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Page 1
Adult Common Variable Immunodeficiency.
Dong J, Liang H, Wen D, Wang J. Dong J, et al. Am J Med Sci. 2016 Mar;351(3):239-43. doi: 10.1016/j.amjms.2015.12.010. Am J Med Sci. 2016. PMID: 26992251
BACKGROUND: Common variable immunodeficiency (CVID) is characterized by hypogammaglobulinemia, defective antibody production and recurrent upper and lower respiratory tract infections. The diagnosis in adult patients is often thoug …
BACKGROUND: Common variable immunodeficiency (CVID) is characterized by hypogammaglobulinemia, defective antibody production and recurren
Primary ciliary dyskinesia, an orphan disease.
Boon M, Jorissen M, Proesmans M, De Boeck K. Boon M, et al. Eur J Pediatr. 2013 Feb;172(2):151-62. doi: 10.1007/s00431-012-1785-6. Epub 2012 Jul 10. Eur J Pediatr. 2013. PMID: 22777640 Review.
In the respiratory tract epithelium, impaired mucociliary clearance leads to chronic and/or recurrent upper and lower respiratory tract infections. In up to 75 % of the patients, respiratory manifestations start in the newborn peri …
In the respiratory tract epithelium, impaired mucociliary clearance leads to chronic and/or recurrent upper and lowe
Primary ciliary dyskinesia: when to suspect the diagnosis and how to confirm it.
Hogg C. Hogg C. Paediatr Respir Rev. 2009 Jun;10(2):44-50. doi: 10.1016/j.prrv.2008.10.001. Epub 2009 Apr 9. Paediatr Respir Rev. 2009. PMID: 19410200 Review.
As a consequence, the patient typically presents with a range of features, including recurrent upper and lower respiratory tract infections, persistent glue ear and possible hearing deficit. ...
As a consequence, the patient typically presents with a range of features, including recurrent upper and lower
Comprehensive assessment of respiratory complications in patients with common variable immunodeficiency.
Moazzami B, Mohayeji Nasrabadi MA, Abolhassani H, Olbrich P, Azizi G, Shirzadi R, Modaresi M, Sohani M, Delavari S, Shahkarami S, Yazdani R, Aghamohammadi A. Moazzami B, et al. Ann Allergy Asthma Immunol. 2020 May;124(5):505-511.e3. doi: 10.1016/j.anai.2020.01.019. Epub 2020 Jan 30. Ann Allergy Asthma Immunol. 2020. PMID: 32007567 Free article.
BACKGROUND: Common variable immunodeficiency (CVID) is a heterogeneous group of disorders, characterized by recurrent upper and lower respiratory tract infections and some noninfectious clinical complications. ...
BACKGROUND: Common variable immunodeficiency (CVID) is a heterogeneous group of disorders, characterized by recurrent upper
Kartagener's syndrome: a classical case.
Arunabha DC, Sumit RT, Sourin B, Sabyasachi C, Subhasis M. Arunabha DC, et al. Ethiop J Health Sci. 2014 Oct;24(4):363-8. doi: 10.4314/ejhs.v24i4.13. Ethiop J Health Sci. 2014. PMID: 25489202 Free PMC article.
CASE DETAILS: among the various causes of recurrent LRTI, the most frequent causes are abnormalities of general or local impairment of immune mechanism and abnormalities of cilia or mucus of respiratory tract. We report an adult case of recurrent upper and
CASE DETAILS: among the various causes of recurrent LRTI, the most frequent causes are abnormalities of general or local impairment of immun …
Nasal Nitric Oxide in Primary Immunodeficiency and Primary Ciliary Dyskinesia: Helping to Distinguish Between Clinically Similar Diseases.
Zysman-Colman ZN, Kaspy KR, Alizadehfar R, NyKamp KR, Zariwala MA, Knowles MR, Vinh DC, Shapiro AJ. Zysman-Colman ZN, et al. J Clin Immunol. 2019 Feb;39(2):216-224. doi: 10.1007/s10875-019-00613-8. Epub 2019 Mar 26. J Clin Immunol. 2019. PMID: 30911954 Free PMC article.
