Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Arun Paul Charlu"'
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 18, Iss 04, Pp 04-06 (2024)
Pyogenic Granuloma (PG) is a benign vascular lesion that rapidly grows, is painless, and presents as a friable, smooth, or lobulated exophytic lesion, manifesting as small, red, erythematous papules with a pedunculated or sessile base. The most commo
Externí odkaz:
https://doaj.org/article/54386d7b479a4dc3a73f7b235c310049
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 17, Iss 11, Pp 15-18 (2023)
Pyogenic Granuloma (PG) is a benign reactive lesion characterised by tissue hyperplasia caused by local irritants. The gingiva is the most common site of occurrence in the oral cavity, followed by the tongue and buccal mucosa. It typically presents a
Externí odkaz:
https://doaj.org/article/b446d16ca64c41578240fe7454826afd
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 12, Iss 4, Pp ZC11-ZC14 (2018)
Introduction: Various biologic and non biologic graft materials are considered in the past as Intraoral wound dressing material. While autografts have issues related to donor site morbidity, allografts like collagen have limited intraoral usage due t
Externí odkaz:
https://doaj.org/article/3607e36e4fe34bce9098a82d971aa5a3
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 10, Iss 4, Pp ZD09-ZD11 (2016)
Dental malocclusion and facial deformity are frequent observations in patients with clefts of the orofacial region. These patients have a low self perception secondary to their aesthetic appearance. Cleft palate patients are further affected in thei
Externí odkaz:
https://doaj.org/article/30811cdca472431ba925741560f3a267
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 10, Iss 1, Pp ZD11-ZD12 (2016)
Glanzmann’s Thrombasthenia (GT) is a rare autosomal recessive bleeding disorder affecting the megakaryocyte lineage and is characterized by lack of platelet aggregation on stimulation. The molecular basis is linked to quantitative and qualitative
Externí odkaz:
https://doaj.org/article/272d6651828543a2ab731aa5da276f2f
Autor:
Venkata Sandeep Nandipati, Aaron Chapla, Felix K Jebasingh, Arun Paul Charlu, Thilak Samuel Jepegnanam, Kripa Elizabeth Cherian, Thomas V Paul, Nihal Thomas
Publikováno v:
Journal of the Endocrine Society. 6
Context Pyknodysostosis is an uncommon inherited disorder associated with consanguinity, often presenting with sclerotic bone disease, short stature, dysmorphic features, and recurrent fragility fractures at an early age. Case A 34-year-old woman was
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3b38e4955fcfc30fa648e108424d56c6
https://doi.org/10.1210/jendso/bvac102
https://doi.org/10.1210/jendso/bvac102
Publikováno v:
BMJ Case Reports. 16:e254074
A man in his 20s came for maxillofacial consultation with a pus discharge from the left preauricular region for the last 1 year. He had met with a road traffic accident 2 years earlier and had received surgical treatment for injuries associated with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5d49db15023b4d4c2bfae92ecbfeabde
https://doi.org/10.1136/bcr-2022-254074
https://doi.org/10.1136/bcr-2022-254074
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 12, Iss 4, Pp ZC11-ZC14 (2018)
Introduction: Various biologic and non biologic graft materials are considered in the past as Intraoral wound dressing material. While autografts have issues related to donor site morbidity, allografts like collagen have limited intraoral usage due t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2ab5394cde7754c6a6ee03eb8e9b5b4f
https://doi.org/10.7860/jcdr/2018/30867.11423
https://doi.org/10.7860/jcdr/2018/30867.11423
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 10, Iss 4, Pp ZD09-ZD11 (2016)
Dental malocclusion and facial deformity are frequent observations in patients with clefts of the orofacial region. These patients have a low self perception secondary to their aesthetic appearance. Cleft palate patients are further affected in their
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::13623d9e985d9e2c86830559bce26e71
https://doi.org/10.7860/jcdr/2016/16599.7639
https://doi.org/10.7860/jcdr/2016/16599.7639
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 10, Iss 1, Pp ZD11-ZD12 (2016)
Glanzmann’s Thrombasthenia (GT) is a rare autosomal recessive bleeding disorder affecting the megakaryocyte lineage and is characterized by lack of platelet aggregation on stimulation. The molecular basis is linked to quantitative and qualitative a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0d8b854dc723b6563d928c0bfbe47c41
https://doi.org/10.7860/jcdr/2016/16383.7123
https://doi.org/10.7860/jcdr/2016/16383.7123