PHARMACOECONOMICAL ASPECTS OF SELF-MEDICATION; A COMMUNITY PHARMACY SURVEY IN NORTHERN KERALA

Autor: NAINA LIZ PUTHIYEDAM, ANJANA SAJAN, ARUNA T, VINEETH VS, KIRON SS, SMRITHY SUNNY

Publikováno v: ORCID

Objectives: The main objectives of the study are to identify the socio-economic characteristics of lay persons who engage in self-medication activities, to determine the economic aspects of self-medication, to conduct cost minimization analysis, and

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::73930e7e2406409c4ea52d5f70bd5d8b
https://doi.org/10.22159/ajpcr.2022.v15i12.45982

Next Generation Sequencing for Rare Mendelian Disorders: An Indian Scenario

Autor: Aneek Das Bhowmik, Kar, Anjana, Vineeth Vs, Shagun Aggarwal, Prajyna Ranganath, Phadke, Shubha, Bharadwaj, Karthik, Dutta, Usha R, Sharda, Sheetal, Girisha Km, Sj Patil, Gupta, Neerja, Ashwin B Dalal

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::1a00c8e5d7db16c0f00fcc3c97e5b993

SERPINA11 related novel serpinopathy - A perinatal lethal disorder.

Autor: Aggarwal S; Department of Medical Genetics, Nizam's Institute of Medical Sciences, Hyderabad, India.; Laboratory of Human and Medical Genetics, Centre for DNA Fingerprinting and Diagnostics, Hyderabad, India., Vineeth VS; Laboratory of Human and Medical Genetics, Centre for DNA Fingerprinting and Diagnostics, Hyderabad, India., Padwal SS; Laboratory of Human and Medical Genetics, Centre for DNA Fingerprinting and Diagnostics, Hyderabad, India.; Laboratory of Cell Signalling, Centre for DNA Fingerprinting and Diagnostics, Hyderabad, India.; Manipal Academy of Higher Education, Manipal, India., Bhat SA; Laboratory of Cell Signalling, Centre for DNA Fingerprinting and Diagnostics, Hyderabad, India., Singh A; Laboratory of Cell Signalling, Centre for DNA Fingerprinting and Diagnostics, Hyderabad, India.; Regional Centre for Biotechnology, Faridabad, India., Kulkarni A; Department of Histopathology, Apollo Hospitals, Hyderabad, India., Patil M; Department of Medical Genetics, Nizam's Institute of Medical Sciences, Hyderabad, India., Tallapaka K; CSIR-Centre for Cellular and Molecular Biology, Hyderabad, India., Pasumarthi D; Laboratory of Human and Medical Genetics, Centre for DNA Fingerprinting and Diagnostics, Hyderabad, India., Venkatapuram V; Department of Medical Genetics, Nizam's Institute of Medical Sciences, Hyderabad, India.; Laboratory of Human and Medical Genetics, Centre for DNA Fingerprinting and Diagnostics, Hyderabad, India., Thotakura PL; Laboratory of Human and Medical Genetics, Centre for DNA Fingerprinting and Diagnostics, Hyderabad, India., Dalal A; Laboratory of Human and Medical Genetics, Centre for DNA Fingerprinting and Diagnostics, Hyderabad, India., Bhandari R; Laboratory of Cell Signalling, Centre for DNA Fingerprinting and Diagnostics, Hyderabad, India.

Publikováno v: Clinical genetics [Clin Genet] 2024 Sep; Vol. 106 (3), pp. 367-373. Date of Electronic Publication: 2024 Jun 03.

Fetal phenotypes of Mendelian disorders: A descriptive study from India.

Autor: Saini N; Department of Medical Genetics, Nizam's Institute of Medical Sciences, Hyderabad, India., Venkatapuram VS; Department of Medical Genetics, Nizam's Institute of Medical Sciences, Hyderabad, India., Vineeth VS; Diagnostics Division, Centre for DNA Fingerprinting & Diagnostics, Hyderabad, India., Kulkarni A; Department of Pathology, Apollo Hospitals, Hyderabad, India., Tandon A; Department of Pathology, All India Institute of Medical Sciences, Bhopal, India., Koppolu G; The Lotus Ultrasound and Fetal Care Centre, Kurnool, India., Patil SJ; Division of Medical Genetics, Mazumdar Shaw Medical Center, Narayana Hrudayalaya Hospitals, Bangalore, India., Dalal A; Diagnostics Division, Centre for DNA Fingerprinting & Diagnostics, Hyderabad, India., Aggarwal S; Department of Medical Genetics, Nizam's Institute of Medical Sciences, Hyderabad, India.; Diagnostics Division, Centre for DNA Fingerprinting & Diagnostics, Hyderabad, India.

Publikováno v: Prenatal diagnosis [Prenat Diagn] 2022 Jun; Vol. 42 (7), pp. 911-926. Date of Electronic Publication: 2022 Jun 01.

Report of an Asian-Indian patient with Okur-Chung Syndrome and comparison of the clinical phenotype in different ethnic groups.

Autor: Ranganath P; Department of Medical genetics, Nizam's Institute of Medical Sciences., Ranganath P; Department of Medical genetics, Nizam's Institute of Medical Sciences., Vineeth VS; Diagnostics Division, Centre for DNA Fingerprinting and Diagnostics, Hyderabad, Telangana., Dalal A; Diagnostics Division, Centre for DNA Fingerprinting and Diagnostics, Hyderabad, Telangana., Patil SJ; Division of Medical Genetics, Mazumdar Shaw Medical Centre, Narayana Hrudayalaya Hospitals, Bangalore, Karnataka, India.

Publikováno v: Clinical dysmorphology [Clin Dysmorphol] 2021 Oct 01; Vol. 30 (4), pp. 209-212.