Zobrazeno 1 - 10
of 210
pro vyhledávání: '"Jyotsna M Joshi"'
Publikováno v:
Medical Journal of Dr. D.Y. Patil Vidyapeeth, Vol 14, Iss 3, Pp 255-264 (2021)
Pulmonary hypertension (PH) is a progressive disorder of the pulmonary vasculature caused due to vasoconstriction, vasodestruction, or vaso-obliteration. PH results from heterogeneous pathophysiologic mechanisms culminating in elevation of mean pulmo
Externí odkaz:
https://doaj.org/article/4730803e6e7d45e5b9c79100783d5b9c
Autor:
Sheetu Singh, Bharat Bhushan Sharma, Mohan Bairwa, Dipti Gothi, Unnati Desai, Jyotsna M Joshi, Deepak Talwar, Abhijeet Singh, Raja Dhar, Ambika Sharma, Bineet Ahluwalia, Daya K Mangal, Nirmal K Jain, Khushboo Pilania, Vijay Hadda, Parvaiz A Koul, Shanti Kumar Luhadia, Rajesh Swarnkar, Shailender Nath Gaur, Aloke G Ghoshal, Amita Nene, Arpita Jindal, Bhavin Jankharia, Chetambath Ravindran, Dhruv Choudhary, Digambar Behera, D J Christopher, Gopi C Khilnani, Jai Kumar Samaria, Harpreet Singh, Krishna Bihari Gupta, Manju Pilania, Manohar L Gupta, Narayan Misra, Nishtha Singh, Prahlad R Gupta, Prashant N Chhajed, Raj Kumar, Rajesh Chawla, Rajendra K Jenaw, Rakesh Chawla, Randeep Guleria, Ritesh Agarwal, R Narsimhan, Sandeep Katiyar, Sanjeev Mehta, Sahajal Dhooria, Sushmita R Chowdhury, Surinder K Jindal, Subodh K Katiyar, Sudhir Chaudhri, Neeraj Gupta, Sunita Singh, Surya Kant, Zarir Udwadia, Virendra Singh, Ganesh Raghu
Publikováno v:
Lung India, Vol 37, Iss 4, Pp 359-378 (2020)
Background: Interstitial lung disease (ILD) is a complex and heterogeneous group of acute and chronic lung diseases of several known and unknown causes. While clinical practice guidelines (CPG) for idiopathic pulmonary fibrosis (IPF) have been recent
Externí odkaz:
https://doaj.org/article/780359bc9ef34f2ea4b078f714704bcf
Publikováno v:
Lung India, Vol 37, Iss 5, Pp 415-420 (2020)
Background: Sleep-disordered breathing (SDB), predominantly obstructive sleep apnea (OSA), is a frequent phenomenon in interstitial lung disease (ILD) and may be associated with significant morbidity and mortality. Methodology: A prospective, observa
Externí odkaz:
https://doaj.org/article/4066677ea76b477782538fb7ee8e3588
Autor:
Unnati Desai, Jyotsna M Joshi
Publikováno v:
Lung India, Vol 36, Iss 1, Pp 3-7 (2019)
Background: Drug-resistant tuberculosis (DR-TB) is a global problem with only 52% reported cure rate. Extrapulmonary (EP) DR-TB poses a formidable diagnostic, therapeutic challenge. We aimed to study their clinical profile and treatment outcomes unde
Externí odkaz:
https://doaj.org/article/3a4749955d2449caa328c903c0f726bf
Publikováno v:
Lung India, Vol 36, Iss 4, Pp 345-348 (2019)
Hermansky-Pudlak syndrome (HPS) is an extremely subtile autosomal recessive disorder characterized by tyrosinase-positive oculocutaneous albinism (Ty-pos OCA), bleeding tendencies, and systemic complications associated to lysosomal dysfunction. The m
Externí odkaz:
https://doaj.org/article/4e595df5d19f4932a8c93f0f4cbf5587
Publikováno v:
Lung India, Vol 36, Iss 4, Pp 313-318 (2019)
Background: Obliterative bronchiolitis (OB) forms a major proportion of chronic airway diseases (CADs). OB is often misdiagnosed and included under the umbrella term 'chronic obstructive pulmonary disease'. We set out to identify the proportion of OB
Externí odkaz:
https://doaj.org/article/ca06d9ec49c74c5ea285371a7fcb0cce
Autor:
Unnati Desai, Jyotsna M Joshi
Publikováno v:
Lung India, Vol 35, Iss 6, Pp 488-493 (2018)
Background: The World Health Organization drug-resistant tuberculosis (DR-TB) 2016 guidelines reclassified para-aminosalicylic acid (PAS) as Group D3 “add-on” drug. We studied our DR-TB data wherein PAS was widely and preferably used as a substit
Externí odkaz:
https://doaj.org/article/dec2371771ef49489163cd9264e55ec4
Publikováno v:
Indian Journal of Pathology and Microbiology, Vol 61, Iss 1, Pp 85-89 (2018)
A 60-year-old female presented with dyspnea, cough, and chest pain with a left hilar mass lesion. In our case, clinicoradiological correlation, bronchoscopy, and computed tomography-guided biopsy revealed the diagnosis of primary pulmonary non-Hodgki
Externí odkaz:
https://doaj.org/article/8f026859f1af40e79ab449d4ef8ec5d2
Autor:
Unnati Desai, Jyotsna M Joshi
Publikováno v:
Lung India, Vol 35, Iss 5, Pp 395-400 (2018)
Background: Intercostal chest drainage is required for varied lung diseases with the pleural involvement. While the conventional method of intercostal drainage (ICD) insertion with the bulky underwater drain (UWD) was the gold standard for management
Externí odkaz:
https://doaj.org/article/d2f251aea5544d83ad1e1e947937617a
Publikováno v:
Medical Journal of Dr. D.Y. Patil Vidyapeeth, Vol 11, Iss 2, Pp 115-120 (2018)
Background: Idiopathic pulmonary fibrosis (IPF) is a progressive idiopathic interstitial pneumonia. Gender-Age-Physiology (GAP) is the first prognostic staging system for IPF which predicts mortality. Disadvantage is the cumbersome diffusion lung cap
Externí odkaz:
https://doaj.org/article/032a502d56194943bf07d36052806f7a