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TU‐E‐210A‐03: A Double‐Layer Detector, Dual‐Energy CT — Principles, Advantages and Applications

Medical Physics, 2009-06, Vol.36 (6), p.2750-2750

2009

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Static Var Compensator and Active Power Filter With Power Injection Capability, Using 27-Level Inverters and Photovoltaic Cells

IEEE transactions on industrial electronics (1982), 2009-01, Vol.56 (1), p.130-138

2009

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IEEE_Xplore

Voltage-source active power filter based on multilevel converter and ultracapacitor DC link

IEEE transactions on industrial electronics (1982), 2006-04, Vol.53 (2), p.477-485

2006

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IEEE_Xplore

Perineal Biodegradable Balloon Is Effective for Both Sparing the Rectum and as a Fiducial Marker in Prostate Cancer Patients Treated With Mild Hypofractionation

International journal of radiation oncology, biology, physics, 2013-10, Vol.87 (2), p.S360-S361

2013

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Dynamic Versus Quasi Static Fracture Toughness of Additively Manufactured AlSi10Mg Alloy by Selective Laser Melting Technique

Annals of "Dunărea de Jos" University of Galaţi. Fascicle XII, Welding Equipment and Technology, 2018-12, Vol.29, p.33-40

2018

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A comparison of the minimum canal wall thickness remaining following preparation using two nickel-titanium rotary systems

International endodontic journal, 2003-09, Vol.36 (9), p.636-642

2003

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Quantifying center bias of observers in free viewing of dynamic natural scenes

Journal of vision (Charlottesville, Va.), 2009-07, Vol.9 (7), p.4-4

2009

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Familial aggregation in the fibromyalgia syndrome

Seminars in arthritis and rheumatism, 1996-12, Vol.26 (3), p.605-611

1996

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Spontaneous macroscopic magnetization at the superconducting transition temperature of YBa2Cu3O(7-delta)

Nature (London), 2000-04, Vol.404 (6780), p.853-855

2000

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EP-2393: The influence of raising patient awareness of physical activity during radiation treatment

Radiotherapy and oncology, 2018-04, Vol.127, p.S1252-S1253

2018

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EP-2337: Comparison between two frameless immobilization techniques for Brain stereotactic radiosurgery

Radiotherapy and oncology, 2018-04, Vol.127, p.S1289-S1290

2018

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Identification of mutations in the connexin 26 gene that cause autosomal recessive nonsyndromic hearing loss

Human mutation, 1998, Vol.11 (5), p.387-394

1998

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Spontaneous macroscopic magnetization at the superconducting transition temperature of YBa2Cu3O7-δ

Nature (London), 2000-04, Vol.404 (6780), p.853-855

2000

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Homozygosity Mapping with SNP Arrays Identifies TRIM32, an E3 Ubiquitin Ligase, as a Bardet-Biedl Syndrome Gene (BBS11)

Proceedings of the National Academy of Sciences - PNAS, 2006-04, Vol.103 (16), p.6287-6292

2006

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Clinical presentation and outcome in primary familial hypomagnesaemia

Archives of disease in childhood, 1998-02, Vol.78 (2), p.127-130

1998

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Bbs2-Null Mice Have Neurosensory Deficits, a Defect in Social Dominance, and Retinopathy Associated with Mislocalization of Rhodopsin

Proceedings of the National Academy of Sciences - PNAS, 2004-11, Vol.101 (47), p.16588-16593

2004

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Use of a DNA pooling strategy to identify a human obesity syndrome locus on chromosome 15

Human molecular genetics, 1995-01, Vol.4 (1), p.9-13

1995

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Familial Hypomagnesemia Maps to Chromosome 9q, not to the X Chromosome: Genetic Linkage Mapping and Analysis of a Balanced Translocation Breakpoint

Human molecular genetics, 1997-09, Vol.6 (9), p.1491-1497

1997

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Mutation of TRPM6 causes familial hypomagnesemia with secondary hypocalcemia

Nature genetics, 2002-06, Vol.31 (2), p.171-174

2002

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Comparative Genomic Analysis Identifies an ADP-Ribosylation Factor–like Gene as the Cause of Bardet-Biedl Syndrome (BBS3)

American journal of human genetics, 2004-09, Vol.75 (3), p.475-484

2004

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From eye-tracking data to information: Lessons from dynamic scenes

Journal of vision (Charlottesville, Va.), 2010-03, Vol.6 (6), p.493-493

2010

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Why do we fail to perceive jump-cuts in motion pictures?

