Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Tapan Dhibar"'
Publikováno v:
Medical Journal of Dr. D.Y. Patil University, Vol 9, Iss 6, Pp 753-755 (2016)
We hereby describe a 7-month-old female baby, born to first-degree cousins, who was initially diagnosed as meningitis based on the features of seizures and dystonia with fever. Detailed review of brain imaging and high urinary 3-hydroxy (3-OH) glutar
Externí odkaz:
https://doaj.org/article/d9eca76fd2e247b38678dc2b8b796464
Publikováno v:
Medical Journal of Dr. D.Y. Patil University, Vol 6, Iss 3, Pp 308-309 (2013)
Abnormal hyperdensity of intracranial blood vessels on non-contrast computed tomography scan (NCCT) may be found in cases with raised hematocrit. This finding not only simulates the appearance of a contrast enhanced CT scan but also may mimic dural v
Externí odkaz:
https://doaj.org/article/75e11cccea1247669ee523e220c0afae
Publikováno v:
Indian Journal of Musculoskeletal Radiology. 4:124-127
The other name for Van Buchem disease is hyperostosis corticalis generalisata. It is an uncommon genetic bone condition characterized by aberrant metaphyseal expansion of the tubular bones and hyperostosis and sclerosis of the craniofacial bones. It
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::09961eaf4125387ca7e84b99f7531e19
https://doi.org/10.25259/ijmsr_29_2022
https://doi.org/10.25259/ijmsr_29_2022
Autor:
Aprateem Mukherjee, Amitabha Chattopadhyay, Amit Kumar Das, Kiran Sankar Saha, Bhaskar Bhattacharyya, Tapan Dhibar, Arijit Roy
Publikováno v:
Journal of Evidence Based Medicine and Healthcare, Vol 7, Iss 46, Pp 2730-2734 (2020)
BACKGROUND Chordomas are tumours presumed to originate from the remnants of embryonic notochord. They present a diagnostic challenge as they can occur in any region within the craniospinal axis and are rare with an incidence of less than 0.1 / 100,00
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::17de9ca376af5cc76c7e4cdfe8e54c61
https://doi.org/10.18410/jebmh/2020/561
https://doi.org/10.18410/jebmh/2020/561
Publikováno v:
Journal of Evolution of Medical and Dental Sciences. 8:2041-2044
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1748110f5c1ec273afe8f4f9a7515d7a
https://doi.org/10.14260/jemds/2019/450
https://doi.org/10.14260/jemds/2019/450
Publikováno v:
Journal of Pediatric Neurology. :415-417
Marinesco-Sjogren syndrome (MSS) is a rare autosomal recessive disorder characterized clinically by cerebellar ataxia, congenitalBRcataracts, mental and physical retardation, skeletal anomalies, motor and sensory neuropathy and myopathy. Cerebellar a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::63174f604787ea2dcb59e27e51719271
https://doi.org/10.3233/jpn-2009-0323
https://doi.org/10.3233/jpn-2009-0323
Autor:
Rakesh Mondal, Supratim Datta, Madhumita Nandi, Tapan Dhibar, Balai Chandra Karmakar, Krishnendu Mukherjee
Publikováno v:
The Indian Journal of Pediatrics. 75:290-294
We describe two cases of Rosai-Dorfman disease. One of them had commonly described cervical adenopathy and the second with the very rare bilateral orbital involvement. Both our cases required treatment with steroids because of the danger of pressure
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::77dba1c1902737d3423e9b8c80afb17e
https://doi.org/10.1007/s12098-008-0063-0
https://doi.org/10.1007/s12098-008-0063-0
Publikováno v:
South African Journal of Child Health, Volume: 9, Issue: 4, Pages: 137-139, Published: NOV 2015
South African Journal of Child Health; Vol 9, No 4 (2015); 137-139
South African Journal of Child Health; Vol 9, No 4 (2015); 137-139
Posterior reversible encephalopathy syndrome (PRES) (also called reversible posterior leukoencephalopathy syndrome) is a mostly transient and reversible neurological disorder clinically characterised by headache, seizures, blindness and altered consc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1efb3d87ce583e89a30003c0c50350ba
http://www.scielo.org.za/scielo.php?script=sci_arttext&pid=S1999-76712015000400009&lng=en&tlng=en
http://www.scielo.org.za/scielo.php?script=sci_arttext&pid=S1999-76712015000400009&lng=en&tlng=en
Autor:
Bhaskar, Bhattacharyya, Soumitra Kumar, Ghosh, Tapan, Dhibar, Amitabha, Chattopadhyay, Samarendra Nath, Ghosh, Ashok Kumar, Bhadra, Prabhat Kumar, Ghorai
Publikováno v:
Journal of the Indian Medical Association. 111(5)
Extramedullary haematopoiesis leading to spinal cord compression is a rare complication of thalassaemia. An interesting case has been reported where a diagnosis of thalassaemia intermedia was made at the age of 35 years in a male patient with no hist
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::393501f69f48363f65c4c30b00d0e3ca
https://pubmed.ncbi.nlm.nih.gov/24765699
https://pubmed.ncbi.nlm.nih.gov/24765699
Publikováno v:
Indian pediatrics. 47(2)
We report a 7 year old girl with deep vein thrombosis due to combined protein C and protein S deficiency, who presented with swollen left thigh and restriction of movement of left hip joint.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4447f5d88922ddd4733277e2b8e27994
https://pubmed.ncbi.nlm.nih.gov/20228434
https://pubmed.ncbi.nlm.nih.gov/20228434