Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1968 4
1970 4
1971 1
1972 2
1973 5
1974 4
1975 4
1976 1
1977 5
1978 3
1979 1
1980 3
1981 5
1982 1
1983 4
1984 5
1985 6
1986 7
1987 2
1988 6
1989 5
1990 10
1991 13
1992 15
1993 14
1994 9
1995 16
1996 21
1997 15
1998 12
1999 18
2000 17
2001 16
2002 18
2003 16
2004 21
2005 17
2006 18
2007 19
2008 19
2009 18
2010 22
2011 23
2012 22
2013 40
2014 28
2015 26
2016 38
2017 26
2018 31
2019 41
2020 32
2021 18
2022 14
2023 14
2024 7

Text availability

Article attribute

Article type

Publication date

Search Results

723 results

Results by year

Filters applied: . Clear all
Page 1
Pulmonary arterial hypertension: pathogenesis and clinical management.
Thenappan T, Ormiston ML, Ryan JJ, Archer SL. Thenappan T, et al. BMJ. 2018 Mar 14;360:j5492. doi: 10.1136/bmj.j5492. BMJ. 2018. PMID: 29540357 Free PMC article. Review.
Pulmonary hypertension is defined as a resting mean pulmonary artery pressure of 25 mm Hg or above. This review deals with pulmonary arterial hypertension (PAH), a type of pulmonary hypertension that primarily affects the pulmonary vascul
Pulmonary hypertension is defined as a resting mean pulmonary artery pressure of 25 mm Hg or above. This review deals w
Williams syndrome.
Twite MD, Stenquist S, Ing RJ. Twite MD, et al. Paediatr Anaesth. 2019 May;29(5):483-490. doi: 10.1111/pan.13620. Epub 2019 May 2. Paediatr Anaesth. 2019. PMID: 30811742 Review.
Patients with Williams syndrome have increased morbidity and mortality under sedation and anesthesia, largely as a result of cardiovascular abnormalities. This review article focuses on new information about Williams syndrome and outlines a structured approach to patients …
Patients with Williams syndrome have increased morbidity and mortality under sedation and anesthesia, largely as a result of cardiovascular …
Alagille syndrome: pathogenesis, diagnosis and management.
Turnpenny PD, Ellard S. Turnpenny PD, et al. Eur J Hum Genet. 2012 Mar;20(3):251-7. doi: 10.1038/ejhg.2011.181. Epub 2011 Sep 21. Eur J Hum Genet. 2012. PMID: 21934706 Free PMC article. Review.
The main clinical and pathological features are chronic cholestasis due to paucity of intrahepatic bile ducts, peripheral pulmonary artery stenosis, minor vertebral segmentation anomalies, characteristic facies, posterior embryotoxon/anterior segment abnormalitie
The main clinical and pathological features are chronic cholestasis due to paucity of intrahepatic bile ducts, peripheral pulmonary
BMPR2 Mutation and Metabolic Reprogramming in Pulmonary Arterial Hypertension.
Cuthbertson I, Morrell NW, Caruso P. Cuthbertson I, et al. Circ Res. 2023 Jan 6;132(1):109-126. doi: 10.1161/CIRCRESAHA.122.321554. Epub 2023 Jan 5. Circ Res. 2023. PMID: 36603064 Review.
Pulmonary arterial hypertension forms the first and most severe of the 5 categories of pulmonary hypertension. ...Widespread metabolic abnormalities are observed in the heart, pulmonary vasculature, and systemic tissues, and may underpin heterogeneity
Pulmonary arterial hypertension forms the first and most severe of the 5 categories of pulmonary hypertension. ...Widespread m
Metabolic reprogramming, oxidative stress, and pulmonary hypertension.
Pokharel MD, Marciano DP, Fu P, Franco MC, Unwalla H, Tieu K, Fineman JR, Wang T, Black SM. Pokharel MD, et al. Redox Biol. 2023 Aug;64:102797. doi: 10.1016/j.redox.2023.102797. Epub 2023 Jun 24. Redox Biol. 2023. PMID: 37392518 Free PMC article. Review.
