Satish Chandra Girimaji
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Explore the profile of Satish Chandra Girimaji including associated specialties, affiliations and a list of published articles.
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31
Citations
344
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Recent Articles
1.
Yadav A, Rajendra K, Sravanti L, Kommu J, Seshadri S, Girimaji S
Ind Psychiatry J
. 2025 Feb;
33(2):305-311.
PMID: 39898065
Background: School refusal behaviour is an umbrella term that often subsumes constructs such as truancy, school refusal, and school phobia. It is influenced by various psychological and psychosocial factors and...
2.
Sravanti L, Madegowda R, Velusamy A, Kommu J, Girimaji S, Seshadri S
Child Adolesc Psychiatry Ment Health
. 2024 Dec;
18(1):160.
PMID: 39695802
Objective: The objective is to examine barriers and facilitators to recovery in children and adolescents with obsessive-compulsive disorder (OCD) using a qualitative approach. Methods: Ten semi-structured interviews were conducted, audio-recorded,...
3.
Sravanti L, Velusamy A, Karki U, Kommu J, Girimaji S
Indian J Psychol Med
. 2024 Jul;
46(4):323-329.
PMID: 39056033
Background: Anorexia nervosa is one of the least studied mental health conditions in the Indian setting. The objective of this study was to assess the course and outcome of anorexia...
4.
Sravanti L, Kommu J, Girimaji S, Seshadri S
Child Adolesc Psychiatry Ment Health
. 2022 Jun;
16(1):44.
PMID: 35710566
Background: Childhood obsessive-compulsive disorder (OCD) is distinct from OCD in adults. It can be severely disabling and there is little qualitative research on OCD in children. The present study aims...
5.
Sravanti L, Velusamy A, Karki U, Kommu J, Girimaji S
Asian J Psychiatr
. 2022 Mar;
71:103077.
PMID: 35299144
Objective: This study was conducted to assess the trends observed in the prevalence pattern, clinical presentation, psychosocial profile and treatment profile of anorexia nervosa in children and adolescents who presented...
6.
Shere S, Mehta U, Girimaji S
Brain Stimul
. 2021 Jul;
14(4):1051-1053.
PMID: 34229115
No abstract available.
7.
Bellad A, Girimaji S, Muthusamy B
Neurol Sci
. 2021 Apr;
42(12):5311-5319.
PMID: 33884525
Background: Spastic paraplegia 50 (SPG50) is a rare autosomal recessive inherited disorder characterized by spasticity, severe intellectual disability and delayed or absent speech. Loss-of-function pathogenic mutations in the AP4M1 gene...
8.
Muthusamy B, Bellad A, Girimaji S, Pandey A
Genes (Basel)
. 2021 Apr;
12(3).
PMID: 33810051
Shukla-Vernon syndrome (SHUVER) is an extremely rare neurodevelopmental disorder characterized by global developmental delay, intellectual disability, behavioral anomalies, and dysmorphic features. Pathogenic variants in the gene have been identified as...
9.
Kumar K, Bellad A, Prasad P, Girimaji S, Muthusamy B
BMC Med Genet
. 2020 Jun;
21(1):136.
PMID: 32590954
Background: Alkuraya-Kučinskas syndrome is an autosomal recessive disorder characterized by brain abnormalities associated with cerebral parenchymal underdevelopment, arthrogryposis, club foot and global developmental delay. KIAA1109, a functionally uncharacterized gene is...
10.
Bellad A, Bandari A, Pandey A, Girimaji S, Muthusamy B
J Mol Neurosci
. 2020 May;
70(9):1403-1409.
PMID: 32399860
Börjeson-Forssman-Lehman Syndrome (BFLS) is a rare X-linked recessive syndrome characterized by intellectual disability, developmental delay, obesity, epilepsy, swelling of the subcutaneous tissues of the face, large but not deformed ears,...