Journal of vision (Charlottesville, Va.), 2010-03, Vol.5 (8), p.548-548

2010

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Observation of spontaneous flux generation in a multi-josephson-junction loop

Physical review letters, 2000-05, Vol.84 (21), p.4966-4969

2000

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An autosomal recessive nonsyndromic-hearing-loss locus identified by DNA pooling using two inbred bedouin kindreds

American journal of human genetics, 1996-08, Vol.59 (2), p.385-391

1996

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Mutation of a nuclear receptor gene, NR2E3 , causes enhanced S cone syndrome, a disorder of retinal cell fate

Nature genetics, 2000-02, Vol.24 (2), p.127-131

2000

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TU‐E‐210A‐03: A Double‐Layer Detector, Dual‐Energy CT — Principles, Advantages and Applications

Static Var Compensator and Active Power Filter With Power Injection Capability, Using 27-Level Inverters and Photovoltaic Cells

Voltage-source active power filter based on multilevel converter and ultracapacitor DC link

Perineal Biodegradable Balloon Is Effective for Both Sparing the Rectum and as a Fiducial Marker in Prostate Cancer Patients Treated With Mild Hypofractionation

Dynamic Versus Quasi Static Fracture Toughness of Additively Manufactured AlSi10Mg Alloy by Selective Laser Melting Technique

A comparison of the minimum canal wall thickness remaining following preparation using two nickel-titanium rotary systems

Quantifying center bias of observers in free viewing of dynamic natural scenes

Familial aggregation in the fibromyalgia syndrome

Spontaneous macroscopic magnetization at the superconducting transition temperature of YBa2Cu3O(7-delta)

EP-2393: The influence of raising patient awareness of physical activity during radiation treatment

EP-2337: Comparison between two frameless immobilization techniques for Brain stereotactic radiosurgery

Identification of mutations in the connexin 26 gene that cause autosomal recessive nonsyndromic hearing loss

Spontaneous macroscopic magnetization at the superconducting transition temperature of YBa2Cu3O7-δ

Homozygosity Mapping with SNP Arrays Identifies TRIM32, an E3 Ubiquitin Ligase, as a Bardet-Biedl Syndrome Gene (BBS11)

Clinical presentation and outcome in primary familial hypomagnesaemia

Bbs2-Null Mice Have Neurosensory Deficits, a Defect in Social Dominance, and Retinopathy Associated with Mislocalization of Rhodopsin

Use of a DNA pooling strategy to identify a human obesity syndrome locus on chromosome 15

Familial Hypomagnesemia Maps to Chromosome 9q, not to the X Chromosome: Genetic Linkage Mapping and Analysis of a Balanced Translocation Breakpoint

Mutation of TRPM6 causes familial hypomagnesemia with secondary hypocalcemia

Comparative Genomic Analysis Identifies an ADP-Ribosylation Factor–like Gene as the Cause of Bardet-Biedl Syndrome (BBS3)

From eye-tracking data to information: Lessons from dynamic scenes

Why do we fail to perceive jump-cuts in motion pictures?

Observation of spontaneous flux generation in a multi-josephson-junction loop

An autosomal recessive nonsyndromic-hearing-loss locus identified by DNA pooling using two inbred bedouin kindreds

Mutation of a nuclear receptor gene, NR2E3 , causes enhanced S cone syndrome, a disorder of retinal cell fate

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