Zobrazeno 1 - 10
of 23
pro vyhledávání: '"Shatanik Sarkar"'
Publikováno v:
The Egyptian Journal of Bronchology, Vol 11, Iss 1, Pp 62-65 (2017)
Abstract A 7-year-old girl presented with severe pallor, cough, and massive hemoptysis. She had been previously hospitalized twice within the time span of 2 years for severe pallor and hemoptysis, each time requiring 2U of blood transfusion. In the r
Externí odkaz:
https://doaj.org/article/ad89f71fceeb4f42a418018739e24190
Publikováno v:
Indian Journal of Health Sciences and Biomedical Research KLEU, Vol 11, Iss 1, Pp 86-88 (2018)
Acquired epileptic aphasia, otherwise known as Landau–Kleffner syndrome, is a childhood epilepsy syndrome, characterized by acquired aphasia, seizures, behavioral abnormalities, and abnormal electroencephalography (EEG), in various combinations. So
Externí odkaz:
https://doaj.org/article/efac11bfda5d408a891a2c9ebbfb350a
Publikováno v:
Indian Journal of Health Sciences and Biomedical Research KLEU, Vol 9, Iss 3, Pp 297-302 (2016)
Background: In spite of major advances in the knowledge of fetal and perinatal medicine, perinatal asphyxia is one of the significant causes of mortality and long-term morbidity. Outcome of asphyxiated babies depends on the severity of hypoxia which
Externí odkaz:
https://doaj.org/article/b8be7e05515440bb90e13be4a2650758
Publikováno v:
Indian Journal of Paediatric Dermatology, Vol 17, Iss 2, Pp 154-156 (2016)
Externí odkaz:
https://doaj.org/article/6bcca87c47ea429b83b2ec2401f9aadf
Publikováno v:
Indian Dermatology Online Journal, Vol 5, Iss 2, Pp 170-172 (2014)
Morphea is a variant of localized scleroderma in which lesions are usually limited to the skin and subcutaneous tissue. Pansclerotic morphea is a rare atrophying and sclerosing type of morphea. It can follow a comparatively benign course with spontan
Externí odkaz:
https://doaj.org/article/2e8bb7c93abe490c95a43e6778efd129
Publikováno v:
Indian Journal of Dermatology, Vol 60, Iss 2, Pp 215-215 (2015)
Goltz syndrome or Focal Dermal Hypoplasia is a rare multisystem disorder, involving all the three germ cell layers. The disease is thought to be inherited in X-linked dominant fashion with heterogeneous mutations of the PORCN gene at Xp11.23 locus. M
Externí odkaz:
https://doaj.org/article/4141988c2e3b4332b38d5b5d6fbf39e4
Publikováno v:
Journal of Nepal Paediatric Society. 42:80-86
Introduction: This study was undertaken to evaluate the effect of nutrition on kidney size and to determine the correlation between renal parameters and different anthropometric parameters. Methods: This hospital-based descriptive observational study
Publikováno v:
Journal of Nepal Paediatric Society. 41:111-114
Recurrent respiratory tract infections, a cause of concern for both parents and paediatricians, can have various etiologies entitled to different organ systems. Diagnosing the exact cause warrants both clinical acumen and timely investigations. Here,
Publikováno v:
Journal of Nepal Paediatric Society. 39:123-126
Recurrent nasal obstruction, a common symptom in pediatric practice, can lead to some unusual diagnosis rarely. Non- response to standard treatment warrants further delineation of local anatomy, particularly if symptoms occur unilaterally. Here, we r
Publikováno v:
The Egyptian Journal of Bronchology, Vol 11, Iss 1, Pp 62-65 (2017)
A 7-year-old girl presented with severe pallor, cough, and massive hemoptysis. She had been previously hospitalized twice within the time span of 2 years for severe pallor and hemoptysis, each time requiring 2U of blood transfusion. In the recent epi