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
1959 1
1964 1
1967 5
1968 8
1969 12
1970 12
1971 14
1972 14
1973 20
1974 16
1975 41
1976 21
1977 22
1978 27
1979 30
1980 31
1981 19
1982 27
1983 48
1984 54
1985 45
1986 49
1987 40
1988 47
1989 60
1990 62
1991 56
1992 67
1993 65
1994 95
1995 81
1996 102
1997 101
1998 130
1999 121
2000 114
2001 103
2002 101
2003 111
2004 140
2005 140
2006 120
2007 117
2008 115
2009 154
2010 156
2011 169
2012 177
2013 182
2014 171
2015 175
2016 201
2017 167
2018 171
2019 208
2020 187
2021 126
2022 58
2023 40
2024 24

Text availability

Article attribute

Article type

Publication date

Search Results

4,578 results

Results by year

Filters applied: . Clear all
Quoted phrase not found in phrase index: "Abnormal respiratory system physiology"
Page 1
Congenital diaphragmatic hernia.
Zani A, Chung WK, Deprest J, Harting MT, Jancelewicz T, Kunisaki SM, Patel N, Antounians L, Puligandla PS, Keijzer R. Zani A, et al. Nat Rev Dis Primers. 2022 Jun 1;8(1):37. doi: 10.1038/s41572-022-00362-w. Nat Rev Dis Primers. 2022. PMID: 35650272 Review.
Congenital diaphragmatic hernia (CDH) is a rare birth defect characterized by incomplete closure of the diaphragm and herniation of fetal abdominal organs into the chest that results in pulmonary hypoplasia, postnatal pulmonary hypertension owing to vascular remodelling an
Congenital diaphragmatic hernia (CDH) is a rare birth defect characterized by incomplete closure of the diaphragm and herniation of f
Persistent pulmonary hypertension of the newborn.
Mandell E, Kinsella JP, Abman SH. Mandell E, et al. Pediatr Pulmonol. 2021 Mar;56(3):661-669. doi: 10.1002/ppul.25073. Pediatr Pulmonol. 2021. PMID: 32930508 Review.
Persistent pulmonary hypertension of the newborn (PPHN) is a significant clinical problem characterized by refractory and severe hypoxemia secondary to elevated pulmonary vascular resistance resulting in right-to-left extrapulmonary shunting of deoxygenated blood. ...Survi …
Persistent pulmonary hypertension of the newborn (PPHN) is a significant clinical problem characterized by refractory and severe hypo …
Current and Future Treatments in Primary Ciliary Dyskinesia.
Paff T, Omran H, Nielsen KG, Haarman EG. Paff T, et al. Int J Mol Sci. 2021 Sep 11;22(18):9834. doi: 10.3390/ijms22189834. Int J Mol Sci. 2021. PMID: 34575997 Free PMC article. Review.
Primary ciliary dyskinesia (PCD) is a rare genetic ciliopathy in which mucociliary clearance is disturbed by the abnormal motion of cilia or there is a severe reduction in the generation of multiple motile cilia. Lung damage ensues due to recurrent airway infections, somet …
Primary ciliary dyskinesia (PCD) is a rare genetic ciliopathy in which mucociliary clearance is disturbed by the abnormal motion of c …
Ambroxol in the 21st century: pharmacological and clinical update.
Malerba M, Ragnoli B. Malerba M, et al. Expert Opin Drug Metab Toxicol. 2008 Aug;4(8):1119-29. doi: 10.1517/17425255.4.8.1119. Expert Opin Drug Metab Toxicol. 2008. PMID: 18680446 Review.
Therefore, ambroxol's indication is 'secretolytic therapy in acute and chronic bronchopulmonary diseases associated with abnormal mucus secretion and impaired mucus transport'. OBJECTIVE: The aim of this review is to evaluate the pharmacological and clinical data on …
Therefore, ambroxol's indication is 'secretolytic therapy in acute and chronic bronchopulmonary diseases associated with abnormal muc …
Primary ciliary dyskinesia.
Lobo LJ, Zariwala MA, Noone PG. Lobo LJ, et al. QJM. 2014 Sep;107(9):691-9. doi: 10.1093/qjmed/hcu063. Epub 2014 Mar 19. QJM. 2014. PMID: 24652656 Review.
