Zobrazeno 1 - 10
of 59
pro vyhledávání: '"Lyubov Yevtushok"'
Autor:
Mika Gissler, Maria Loane, Ingeborg Barisic, Hermien E K de Walle, Miriam Gatt, Kari Klungsoyr, Anna Pierini, Anke Rissmann, Oscar Zurriaga, Diana G Wellesley, Clara Cavero-Carbonell, Olatz Mokoroa, Judith Rankin, Ester Garne, Sue Jordan, Anna Heino, Michele Santoro, Alessio Coi, Joan Morris, Svetlana V Glinianaia, Elisa Ballardini, Joachim Tan, Abigail Reid, Stine Kjaer Urhoj, Lyubov Yevtushok, Diana Akhmedzhanova, Joanne Given, Amanda Julie Neville, Amaia Aizpurua, Renee Lutke, Daniel S Thayer
Publikováno v:
BMJ Paediatrics Open, Vol 7, Iss 1 (2023)
Background Congenital anomalies (CAs) increase the risk of death during infancy and childhood. This study aimed to evaluate the accuracy of using death certificates to estimate the burden of CAs on mortality for children under 10 years old.Methods Ch
Externí odkaz:
https://doaj.org/article/f42c5f88e93644388fcf44d53460a7f0
Autor:
Liliya Fishchuk, Zoia Rossokha, Natalia Olkhovich, Nataliia Pichkur, Olena Popova, Nataliia Medvedieva, Viktoriia Vershyhora, Olha Dubitska, Tetiana Shkurko, Larysa Popovych, Olga Bondar, Irina Morozuk, Svitlana Onyshchenko, Lyubov Yevtushok, Oksana Tsizh, Iryna Bryl, Olena Tul, Svitlana Kalynka, Iryna Zinkina, Svitlana Matviiuk, Yulianna Riabova, Nataliia Gorovenko
Publikováno v:
Molecular Genetics and Metabolism Reports, Vol 32, Iss , Pp 100907- (2022)
Phenylketonuria (PKU) is hyperphenylalaninemia that develops due to a deficiency of the phenylalanine hydroxylase enzyme (PAH). Identification of variants in the PAH gene is necessary for verification of the diagnosis, choice of treatment tactics, de
Externí odkaz:
https://doaj.org/article/64d845bbcd84433a8f543d42762f9a05
Autor:
Nihal A. Salem, Amanda H. Mahnke, Alan B. Wells, Alexander M. Tseng, Lyubov Yevtushok, Natalya Zymak-Zakutnya, Wladimir Wertlecki, Christina D. Chambers, Rajesh C. Miranda, Collaborative Initiative on Fetal Alcohol Spectrum Disorders (CIFASD)
Publikováno v:
Biology of Sex Differences, Vol 11, Iss 1, Pp 1-17 (2020)
Abstract Most persons with fetal alcohol spectrum disorders (FASDs) remain undiagnosed or are diagnosed in later life. To address the need for earlier diagnosis, we previously assessed miRNAs in the blood plasma of pregnant women who were classified
Externí odkaz:
https://doaj.org/article/f02315f86070432eb69f640876acc9e6
Autor:
Tamara S. Bodnar, Charlis Raineki, Wladimir Wertelecki, Lyubov Yevtushok, Larisa Plotka, Irina Granovska, Natalya Zymak-Zakutnya, Alla Pashtepa, Alan Wells, Gordon Honerkamp-Smith, Claire D. Coles, Julie A. Kable, Christina D. Chambers, Joanne Weinberg, and the CIFASD
Publikováno v:
Journal of Neuroinflammation, Vol 17, Iss 1, Pp 1-14 (2020)
Abstract Background Evidence suggests that cytokine imbalances may be at the root of deficits that occur in numerous neurodevelopmental disorders, including schizophrenia and autism spectrum disorder. Notably, while clinical studies have demonstrated
Externí odkaz:
https://doaj.org/article/319bf4eebc5943b787ec8c1b41c94184
Autor:
Marcelo Aguilar-Rivera, Julie A. Kable, Lyubov Yevtushok, Yaroslav Kulikovsky, Natalya Zymak-Zakutnya, Iryna Dubchak, Diana Akhmedzhanova, Wladimir Wertelecki, Christina Chambers, Todd P. Coleman
Publikováno v:
Sensors, Vol 22, Iss 23, p 9140 (2022)
Early identification of infants at risk of neurodevelopmental delay is an essential public health aim. Such a diagnosis allows early interventions for infants that maximally take advantage of the neural plasticity in the developing brain. Using stand
Externí odkaz:
https://doaj.org/article/a0d41782ca1749eea48349e01cbb65d7
Autor:
