and syndromic optic atrophy explained by deep intronic OPA1 mutations and an intralocus modifier

Brain (London, England : 1878), 2014-08, Vol.137 (Pt 8), p.2164-2177

2014

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MFN2 mutation distribution and genotype/phenotype correlation in Charcot–Marie–Tooth type 2

Brain (London, England : 1878), 2006-08, Vol.129 (8), p.2093-2102

2006

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C9ORF72 Intermediate Repeat Copies Are a Significant Risk Factor for Parkinson Disease

Annals of human genetics, 2013-09, Vol.77 (5), p.351-363

2013

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Phenotypic spectrum of dynamin 2 mutations in Charcot-Marie-Tooth neuropathy

Brain (London, England : 1878), 2009-07, Vol.132 (7), p.1741-1752

2009

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SLITRK1 mutations in Trichotillomania

Molecular psychiatry, 2006-10, Vol.11 (10), p.888-889

2006

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The COMT Val158Met polymorphism and temporal lobe morphometry in healthy adults

Psychiatry research, 2007-07, Vol.155 (2), p.173-177

2007

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Prevalence, kinetics, and therapeutic modulation of autoantibodies against Sp100 and promyelocytic leukemia protein in a large cohort of patients with primary biliary cirrhosis

Hepatology (Baltimore, Md.), 1997-11, Vol.26 (5), p.1123-1130

1997

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A CCG expansion in ABCD3 causes oculopharyngodistal myopathy in individuals of European ancestry

Nature communications, 2024-07, Vol.15 (1), p.6327-15, Article 6327

2024

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A CADM3 variant causes Charcot-Marie-Tooth disease with marked upper limb involvement

Brain (London, England : 1878), 2021-05, Vol.144 (4), p.1197-1213

2021

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Phenotypic and molecular insights into spinal muscular atrophy due to mutations in BICD2

Brain (London, England : 1878), 2015-02, Vol.138 (Pt 2), p.293-310

2015

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Clinical and neuroradiological spectrum of biallelic variants in NOTCH3

EBioMedicine, 2024-09, Vol.107, p.105297, Article 105297

2024

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The effect of hemodynamic changes in atrial septum defects on the electrocardiogram

Archiv für Kreislaufforschung, 1966-06, Vol.50 (1), p.111

1966

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Population pharmacokinetics of sevoflurane in conjunction with the AnaConDa®: toward target-controlled infusion of volatiles into the breathing system

Influence of intrinsic noise generated by a thermotesting device on thermal sensory detection and thermal pain detection thresholds

Prevention of patient bacterial contamination of anaesthesia-circle-systems: A clinical study of the contamination risk and performance of different heat and moisture exchangers with electret filter (HMEF)

Measurement of water vapour pressure in the airways of mechanically ventilated patient using different types of humidifiers

Evaluation of the new supraglottic airway devices Ambu AuraOnce and Intersurgical i-gel. Positioning, sealing, patient comfort and airway morbidity

Heat and moisture exchangers for conditioning of inspired air of intubated patients in intensive care. The humidification properties of passive air exchangers under clinical conditions

Is the lithium chloride-coated heat and moisture exchanger a danger for patients?

Exome sequencing allows for rapid gene identification in a Charcot-Marie-Tooth family

Mutations in a Gene Encoding a Novel SH3/TPR Domain Protein Cause Autosomal Recessive Charcot-Marie-Tooth Type 4C Neuropathy

Hereditary spastic paraplegia type 5: natural history, biomarkers and a randomized controlled trial

Whole exome sequencing of rare variants in EIF4G1 and VPS35 in Parkinson disease

Early-onset stroke associated with a mutation in mitofusin 2

Axonal neuropathy with optic atrophy is caused by mutations in mitofusin 2

Pure and syndromic optic atrophy explained by deep intronic OPA1 mutations and an intralocus modifier

MFN2 mutation distribution and genotype/phenotype correlation in Charcot–Marie–Tooth type 2

C9ORF72 Intermediate Repeat Copies Are a Significant Risk Factor for Parkinson Disease

Phenotypic spectrum of dynamin 2 mutations in Charcot-Marie-Tooth neuropathy

SLITRK1 mutations in Trichotillomania

The COMT Val158Met polymorphism and temporal lobe morphometry in healthy adults

Prevalence, kinetics, and therapeutic modulation of autoantibodies against Sp100 and promyelocytic leukemia protein in a large cohort of patients with primary biliary cirrhosis

A CCG expansion in ABCD3 causes oculopharyngodistal myopathy in individuals of European ancestry

A CADM3 variant causes Charcot-Marie-Tooth disease with marked upper limb involvement

Phenotypic and molecular insights into spinal muscular atrophy due to mutations in BICD2

Clinical and neuroradiological spectrum of biallelic variants in NOTCH3

The effect of hemodynamic changes in atrial septum defects on the electrocardiogram

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