Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Neluwa-Liyanage R. Indika"'
Autor:
Neluwa-Liyanage R. Indika, Richard E. Frye, Daniel A. Rossignol, Susan C. Owens, Udara D. Senarathne, Andreas M. Grabrucker, Rasika Perera, Marielle P. K. J. Engelen, Nicolaas E. P. Deutz
Children with autism spectrum disorder may exhibit nutritional deficiencies due to reduced intake, genetic variants, autoantibodies interfering with vitamin transport, and the accumulation of toxic compounds that consume vitamins. Importantly, vitami
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b1d956c1afbbf3bcbb8942ffd6232089
https://figshare.com/articles/journal_contribution/The_Rationale_for_vitamin_mineral_and_cofactor_treatment_in_the_precision_medical_care_of_autism_spectrum_disorder/23627340
https://figshare.com/articles/journal_contribution/The_Rationale_for_vitamin_mineral_and_cofactor_treatment_in_the_precision_medical_care_of_autism_spectrum_disorder/23627340
Publikováno v:
Genetic Syndromes ISBN: 9783319668161
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1398fd146099857bb7b6f14665ea5cb9
https://doi.org/10.1007/978-3-319-66816-1_1752-1
https://doi.org/10.1007/978-3-319-66816-1_1752-1
Publikováno v:
Genetic Syndromes ISBN: 9783319668161
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8ea5b6eeb5f4ac18504210b52c3233a3
https://doi.org/10.1007/978-3-319-66816-1_1787-1
https://doi.org/10.1007/978-3-319-66816-1_1787-1
Autor:
Udara D. Senarathne, Neluwa-Liyanage R. Indika, Aleksandra Jezela-Stanek, Elżbieta Ciara, Richard E. Frye, Cliff Chen, Karolina M. Stepien
Publikováno v:
Genes. 14:803
Autism spectrum disorders (ASD) are a heterogeneous group of neurodevelopmental disorders characterized by impaired social interaction, limited communication skills, and restrictive and repetitive behaviours. The pathophysiology of ASD is multifactor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::07bfa36682102666647b0519073ca35d
https://doi.org/10.3390/genes14040803
https://doi.org/10.3390/genes14040803
Autor:
Iván Pérez-Neri, Hugo Sandoval, Antonio Malvaso, Neluwa-Liyanage R. Indika, Christoper A. Alarcon-Ruiz, Manoochehr Ebrahimian, Camilo Ríos
Publikováno v:
Archivos de Neurociencias. 28
Introduction: Hepatic encephalopathy (HE) is a neuropsychiatric complication of liver disease and/or portosystemic blood shunting, characterized by alterations of alertness, personality, cognition, and motor functions. Its severity is defined from mi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6024e1ba7ab58384c99f3dd801413603
https://doi.org/10.31157/an.v28i1.354
https://doi.org/10.31157/an.v28i1.354