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Judit Bene

Showing results (41-50 of 77) with videos related to

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Journal of Human Genetics|December 17, 2010
Analysis of Hungarian patients with Rett syndrome phenotype for MECP2, CDKL5 and FOXG1 gene mutationsKinga Hadzsiev, Noemi Polgar, Judit Bene, et al.
World Journal of Gastroenterology|September 29, 2006
Prevalence of SLC22A4, SLC22A5 and CARD15 gene mutations in Hungarian pediatric patients with Crohn's diseaseJudit Bene, Lili Magyari, Gábor Talián, et al.
The Journal of Pediatrics|December 26, 2006
Histopathologic abnormalities of the lymphoreticular tissues in organic cation transporter 2 deficiency: evidence for impaired B cell maturationKatalin Komlósi, Viktória Havasi, Judit Bene, et al.
International Journal of Molecular Sciences|August 26, 2023
Three-Year Follow-Up after Intrauterine mTOR Inhibitor Administration for Fetus with TSC-Associated RhabdomyomaAnita Maász, Tímea Bodó, Ágnes Till, et al.
American Journal of Medical Genetics. Part A|September 25, 2004
Mutation analysis of MECP2 and determination of the X-inactivation pattern in Hungarian Rett syndrome patientsJudit Kárteszi, Katalin Hollódy, Judit Bene, et al.
Annals of Nutrition & Metabolism|January 9, 2013
Similarities in serum acylcarnitine patterns in type 1 and type 2 diabetes mellitus and in metabolic syndromeJudit Bene, Magdolna Márton, Márton Mohás, et al.
Pathology Oncology Research : POR|August 16, 2024
Molecular genetic investigation of hereditary breast and ovarian cancer patients in the Southern Transdanubian region: widening the mutation spectrum and searching for new pathogenic variants using next-generation methodsLászló Baráti, Anita Maász, Alexandra Mikó, et al.
Molecular Biology Reports|November 5, 2014
Erratum to: Significant interethnic differences in functional variants of PON1 and P2RY12 genes in Roma and Hungarian population samplesIngrid Janicsek, Csilla Sipeky, Judit Bene, et al.
International Journal of Molecular Sciences|September 9, 2023
Identification of an <i>NF1</i> Microdeletion with Optical Genome MappingGergely Büki, Anna Bekő, Csaba Bödör, et al.
Drugs & Aging|April 17, 2007
Does glycoprotein IIIa gene (Pl(A)) polymorphism influence clopidogrel resistance? : a study in older patientsElod Papp, Viktoria Havasi, Judit Bene, et al.
Pageof 8

Showing results (41-50 of 77) with videos related to

Sort By:
Pageof 8
Journal of Human Genetics|December 17, 2010
Analysis of Hungarian patients with Rett syndrome phenotype for MECP2, CDKL5 and FOXG1 gene mutationsKinga Hadzsiev, Noemi Polgar, Judit Bene, et al.
World Journal of Gastroenterology|September 29, 2006
Prevalence of SLC22A4, SLC22A5 and CARD15 gene mutations in Hungarian pediatric patients with Crohn's diseaseJudit Bene, Lili Magyari, Gábor Talián, et al.
The Journal of Pediatrics|December 26, 2006
Histopathologic abnormalities of the lymphoreticular tissues in organic cation transporter 2 deficiency: evidence for impaired B cell maturationKatalin Komlósi, Viktória Havasi, Judit Bene, et al.
International Journal of Molecular Sciences|August 26, 2023
Three-Year Follow-Up after Intrauterine mTOR Inhibitor Administration for Fetus with TSC-Associated RhabdomyomaAnita Maász, Tímea Bodó, Ágnes Till, et al.
American Journal of Medical Genetics. Part A|September 25, 2004
Mutation analysis of MECP2 and determination of the X-inactivation pattern in Hungarian Rett syndrome patientsJudit Kárteszi, Katalin Hollódy, Judit Bene, et al.
Annals of Nutrition & Metabolism|January 9, 2013
Similarities in serum acylcarnitine patterns in type 1 and type 2 diabetes mellitus and in metabolic syndromeJudit Bene, Magdolna Márton, Márton Mohás, et al.
Pathology Oncology Research : POR|August 16, 2024
Molecular genetic investigation of hereditary breast and ovarian cancer patients in the Southern Transdanubian region: widening the mutation spectrum and searching for new pathogenic variants using next-generation methodsLászló Baráti, Anita Maász, Alexandra Mikó, et al.
Molecular Biology Reports|November 5, 2014
Erratum to: Significant interethnic differences in functional variants of PON1 and P2RY12 genes in Roma and Hungarian population samplesIngrid Janicsek, Csilla Sipeky, Judit Bene, et al.
International Journal of Molecular Sciences|September 9, 2023
Identification of an <i>NF1</i> Microdeletion with Optical Genome MappingGergely Büki, Anna Bekő, Csaba Bödör, et al.
Drugs & Aging|April 17, 2007
Does glycoprotein IIIa gene (Pl(A)) polymorphism influence clopidogrel resistance? : a study in older patientsElod Papp, Viktoria Havasi, Judit Bene, et al.
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