205 related articles for article (PubMed ID: 30523160)
41. Idiopathic Interstitial Pneumonia Associated With Autoantibodies: A Large Case Series Followed Over 1 Year.
Collins BF; Spiekerman CF; Shaw MA; Ho LA; Hayes J; Spada CA; Stamato CM; Raghu G
Chest; 2017 Jul; 152(1):103-112. PubMed ID: 28300570
[TBL] [Abstract][Full Text] [Related]
42. A Rare Missense Variant in Telomerase Reverse Transcriptase is Associated with Idiopathic Pulmonary Fibrosis in a Chinese Han Family.
Zheng CM; Zhan X; Yang YH; Jiang T; Ye Q; Lu Y
Chin Med J (Engl); 2018 Sep; 131(18):2205-2209. PubMed ID: 30203795
[TBL] [Abstract][Full Text] [Related]
43. Telomerase Variants in Patients with Cirrhosis Awaiting Liver Transplantation.
Chiu V; Hogen R; Sher L; Wadé N; Conti D; Martynova A; Li H; Liang G; O'Connell C
Hepatology; 2019 Jun; 69(6):2652-2663. PubMed ID: 30964210
[TBL] [Abstract][Full Text] [Related]
44. An RTEL1 Mutation Links to Infantile-Onset Ulcerative Colitis and Severe Immunodeficiency.
Ziv A; Werner L; Konnikova L; Awad A; Jeske T; Hastreiter M; Mitsialis V; Stauber T; Wall S; Kotlarz D; Klein C; Snapper SB; Tzfati Y; Weiss B; Somech R; Shouval DS
J Clin Immunol; 2020 Oct; 40(7):1010-1019. PubMed ID: 32710398
[TBL] [Abstract][Full Text] [Related]
45. Synergistic effects of telomerase reverse transcriptase and regulator of telomere elongation helicase 1 on aggressiveness and outcomes in adrenocortical carcinoma.
Yuan H; Wu Y; Wang J; Qin X; Huang Y; Yan L; Fana Y; Zedenius J; Juhlin CC; Larsson C; Lui WO; Xu D
Biomed Pharmacother; 2022 May; 149():112796. PubMed ID: 35279598
[TBL] [Abstract][Full Text] [Related]
46. Compound heterozygous mutation of RTEL1 in interstitial lung disease complicated with pneumothorax and emphysema: A case report and literature review.
Luo M; Wang JL
Respirol Case Rep; 2022 Oct; 10(10):e01032. PubMed ID: 36090019
[TBL] [Abstract][Full Text] [Related]
47. Genetic interstitial lung disease.
Devine MS; Garcia CK
Clin Chest Med; 2012 Mar; 33(1):95-110. PubMed ID: 22365249
[TBL] [Abstract][Full Text] [Related]
48. The many faces of the helicase RTEL1 at telomeres and beyond.
Hourvitz N; Awad A; Tzfati Y
Trends Cell Biol; 2024 Feb; 34(2):109-121. PubMed ID: 37532653
[TBL] [Abstract][Full Text] [Related]
49. Clinical Characteristics and Natural History of Autoimmune Forms of Interstitial Lung Disease: A Single-Center Experience.
Chartrand S; Lee JS; Swigris JJ; Stanchev L; Fischer A
Lung; 2019 Dec; 197(6):709-713. PubMed ID: 31583453
[TBL] [Abstract][Full Text] [Related]
50. Clinical profile of unclassifiable interstitial lung disease: Comparison with chronic fibrosing idiopathic interstitial pneumonias.
Traila D; Oancea C; Tudorache E; Mladinescu OF; Timar B; Tudorache V
J Int Med Res; 2018 Jan; 46(1):448-456. PubMed ID: 28758849
[TBL] [Abstract][Full Text] [Related]
51. Telomerase gene mutations and telomere length shortening in patients with idiopathic pulmonary fibrosis in a Chinese population.
