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Postoperative residual curarization from intermediate-acting neuromuscular blocking agents delays recovery room discharge

British journal of anaesthesia : BJA, 2010-09, Vol.105 (3), p.304-309

2010

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Relating free energy and open-circuit voltage to disorder in organic photovoltaic systems

The Journal of chemical physics, 2018-12, Vol.149 (24), p.244123-244123

2018

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Spectroscopic Investigation of the Effect of Microstructure and Energetic Offset on the Nature of Interfacial Charge Transfer States in Polymer: Fullerene Blends

Journal of the American Chemical Society, 2019-03, Vol.141 (11), p.4634-4643

2019

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Disruptive SCYL1 Mutations Underlie a Syndrome Characterized by Recurrent Episodes of Liver Failure, Peripheral Neuropathy, Cerebellar Atrophy, and Ataxia

American journal of human genetics, 2015-12, Vol.97 (6), p.855-861

2015

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A recurrent single-amino acid deletion (p.Glu500del) in the head domain of ß-cardiac myosin in two unrelated boys presenting with polyhydramnios, congenital axial stiffness and skeletal myopathy

Orphanet journal of rare diseases, 2022-07, Vol.17 (1), p.1-279, Article 279

2022

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Mutations in FKBP14 Cause a Variant of Ehlers-Danlos Syndrome with Progressive Kyphoscoliosis, Myopathy, and Hearing Loss

American journal of human genetics, 2012-02, Vol.90 (2), p.201-216

2012

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DNA damage, somatic aneuploidy, and malignant sarcoma susceptibility in muscular dystrophies

PLoS genetics, 2011-04, Vol.7 (4), p.e1002042-e1002042

2011

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Overlapping and Distinct Features of Cardiac Pathology in Inherited Human and Murine Ether Lipid Deficiency

International journal of molecular sciences, 2023-01, Vol.24 (3), p.1884

2023

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Voltage-gated ion channel dysfunction precedes cardiomyopathy development in the dystrophic heart

PloS one, 2011-05, Vol.6 (5), p.e20300-e20300

2011

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Characterization of stargardt disease using polarization-sensitive optical coherence tomography and fundus autofluorescence imaging

Investigative ophthalmology & visual science, 2013-09, Vol.54 (9), p.6416-6425

2013

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Mutant glycosyltransferase and altered glycosylation of α-dystroglycan in the myodystrophy mouse

Nature genetics, 2001-06, Vol.28 (2), p.151-154

2001

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Inclusion body myopathy and Paget disease is linked to a novel mutation in the VCP gene

Neurology, 2005-10, Vol.65 (8), p.1304

2005

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Dysferlin Is a New Marker for Leaky Brain Blood Vessels in Multiple Sclerosis

Journal of neuropathology and experimental neurology, 2006-09, Vol.65 (9), p.855-865

2006

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Recruitment of bone-marrow-derived cells by skeletal and cardiac muscle in adult dystrophic mdx mice

Anatomy and Embryology, 1999-05, Vol.199 (5), p.391-396

1999

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Evaluation of the association between quality of handover and length of stay in the post anaesthesia care unit: a pilot study

Anaesthesia, 2012-05, Vol.67 (5), p.548-549

2012

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Targeted disruption of Hspa4 gene leads to cardiac hypertrophy and fibrosis

Journal of molecular and cellular cardiology, 2012-10, Vol.53 (4), p.459-468

2012

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Monte Carlo study of the evaporation/condensation transition of Ising droplets

Europhysics letters, 2006-09, Vol.75 (5), p.716-722

2006

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Football fever: goal distributions and non-Gaussian statistics

The European physical journal. B, Condensed matter physics, 2009-02, Vol.67 (3), p.459-471

2009

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MAP1B Is Required for Axon Guidance and Is Involved in the Development of the Central and Peripheral Nervous System

The Journal of cell biology, 2000-12, Vol.151 (6), p.1169-1178

2000

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Impaired muscle spindle function in murine models of muscular dystrophy

