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1964
2025

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

Year Number of Results
1964 1
1967 1
1968 7
1969 4
1970 9
1971 7
1972 5
1973 16
1974 13
1975 14
1976 9
1977 12
1978 11
1979 13
1980 10
1981 19
1982 20
1983 22
1984 31
1985 26
1986 38
1987 29
1988 35
1989 32
1990 42
1991 41
1992 44
1993 39
1994 54
1995 55
1996 62
1997 67
1998 74
1999 64
2000 112
2001 82
2002 91
2003 102
2004 99
2005 97
2006 93
2007 106
2008 102
2009 95
2010 130
2011 118
2012 127
2013 119
2014 125
2015 117
2016 134
2017 115
2018 115
2019 116
2020 153
2021 129
2022 77
2023 85
2024 91
2025 5

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3,390 results

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Page 1
Joubert syndrome: Molecular basis and treatment.
Spahiu L, Behluli E, Grajçevci-Uka V, Liehr T, Temaj G. Spahiu L, et al. J Mother Child. 2023 Feb 22;26(1):118-123. doi: 10.34763/jmotherandchild.20222601.d-22-00034. eCollection 2022 Mar 1. J Mother Child. 2023. PMID: 36803942 Free PMC article. Review.
Other characteristic features are hypotonia with lateral ataxia, intellectual disability/mental retardation, oculomotor apraxia, retinal dystrophy, abnormalities in the respiratory system, renal cysts, hepatic fibrosis, and skeletal changes. ...
Other characteristic features are hypotonia with lateral ataxia, intellectual disability/mental retardation, oculomotor apraxia, retinal dys …
Lung disease manifestations in Down syndrome.
Danopoulos S, Deutsch GH, Dumortier C, Mariani TJ, Al Alam D. Danopoulos S, et al. Am J Physiol Lung Cell Mol Physiol. 2021 Nov 1;321(5):L892-L899. doi: 10.1152/ajplung.00434.2020. Epub 2021 Sep 1. Am J Physiol Lung Cell Mol Physiol. 2021. PMID: 34469245 Free PMC article. Review.
Down syndrome (DS) is one of the most prevalent chromosomal abnormalities worldwide, affecting 1 in 700 live births. Although multiple organ systems are affected by the chromosomal defects, respiratory failure and lung disease are the leading causes of morbidity and …
Down syndrome (DS) is one of the most prevalent chromosomal abnormalities worldwide, affecting 1 in 700 live births. Although multipl …
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.
Surviving infants with PPHN have an increased risk of long-term morbidities. PPHN physiology can be categorized by (1) maladaptation: pulmonary vessels have normal structure and number but have abnormal vasoreactivity; (2) excessive muscularization: increased smooth …
Surviving infants with PPHN have an increased risk of long-term morbidities. PPHN physiology can be categorized by (1) maladaptation: …
Lung development.
Mullassery D, Smith NP. Mullassery D, et al. Semin Pediatr Surg. 2015 Aug;24(4):152-5. doi: 10.1053/j.sempedsurg.2015.01.011. Epub 2015 Feb 2. Semin Pediatr Surg. 2015. PMID: 26051046 Review.
Survival at birth is dependent on adequate development and maturation of the lung in utero. Abnormal bronchopulmonary development results in congenital lung malformations, and inadequate development is thought to contribute to bronchopulmonary dysplasia. ...
Survival at birth is dependent on adequate development and maturation of the lung in utero. Abnormal bronchopulmonary development res …
VACTERL/VATER Association.
Solomon BD. Solomon BD. Orphanet J Rare Dis. 2011 Aug 16;6:56. doi: 10.1186/1750-1172-6-56. Orphanet J Rare Dis. 2011. PMID: 21846383 Free PMC article. Review.
VACTERL/VATER association is typically defined by the presence of at least three of the following congenital malformations: vertebral defects, anal atresia, cardiac defects, tracheo-esophageal fistula, renal anomalies, and limb abnormalities. ...The management of pa …
VACTERL/VATER association is typically defined by the presence of at least three of the following congenital malformations: vertebral …
Secondary Rhinoplasty for Unilateral Cleft Nasal Deformity.
Rohrich RJ, Benkler M, Avashia YJ, Savetsky IL. Rohrich RJ, et al. Plast Reconstr Surg. 2021 Jul 1;148(1):133-143. doi: 10.1097/PRS.0000000000008124. Plast Reconstr Surg. 2021. PMID: 34076624 Free PMC article. Review.
Understanding the anatomy and growth abnormality seen with the cleft nasal deformity helps to tailor surgical management. This article seeks to expand on the application of current concepts in secondary rhinoplasty for unilateral cleft lip nasal deformity. ...
Understanding the anatomy and growth abnormality seen with the cleft nasal deformity helps to tailor surgical management. This articl …
The multiple dimensions of Platypnea-Orthodeoxia syndrome: A review.
Agrawal A, Palkar A, Talwar A. Agrawal A, et al. Respir Med. 2017 Aug;129:31-38. doi: 10.1016/j.rmed.2017.05.016. Epub 2017 May 31. Respir Med. 2017. PMID: 28732833 Free article. Review.
The primary mechanisms of POS in these patients can be broadly classified based on intracardiac abnormalities, extracardiac abnormalities and miscellaneous etiologies. A Patent Foramen Ovale (PFO) was the most common reported site of an intracardiac shunt. ...
The primary mechanisms of POS in these patients can be broadly classified based on intracardiac abnormalities, extracardiac abnorm
Congenital Pulmonary Airway Malformations With a Reconsideration and Current Perspective on the Stocker Classification.
Dehner LP, Schultz KAP, Hill DA. Dehner LP, et al. Pediatr Dev Pathol. 2023 May-Jun;26(3):241-249. doi: 10.1177/10935266221146823. Epub 2023 Feb 21. Pediatr Dev Pathol. 2023. PMID: 37334833 Review.
Congenital cystic pulmonary lesions (CCPLs) are represented by the following entities: congenital pulmonary airway malformation (CPAM), formerly congenital cystic adenomatoid malformation, extra- and intralobar sequestration (EIS), congenital lobar emp
Congenital cystic pulmonary lesions (CCPLs) are represented by the following entities: congenital pulmonary airway malformatio
Epithelial cell dysfunction, a major driver of asthma development.
Heijink IH, Kuchibhotla VNS, Roffel MP, Maes T, Knight DA, Sayers I, Nawijn MC. Heijink IH, et al. Allergy. 2020 Aug;75(8):1902-1917. doi: 10.1111/all.14421. Epub 2020 Jun 16. Allergy. 2020. PMID: 32460363 Free PMC article. Review.
The physical barrier function of the airway epithelium is tightly interwoven with its immunomodulatory actions, while abnormal epithelial repair responses may contribute to remodelling of the airway wall. We propose that abnormalities in the airway epithelial barrie …
The physical barrier function of the airway epithelium is tightly interwoven with its immunomodulatory actions, while abnormal epithe …
3,390 results