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Foam Sclerotherapy of the Saphenous Veins: Randomised Controlled Trial with or without Compression

European journal of vascular and endovascular surgery, 2010-04, Vol.39 (4), p.500-507

2010

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Perspective: Machine learning in experimental solid mechanics

Journal of the mechanics and physics of solids, 2023-04, Vol.173 (C), p.105231, Article 105231

2023

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In Vivo Biological Effects of Foam Sclerotherapy

European journal of vascular and endovascular surgery, 2011-08, Vol.42 (2), p.238-245

2011

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In Vivo Biological Effects of Foam Sclerotherapy

Journal of vascular surgery, 2011, Vol.54 (2), p.584-585

2011

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Great Saphenous Vein Diameters in Phlebological Practice in France: A Report of the DIAGRAVES Study by the French Society of Phlebology

Journal of vascular surgery, 2019-08, Vol.70 (2), p.655-655

2019

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Partner anxiety prior to elective Caesarean section under regional anaesthesia

Anaesthesia, 2002-06, Vol.57 (6), p.584-605

2002

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Obstetric anaesthesia training in the Wessex region before and after introduction of Calman training

International journal of obstetric anesthesia, 2003-04, Vol.12 (2), p.102-106

2003

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Synchronised spiking activity underlies phase amplitude coupling in the subthalamic nucleus of Parkinson's disease patients

Neurobiology of disease, 2019-07, Vol.127, p.101-113

2019

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An improved high-power battery with increased thermal operating range: C–LiFePO4//C–Li4Ti5O12

Journal of power sources, 2012-10, Vol.216, p.192-200

2012

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Heterozygous Germline Mutations in the p53 Homolog p63 Are the Cause of EEC Syndrome

Cell, 1999-10, Vol.99 (2), p.143-153

1999

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Synthesis of pure phase disordered LiMn1.45Cr0.1Ni0.45O4 by a post-annealing method

Journal of power sources, 2012-11, Vol.217, p.400-406

2012

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Identification of Inherited Retinal Disease-Associated Genetic Variants in 11 Candidate Genes

Genes, 2018-01, Vol.9 (1), p.21

2018

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Brevetoxin composition in water and marine aerosol along a Florida beach: Assessing potential human exposure to marine biotoxins

Harmful algae, 2005-11, Vol.4 (6), p.965-972

2005

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A mutation in the gene encoding the α2 chain of the fibril-associated collagen IX, COL9A2 , causes multiple epiphyseal dysplasia (EDM2)

Nature genetics, 1996-01, Vol.12 (1), p.103-105

1996

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Cerulean Warbler Reproduction, Survival, and Models of Population Decline

The Journal of wildlife management, 2008-04, Vol.72 (3), p.646-653

2008

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An improved high-power battery with increased thermal operating range: CeLiFePO4//CeLi4Ti5O12

Journal of power sources, 2012, Vol.216, p.192-200

2012

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Localization of a Gene for Möbius Syndrome to Chromosome 3q by Linkage Analysis in a Dutch Family

Human molecular genetics, 1996-09, Vol.5 (9), p.1367-1371

1996

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Limb Mammary Syndrome: A New Genetic Disorder with Mammary Hypoplasia, Ectrodactyly, and Other Hand/Foot Anomalies Maps to Human Chromosome 3q27

American journal of human genetics, 1999-02, Vol.64 (2), p.538-546

1999

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Identification and Characterization of an Xq26–q27 Duplication in a Family with Spina Bifida and Panhypopituitarism Suggests the Involvement of Two Distinct Genes

Genomics (San Diego, Calif.), 2000-10, Vol.69 (2), p.174-181

2000

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Pure Phase Disordered LiMn 1.45 Cr 0.1 Ni 0.45 O 4 by Post-Annealing Treatment

ECS transactions, 2013-04, Vol.50 (24), p.155-161

2013

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Rubinstein-Taybi syndrome caused by submicroscopic deletions within 16p13.3

American journal of human genetics, 1993-02, Vol.52 (2), p.249-254

1993

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PAX genes and human neural tube defects: an amino acid substitution in PAX1 in a patient with spina bifida

Journal of medical genetics, 1996-08, Vol.33 (8), p.655-660

1996

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Growth-Reductive Therapy in Children with Marfan Syndrome

The Journal of pediatrics, 2005-11, Vol.147 (5), p.674-679

2005

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Altered Regulation of Platelet-Derived Growth Factor receptor-α Gene-Transcription in vitro by Spina Bifida-Associated Mutant Pax1 Proteins

Proceedings of the National Academy of Sciences - PNAS, 1998-11, Vol.95 (24), p.14459-14463

1998

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A frameshift mutation in the gene for PAX3 in a girl with spina bifida and mild signs of Waardenburg syndrome

Journal of medical genetics, 1995-01, Vol.32 (1), p.52-56

1995

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Foam Sclerotherapy of the Saphenous Veins: Randomised Controlled Trial with or without Compression

Perspective: Machine learning in experimental solid mechanics

In Vivo Biological Effects of Foam Sclerotherapy

In Vivo Biological Effects of Foam Sclerotherapy

Great Saphenous Vein Diameters in Phlebological Practice in France: A Report of the DIAGRAVES Study by the French Society of Phlebology

Partner anxiety prior to elective Caesarean section under regional anaesthesia

Obstetric anaesthesia training in the Wessex region before and after introduction of Calman training

Synchronised spiking activity underlies phase amplitude coupling in the subthalamic nucleus of Parkinson's disease patients

An improved high-power battery with increased thermal operating range: C–LiFePO4//C–Li4Ti5O12

Heterozygous Germline Mutations in the p53 Homolog p63 Are the Cause of EEC Syndrome

Synthesis of pure phase disordered LiMn1.45Cr0.1Ni0.45O4 by a post-annealing method

Identification of Inherited Retinal Disease-Associated Genetic Variants in 11 Candidate Genes

Brevetoxin composition in water and marine aerosol along a Florida beach: Assessing potential human exposure to marine biotoxins

A mutation in the gene encoding the α2 chain of the fibril-associated collagen IX, COL9A2 , causes multiple epiphyseal dysplasia (EDM2)

Cerulean Warbler Reproduction, Survival, and Models of Population Decline

An improved high-power battery with increased thermal operating range: CeLiFePO4//CeLi4Ti5O12

Localization of a Gene for Möbius Syndrome to Chromosome 3q by Linkage Analysis in a Dutch Family

Limb Mammary Syndrome: A New Genetic Disorder with Mammary Hypoplasia, Ectrodactyly, and Other Hand/Foot Anomalies Maps to Human Chromosome 3q27

Identification and Characterization of an Xq26–q27 Duplication in a Family with Spina Bifida and Panhypopituitarism Suggests the Involvement of Two Distinct Genes

Pure Phase Disordered LiMn 1.45 Cr 0.1 Ni 0.45 O 4 by Post-Annealing Treatment

Rubinstein-Taybi syndrome caused by submicroscopic deletions within 16p13.3

PAX genes and human neural tube defects: an amino acid substitution in PAX1 in a patient with spina bifida

Growth-Reductive Therapy in Children with Marfan Syndrome

Altered Regulation of Platelet-Derived Growth Factor receptor-α Gene-Transcription in vitro by Spina Bifida-Associated Mutant Pax1 Proteins

A frameshift mutation in the gene for PAX3 in a girl with spina bifida and mild signs of Waardenburg syndrome

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