Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Fatima Neemuchwala"'
Publikováno v:
Frontiers in Pediatrics, Vol 9 (2021)
In response to the novel coronavirus (COVID-19) pandemic, all in-person cystic fibrosis (CF) appointments were converted to telemedicine visits at UCSF Benioff Children's Hospital. The purpose of our study was to learn about the experiences that pati
Externí odkaz:
https://doaj.org/article/de1cc5d3e3384bc7b4fb4cbb18921fde
Autor:
Caroline T. Simon, MD, Toby C. Lewis, MD, MPH, Fatima Neemuchwala, MD, Manuel Arteta, MD, Raja Rabah, MD
Publikováno v:
Human Pathology: Case Reports, Vol 13, Iss , Pp 33-35 (2018)
Pulmonary alveolar microlithiasis (PAM) is a rare autosomal recessive genetic disease characterized by intraalveolar psammomatous calcium phosphate deposition. Patients with PAM are often asymptomatic until the third or fourth decade, when they most
Externí odkaz:
https://doaj.org/article/6f18d463cd8944798e5a40eafa2af2ae
Publikováno v:
Global Pediatric Health, Vol 4 (2017)
Cystic fibrosis (CF) patients are at risk for developing pelvic (urinary and/or fecal) incontinence due to progressive weakness of pelvic floor muscles secondary to recurrent episodes of coughing and respiratory infections. Many patients do not bring
Externí odkaz:
https://doaj.org/article/33bf08182f2c46feac48f8c0b07dd324
Autor:
Janet T. Lim, Ngoc P. Ly, Shaina M. Willen, Kensho Iwanaga, Elizabeth R. Gibb, Marilynn Chan, Gwynne D. Church, Fatima Neemuchwala, Meghan E. McGarry
Publikováno v:
Pediatric Pulmonology. 57:1238-1244
The COVID-19 pandemic impacted many households due to shelter-in-place orders and economic hardship. People with cystic fibrosis (CF) experienced increased food insecurity compared to the general population before the pandemic, even though adequate f
Publikováno v:
Frontiers in Pediatrics
Frontiers in Pediatrics, Vol 9 (2021)
Frontiers in Pediatrics, Vol 9 (2021)
In response to the novel coronavirus (COVID-19) pandemic, all in-person cystic fibrosis (CF) appointments were converted to telemedicine visits at UCSF Benioff Children's Hospital. The purpose of our study was to learn about the experiences that pati
Publikováno v:
Case Reports in Pediatrics
Case Reports in Pediatrics, Vol 2018 (2018)
Case Reports in Pediatrics, Vol 2018 (2018)
Newborn screening for cystic fibrosis (CF) enables early diagnosis and treatment leading to improved health outcomes for patients with CF. Although the sensitivity of newborn screening is high, false-negative results can still occur which can be misl
Autor:
Fatima Neemuchwala, Timothy D. Johnson, Ramon Sanchez-Jacob, Christopher A Flask, Eunjee Lee, Samya Z. Nasr, Yuxi Pang, Craig J. Galbán, Aleksa B. Fortuna, Maryam Ghadimi Mahani
Publikováno v:
Pediatric radiology. 50(7)
Assessment tools for early cystic fibrosis (CF) lung disease are limited. Detecting early pulmonary disease is crucial to increasing life expectancy by starting interventions to slow the progression of the pulmonary disease with the many treatment op
Autor:
Fatima Neemuchwala, Rama Jasty, Antonia P Popova, Raja Rabah, Amanda Sankar, Moaaz Soliman, Erika A. Newman
Publikováno v:
Journal of pediatric hematology/oncology. 40(7)
A 14-year-old male patient presented with a nonproductive cough, weight loss, fatigue, and malaise. A chest radiograph showed large bilateral cavitary lung lesions in both upper and lower lobes that failed to improve with antibiotics and anti-inflamm