Dai J; Cai H; Zhuang Y; Wu Y; Min H; Li J; Shi Y; Gao Q; Yi L
Respirology; 2015 Jan; 20(1):122-8. PubMed ID: 25346280
[TBL] [Abstract][Full Text] [Related]
52. A cohort study of Danish patients with interstitial lung diseases: burden, severity, treatment and survival.
Hyldgaard C
Dan Med J; 2015 Apr; 62(4):B5069. PubMed ID: 25872544
[TBL] [Abstract][Full Text] [Related]
53. Comparison of clinical courses and mortality of connective tissue disease-associated interstitial pneumonias and chronic fibrosing idiopathic interstitial pneumonias.
Yıldırım F; Türk M; Bitik B; Erbaş G; Köktürk N; Haznedaroğlu Ş; Türktaş H
Kaohsiung J Med Sci; 2019 Jun; 35(6):365-372. PubMed ID: 30913371
[TBL] [Abstract][Full Text] [Related]
54. Familial forms of nonspecific interstitial pneumonia/idiopathic pulmonary fibrosis: clinical course and genetic background.
Borie R; Kannengiesser C; Crestani B
Curr Opin Pulm Med; 2012 Sep; 18(5):455-61. PubMed ID: 22781209
[TBL] [Abstract][Full Text] [Related]
55. Ultrastructural characterization of genetic diffuse lung diseases in infants and children: a cohort study and review.
Citti A; Peca D; Petrini S; Cutrera R; Biban P; Haass C; Boldrini R; Danhaive O
Ultrastruct Pathol; 2013 Oct; 37(5):356-65. PubMed ID: 24047351
[TBL] [Abstract][Full Text] [Related]
56. Pulmonary fibrosis in dyskeratosis congenita: report of 2 cases.
Dvorak LA; Vassallo R; Kirmani S; Johnson G; Hartman TE; Tazelaar HD; Leslie KO; Colby TV; Cockcroft DW; Churg AM; Yi ES
Hum Pathol; 2015 Jan; 46(1):147-52. PubMed ID: 25455995
[TBL] [Abstract][Full Text] [Related]
57. [Genetic basis in chronic interstitial familial pneumopathy. Familial study of SFTPC].
Somaschini M; Cavazza A; Riva S; Sassi I; Carrera P
Pediatr Med Chir; 2005; 27(3-4):103-7. PubMed ID: 16910460
[TBL] [Abstract][Full Text] [Related]
58. Heterogeneity of lung disease associated with NK2 homeobox 1 mutations.
Nattes E; Lejeune S; Carsin A; Borie R; Gibertini I; Balinotti J; Nathan N; Marchand-Adam S; Thumerelle C; Fauroux B; Bosdure E; Houdouin V; Delestrain C; Louha M; Couderc R; De Becdelievre A; Fanen P; Funalot B; Crestani B; Deschildre A; Dubus JC; Epaud R
Respir Med; 2017 Aug; 129():16-23. PubMed ID: 28732825
[TBL] [Abstract][Full Text] [Related]
59. Rare and Common Variants in
Zhang D; Povysil G; Kobeissy PH; Li Q; Wang B; Amelotte M; Jaouadi H; Newton CA; Maher TM; Molyneaux PL; Noth I; Martinez FJ; Raghu G; Todd JL; Palmer SM; Haefliger C; Platt A; Petrovski S; Garcia JA; Goldstein DB; Garcia CK
Am J Respir Crit Care Med; 2022 Jul; 206(1):56-69. PubMed ID: 35417304
[No Abstract] [Full Text] [Related]
60. Exome sequencing identifies mutant TINF2 in a family with pulmonary fibrosis.
Alder JK; Stanley SE; Wagner CL; Hamilton M; Hanumanthu VS; Armanios M
Chest; 2015 May; 147(5):1361-1368. PubMed ID: 25539146
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
