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Hereditary Folate Malabsorption: A Rare Treatable Disorder with Hematological and Neurological Manifestations.
Kumar, Madhan; Yoganathan, Sangeetha; Todari, Siddarth; Suresh, Parvathy; Chandran, Mahalakshmi; Danda, Sumita; Mathew, Leni Grace; Koshy, Beena; Thomas, Maya.
Affiliation
  • Kumar M; Department of Pediatrics, Christian Medical College, Vellore, Tamil Nadu, India.
  • Yoganathan S; Pediatric Neurology Unit, Department of Neurological Sciences, Christian Medical College, Vellore, Tamil Nadu, India.
  • Todari S; Pediatric Hematology Oncology Unit, Department of Pediatrics, Christian Medical College, Vellore, Tamil Nadu, India.
  • Suresh P; Department of Radiodiagnosis, Christian Medical College, Vellore, Tamil Nadu, India.
  • Chandran M; Pediatric Neurology Unit, Department of Neurological Sciences, Christian Medical College, Vellore, Tamil Nadu, India.
  • Danda S; Department of Medical Genetics, Christian Medical College, Vellore, Tamil Nadu, India.
  • Mathew LG; Pediatric Hematology Oncology Unit, Department of Pediatrics, Christian Medical College, Vellore, Tamil Nadu, India.
  • Koshy B; Developmental Pediatrics Unit, Department of Pediatrics, Christian Medical College, Vellore, Tamil Nadu, India.
  • Thomas M; Pediatric Neurology Unit, Department of Neurological Sciences, Christian Medical College, Vellore, Tamil Nadu, India.
Ann Indian Acad Neurol ; 25(6): 1238-1241, 2022.
Article in En | MEDLINE | ID: mdl-36911455

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Ann Indian Acad Neurol Year: 2022 Document type: Article Affiliation country: India

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Ann Indian Acad Neurol Year: 2022 Document type: Article Affiliation country: India