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au.\*:("CHRISTOPHER, Rita")

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Janus kinase (JAK) 2 V617F mutation in Asian Indians with cerebral venous thrombosis and without overt myeloproliferative disordersTANIMA DE; PRABHAKAR, Puttachandra; NAGARAJA, Dindagur et al.Journal of the neurological sciences. 2012, Vol 323, Num 1-2, pp 178-182, issn 0022-510X, 5 p.Article

Factor V gene A4070G mutation and the risk of cerebral veno-sinus thrombosis occurring during puerperiumDINDAGUR, Nagaraja; KRUTHIKA-VINOD, T. P; CHRISTOPHER, Rita et al.Thrombosis research. 2007, Vol 119, Num 4, pp 497-500, issn 0049-3848, 4 p.Article

Type I hyperprolinemiaSHIVANANDA; CHRISTOPHER, Rita; KUMAR, Prem et al.Indian journal of pediatrics. 2000, Vol 67, Num 7, pp 541-543, issn 0019-5456Conference Paper

Neuropharmacology of schizophrenia: is there a role for leptin?VENKATASUBRAMANIAN, Ganesan; ARASAPPA, Rashmi; CHRISTOPHER, Rita et al.Clinical chemistry and laboratory medicine. 2010, Vol 48, Num 6, pp 895-896, issn 1434-6621, 2 p.Article

Profile of Inborn Errors of Metabolism in a Tertiary Care Centre PICUKAMATE, Mahesh; CHETAL, Vivek; KULGOD, Vijaylaxmi et al.Indian journal of pediatrics. 2010, Vol 77, Num 1, pp 57-60, issn 0019-5456, 4 p.Article

Screening for inborn errors of metabolism using automated electrospray tandem mass spectrometry: Study in high-risk Indian populationNAGARAJA, Dindagur; SOPANAHALLI NARASIMHAMURTHY MAMATHA; DE, Tanima et al.Clinical biochemistry. 2010, Vol 43, Num 6, pp 581-588, issn 0009-9120, 8 p.Article

Homocysteine, folate and vitamin B12 in puerperal cerebral venous thrombosisNAGARAJA, Dindagur; MOHAN LESLIE NOONE; VENKATA PINNELLI BHARATKUMAR et al.Journal of the neurological sciences. 2008, Vol 272, Num 1-2, pp 43-47, issn 0022-510X, 5 p.Article

Cranial MRI in Acute Hyperammonemic EncephalopathyBINDU, Parayil S; SINHA, Sanjib; TALY, Arun B et al.Pediatric neurology. 2009, Vol 41, Num 2, pp 139-142, issn 0887-8994, 4 p.Article

Nuclear localization of Munc18-1 (p67) in the adult rat brain and PC12 cellsSHARMA, Vandana M; SHAREEF, Momin M; BHASKAR, Kiran et al.Neurochemistry international. 2005, Vol 47, Num 3, pp 225-234, issn 0197-0186, 10 p.Article

Impact of 5,10-methylenetetrahydrofolate reductase gene polymorphism on neural tube defects: Laboratory investigationPOOMAGAME NARASIMHAMURTHY HARISHA; INDIRA DEVI, B; CHRISTOPHER, Rita et al.Journal of neurosurgery. Pediatrics. 2010, Vol 6, Num 4, pp 364-367, issn 1933-0707, 4 p.Article

Clinical features of adult GM1 gangliosidosis: Report of three Indian patients and review of 40 casesMUTHANE, Uday; CHICKABASAVIAH, Yasha; KANESKI, Chris et al.Movement disorders. 2004, Vol 19, Num 11, pp 1334-1341, issn 0885-3185, 8 p.Article

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