Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Syed Athhar Saqqaf"'
Autor:
Syed Athhar Saqqaf, Shantanu Vijay Gomase, Rajendra Borkar, Amar Taksande, Rupesh Rao, Sachin Yedve
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 17, Iss 09, Pp 10-14 (2023)
Introduction: Sickle Cell Disease (SCD) is one of the most common inherited haemoglobinopathies and is associated with high morbidity and mortality, particularly in early childhood among the affected population. Infection is a significant contrib
Externí odkaz:
https://doaj.org/article/bfdb450569fd4647a63cddc6670130dc
Publikováno v:
Journal of Neonatology. 36:194-198
Background Neurosonography has been commonly used for screening in neonatal intensive care unit (NICU), for early detection of defects in the central nervous system (CNS) which include findings like intracranial hemorrhage, hydrocephalus, cerebral ed
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a4b950e54c563724316bb0972ab51e0d
https://doi.org/10.1177/09732179221113674
https://doi.org/10.1177/09732179221113674
Autor:
Rajendra Borkar, Syed Athhar Saqqaf
Publikováno v:
Journal of Pharmaceutical Research International. :679-685
Sickle cell disease is a very common inherited disorder of the hemoglobin. It is inherited in an autosomal recessive manner. Most affected are the people of African, Indian and Arabian origin. It occurs due to change in the single base pair gene wher
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3a506878c30a9c95679ea3903f817040
https://doi.org/10.9734/jpri/2021/v33i59a34319
https://doi.org/10.9734/jpri/2021/v33i59a34319
Publikováno v:
Journal of Evolution of Medical and Dental Sciences. 11:326-328
Sturge - Weber Syndrome (SWS) is an uncommon neuro-oculocutaneous disorder. It is, also known as encephalotrigeminal angiomatosis, which is characterized by angiomas involving the face, choroid, and leptomeninges. Vascular malformation in conjunctiva
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3818b9e33025e099c47bc1714406582b
https://doi.org/10.14260/jemds/2022/63
https://doi.org/10.14260/jemds/2022/63
Publikováno v:
Journal of Evolution of Medical and Dental Sciences. 10:2684-2686
Beckwith - Wiedemann Syndrome (BWS) usually present at birth is an overgrowth disorder, characterized by variable spectrum of clinical findings. The classical features include macrosomia, macroglossia, midline abdominal wall defects, hypoglycaemia in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1e2759a454430d463ecb317e8a6ea6e3
https://doi.org/10.14260/jemds/2021/547
https://doi.org/10.14260/jemds/2021/547
Publikováno v:
Journal of Evolution of Medical and Dental Sciences. 10:2689-2691
Encephalocele is a form of neural tube defect affecting many children, more common in the occipital regions. The frontoethmoidal encephaloceles (FEE) are rare and the aetiology is unclear since it varies genetically and is linked to multiple reasons.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8aecd274a5c2ad0dcbf341811e2b1419
https://doi.org/10.14260/jemds/2021/549
https://doi.org/10.14260/jemds/2021/549
Publikováno v:
Journal of Evolution of Medical and Dental Sciences. 10:2535-2537
It is difficult to diagnose pancreatic cysts in children. Any previous history of acute pancreatitis is very important because it can lead to a wide set of complications like pseudocyst, pancreatic necrosis, splenic venous thrombosis etc. The most kn
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::90439c03ccaf514d5781a0cb46d625ec
https://doi.org/10.14260/jemds/2021/520
https://doi.org/10.14260/jemds/2021/520