Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Swetlana Mukherjee"'
Publikováno v:
Pediatric Hematology Oncology Journal, Vol 7, Iss 4, Pp S42-S43 (2022)
Externí odkaz:
https://doaj.org/article/92a72c71c7884be4a99516ef79d54b7d
Publikováno v:
Pediatric Hematology Oncology Journal, Vol 7, Iss 4, Pp S43- (2022)
Externí odkaz:
https://doaj.org/article/f1e03d38b81c47a792eb50780d1842e4
Publikováno v:
European Journal of Rheumatology, Vol 9, Iss 1, Pp 58-59 (2022)
Externí odkaz:
https://doaj.org/article/4adf018534b44d80943f48f6b205c966
Autor:
Swetlana Mukherjee, Pradeep Kumar Gunasekaran, Lokesh Saini, Arushi Gahlot Saini, Dipankar De, Prahbhjot Malhi
Publikováno v:
Tropical Doctor. 52:572-575
The phenotypical profile of cutaneous and ocular manifestations in neurocutaneous syndromes is inconstant. We made a cross-sectional study over 18 months of children with neurocutaneous syndromes aged between 1–15 years. A varied presentation was f
Autor:
Nandita Kakkar, Rajni Kumrah, Yamini Sharma, Himanshi Chaudhary, Avinash Sharma, Nameirakpam Johnson, Rakesh Kumar Pilania, Swetlana Mukherjee, Amanpreet Kaur, Pandiarajan Vignesh
Publikováno v:
Rheumatology International. 41:1875-1882
Camptodactyly-arthropathy-coxa vara-pericarditis (CACP) syndrome is a rare familial arthropathy of childhood, commonly misdiagnosed as juvenile idiopathic arthritis. It is characterized by non-inflammatory arthropathy, coxa vara deformity, and steril
Publikováno v:
Med J Armed Forces India
BACKGROUND: The variation in heights beyond high altitude has different effects on the cardiorespiratory profile of individuals because of variation in oxygen density with every thousand feet. This study was planned to analyze and compare the effects
Publikováno v:
European Journal of Rheumatology, Vol 9, Iss 1, Pp 58-59 (2022)
Publikováno v:
Archives of disease in childhood. 106(1)
A boy aged 3 years presented with mild motor delay. He could walk independently but could not run. On examination, he was hypotonic and had multiple cafe-au-lait spots (CALS; >6) on the back (figure 1). There was no family history and/or other featur
Publikováno v:
Pediatric neurology. 96
Autor:
Dipankar De, Chirag Kamal Ahuja, Priyanka Madaan, Lokesh Saini, Kim Vaiphei, Naveen Sankhyan, Swetlana Mukherjee, Shivan Kesavan
Publikováno v:
Archives of Disease in Childhood. 105:797-797
An 18-month-old boy presented with a swelling on his back, global developmental delay, and seizures. At birth, he had a tuft of hair on his left lower back which developed into an ill-defined, doughy plaque with patchy hyperpigmentation and hypopigme