The more we uncover the role mitochondria play in pulmonary vascular disease, the more apparent it becomes that multiple pathways are involved. ...We know that nitric oxide signaling, glucose metabolism, fatty acid oxidation, and the TCA cycle are abnormal in PAH, a …
The more we uncover the role mitochondria play in pulmonary vascular disease, the more apparent it becomes that multiple pathways are …
Understanding the Pathophysiology, Implications, and Treatment Options of Patent Ductus Arteriosus in the Neonatal Population.
Conrad C, Newberry D. Conrad C, et al. Adv Neonatal Care. 2019 Jun;19(3):179-187. doi: 10.1097/ANC.0000000000000590. Adv Neonatal Care. 2019. PMID: 30720481 Review.
BACKGROUND: Patent ductus arteriosus (PDA) is the persistence of a fetal shunt between the pulmonary artery and the aorta. This structure normally closes in the first 3 days after birth; however, closure is delayed in up to 80% of infants born at 25 to 28 weeks of g …
BACKGROUND: Patent ductus arteriosus (PDA) is the persistence of a fetal shunt between the pulmonary artery and the aorta. Thi …
Hermansky-Pudlak Syndrome.
El-Chemaly S, Young LR. El-Chemaly S, et al. Clin Chest Med. 2016 Sep;37(3):505-11. doi: 10.1016/j.ccm.2016.04.012. Epub 2016 Jun 30. Clin Chest Med. 2016. PMID: 27514596 Free PMC article. Review.
HPS pulmonary fibrosis shows many of the clinical, radiologic, and histologic features found in idiopathic pulmonary fibrosis, but occurs at a younger age. Despite knowledge of the underlying genetic defects, there are currently no definitive therapeutic or preventi …
HPS pulmonary fibrosis shows many of the clinical, radiologic, and histologic features found in idiopathic pulmonary fibrosis, …
Pulmonary arteriovenous malformations.
Tellapuri S, Park HS, Kalva SP. Tellapuri S, et al. Int J Cardiovasc Imaging. 2019 Aug;35(8):1421-1428. doi: 10.1007/s10554-018-1479-x. Epub 2018 Nov 1. Int J Cardiovasc Imaging. 2019. PMID: 30386957 Review.
Pulmonary arteriovenous malformation, a condition most commonly associated with hereditary hemorrhagic telangiectasia, is an abnormal communication between the pulmonary artery and pulmonary vein without an intervening capillary communication. .
Pulmonary arteriovenous malformation, a condition most commonly associated with hereditary hemorrhagic telangiectasia, is an abnor
Congenitally Corrected Transposition of the Great Arteries: Anatomic, Physiologic Repair, and Palliation.
Spigel Z, Binsalamah ZM, Caldarone C. Spigel Z, et al. Semin Thorac Cardiovasc Surg Pediatr Card Surg Annu. 2019;22:32-42. doi: 10.1053/j.pcsu.2019.02.008. Semin Thorac Cardiovasc Surg Pediatr Card Surg Annu. 2019. PMID: 31027562 Review.
Congenitally corrected transposition of the great arteries (ccTGA) is a lesion that rarely occurs in isolation. The presenting physiology of ccTGA is predominantly secondary to the concurrent cardiac lesions; however, as the child ages, unrepaired ccTGA results in progress …
Congenitally corrected transposition of the great arteries (ccTGA) is a lesion that rarely occurs in isolation. The presenting physiology
Pediatric Pulmonary Arterial Hypertension.
Frank BS, Ivy DD. Frank BS, et al. Pediatr Clin North Am. 2020 Oct;67(5):903-921. doi: 10.1016/j.pcl.2020.06.005. Pediatr Clin North Am. 2020. PMID: 32888689 Review.
Pulmonary hypertension (PH), the syndrome of increased pressure in the pulmonary arteries, is associated with significant morbidity and mortality for affected children and is associated with a variety of potential underlying causes. Several pulmonary arterial
Pulmonary hypertension (PH), the syndrome of increased pressure in the pulmonary arteries, is associated with significant morb
723 results