Lactate Dehydrogenase and Hepatic Transaminases as Prognostic Markers of Hypoxic Ischaemic Encephalopathy in Neonates with Perinatal Asphyxia

Autor: VIJAYAKUMAR BALAKRISHNAN, SHAHIN MOHAMMED, KALPANA DEVADATHAN, LALITHA KAILAS

Publikováno v: Indian Journal of Neonatal Medicine and Research, Vol 8, Iss 4, Pp 24-28 (2020)

Introduction: Hypoxic Ischaemic Encephalopathy (HIE) following perinatal asphyxia, due to cerebral hypoxia is an important cause of neonatal morbidly and mortality. Hypoxia causes cell death in various tissues like liver, kidney and muscles also. The

Externí odkaz: https://doaj.org/article/ebd03bd923764f61b2277a650895fc71

Amantadine for the Treatment of Refractory Absence Seizures in Children

Autor: Habib K Pathan, Kunju P. A. Mohammed, Mini Sreedharan, Shiji Chalipat, Kalpana Devadathan

Publikováno v: Journal of Pediatric Neurosciences

Introduction: Childhood epilepsy is a generalized epilepsy syndrome with a favorable response to antiepileptic drugs; however, a small percentage of typical absence seizures remain refractory to drugs. We studied the safety and efficacy of amantadine

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8677fd6c7811cd7ea1ddf64b61f5ff54
https://pubmed.ncbi.nlm.nih.gov/30090124

Loss of function mutations in VARS encoding cytoplasmic valyl-tRNA synthetase cause microcephaly, seizures, and progressive cerebral atrophy

Autor: Ullrich Elling, Susan A. Martinis, William A. Gahl, Josef M. Penninger, Yan Huang, Rajesh Kannan, Joshi Stephen, Sheela Nampoothiri, Peter J. Steinbach, Aditi Banerjee, Chukwuma A. Agu, Nathanial J. Tolman, May Christine V. Malicdan, John Douglas Burke, Kalpana Devadathan

Publikováno v: Hum Genet

Progressive microcephaly and neurodegeneration are genetically heterogenous conditions, largely associated with genes that are essential for the survival of neurons. In this study, we interrogate the genetic etiology of two siblings from a non-consan

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2f4c7c4cd0a36418f2dea1a17333aedd
https://pubmed.ncbi.nlm.nih.gov/29691655

A Mild Variant of Pontocerebellar Hypoplasia Type 1 in a 12-Year-Old Indian Boy

Autor: Kalpana, Devadathan, Parvathy, Lalitha, Ahamed, Shahanaz M., Iype, Mary, Kunju, Mohammed P.A.

Publikováno v: In Pediatric Neurology 2009 40(4):302-305

Vitamin D Deficiency in Ambulant Children on Carbamazepine or Sodium Valproate Monotherapy.

Autor: Sreedharan M; Departments of Pediatric Neurology, Government Medical College, Thiruvananthapuram, India., Devadathan K; Departments of Pediatric Neurology, Government Medical College, Thiruvananthapuram, India. Correspondence to: Dr Kalpana Devadathan, Additional Professor, Department of Pediatric Neurology, Government Medical College, Thiruvananthapuram, Kerala, India. vijaykalpana10@gmail.com., Mohammed Kunju PA; Departments of Pediatric Neurology, Government Medical College, Thiruvananthapuram, India., Sasidharan B; Departments of Pediatrics, Government Medical College, Thiruvananthapuram, India., Pillai JP; Departments of Biochemistry; Government Medical College, Thiruvananthapuram, India., Vasumathy Amma MA; Departments of Biochemistry; Government Medical College, Thiruvananthapuram, India., Muthubeevi S; Departments of Biochemistry; Government Medical College, Thiruvananthapuram, India.

Publikováno v: Indian pediatrics [Indian Pediatr] 2018 Apr 15; Vol. 55 (4), pp. 307-310. Date of Electronic Publication: 2018 Feb 09.