PURPOSE: Primary ciliary dyskinesia (PCD) is a rare disorder of the mucociliary clearance leading to recurrent upper and lower respiratory tract infections. PCD is difficult to clinically distinguish from other entities leading to …
PURPOSE: Primary ciliary dyskinesia (PCD) is a rare disorder of the mucociliary clearance leading to recurrent upper and
Clinical evaluation and treatment of the adult patient with suspected primary immunodeficiency disease: a case analysis.
Ciesielka D. Ciesielka D. J Am Acad Nurse Pract. 2004 Apr;16(4):158-65. doi: 10.1111/j.1745-7599.2004.tb00437.x. J Am Acad Nurse Pract. 2004. PMID: 15137474 Review.
CONCLUSIONS: Consideration should be given to primary immunodeficiency diseases as one possible cause of recurrent upper and lower respiratory tract infections in patients at any age. ...
CONCLUSIONS: Consideration should be given to primary immunodeficiency diseases as one possible cause of recurrent upper an
The involvement of musculoskeletal system and its influence on postural stability in children and young adults with cystic fibrosis.
Kenis-Coskun O, Karadag-Saygi E, Bahar-Ozdemir Y, Gokdemir Y, Karadag B, Kayhan O. Kenis-Coskun O, et al. Ital J Pediatr. 2017 Nov 21;43(1):106. doi: 10.1186/s13052-017-0426-0. Ital J Pediatr. 2017. PMID: 29162121 Free PMC article.
BACKGROUND: Cystic fibrosis (CF) affects the musculoskeletal system via a multifactorial pathway that includes vitamin D deficiency and involvement of respiratory muscles such as intercostals due to recurrent upper and lower respiratory tract
BACKGROUND: Cystic fibrosis (CF) affects the musculoskeletal system via a multifactorial pathway that includes vitamin D deficiency and invo …
Novel Hemizygous IL2RG p.(Pro58Ser) Mutation Impairs IL-2 Receptor Complex Expression on Lymphocytes Causing X-Linked Combined Immunodeficiency.
Tuovinen EA, Grönholm J, Öhman T, Pöysti S, Toivonen R, Kreutzman A, Heiskanen K, Trotta L, Toiviainen-Salo S, Routes JM, Verbsky J, Mustjoki S, Saarela J, Kere J, Varjosalo M, Hänninen A, Seppänen MRJ. Tuovinen EA, et al. J Clin Immunol. 2020 Apr;40(3):503-514. doi: 10.1007/s10875-020-00745-2. Epub 2020 Feb 19. J Clin Immunol. 2020. PMID: 32072341 Free PMC article.
We studied the patient's clinical phenotype, B, T, NK, and dendritic cell phenotypes, IL2RG and CD25 cell surface expression, and IL-2 target gene expression, STAT tyrosine phosphorylation, PBMC proliferation, and blast formation in response to IL-2 stimulation, as well as protei …
We studied the patient's clinical phenotype, B, T, NK, and dendritic cell phenotypes, IL2RG and CD25 cell surface expression, and IL-2 targe …
Coexistent yellow nail syndrome and selective antibody deficiency.
Bokszczanin A, Levinson AI. Bokszczanin A, et al. Ann Allergy Asthma Immunol. 2003 Nov;91(5):496-500. doi: 10.1016/S1081-1206(10)61521-9. Ann Allergy Asthma Immunol. 2003. PMID: 14692436
OBJECTIVE: To present the case of a patient with YNS whose recurrent upper and lower respiratory tract infections may have been caused by an underlying selective antibody deficiency that manifests as impaired IgG antibody response …
OBJECTIVE: To present the case of a patient with YNS whose recurrent upper and lower respiratory tract
11 results