Zobrazeno 1 - 10
of 25
pro vyhledávání: '"Hugar, Deepa"'
Autor:
Hugar, Deepa, Zainab, Heena, Sultana, Ameena, khajamoinuddin, Mohammed, Hugar, Santosh, G. H., Divya
Publikováno v:
International Journal of Pure Medical Research; Jan2024, Vol. 9 Issue 1, p1-3, 3p
Publikováno v:
Indian Journal of Forensic Medicine & Toxicology; Jan-Mar2022, Vol. 16 Issue 1, p213-223, 11p
Publikováno v:
Egyptian Journal of Forensic Sciences; 11/24/2021, Vol. 11 Issue 1, p1-9, 9p
Publikováno v:
Journal of Oral & Maxillofacial Pathology (0973029X); Jan-Apr2021, Vol. 25 Issue 1, p118-123, 6p
Autor:
HUGAR, DEEPA1 drdeepahugar@gmail.com, SAJJANSHETTY, SANGAMESHWAR2, HUGAR, SANTOSH3, KADANI, MEGHA4
Publikováno v:
Journal of Clinical & Diagnostic Research. Oct2014, Vol. 8 Issue 10, p28-30. 3p.
Autor:
SAJJANSHETTY, SANGAMESHWAR1 sajjanshettysangamesh@yahoo.com, HUGAR, DEEPA2, HUGAR, SANTOSH3, RANJAN, SHASHI4, KADANI, MEGHA5
Publikováno v:
Journal of Clinical & Diagnostic Research. Jun2014, Vol. 8 Issue 6, p39-41. 3p.
General dentists most commonly encounter one or more congenitally missing teeth on routine oral examination. Hypodontia and oligodontia are the two most commonly encountered genetic disorders. When one or less than six teeth are missing congenitally
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::81d288e7039b66b560d919b6b5f66a3e
https://europepmc.org/articles/PMC4109254/
https://europepmc.org/articles/PMC4109254/
Autor:
Satish, B N V S, Srikala, P, Maharudrappa, B, Awanti, Sharanabasappa M, Kumar, Prashant, Hugar, Deepa
Background: Diabetes mellitus is a metabolic disorder affecting people worldwide, which require constant monitoring of their glucose levels. Commonly employed procedures include collection of blood or urine samples causing discomfort to the patients.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::b58636f27be26c9f1526cc32590e9be8
https://europepmc.org/articles/PMC4037799/
https://europepmc.org/articles/PMC4037799/
Autor:
Deshmukh, Pallavi K., Deshmukh, Kiran, Mangalgi, Anand, Patil, Subhash, Hugar, Deepa, Kodangal, Saraswathi Fakirappa
Publikováno v:
Case Reports in Dentistry.
Van der Woude syndrome (VWS) is a rare autosomal dominant condition with high penetrance and variable expression. Clinical manifestation of this autosomal dominant clefting syndrome includes bilateral midline lower lip pits, cleft lip, and cleft pala
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=hindawi_publ::a0f24d2952d42a9a9e809cb5d4aa96ef
Publikováno v:
JIDA: Journal of Indian Dental Association; Aug2016, Vol. 10 Issue 8, p28-36, 9p, 1 Color Photograph, 1 Black and White Photograph