Zobrazeno 1 - 10
of 141
pro vyhledávání: '"Csaba, Galambos"'
Autor:
Courtney Breckenfelder, BS, Catherine C. Dawson-Gore, MD, MS, Csaba Galambos, MD, PhD, Kristine S. Corkum, MD, David Partrick, MD, S. Christopher Derderian, MD
Publikováno v:
Annals of Thoracic Surgery Short Reports, Vol 2, Iss 3, Pp 400-403 (2024)
Congenital pulmonary airway malformations (CPAMs) are cystic lung lesions often detected prenatally. Resection is often recommended for potential recurrent infections and malignancy. This report describes a case of a 14-year-old female patient who pr
Externí odkaz:
https://doaj.org/article/9ae4e8c47beb42f3847d826b04240610
Autor:
Esra Yıldız Bölükbaşı, Justyna A. Karolak, Przemyslaw Szafranski, Tomasz Gambin, Nicholas Willard, Steven H. Abman, Csaba Galambos, John P. Kinsella, Paweł Stankiewicz
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 10, Iss 11, Pp n/a-n/a (2022)
Abstract Background Alveolar capillary dysplasia with misalignment of pulmonary veins (ACDMPV) results from haploinsufficiency of the mesenchymal transcription factor FOXF1 gene. To date, only one case of an ACDMPV‐causative CNV deletion inherited
Externí odkaz:
https://doaj.org/article/0451161a9ae846f480b268911a95f375
Autor:
Jessica L. Bloom, Benjamin Frank, Jason P. Weinman, Csaba Galambos, Sean T. O’Leary, Deborah R. Liptzin, Robert C. Fuhlbrigge
Publikováno v:
Pediatric Rheumatology Online Journal, Vol 19, Iss 1, Pp 1-8 (2021)
Abstract Background Respiratory conditions are the leading cause of hospitalization and death in children with Trisomy 21 (T21). Diffuse alveolar hemorrhage (DAH) occurs at higher frequency in children with T21; yet, it is not widely studied nor is t
Externí odkaz:
https://doaj.org/article/e1bf74592ef549709a860d7439baea72
Autor:
Lindel C. Dewberry, Andrew Trecartin, Csaba Galambos, Sarah A. Hilton, Kimberly Dannull, Michael V. Zaretsky, Nicholas Behrendt, Henry L. Galan, Ahmed I. Marwan, Kenneth W. Liechty
Publikováno v:
Clinical Case Reports, Vol 8, Iss 1, Pp 18-23 (2020)
Abstract A foregut duplication cyst occurring together with both a congenital cystic pulmonary airway malformation and extralobar pulmonary sequestration is an unusual combination. Prenatal ultrasound, MRI, and postnatal CT are helpful for operative
Externí odkaz:
https://doaj.org/article/04b93191397346d188f6435c66144fb7
Autor:
Justyna A. Karolak, Carrie L. Welch, Christian Mosimann, Katarzyna Bzdęga, James D. West, David Montani, Mélanie Eyries, Mary P. Mullen, Steven H. Abman, Matina Prapa, Stefan Gräf, Nicholas W. Morrell, Anna R. Hemnes, Frédéric Perros, Rizwan Hamid, Malcolm P. O. Logan, Jeffrey Whitsett, Csaba Galambos, Paweł Stankiewicz, Wendy K. Chung, Eric D. Austin
Publikováno v:
American Journal of Respiratory and Critical Care Medicine. 207:855-864
Autor:
Lindel Dewberry, MD, Jason Bunn, BS, Csaba Galambos, MD, PhD, Henry L. Galan, MD, Michael V. Zaretsky, MD, Nicholas Behrendt, MD, Regina Reynolds, MD, Mariana Meyers, MD, Ahmed I. Marwan, MD, Kenneth W. Liechty, MD
Publikováno v:
Journal of Pediatric Surgery Case Reports, Vol 34, Iss C, Pp 13-16 (2018)
A prenatal ultrasound (US) at 21 weeks estimated gestational age (EGA) identified a left intrathoracic homogenously echogenic microcystic mass with mediastinal shift and a CPAM volume ratio (CVR) of 0.78 (Fig. 1). A fetal magnetic resonance imaging (
Externí odkaz:
https://doaj.org/article/cb55a7780b514291b00a2f0e1eee9e4d
Autor:
Jessica L. Bloom, Clara Lin, Lisa Imundo, Stephen Guthery, Shelly Stepenaskie, Csaba Galambos, Amy Lowichik, John F. Bohnsack
Publikováno v:
Pediatric Rheumatology Online Journal, Vol 15, Iss 1, Pp 1-12 (2017)
Abstract Background H Syndrome is an autosomal recessive disorder characterized by cutaneous hyperpigmentation, hypertrichosis, and induration with numerous systemic manifestations. The syndrome is caused by mutations in SLC29A3, a gene located on ch
Externí odkaz:
https://doaj.org/article/03ecd118f0934d75a9d73088b84b55b9
Autor:
Jason P. Weinman, David A. Mong, LaDonna J. Malone, Dunbar D. Ivy, Robin R. Deterding, Csaba Galambos
Publikováno v:
Pediatric Radiology. 52:2549-2556
Autor:
Douglas Bush, Kristine Wolter-Warmerdam, Brandie D. Wagner, Csaba Galambos, D.Dunbar Ivy, Steven H. Abman, Deven McMorrow, Francis Hickey
Publikováno v:
Pulmonary Circulation, Vol 9 (2019)
Past studies have shown that lung angiogenic signaling may be abnormal in children with Down syndrome, but whether differences in circulating angiogenic proteins can identify pulmonary hypertension in children with Down syndrome is unknown. A prospec
Externí odkaz:
https://doaj.org/article/27c9f351a20943599ce10f4aadef0796
Autor:
Justyna A, Karolak, Carrie L, Welch, Christian, Mosimann, Katarzyna, Bzdega, James D, West, David, Montani, Mélanie, Eyries, Mary P, Mullen, Steven H, Abman, Matina, Prapa, Stefan, Gräf, Nicholas W, Morrell, Anna R, Hemnes, Frédéric, Perros, Rizwan, Hamid, Malcolm P O, Logan, Jeffrey, Whitsett, Csaba, Galambos, Paweł, Stankiewicz, Wendy K, Chung, Eric D, Austin
Publikováno v:
American journal of respiratory and critical care medicine.
Over the past decade recognition of the profound impact of the T-box 4 (TBX4) gene, which encodes a member of the evolutionarily conserved family of T-box-containing transcription factors, upon respiratory diseases has emerged. The developmental impo