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130 éve született Pető András. Mozaikok

Kaleidoscope (Budapest), 2023, Vol.13 (27), p.13-91

Balogh, Erzsébet

2023

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Lissencephaly and Band Heterotopia: LIS1, TUBA1A, and DCX Mutations in Hungary

Journal of child neurology, 2012-12, Vol.27 (12), p.1534-1540

2012

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Dark and Strong?! The associations between dark personality traits, mental toughness and resilience in Hungarian student, employee, leader, and military samples

Personality and individual differences, 2022-02, Vol.186, p.111339, Article 111339

2022

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Grammatical errors in Hungarian EFL learners’ argumentative essays

Argumentum, 2024-01, Vol.20, p.114-127

2024

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Clinical and genetic characteristics of craniosynostosis in Hungary

American journal of medical genetics. Part A, 2015-12, Vol.167A (12), p.2985-2991

2015

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Iskolázottsági helyzetkép – Nyíregyházán telepi körülmények között élők körében

Acta medicinae et sociologica, 2019-12, Vol.10 (29), p.55

Balogh Erzsébet

2019

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Correlation study between sperm concentration, hyaluronic acid-binding capacity and sperm aneuploidy in Hungarian patients

Reproductive biomedicine online, 2012-12, Vol.25 (6), p.620-626

2012

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Achondroplasia with multiple-suture craniosynostosis: A report of a new case of this rare association

American journal of medical genetics. Part A, 2013-10, Vol.161A (10), p.2641-2644

2013

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A patient with Smith–Lemli–Opitz syndrome: novel mutation of the DHCR7 gene and effects of therapy with simvastatin and cholesterol supplement

European journal of pediatrics, 2010, Vol.169 (1), p.121-123

2010

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Subtelomeric 6.7 Mb trisomy 10p and 5.6 Mb monosomy 21q detected by FISH and array‐CGH in three related patients

American journal of medical genetics. Part A, 2012-04, Vol.158A (4), p.869-876

2012

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Subtelomeric 6.7Mb trisomy 10p and 5.6Mb monosomy 21q detected by FISH and array-CGH in three related patients

American journal of medical genetics. Part A, 2012-04, Vol.158A (4), p.869-876

2012

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Blepharophimosis mental retardation syndrome Say‐Barber/Biesecker/Young‐Simpson type – New findings with neuroimaging

American journal of medical genetics. Part A, 2011-03, Vol.155 (3), p.634-637

2011

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Results of clinical and genetic diagnosis of rare diseases in the Eastern region of Hungary (2007-2013)

Orvosi hetilap, 2014-03, Vol.155 (9), p.348

2014

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Endocrine and anatomical findings in a case of Solitary Median Maxillary Central Incisor Syndrome

European journal of medical genetics, 2012-02, Vol.55 (2), p.109-111

2012

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Meiotic segregation study of a novel t(3;6)(q21;q23) in an infertile man using fluorescence in situ hybridization (FISH)

Systems biology in reproductive medicine, 2012-06, Vol.58 (3), p.160-164, Article 160

2012

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Felsőoktatási szociális képzések a képzési és kimeneti követelmények tükrében

Educatio : pedagógia, szociológia, história, ökonómia, pszichológia, politológia, 2014, Vol.23 (4), p.668-675

Balogh, Erzsébet

2014

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Conductive education for children with neurological diseases

Ideggyógyászati szemle, 2009-01, Vol.62 (1-2), p.12

2009

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Deletion 15q26 syndrome

Orvosi hetilap, 2014-03, Vol.155 (9), p.362

2014

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Population-based stroke screening days in the 12th district of Budapest in 2011 and 2016 - What have and what have not changed?

Ideggyógyászati szemle, 2019-05, Vol.72 (5-6), p.195

2019

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Quality Versus Equality. The Integration as the Component of Primarly School’s Excellence – a Cross-Cultural Perspective

Przegląd badań edukacyjnych, 2017-02, Vol.2 (23), p.105

2017

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Language Attitudes Towards English Accent Varieties: Hungarian Secondary School Students' Labeling, Evaluating and Commenting on Foreign Accented Englishes

Erzsébet, Balogh

2014

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ProQuest

A patient with Smith-Lemli-Opitz syndrome: novel mutation of the DHCR 7 gene and effects of therapy with simvastatin and cholesterol supplement

European journal of pediatrics, 2010, Vol.169 (1), p.121-123

2010

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Citogenetic and molecular genetic studies in infertility in eastern Hungary

Orvosi hetilap, 2013-01, Vol.154 (2), p.52

2013

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Dysgenetic male pseudohermaphroditism

Orvosi hetilap, 2012-02, Vol.153 (8), p.303

2012

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Early Intervention in Budapest

Infants and young children, 2000, Vol.12 (3), p.71-79

2000

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130 éve született Pető András. Mozaikok

Lissencephaly and Band Heterotopia: LIS1, TUBA1A, and DCX Mutations in Hungary

Dark and Strong?! The associations between dark personality traits, mental toughness and resilience in Hungarian student, employee, leader, and military samples

Grammatical errors in Hungarian EFL learners’ argumentative essays

Clinical and genetic characteristics of craniosynostosis in Hungary

Iskolázottsági helyzetkép – Nyíregyházán telepi körülmények között élők körében

Correlation study between sperm concentration, hyaluronic acid-binding capacity and sperm aneuploidy in Hungarian patients

Achondroplasia with multiple-suture craniosynostosis: A report of a new case of this rare association

A patient with Smith–Lemli–Opitz syndrome: novel mutation of the DHCR7 gene and effects of therapy with simvastatin and cholesterol supplement

Subtelomeric 6.7 Mb trisomy 10p and 5.6 Mb monosomy 21q detected by FISH and array‐CGH in three related patients

Subtelomeric 6.7Mb trisomy 10p and 5.6Mb monosomy 21q detected by FISH and array-CGH in three related patients

Blepharophimosis mental retardation syndrome Say‐Barber/Biesecker/Young‐Simpson type – New findings with neuroimaging

Results of clinical and genetic diagnosis of rare diseases in the Eastern region of Hungary (2007-2013)

Endocrine and anatomical findings in a case of Solitary Median Maxillary Central Incisor Syndrome

Meiotic segregation study of a novel t(3;6)(q21;q23) in an infertile man using fluorescence in situ hybridization (FISH)

Felsőoktatási szociális képzések a képzési és kimeneti követelmények tükrében

Conductive education for children with neurological diseases

Deletion 15q26 syndrome

Population-based stroke screening days in the 12th district of Budapest in 2011 and 2016 - What have and what have not changed?

Quality Versus Equality. The Integration as the Component of Primarly School’s Excellence – a Cross-Cultural Perspective

Language Attitudes Towards English Accent Varieties: Hungarian Secondary School Students' Labeling, Evaluating and Commenting on Foreign Accented Englishes

A patient with Smith-Lemli-Opitz syndrome: novel mutation of the DHCR 7 gene and effects of therapy with simvastatin and cholesterol supplement

Citogenetic and molecular genetic studies in infertility in eastern Hungary

Dysgenetic male pseudohermaphroditism

Early Intervention in Budapest

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