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Association of monocyte/HDL-C ratio with SYNTAX scores in patients with stable coronary artery disease

Herz, 2016-09, Vol.41 (6), p.523-529

2016

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The relationship between the serum uric acid/creatinine ratio and prognosis in patients with transcatheter aortic valve implantation

European review for medical and pharmacological sciences, 2023-06, Vol.27 (11), p.5145

2023

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A novel risk prediction tool for contrast-induced nephropathy in patients with chronic kidney disease who underwent diagnostic coronary angiography

European review for medical and pharmacological sciences, 2023-04, Vol.27 (8), p.3430

2023

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AUTOMATIC 3D BUILDING MODEL GENERATIONS WITH AIRBORNE LiDAR DATA

ISPRS annals of the photogrammetry, remote sensing and spatial information sciences, 2017-01, Vol.IV-4/W4, p.411-414

2017

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Chile Crece Contigo: Implementation, results, and scaling‐up lessons

Child : care, health & development, 2018-01, Vol.44 (1), p.4-11

2018

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CLASSIFICATION OF LiDAR DATA WITH POINT BASED CLASSIFICATION METHODS

International archives of the photogrammetry, remote sensing and spatial information sciences., 2016-06, Vol.XLI-B3, p.441-445

2016

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Dose-Volume Effects of Radiation to Swallowing Function in the Radiation Therapy of Head and Neck Cancers

International journal of radiation oncology, biology, physics, 2014-09, Vol.90 (1), p.S541-S541

2014

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Ring chromosome 21 and monosomy 21 mosaicism in a patient with azoospermia

Andrologia, 2015-02, Vol.47 (1), p.112-115

2015

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Selective IgM deficiency in a boy with ring chromosome 18

Journal of investigational allergology & clinical immunology, 2014, Vol.24 (6), p.442-444

2014

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Prenatal diagnosis of isochromosome 21p and isochromosome 21q in a fetus with Down syndrome

Genetic counseling, 2014-01, Vol.25 (3), p.257

2014

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A PATIENT WITH AZOOSPERMIA AND 45,X/46,X,r(Y) (p11.2q11.2) MOSAICISM WITHOUT AZF DELETIONS

Genetic counseling, 2015-01, Vol.26 (3), p.347

2015

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A MOLECULARLY CHARACTERIZED INTERSTITIAL DELETION ENCOMPASSING THE 11q14.1-q23.3 REGION IN A CASE WITH MULTIPLE CONGENITAL ABNORMALITIES

Genetic counseling, 2016, Vol.27 (1), p.51

2016

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PRENATAL DIAGNOSIS OF DE NOVO PERICENTRIC INVERSION INV(2)(p11.2z13)

Genetic counseling, 2015-01, Vol.26 (2), p.243

2015

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PRENATAL DIAGNOSIS OF DE NOVO SUPERNUMERARY MARKER CHROMOSOME ORIGINATED FROM CHROMOSOME 16 BY ARRAY-CGH

Genetic counseling, 2015-01, Vol.26 (3), p.299

2015

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22q11.2 syndrome due to maternal translocation t(18;22) (pl1.2;q11.2)

Genetic counseling, 2015, Vol.26 (1), p.67

2015

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Investing in the foundation of sustainable development: pathways to scale up for early childhood development

The Lancet (British edition), 2017-01, Vol.389 (10064), p.103-118

2017

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Fully three-dimensional analysis of a photonic crystal assisted silicon on insulator waveguide bend

International journal of modern physics. B, Condensed matter physics, statistical physics, applied physics, 2018-12, Vol.32 (31), p.1850344

2018

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Prenatal diagnosis of isolated ventriculomegaly as a second trimester manifestation of de novo terminal 6q25 deletion

Genetic counseling, 2013, Vol.24 (4), p.427

2013

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CLASSIFICATION OF LiDAR DATA WITH POINT BASED CLASSIFICATION METHODS

International archives of the photogrammetry, remote sensing and spatial information sciences., 2016, Vol.XLI-B3, p.441-445

2016

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In situ stabilization of chromium(VI) in polluted soils using organic ligands: The role of galacturonic, glucuronic and alginic acids

