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Graduate medical education: variation of program and training duration

Das KK

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A Prospective, Single-Blinded, Bicentric Study, and Literature Review to Assess the Need of C2-Ganglion Preservation - SAVIOUR’s Criteria

Singh S, Srivastava AK, Sardhara J, Bhaisora KS, Das KK, Mehrotra A, Jaiswal AK, Panigrahi MK, Behari S

Objective: Joint manipulation for craniovertebral junction instability is often hindered by the C2-ganglion (C2G). Our study aims to compare the surgical outcome among patients with or without C2G preservation and...
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Genetic analysis of the postsynaptic transmembrane X-linked neuroligin 3 gene in autism

Hegde R, Hegde S, Kulkarni SS, Pandurangi A, Gai PB, Das KK

Autism is a complex neurodevelopmental disorder, the prevalence of which has increased drastically in India in recent years. Neuroligin is a type I transmembrane protein that plays a crucial role...
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A Universal Craniometric Index for Establishing the Diagnosis of Basilar Invagination

Sardhara J, Behari S, Singh S, Srivastava AK, Chauhan G, Lal H, Das KK, Bhaisora KS, Mehrotra A, Mishra P, Jaiswal AK

Objective: The conventional criteria for defining the basilar invagination (BI) focus on the relationship of odontoid tip to basion and opisthion, landmarks that are intrinsically variable especially in presence of...
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Type I Chiari Malformation Without Concomitant Bony Instability: Assessment of Different Surgical Procedures and Outcomes in 73 Patients

Rangari K, Das KK, Singh S, Kumar KG, Bhaisora KS, Sardhara J, Mehrotra A, Srivastava AK, Jaiswal AK, Behari S

Objective: Posterior fossa decompression is the treatment of choice in type 1 Chiari malformation (CM-1) without bony instability. Although surgical fixation has been recommended by a few authors recently, comparative...
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Mutation analysis and characterisation of F9 gene in haemophilia- B population of India

Kulkarni S, Hegde R, Hegde S, Kulkarni SS, Hanagvadi S, Das KK, Kolagi S, Gai PB, Bulagouda R

Background Hemophilia B (HB) is an X-linked bleeding disorder resulting from coagulation factor IX defects. Over 3,000 pathogenic, HB-associated mutations in the F9 gene have been identified. We aimed to investigate...
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