Nathalie Lelong, Babak Khoshnood, David Tucker, Mika Gissler, Maria Loane, Ingeborg Barisic, Miriam Gatt, Kari Klungsoyr, Amanda Neville, Anna Pierini, Anke Rissmann, Oscar Zurriaga, Joan K Morris, Paula Braz, Vera Nelen, Judith Rankin, Ester Garne, Sue Jordan, Anna Heino, Silvia Baldacci, Michele Santoro, Alessio Coi, Lorena Mezzasalma, Daniel Thayer, Svetlana V Glinianaia, Hermien de Walle, Guy Thys, Anna Latos-Bielenska, Aurora Puccini, Elisa Ballardini, Wladimir Wertelecki, Carlos Matias Dias, Gianni Astolfi, James Densem, Joachim Tan, Joanne Emma Given, Hugh Claridge, Abigail Reid, Liz Limb, Gillian Briggs, Nicholas Connor, Stine Kjaer Urhoj, Mads Damkjær, Christina Neergaard Pedersen, Annarita Armaroli, Ljubica Boban, L Renée Lutke, Nicole H A Siemensma-Mühlenberg, Nathalie Bertille, Makan Rahshenas, Clara Cavero Carbonell, Laia Barrachina Bonet, Laura García Villodre, Anna Jamry-Dziurla, Sonja Kiuru-Kuhlefelt, Lyubov Yevtushok, Nataliia Zymak-Zakutnia, Diana Akhmedzhanova, Lyubov Ostapchuk, Oksana Tsizh, Serhii Lapchenko, Ausenda Machado, Ana João Santos, Liliana Antunes, Hanitra Randrianaivo-Ranjatoelina, Elly Den Hond, Olatz Mokoroa Carollo, Ieuan Scanlon
Publikováno v:
BMJ Open, Vol 11, Iss 6 (2021)
Introduction Congenital anomalies (CAs) are a major cause of infant mortality, childhood morbidity and long-term disability. Over 130 000 children born in Europe every year will have a CA. This paper describes the EUROlinkCAT study, which is investig
Externí odkaz:
https://doaj.org/article/71d0d10a7c8340b8864daf7f71f7e0a9
Publikováno v:
Праці Наукового товариства імені Шевченка. Медичні науки, Vol 47, Iss 2, Pp 47-56 (2016)
Ukraine suffers from the neural tube defects epidemic. According to“Omni-Net” data (“Omni-Net” is the only Ukrainian International Charitable Organization that runs population-based monitoring of birth defects according to the international s
Externí odkaz:
https://doaj.org/article/cf50bb8166094169b08965c0ade3781f
Plasma miRNA Profiles in Pregnant Women Predict Infant Outcomes following Prenatal Alcohol Exposure.
Autor:
Sridevi Balaraman, Jordan J Schafer, Alexander M Tseng, Wladimir Wertelecki, Lyubov Yevtushok, Natalya Zymak-Zakutnya, Christina D Chambers, Rajesh C Miranda
Publikováno v:
PLoS ONE, Vol 11, Iss 11, p e0165081 (2016)
Fetal alcohol spectrum disorders (FASD) are difficult to diagnose since many heavily exposed infants, at risk for intellectual disability, do not exhibit craniofacial dysmorphology or growth deficits. Consequently, there is a need for biomarkers that
Externí odkaz:
https://doaj.org/article/7341418822b742389591dc0fc9f562ac
Autor:
Gretchen, Bandoli, Claire, Coles, Julie, Kable, Kenneth Lyons, Jones, Erin, Delker, Wladimir, Wertelecki, Lyubov, Yevtushok, Natalya, Zymak-Zakutnya, Iryna, Granovska, Larysa, Plotka, Christina, Chambers
Publikováno v:
Alcoholism: Clinical and Experimental Research. 46:2236-2244
Cardinal and non-cardinal dysmorphic features are associated with prenatal alcohol exposure (PAE); however, their association with neurodevelopment is less clear. The objective of this study was to determine whether alcohol-related dysmorphic feature
Autor:
Alessio Coi, Ingeborg Barisic, Ester Garne, Anna Pierini, Marie‐Claude Addor, Amaia Aizpurua Atxega, Elisa Ballardini, Paula Braz, Jennifer M. Broughan, Clara Cavero‐Carbonell, Hermien E. K. de Walle, Elizabeth S. Draper, Miriam Gatt, Martin Häusler, Agnieszka Kinsner‐Ovaskainen, Jennifer J. Kurinczuk, Nathalie Lelong, Karen Luyt, Lorena Mezzasalma, Carmel Mullaney, Vera Nelen, Ljubica Odak, Mary T. O'Mahony, Isabelle Perthus, Hanitra Randrianaivo, Judith Rankin, Anke Rissmann, Florence Rouget, Bruno Schaub, David Tucker, Diana Wellesley, Katarzyna Wiśniewska, Lyubov Yevtushok, Michele Santoro
Publikováno v:
Journal of the European Academy of Dermatology and Venereology
Journal of the European Academy of Dermatology and Venereology, 2022, ⟨10.1111/jdv.18690⟩
JOURNAL OF THE EUROPEAN ACADEMY OF DERMATOLOGY AND VENEREOLOGY
r-FISABIO. Repositorio Institucional de Producción Científica
instname
Journal of the European Academy of Dermatology and Venereology. Wiley
Journal of the European Academy of Dermatology and Venereology, 2022, ⟨10.1111/jdv.18690⟩
JOURNAL OF THE EUROPEAN ACADEMY OF DERMATOLOGY AND VENEREOLOGY
r-FISABIO. Repositorio Institucional de Producción Científica
instname
Journal of the European Academy of Dermatology and Venereology. Wiley
Background Aplasia cutis congenita (ACC) is a rare congenital anomaly characterized by localized or widespread absence of skin at birth, mainly affecting the scalp. Most information about ACC exists as individual case reports and medium-sized studies