Zobrazeno 1 - 10
of 31
pro vyhledávání: '"GN Sanjeeva"'
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 18, Iss 10, Pp 01-03 (2024)
Crouzon Syndrome (CS) with Acanthosis Nigricans is a disorder characterised by the premature joining of certain bones of the skull {Craniosynostosis (CSO)} during development and a skin condition called Acanthosis Nigricans. Two cases of CSO with abn
Externí odkaz:
https://doaj.org/article/cff7ae630f334be3861331b6925a6a9b
Autor:
Thomas Semple, Samatha Sonnappa, Catherine M. Owens, Kani Varshneya, RL Ramesh, HB Pavithra, GN Sanjeeva
Publikováno v:
Pediatric Infectious Disease. 1:45-51
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8181a78d493f27a5b523ddba5f5cc7e7
https://doi.org/10.5005/jp-journals-10081-1204
https://doi.org/10.5005/jp-journals-10081-1204
Autor:
Rao, Nivedita, Kanago, Dhanashree, Morris, Monisha, Narayan, Vinu, Varshney, Kruti, GN, Sanjeeva, Bhat, Meenakshi
Publikováno v:
Journal of Genetic Counseling; Oct2021, Vol. 30 Issue 5, p1224-1232, 9p
Publikováno v:
Community Acquired Infection. 4:51
Background and Objective: The life span of the children living with Hiv/AIDS has increased with the invention of Retroviral drugs. As they are entering in to late adolescents and early adulthood, it becomes necessary to understand their expectations.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4f3279c0d34231d5e7834725a629f0b0
https://doi.org/10.4103/cai.cai_3_18
https://doi.org/10.4103/cai.cai_3_18
Autor:
S Shivananda, K. S. Sanjay, M Govindaraju, N Benakappa, GC Bharmappanavara, S Pragalathakumar, GN Sanjeeva, KN Vykuntaraju
Publikováno v:
Archives of Disease in Childhood. 99:A167-A168
To study Prevalence and Clinical spectrum of Tuberculosis in Paediatric HIV/AIDS. Methods 320 children with HIV/AIDS enrolled in this study between September 2004 and September 2007. History, Examination, relevant investigations done and classified a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6651f78f1cb16b5b95e399addae20c6f
https://doi.org/10.1136/archdischild-2014-306237.383
https://doi.org/10.1136/archdischild-2014-306237.383
Publikováno v:
Clinical Dysmorphology; Oct2015, Vol. 24 Issue 4, p159-162, 4p
Publikováno v:
Clinical Dysmorphology; October 2015, Vol. 24 Issue: 4 p159-162, 4p
Autor:
Mishra S; Molecular Biology and Genetics Unit, Jawaharlal Nehru Centre for Advanced Scientific Research, Bengaluru, Karnataka, India., Gohil Y; Molecular Biology and Genetics Unit, Jawaharlal Nehru Centre for Advanced Scientific Research, Bengaluru, Karnataka, India., Mehta K; Molecular Biology and Genetics Unit, Jawaharlal Nehru Centre for Advanced Scientific Research, Bengaluru, Karnataka, India., D'silva A; Molecular Biology and Genetics Unit, Jawaharlal Nehru Centre for Advanced Scientific Research, Bengaluru, Karnataka, India., Amanullah A; Molecular Biology and Genetics Unit, Jawaharlal Nehru Centre for Advanced Scientific Research, Bengaluru, Karnataka, India., Selvam D; Molecular Biology and Genetics Unit, Jawaharlal Nehru Centre for Advanced Scientific Research, Bengaluru, Karnataka, India., Pargain N; Molecular Biology and Genetics Unit, Jawaharlal Nehru Centre for Advanced Scientific Research, Bengaluru, Karnataka, India., Nala N; Molecular Biology and Genetics Unit, Jawaharlal Nehru Centre for Advanced Scientific Research, Bengaluru, Karnataka, India., Sanjeeva GN; Department of Pediatric Genetics, Indira Gandhi Institute of Child Health, Bengaluru, India., Ranga U; Molecular Biology and Genetics Unit, Jawaharlal Nehru Centre for Advanced Scientific Research, Bengaluru, Karnataka, India.
Publikováno v:
Bio-protocol [Bio Protoc] 2022 Jun 05; Vol. 12 (11). Date of Electronic Publication: 2022 Jun 05 (Print Publication: 2022).