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Unveiling the Structure–Property Relationship of MgO-Supported Ni Ammonia Decomposition Catalysts from Bulk to Atomic Structure by In Situ/Operando Studies

ACS catalysis, 2024-03, Vol.14 (5), p.2828-2841

2024

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Correction to: The Anomalous Nucleation in Al-Tb Metallic Glasses

Metallurgical and materials transactions. A, Physical metallurgy and materials science, 2021-12, Vol.52 (12), p.5457-5457

2021

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The Anomalous Nucleation in Al-Tb Metallic Glasses

Metallurgical and materials transactions. A, Physical metallurgy and materials science, 2021-02, Vol.52 (2), p.700-710

2021

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DNA repair gene XPD Asp312Asn and XRCC4 G-1394T polymorphisms and the risk of autism spectrum disorder

Cellular and molecular biology (Noisy-le-Grand, France), 2016-03, Vol.62 (3), p.46

2016

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Transient neonatal diabetes mellitus: a patient report

Journal of Pediatric Endocrinology and Metabolism, 2003-09, Vol.16 (7), p.1057

2003

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Segregational fidelity of chromosomes in human thyroid tumour cells

Chromosoma, 1998-12, Vol.107 (6-7), p.491-497

1998

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What Is the Important Point Related to Follow-Up Sonographic Evaluation for the Developmental Dysplasia of the Hip?

Journal of child science, 2017-01, Vol.7 (1), p.e123-e126

2017

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De novo pericentric inversion of chromosome 5 in a girl with mental retardation and unilateral ear malformation

American journal of medical genetics. Part A, 2006-02, Vol.140A (3), p.298-299

2006

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Investigation of DNA damage in lymphocytes exposed to benzathine penicillin G

Pediatrics international, 2004-08, Vol.46 (4), p.415-418

2004

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Preliminary study on DNA damage in non breast-fed infants

Pediatrics international, 2002-04, Vol.44 (2), p.127-130

2002

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Analysis of DNA damage using the comet assay in infants fed cow's milk

Biology of the neonate, 2003-01, Vol.84 (2), p.135-141

2003

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Evaluation of DNA damage using the comet assay in children on long-term benzathine penicillin for secondary prophylaxis of rheumatic fever

Pediatrics international, 2001-06, Vol.43 (3), p.276-280

2001

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Acrocallosal syndrome: report of five Turkish patients

Clinical dysmorphology, 2004-10, Vol.13 (4), p.241-246

2004

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A large deletion (1.5 Mb) encompassing the neurofibromatosis type 1 (NF1) gene in a patient with sporadic NF1 associated with dysmorphism, mental retardation, and unusual ocular and skeletal features

Clinical dysmorphology, 2003-07, Vol.12 (3), p.199-201

2003

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Unilateral split foot, torticollis, congenital heart defect and hydrocephaly: a new syndrome?

Clinical dysmorphology, 2002-04, Vol.11 (2), p.141-142

2002

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Camptodactyly, skeletal changes, ptosis and infertility in a male: a new syndrome?

Clinical dysmorphology, 2001-10, Vol.10 (4), p.295-297

2001

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Comparative analysis of two thyroid tumor cell lines by fluorescence in situ hybridization and comparative genomic hybridization

Cancer genetics and cytogenetics, 2002-09, Vol.137 (2), p.108-118

2002

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Camptodactyly, skeletal changes, ptosis and infertility in a male: a new syndrome?

Clinical dysmorphology, 2001, Vol.10 (4), p.295-297

2001

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Health-led growth hypothesis and health financing systems: an econometric synthesis for OECD countries

Frontiers in public health, 2024-07, Vol.12, p.1437304

2024

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Single nucleotide polymorphisms in IL-1A RS1800587, IL-1B RS1143634 and vitamin D receptor rs731236 in stage III grade B/C periodontitis

Balkan journal of medical genetics, 2023-03, Vol.25 (1), p.51-60

2023

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Tachycardia-Induced Cardiomyopathy in Patients With Idiopathic Ventricular Arrhythmias: The Incidence, Clinical and Electrophysiologic Characteristics, and the Predictors

Journal of cardiovascular electrophysiology, 2011-06, Vol.22 (6), p.663-668

2011

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Screening of coronary artery anomalies in 11,707 patients reveals that the radial approach is safe for cannulating coronary anomalies

European review for medical and pharmacological sciences, 2016, Vol.20 (6), p.1161

2016

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Effects of ACE polymorphisms and other risk factors on the severity of coronary artery disease

Genetics and molecular research, 2013-12, Vol.12 (4), p.6895-6906

2013

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Investigation of the N-terminal coding region of MUC7 alterations in dentistry students with and without caries

Balkan journal of medical genetics, 2016-07, Vol.19 (1), p.71-76

2016

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Detection of mitochondrial DNA mutations in nonmuscle invasive bladder cancer

Genetic testing and molecular biomarkers, 2012-07, Vol.16 (7), p.672-678

2012

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Unveiling the Structure–Property Relationship of MgO-Supported Ni Ammonia Decomposition Catalysts from Bulk to Atomic Structure by In Situ/Operando Studies

Correction to: The Anomalous Nucleation in Al-Tb Metallic Glasses

The Anomalous Nucleation in Al-Tb Metallic Glasses

DNA repair gene XPD Asp312Asn and XRCC4 G-1394T polymorphisms and the risk of autism spectrum disorder

Transient neonatal diabetes mellitus: a patient report

Segregational fidelity of chromosomes in human thyroid tumour cells

What Is the Important Point Related to Follow-Up Sonographic Evaluation for the Developmental Dysplasia of the Hip?

De novo pericentric inversion of chromosome 5 in a girl with mental retardation and unilateral ear malformation

Investigation of DNA damage in lymphocytes exposed to benzathine penicillin G

Preliminary study on DNA damage in non breast-fed infants

Analysis of DNA damage using the comet assay in infants fed cow's milk

Evaluation of DNA damage using the comet assay in children on long-term benzathine penicillin for secondary prophylaxis of rheumatic fever

Acrocallosal syndrome: report of five Turkish patients

A large deletion (1.5 Mb) encompassing the neurofibromatosis type 1 (NF1) gene in a patient with sporadic NF1 associated with dysmorphism, mental retardation, and unusual ocular and skeletal features

Unilateral split foot, torticollis, congenital heart defect and hydrocephaly: a new syndrome?

Camptodactyly, skeletal changes, ptosis and infertility in a male: a new syndrome?

Comparative analysis of two thyroid tumor cell lines by fluorescence in situ hybridization and comparative genomic hybridization

Camptodactyly, skeletal changes, ptosis and infertility in a male: a new syndrome?

Health-led growth hypothesis and health financing systems: an econometric synthesis for OECD countries

Single nucleotide polymorphisms in IL-1A RS1800587, IL-1B RS1143634 and vitamin D receptor rs731236 in stage III grade B/C periodontitis

Tachycardia-Induced Cardiomyopathy in Patients With Idiopathic Ventricular Arrhythmias: The Incidence, Clinical and Electrophysiologic Characteristics, and the Predictors

Screening of coronary artery anomalies in 11,707 patients reveals that the radial approach is safe for cannulating coronary anomalies

Effects of ACE polymorphisms and other risk factors on the severity of coronary artery disease

Investigation of the N-terminal coding region of MUC7 alterations in dentistry students with and without caries

Detection of mitochondrial DNA mutations in nonmuscle invasive bladder cancer

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