The Journal of physiology, 2020-04, Vol.598 (8), p.1591-1609

2020

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The bradycardic agent ivabradine decreases conduction velocity in the AV node and in the ventricles in-vivo

European journal of pharmacology, 2021-02, Vol.893, p.173818-173818, Article 173818

2021

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Glomerular expression of dystroglycans is reduced in minimal change nephrosis but not in focal segmental glomerulosclerosis

Journal of the American Society of Nephrology, 2000-03, Vol.11 (3), p.403-412

2000

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Skeletal, cardiac and tongue muscle pathology, defective retinal transmission, and neuronal migration defects in the Large(myd) mouse defines a natural model for glycosylation-deficient muscle - eye - brain disorders

Human molecular genetics, 2002-10, Vol.11 (21), p.2673-2687

2002

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Mutation in the Scyl1 gene encoding amino-terminal kinase-like protein causes a recessive form of spinocerebellar neurodegeneration

EMBO reports, 2007-07, Vol.8 (7), p.691-697

2007

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Postoperative residual curarization from intermediate-acting neuromuscular blocking agents delays recovery room discharge

Relating free energy and open-circuit voltage to disorder in organic photovoltaic systems

Spectroscopic Investigation of the Effect of Microstructure and Energetic Offset on the Nature of Interfacial Charge Transfer States in Polymer: Fullerene Blends

Disruptive SCYL1 Mutations Underlie a Syndrome Characterized by Recurrent Episodes of Liver Failure, Peripheral Neuropathy, Cerebellar Atrophy, and Ataxia

A recurrent single-amino acid deletion (p.Glu500del) in the head domain of ß-cardiac myosin in two unrelated boys presenting with polyhydramnios, congenital axial stiffness and skeletal myopathy

Mutations in FKBP14 Cause a Variant of Ehlers-Danlos Syndrome with Progressive Kyphoscoliosis, Myopathy, and Hearing Loss

DNA damage, somatic aneuploidy, and malignant sarcoma susceptibility in muscular dystrophies

Biallelic loss-of-function P4HTM gene variants cause hypotonia, hypoventilation, intellectual disability, dysautonomia, epilepsy, and eye abnormalities (HIDEA syndrome)

Overlapping and Distinct Features of Cardiac Pathology in Inherited Human and Murine Ether Lipid Deficiency

Voltage-gated ion channel dysfunction precedes cardiomyopathy development in the dystrophic heart

Characterization of stargardt disease using polarization-sensitive optical coherence tomography and fundus autofluorescence imaging

Mutant glycosyltransferase and altered glycosylation of α-dystroglycan in the myodystrophy mouse

Inclusion body myopathy and Paget disease is linked to a novel mutation in the VCP gene

Dysferlin Is a New Marker for Leaky Brain Blood Vessels in Multiple Sclerosis

Recruitment of bone-marrow-derived cells by skeletal and cardiac muscle in adult dystrophic mdx mice

Evaluation of the association between quality of handover and length of stay in the post anaesthesia care unit: a pilot study

Targeted disruption of Hspa4 gene leads to cardiac hypertrophy and fibrosis

Monte Carlo study of the evaporation/condensation transition of Ising droplets

Football fever: goal distributions and non-Gaussian statistics

MAP1B Is Required for Axon Guidance and Is Involved in the Development of the Central and Peripheral Nervous System

Impaired muscle spindle function in murine models of muscular dystrophy

The bradycardic agent ivabradine decreases conduction velocity in the AV node and in the ventricles in-vivo

Glomerular expression of dystroglycans is reduced in minimal change nephrosis but not in focal segmental glomerulosclerosis

Skeletal, cardiac and tongue muscle pathology, defective retinal transmission, and neuronal migration defects in the Large(myd) mouse defines a natural model for glycosylation-deficient muscle - eye - brain disorders

Mutation in the Scyl1 gene encoding amino-terminal kinase-like protein causes a recessive form of spinocerebellar neurodegeneration

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