These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
180 related articles for article (PubMed ID: 33370995)
1. Hypoxaemia and interstitial lung disease in an infant with hypothyroidism and hypotonia. Lynn MM; Simon D; Kasi AS BMJ Case Rep; 2020 Dec; 13(12):. PubMed ID: 33370995 [TBL] [Abstract][Full Text] [Related]
2. Respiratory Distress, Congenital Hypothyroidism and Hypotonia in a Newborn. Jovien S; Borie R; Doummar D; Clement A; Nathan N Respiration; 2016; 92(3):188-91. PubMed ID: 27595265 [No Abstract] [Full Text] [Related]
3. Combined mutations of NKX2-1 and surfactant protein C genes for refractory low oxyhemoglobin saturation and interstitial pneumonia: A case report. Gu R; Ye G; Zhou Y; Jiang Z Medicine (Baltimore); 2020 Mar; 99(12):e19650. PubMed ID: 32195974 [TBL] [Abstract][Full Text] [Related]
7. The Brain-Lung-Thyroid syndrome (BLTS): A novel deletion in chromosome 14q13.2-q21.1 expands the phenotype to humoral immunodeficiency. Villafuerte B; Natera-de-Benito D; González A; Mori MA; Palomares M; Nevado J; García-Miñaur S; Lapunzina P; González-Granado LI; Allende LM; Moreno JC Eur J Med Genet; 2018 Jul; 61(7):393-398. PubMed ID: 29477862 [TBL] [Abstract][Full Text] [Related]
8. A further case of brain-lung-thyroid syndrome with deletion proximal to NKX2-1. Kharbanda M; Hermanns P; Jones J; Pohlenz J; Horrocks I; Donaldson M Eur J Med Genet; 2017 May; 60(5):257-260. PubMed ID: 28286255 [TBL] [Abstract][Full Text] [Related]
9. [Brain-lung-thyroid syndrome in a newborn with deletion 14q12-q21.1]. Villamil-Osorio M; Yunis LK; Quintero L; Restrepo-Gualteros S; Yunis JJ; Jaramillo L; Agudelo BI; Ladino Y Andes Pediatr; 2021 Dec; 92(6):930-936. PubMed ID: 35506806 [TBL] [Abstract][Full Text] [Related]
10. Insights from European Reference Network for rare neurological disorders study surveys on diagnosis, treatment, and management of NKX2-1-related disorders. Nou-Fontanet L; Nguyen QTR; Bachoud-Levi AC; Reinhard C; ; Ortigoza-Escobar JD Eur J Paediatr Neurol; 2024 Jul; 51():110-117. PubMed ID: 38917695 [TBL] [Abstract][Full Text] [Related]
11. Haploinsufficiency of NKX2-1 in Brain-Lung-Thyroid Syndrome with Additional Multiple Pituitary Dysfunction. Prasad R; Nicholas AK; Schoenmakers N; Barton J Horm Res Paediatr; 2019; 92(5):340-344. PubMed ID: 31707387 [TBL] [Abstract][Full Text] [Related]
12. NKX2.1 run-on mutation associated to familial brain-lung-thyroid syndrome. Cavaliere E; Gortan AJ; Passon N; Fabbro D; Marin D; Carecchio M; Baldan F; Credendino SC; Gallo R; Cogo P; Damante G; De Vita G Clin Genet; 2021 Jul; 100(1):114-116. PubMed ID: 33778944 [TBL] [Abstract][Full Text] [Related]
13. A novel mutation of NKX2-1 affecting 2 generations with hypothyroidism and choreoathetosis: part of the spectrum of brain-thyroid-lung syndrome. Williamson S; Kirkpatrick M; Greene S; Goudie D J Child Neurol; 2014 May; 29(5):666-9. PubMed ID: 24453141 [TBL] [Abstract][Full Text] [Related]
14. The Movement Disorder of Brain-Lung-Thyroid Syndrome Can be Responsive to Methylphenidate. Gauquelin L; Tran LT; Chouinard S; Bernard G Tremor Other Hyperkinet Mov (N Y); 2017; 7():508. PubMed ID: 29109906 [No Abstract] [Full Text] [Related]
16. NKX2-1 mutations in brain-lung-thyroid syndrome: a case series of four patients. Shetty VB; Kiraly-Borri C; Lamont P; Bikker H; Choong CS J Pediatr Endocrinol Metab; 2014 Mar; 27(3-4):373-8. PubMed ID: 24129101 [TBL] [Abstract][Full Text] [Related]
17. Respiratory insufficiency in a newborn with congenital hypothyroidism due to a new mutation of TTF-1/NKX2.1 gene. Salerno T; Peca D; Menchini L; Schiavino A; Petreschi F; Occasi F; Cogo P; Danhaive O; Cutrera R Pediatr Pulmonol; 2014 Mar; 49(3):E42-4. PubMed ID: 23997037 [TBL] [Abstract][Full Text] [Related]
18. A case of brain Liang R; Ou S; Ding Y; Liu C Zhong Nan Da Xue Xue Bao Yi Xue Ban; 2022 Mar; 47(3):396-400. PubMed ID: 35545334 [TBL] [Abstract][Full Text] [Related]
19. Novel Mutations in the NKX2.1 gene and the PAX8 gene in a Boy with Brain-Lung-Thyroid Syndrome. Hermanns P; Kumorowicz-Czoch M; Grasberger H; Refetoff S; Pohlenz J Exp Clin Endocrinol Diabetes; 2018 Feb; 126(2):85-90. PubMed ID: 28954305 [TBL] [Abstract][Full Text] [Related]
20. [Analysis of clinical characteristics and variant of NKX2-1 gene in a Chinese boy with Brain-Lung-Thyroid syndrome]. Dong R; Liu Y; Shi B; Huang Y; Lyu Y; Liu Y Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2024 Aug; 41(8):947-952. PubMed ID: 39097277 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]