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Pathology Oncology Research : POR
|
May 29, 2024
Case report: Initial atypical skeletal symptoms and dental anomalies as first signs of Gardner syndrome: the importance of genetic analysis in the early diagnosis
Gréta Antal, Anna Zsigmond, Ágnes Till, et al.
American Journal of Medical Genetics. Part A
|
October 16, 2004
Phenotypic manifestations of the OCTN2 V295X mutation: sudden infant death and carnitine-responsive cardiomyopathy in Roma families
Béla Melegh, Judit Bene, Gábor Mogyorósy, et al.
World Journal of Gastroenterology
|
January 28, 2006
Changes of plasma fasting carnitine ester profile in patients with ulcerative colitis
Judit Bene, Katalin Komlósi, Viktória Havasi, et al.
World Journal of Gastroenterology
|
May 1, 2007
No association of the cytotoxic T-lymphocyte associated gene CTLA4 +49A/G polymorphisms with Crohn's disease and ulcerative colitis in Hungarian population samples
Lili Magyari, Bernadett Faragó, Judit Bene, et al.
Molecular Biology Reports
|
October 10, 2014
Significant interethnic differencies in functional variants of PON1 and P2RY12 genes in Roma and Hungarian population samples
Ingrid Janicsek, Csilla Sipeky, Judit Bene, et al.
JIMD Reports
|
February 23, 2013
Non-syndromic Hearing Impairment in a Hungarian Family with the m.7510T>C Mutation of Mitochondrial tRNA(Ser(UCN)) and Review of Published Cases
Katalin Komlósi, Anita Maász, Péter Kisfali, et al.
JIMD Reports
|
July 9, 2013
Erratum to: Non-syndromic Hearing Impairment in a Hungarian Family with the m.7510T>C Mutation of Mitochondrial tRNA(Ser(UCN)) and Review of Published Cases
Katalin Komlósi, Anita Maász, Péter Kisfali, et al.
The British Journal of Nutrition
|
March 30, 2007
Plasma carnitine ester profiles in Crohn's disease patients characterized for SLC22A4 C1672T and SLC22A5 G-207C genotypes
Judit Bene, Katalin Komlósi, Lili Magyari, et al.
Journal of Molecular Neuroscience : MN
|
September 28, 2005
Lymphotoxin-alpha gene 252G allelic variant is a risk factor for large-vessel-associated ischemic stroke
Zoltán Szolnoki, Viktória Havasi, Gábor Talián, et al.
Journal of Molecular Neuroscience : MN
|
May 13, 2006
Angiotensin II type-1 receptor A1166C polymorphism is associated with increased risk of ischemic stroke in hypertensive smokers
Zoltán Szolnoki, Viktória Havasi, Gábor Talián, et al.
Page
of 8
Search research articles
Search
Showing results (51-60 of 77) with videos related to
Sort By:
Page
of 8
Pathology Oncology Research : POR
|
May 29, 2024
Case report: Initial atypical skeletal symptoms and dental anomalies as first signs of Gardner syndrome: the importance of genetic analysis in the early diagnosis
Gréta Antal, Anna Zsigmond, Ágnes Till, et al.
American Journal of Medical Genetics. Part A
|
October 16, 2004
Phenotypic manifestations of the OCTN2 V295X mutation: sudden infant death and carnitine-responsive cardiomyopathy in Roma families
Béla Melegh, Judit Bene, Gábor Mogyorósy, et al.
World Journal of Gastroenterology
|
January 28, 2006
Changes of plasma fasting carnitine ester profile in patients with ulcerative colitis
Judit Bene, Katalin Komlósi, Viktória Havasi, et al.
World Journal of Gastroenterology
|
May 1, 2007
No association of the cytotoxic T-lymphocyte associated gene CTLA4 +49A/G polymorphisms with Crohn's disease and ulcerative colitis in Hungarian population samples
Lili Magyari, Bernadett Faragó, Judit Bene, et al.
Molecular Biology Reports
|
October 10, 2014
Significant interethnic differencies in functional variants of PON1 and P2RY12 genes in Roma and Hungarian population samples
Ingrid Janicsek, Csilla Sipeky, Judit Bene, et al.
JIMD Reports
|
February 23, 2013
Non-syndromic Hearing Impairment in a Hungarian Family with the m.7510T>C Mutation of Mitochondrial tRNA(Ser(UCN)) and Review of Published Cases
Katalin Komlósi, Anita Maász, Péter Kisfali, et al.
JIMD Reports
|
July 9, 2013
Erratum to: Non-syndromic Hearing Impairment in a Hungarian Family with the m.7510T>C Mutation of Mitochondrial tRNA(Ser(UCN)) and Review of Published Cases
Katalin Komlósi, Anita Maász, Péter Kisfali, et al.
The British Journal of Nutrition
|
March 30, 2007
Plasma carnitine ester profiles in Crohn's disease patients characterized for SLC22A4 C1672T and SLC22A5 G-207C genotypes
Judit Bene, Katalin Komlósi, Lili Magyari, et al.
Journal of Molecular Neuroscience : MN
|
September 28, 2005
Lymphotoxin-alpha gene 252G allelic variant is a risk factor for large-vessel-associated ischemic stroke
Zoltán Szolnoki, Viktória Havasi, Gábor Talián, et al.
Journal of Molecular Neuroscience : MN
|
May 13, 2006
Angiotensin II type-1 receptor A1166C polymorphism is associated with increased risk of ischemic stroke in hypertensive smokers
Zoltán Szolnoki, Viktória Havasi, Gábor Talián, et al.
Page
of 8