Zobrazeno 1 - 10
of 72
pro vyhledávání: '"Adarshlata Singh"'
Autor:
Diwakar Dhurandhar, Swanand Pathak, Tripti Chandrakar, Vaibhav Anjankar, Adarshlata Singh, Jagriti Agrawal
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 18, Iss 09, Pp 01-05 (2024)
Introduction: Reflection facilitates the enhancement of critical thinking and profound learning through obtaining a greater understanding of oneself and the circumstances at hand. There is a limited amount of published literature evaluating the refle
Externí odkaz:
https://doaj.org/article/f0098eb51e1948789b07bd56a63fdb91
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 18, Iss 07, Pp 01-03 (2024)
Leprosy and Tuberculosis (TB), both significant mycobacterial infections, often affect populations with lowered specific immunity. TB is a widespread and life-threatening mycobacterial infection. Co-infection of these diseases is uncommon in routine
Externí odkaz:
https://doaj.org/article/40b01aa90708425daf0d48ef2aa8517b
Publikováno v:
Journal of Primary Care Specialties, Vol 5, Iss 2, Pp 127-129 (2024)
A form of lichen planus (LP) which follows the Blaschkos line pattern known as linear LP, presents with lichenoid eruptions and violaceous papules in a linear distribution. It is a rare form of LP affecting
Externí odkaz:
https://doaj.org/article/44377fb3bb954cfb9dd7a5bc593abd6b
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 18, Iss 03, Pp 01-06 (2024)
Introduction: Medical conditions can cause the skin to become hypopigmented or depigmented, mainly due to decreased production of melanin. Hypomelanosis is mainly benign and rarely malignant. Depigmentation refers to a complete lack of melanin, with
Externí odkaz:
https://doaj.org/article/542fe5df42e14d0d948ea87bc3c341e2
Publikováno v:
Case Reports in Dermatology, Vol 16, Iss 1, Pp 55-62 (2024)
Introduction: Lucio leprosy is a non-nodular diffuse type of lepromatous leprosy first described by Lucio and Alvarado. Lucio phenomenon is a rare vasculonecrotic reaction characterized by cutaneous necrosis with minimal constitutional features. Case
Externí odkaz:
https://doaj.org/article/c8f5f46f4b5049a1aa3d55e19f35c3b2
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 18, Iss 02, Pp 01-03 (2024)
Introduction: Melasma is a widely prevalent acquired condition characterised by gray-brown pigmentation with a predilection on the face, affecting the quality of life. Tranexamic Acid (TXA) has been used for managing melasma orally and topically, whi
Externí odkaz:
https://doaj.org/article/7b8ddbdd130b47e7879e46cbeb4a0cd4
Publikováno v:
Journal of Family Medicine and Primary Care, Vol 12, Iss 11, Pp 2942-2949 (2023)
Background: During the neonatal life cycle, various dermatological conditions are common. In comparison to the skin of adults, neonates' skins are more susceptible to infections in the first week of their lives. These infections often lead to many de
Externí odkaz:
https://doaj.org/article/51fcc3cb82154051907f171a05becbb9
Autor:
Sanjiv Choudhary, Ankita Srivastava, Vikrant Saoji, Adarshlata Singh, Isha Verma, Shivani Dhande
Publikováno v:
Anais Brasileiros de Dermatologia, Vol 98, Iss 4, Pp 460-465 (2023)
Abstract Background: Globally, few studies have been undertaken to assess the association of acanthosis nigricans (AN) with metabolic syndrome (MS). Most of the available studies have either focused on a particular age group, gender, ethnicity or on
Externí odkaz:
https://doaj.org/article/0c4f624944434badba3b96469a7e5c85
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 17, Iss 3, Pp WD01-WD03 (2023)
Scrofuloderma also called Tuberculosis colliquativa cutis is one of the variants of cutaneous tuberculosis. It can be a skin manifestation of concealed tuberculosis infection. It is most common in countries under development, such as India. It is pos
Externí odkaz:
https://doaj.org/article/365bd355d967408e8b6b168a5f1c94e9
Publikováno v:
Journal of the Scientific Society, Vol 49, Iss 2, Pp 201-203 (2022)
Primary immunodeficiency syndrome represents a heterogeneous group of inherited disorders caused by mutations in genes encoding functional proteins of the immune cells and characterized by an increased risk of infections, autoimmunity, autoinflammati
Externí odkaz:
https://doaj.org/article/72099ade05824a0790ec8bf670be9669