Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Aparna R. Rao"'
Publikováno v:
The Annals of otology, rhinology, and laryngology. 120(11)
Objectives: We describe the clinical presentation of a 7 1/2-year-old boy with a history of mild intermittent asthma who presented with left lung collapse and was found to have plastic bronchitis. Methods: We reviewed the patient chart and imaging re
Autor:
Aparna R. Rao, Hari P.R. Bandla
Publikováno v:
Sleep Disordered Breathing in Children ISBN: 9781607617242
Gastroesophageal reflux (GER) is a common clinical problem in children. Although GER can be physiological in infancy, a significant number of children will develop gastroesophageal reflux disease (GERD), as evidenced by the presence of accompanying
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::450456f4a83eb28c8e92a6f3bfbbedc2
https://doi.org/10.1007/978-1-60761-725-9_31
https://doi.org/10.1007/978-1-60761-725-9_31
Autor:
Gabriela Gheorghe, Peter L. Havens, Anne B. Warwick, Bruce M. Camitta, Swati Kumar, Sweta Gupta, Aparna R. Rao, Christopher H. Cogbill
Publikováno v:
Journal of pediatric hematology/oncology. 33(3)
A 5.5-year-old asymptomatic Hispanic/African American male presented with matted lymph nodes in the neck and reticulonodular opacities in the right upper lung. An extensive diagnostic work up was performed to rule out infectious etiologies. Biopsies
Publikováno v:
Journal of clinical microbiology. 47(8)
Identification of new immunogenic antigens that diagnose initial Pseudomonas aeruginosa infections in patients with cystic fibrosis (CF) alone or as an adjunct to microbiology is needed. In the present study, a proteomic analysis was performed to obt
Publikováno v:
Pediatric emergency care. 22(5)
Dyspnea and tachypnea are common presenting complaints in an emergency department. Respiratory and cardiac causes are the most common etiology. Functional respiratory disorders should be considered in patients with atypical presentation to avoid exte
Publikováno v:
Pediatric transplantation. 9(2)
We report a case of a patient who received a bilateral lung transplant for end-stage lung disease secondary to Gauchers type-1 disease with no evidence of recurrence of the disease in the transplanted lung.
Autor:
Aparna R Rao, Baha Al-Shawwa
Publikováno v:
Journal of Medical Case Reports
Journal of Medical Case Reports, Vol 1, Iss 1, p 24 (2007)
Journal of Medical Case Reports, Vol 1, Iss 1, p 24 (2007)
Background Cystic fibrosis (CF) is an autosomal recessive disease that is predominantly seen in the Caucasian population and involves multiple organs. Traditionally it has been thought that the kidney is the only organ which does not seem to be gener