Cargando…
Hereditary Folate Malabsorption: A Rare Treatable Disorder with Hematological and Neurological Manifestations
Autores principales: | Kumar, Madhan, Yoganathan, Sangeetha, Todari, Siddarth, Suresh, Parvathy, Chandran, Mahalakshmi, Danda, Sumita, Mathew, Leni Grace, Koshy, Beena, Thomas, Maya |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer - Medknow
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9996535/ https://www.ncbi.nlm.nih.gov/pubmed/36911455 http://dx.doi.org/10.4103/aian.aian_1118_21 |
Ejemplares similares
-
Late Onset Multiple Acyl-CoA Dehydrogenase Deficiency: A Rare Treatable Neurometabolic Disorder
por: Korula, Sophy, et al.
Publicado: (2022) -
Attenuated form of Glycine Encephalopathy: An Unusual Cause of Neurodevelopmental Disorder
por: Yoganathan, Sangeetha, et al.
Publicado: (2021) -
Clinico-Etiological Spectrum and Functional Outcomes of Children with Pre-Status Dystonicus and Status Dystonicus (SD): A Descriptive Study
por: Joshi, Shridhar P., et al.
Publicado: (2023) -
Novel Imaging Finding and Novel Mutation in an Infant with Molybdenum Cofactor Deficiency, a Mimicker of Hypoxic-Ischaemic Encephalopathy
por: YOGANATHAN, Sangeetha, et al.
Publicado: (2018) -
Phenotypic Pleiotropy in Arginase Deficiency: A Single Center Cohort
por: Bharathi, Narmadham K., et al.
Publicado: (2022)