Zobrazeno 1 - 10 of 15 pro vyhledávání: '"Shrinath Shetty"'
1
Akademický článek
Lean Cushing's
Autor: Yashendu Sarda, Damodar Shenoy, Shrinath Shetty, Sonali Ullal, Sanyam Katyal
Publikováno v: Journal of Family Medicine and Primary Care, Vol 9, Iss 7, Pp 3759-3761 (2020)
This is a case report of 59 years old male with adrenocorticotropic hormone ACTH-independent macronodular adrenal hyperplasia (AIMAH), which is a rare cause of Cushing's syndrome. He was detected to have adrenal lesions incidentally on imaging. The b
Externí odkaz: https://doaj.org/article/fc29de7a7c8c4a0ca92ae7be1514fb50
Zobrazit plný text záznamu
2
Akademický článek
An unusual presentation of metastatic bone disease in a subject with Paget's disease of bone
Autor: Shrinath Shetty, Sahana Shetty, Annie Jennifer Prabhu, Nitin Kapoor, Julie Hepzibah, Thomas Vizhalil Paul
Publikováno v: Journal of Family Medicine and Primary Care, Vol 5, Iss 2, Pp 488-490 (2016)
Solid organ malignancies involving breast, prostate, and lung frequently metastasize to the skeleton. However, the occurrence of Paget's disease and metastatic bone disease in the same patient is uncommon. We report a case of a 63-year-old man who pr
Externí odkaz: https://doaj.org/article/cc025e4a5d7f45b4a0e36863646906cc
Zobrazit plný text záznamu
3
Akademický článek
Hajdu Cheney Syndrome
Autor: Shini Susan Samuel, Shrinath Shetty, Gautham Arunachal, Santosh Koshy, Thomas Vizhalil Paul
Publikováno v: Journal of Clinical and Diagnostic Research, Vol 10, Iss 2, Pp OD07-OD09 (2016)
Hajdu-Cheney Syndrome is a rare genetic disorder characterised by progressive focal bone destruction. It is known to be an autosomal dominant disorder but there have been reports of sporadic cases as well. Although the disease manifestation is found
Externí odkaz: https://doaj.org/article/d697ab56e2fb441e99c1195af1e5ee1d
Zobrazit plný text záznamu
4
Akademický článek
Next-Generation Sequencing-Based Genetic Testing For Familial Partial Lipodystrophy
Autor: Hesarghatta Shyamasunder Asha, MBBS, MD, DNB (Endo), Aaron Chapla, MSc, Shrinath Shetty, MBBS, MD, Nihal Thomas, MBBS, MD, MNAMS, DNB (Endo), FRACP (Endo), FRCP (Edin), FRCP (Glasg)
Publikováno v: AACE Clinical Case Reports, Vol 1, Iss 1, Pp e28-e31 (2015)
ABSTRACT: Objective: Familial partial lipodystrophy (FPL) of the Dunnigan type (FPLD) is an autosomal dominant condition characterized by fat loss in the limbs and trunk, fat accumulation in the head and neck, and early onset diabetes mellitus. Here
Externí odkaz: https://doaj.org/article/7c39c9ae8cd24b7cb0e43b29be672069
Zobrazit plný text záznamu
6
Clinico-radiological characteristics and not laboratory markers are useful in diagnosing diabetic myonecrosis in Asian Indian patients with type 2 diabetes mellitus: A 10-year experience from South India
Autor: Shrinath Shetty, Anish Krishna, H S Asha, Riddhi Das Gupta, Anil Satyaraddi, Roshna Ramchandran, Surjit Singh Haobam, Nihal Thomas, Thomas V Paul
Publikováno v: Journal of Family Medicine and Primary Care
Introduction: Diabetic myonecrosis or muscle infarction is an unusual complication of Type 2 Diabetes, usually associated with longstanding disease. It commonly presents as an acute non-traumatic palpable swelling of the affected muscle with predilec
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9fa01926b4620b73d525aa1d45b6bd44
https://pubmed.ncbi.nlm.nih.gov/30613504
Zobrazit plný text záznamu
8
Hajdu Cheney Syndrome
Autor: Shrinath Shetty, Thomas V Paul, Santosh Koshy, Shini Susan Samuel, Gautham Arunachal
Publikováno v: Journal of Clinical and Diagnostic Research, Vol 10, Iss 2, Pp OD07-OD09 (2016)
Hajdu-Cheney Syndrome is a rare genetic disorder characterised by progressive focal bone destruction. It is known to be an autosomal dominant disorder but there have been reports of sporadic cases as well. Although the disease manifestation is found
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bce6997cb8692f71d7234a239047abb8
https://jcdr.net/articles/PDF/7203/15782_CE(RA1)_F(T)_PF1(EKAK)_PFA(AK)_PF2(PAG).pdf
Zobrazit plný text záznamu
10
Next generation sequencing approach for molecular genetic diagnosis of familial partial lipodystrophy
Autor: Nihal Thomas, H S Asha, V Manika, Shrinath Shetty, Aaron Chapla
Publikováno v: Endocrine Abstracts.
www.PosterPresentations.com •Lipodystrophies are a heterogeneous group of diseases characterized by abnormal fat distribution. •Familial partial lipodystrophy 2 (FPLD2) is autosomal dominant condition due to mutations in the LMNA gene. •It is c
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::36a015a4bc59c7fa06d01f74da700ba1
https://doi.org/10.1530/endoabs.34.p135
Zobrazit plný text záznamu

Vyhledávací nástroje:

Upřesnit hledání

Omezení vyhledávání
Plný text Recenzováno Digitální knihovna AV ČR
Zdroje