Primary ciliary dyskinesia (PCD) is an autosomal recessive disorder of cilia structure and function, leading to chronic infections of the respiratory tract, fertility problems and disorders of organ laterality. ...In conjunction with the PCD foundation and lead investigato …
Primary ciliary dyskinesia (PCD) is an autosomal recessive disorder of cilia structure and function, leading to chronic infections of the …
Mitochondria signaling pathways in allergic asthma.
Qian L, Mehrabi Nasab E, Athari SM, Athari SS. Qian L, et al. J Investig Med. 2022 Apr;70(4):863-882. doi: 10.1136/jim-2021-002098. Epub 2022 Feb 15. J Investig Med. 2022. PMID: 35168999 Free PMC article. Review.
Asthma pathophysiology has been tightly associated with mitochondrial dysfunction leading to reduced ATP synthase activity, increased oxidative stress, apoptosis induction, and abnormal calcium homeostasis. Defects of the mitochondrial play an essential role in the pro-rem …
Asthma pathophysiology has been tightly associated with mitochondrial dysfunction leading to reduced ATP synthase activity, increased oxidat …
Neonatal Lateral Epiglottic Defects.
Peterson JD, Goyal V, Puricelli MD, Thatcher A, Smith RJ. Peterson JD, et al. Ann Otol Rhinol Laryngol. 2021 Mar;130(3):311-313. doi: 10.1177/0003489420948546. Epub 2020 Aug 8. Ann Otol Rhinol Laryngol. 2021. PMID: 32772542 Review.
INTRODUCTION: Multiple congenital abnormalities of the epiglottis have been reported and iatrogenic injuries to the larynx and subglottis are well known. ...Both have swallowing difficulties and are gastrostomy dependent. Congenital epiglottic defects include …
INTRODUCTION: Multiple congenital abnormalities of the epiglottis have been reported and iatrogenic injuries to the larynx and …
Pathophysiology, evaluation, and management of sleep disorders in the mucopolysaccharidoses.
Rapoport DM, Mitchell JJ. Rapoport DM, et al. Mol Genet Metab. 2017 Dec;122S:49-54. doi: 10.1016/j.ymgme.2017.08.008. Epub 2017 Aug 25. Mol Genet Metab. 2017. PMID: 28964643 Free article. Review.
Sleep disorders are a frequent manifestation of all types of MPS. Underlying causes are diverse and comprised of both respiratory and central nervous system (CNS) abnormalities. Sleep disordered breathing such as obstructive sleep apnea and nocturnal hypovent …
Sleep disorders are a frequent manifestation of all types of MPS. Underlying causes are diverse and comprised of both respiratory and …
Drug-induced apnea.
Boutroy MJ. Boutroy MJ. Biol Neonate. 1994;65(3-4):252-7. doi: 10.1159/000244061. Biol Neonate. 1994. PMID: 8038291 Review.
At these different stages of development, the child may be abnormally vulnerable to respiratory disorders and apnea, and doses of drugs, without any abnormal side effects in adult patients, can be harmful in younger subjects. ...Other pharmacological families …
At these different stages of development, the child may be abnormally vulnerable to respiratory disorders and apnea, and doses …
Congenital diaphragmatic hernia-associated cardiac dysfunction.
Patel N, Massolo AC, Kipfmueller F. Patel N, et al. Semin Perinatol. 2020 Feb;44(1):151168. doi: 10.1053/j.semperi.2019.07.007. Epub 2019 Jul 30. Semin Perinatol. 2020. PMID: 31420110 Review.
Dysfunction in both right and left ventricles is common in the early neonatal period, contributes to clinical disease severity, and is associated with adverse outcomes including death and ECMO use. Early and routine assessment of ventricular function and pulmonary artery p …
Dysfunction in both right and left ventricles is common in the early neonatal period, contributes to clinical disease severity, and i …
4,578 results