Journal of hazardous materials, 2008-11, Vol.159 (2), p.287-293

2008

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Double partial trisomy of 6p23-pter and 9pter-q21.2 in a neonate resulting from 4:2 meiotic segregation of a maternal complex t(6;7;9)(p23;p15;q21.2) translocation

Genetic counseling, 2012-01, Vol.23 (2), p.239

2012

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Mosaic Intrachromosomal Triplication of (12)(p11.2p13) in a Patient with Pallister-Killian Syndrome

Balkan journal of medical genetics, 2012-01, Vol.15 (1), p.61-64

2012

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Turner Syndrome with Isochromosome Xq and Familial Reciprocal Translocation t(4;16)(p15.2;p13.1)

Balkan journal of medical genetics, 2011-01, Vol.14 (1), p.57-60

2011

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Interstitial deletion of 13q22-q32: a case with choanal atresia and mega-cisterna magna and review of the literature

Genetic counseling, 2011, Vol.22 (3), p.313

2011

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De novo supernumerary marker chromosome originating from chromosome 17 resulting in a normal pregnancy outcome

Genetic counseling, 2011, Vol.22 (1), p.63

2011

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Association of monocyte/HDL-C ratio with SYNTAX scores in patients with stable coronary artery disease

The relationship between the serum uric acid/creatinine ratio and prognosis in patients with transcatheter aortic valve implantation

A novel risk prediction tool for contrast-induced nephropathy in patients with chronic kidney disease who underwent diagnostic coronary angiography

AUTOMATIC 3D BUILDING MODEL GENERATIONS WITH AIRBORNE LiDAR DATA

Chile Crece Contigo: Implementation, results, and scaling‐up lessons

CLASSIFICATION OF LiDAR DATA WITH POINT BASED CLASSIFICATION METHODS

Dose-Volume Effects of Radiation to Swallowing Function in the Radiation Therapy of Head and Neck Cancers

Ring chromosome 21 and monosomy 21 mosaicism in a patient with azoospermia

Selective IgM deficiency in a boy with ring chromosome 18

Prenatal diagnosis of isochromosome 21p and isochromosome 21q in a fetus with Down syndrome

A PATIENT WITH AZOOSPERMIA AND 45,X/46,X,r(Y) (p11.2q11.2) MOSAICISM WITHOUT AZF DELETIONS

A MOLECULARLY CHARACTERIZED INTERSTITIAL DELETION ENCOMPASSING THE 11q14.1-q23.3 REGION IN A CASE WITH MULTIPLE CONGENITAL ABNORMALITIES

PRENATAL DIAGNOSIS OF DE NOVO PERICENTRIC INVERSION INV(2)(p11.2z13)

PRENATAL DIAGNOSIS OF DE NOVO SUPERNUMERARY MARKER CHROMOSOME ORIGINATED FROM CHROMOSOME 16 BY ARRAY-CGH

22q11.2 syndrome due to maternal translocation t(18;22) (pl1.2;q11.2)

Investing in the foundation of sustainable development: pathways to scale up for early childhood development

Fully three-dimensional analysis of a photonic crystal assisted silicon on insulator waveguide bend

Prenatal diagnosis of isolated ventriculomegaly as a second trimester manifestation of de novo terminal 6q25 deletion

CLASSIFICATION OF LiDAR DATA WITH POINT BASED CLASSIFICATION METHODS

In situ stabilization of chromium(VI) in polluted soils using organic ligands: The role of galacturonic, glucuronic and alginic acids

Double partial trisomy of 6p23-pter and 9pter-q21.2 in a neonate resulting from 4:2 meiotic segregation of a maternal complex t(6;7;9)(p23;p15;q21.2) translocation

Mosaic Intrachromosomal Triplication of (12)(p11.2p13) in a Patient with Pallister-Killian Syndrome

Turner Syndrome with Isochromosome Xq and Familial Reciprocal Translocation t(4;16)(p15.2;p13.1)

Interstitial deletion of 13q22-q32: a case with choanal atresia and mega-cisterna magna and review of the literature

De novo supernumerary marker chromosome originating from chromosome 17 resulting in a normal pregnancy outcome

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