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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

180 related articles for article (PubMed ID: 24129101)

  • 21. [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]  

  • 22. 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]  

  • 23. Benign hereditary chorea: phenotype, prognosis, therapeutic outcome and long term follow-up in a large series with new mutations in the TITF1/NKX2-1 gene.
    Gras D; Jonard L; Roze E; Chantot-Bastaraud S; Koht J; Motte J; Rodriguez D; Louha M; Caubel I; Kemlin I; Lion-François L; Goizet C; Guillot L; Moutard ML; Epaud R; Héron B; Charles P; Tallot M; Camuzat A; Durr A; Polak M; Devos D; Sanlaville D; Vuillaume I; Billette de Villemeur T; Vidailhet M; Doummar D
    J Neurol Neurosurg Psychiatry; 2012 Oct; 83(10):956-62. PubMed ID: 22832740
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Growth hormone deficiency in a child with benign hereditary chorea caused by a
    Trevisani V; Predieri B; Madeo SF; Fusco C; Garavelli L; Caraffi S; Iughetti L
    J Pediatr Endocrinol Metab; 2022 Mar; 35(3):411-415. PubMed ID: 34710315
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Benign hereditary chorea related to NKX2.1: expansion of the genotypic and phenotypic spectrum.
    Peall KJ; Lumsden D; Kneen R; Madhu R; Peake D; Gibbon F; Lewis H; Hedderly T; Meyer E; Robb SA; Lynch B; King MD; Lin JP; Morris HR; Jungbluth H; Kurian MA
    Dev Med Child Neurol; 2014 Jul; 56(7):642-8. PubMed ID: 24171694
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Differential diagnosis of Huntington's disease- neurological aspects of NKX2-1-related disorders.
    Skwara J; Nowicki M; Sharif L; Milanowski Ł; Dulski J; Elert-Dobkowska E; Skrzypek K; Hoffman-Zacharska D; Koziorowski D; Sławek J
    J Neural Transm (Vienna); 2024 Sep; 131(9):1013-1024. PubMed ID: 38916623
    [TBL] [Abstract][Full Text] [Related]  

  • 27. A Novel Missense Variant in the NKX2-1
    Villafuerte B; Carrasco-López C; Herranz A; Garzón L; Simón R; Natera-de-Benito D; Alikhani P; Tenorio J; García-Santiago F; Solis M; Del-Pozo Á; Lapunzina P; Ortigoza-Escobar JD; Santisteban P; Moreno JC
    Thyroid; 2024 Jul; 34(7):942-948. PubMed ID: 38757609
    [No Abstract]   [Full Text] [Related]  

  • 28. [Chorea due to TITF1/NKX2-1 mutation: phenotypical description and therapeutic response in a family].
    Salvado M; Boronat-Guerrero S; Hernández-Vara J; Álvarez-Sabin J
    Rev Neurol; 2013 May; 56(10):515-20. PubMed ID: 23658034
    [TBL] [Abstract][Full Text] [Related]  

  • 29. 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]  

  • 30. A novel NKX2.1 mutation in a family with hypothyroidism and benign hereditary chorea.
    Ferrara AM; De Michele G; Salvatore E; Di Maio L; Zampella E; Capuano S; Del Prete G; Rossi G; Fenzi G; Filla A; Macchia PE
    Thyroid; 2008 Sep; 18(9):1005-9. PubMed ID: 18788921
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Lethal respiratory failure and mild primary hypothyroidism in a term girl with a de novo heterozygous mutation in the TITF1/NKX2.1 gene.
    Maquet E; Costagliola S; Parma J; Christophe-Hobertus C; Oligny LL; Fournet JC; Robitaille Y; Vuissoz JM; Payot A; Laberge S; Vassart G; Van Vliet G; Deladoëy J
    J Clin Endocrinol Metab; 2009 Jan; 94(1):197-203. PubMed ID: 18957494
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Fatal neonatal respiratory failure in an infant with congenital hypothyroidism due to haploinsufficiency of the NKX2-1 gene: alteration of pulmonary surfactant homeostasis.
    Kleinlein B; Griese M; Liebisch G; Krude H; Lohse P; Aslanidis C; Schmitz G; Peters J; Holzinger A
    Arch Dis Child Fetal Neonatal Ed; 2011 Nov; 96(6):F453-6. PubMed ID: 20584796
    [TBL] [Abstract][Full Text] [Related]  

  • 33. 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]  

  • 34. A novel TITF-1 mutation causes benign hereditary chorea with response to levodopa.
    Asmus F; Horber V; Pohlenz J; Schwabe D; Zimprich A; Munz M; Schöning M; Gasser T
    Neurology; 2005 Jun; 64(11):1952-4. PubMed ID: 15955952
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Screening for mutations in transcription factors in a Czech cohort of 170 patients with congenital and early-onset hypothyroidism: identification of a novel PAX8 mutation in dominantly inherited early-onset non-autoimmune hypothyroidism.
    Al Taji E; Biebermann H; Límanová Z; Hníková O; Zikmund J; Dame C; Grüters A; Lebl J; Krude H
    Eur J Endocrinol; 2007 May; 156(5):521-9. PubMed ID: 17468187
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Functional characterization of two novel mutations in TTF-1/NKX2.1 homeodomain in patients with benign hereditary chorea.
    Provenzano C; Zamboni M; Veneziano L; Mantuano E; Garavaglia B; Zorzi G; Pagonabarraga J; Giunti P; Civitareale D
    J Neurol Sci; 2016 Jan; 360():78-83. PubMed ID: 26723978
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Altered pituitary morphology as a sign of benign hereditary chorea caused by TITF1/NKX2.1 mutations.
    Thust S; Veneziano L; Parkinson MH; Bhatia KP; Mantuano E; Gonzalez-Robles C; Davagnanam I; Giunti P
    Neurogenetics; 2022 Apr; 23(2):91-102. PubMed ID: 35079915
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Hypoperfusion in caudate nuclei in patients with brain-lung-thyroid syndrome.
    Uematsu M; Haginoya K; Kikuchi A; Nakayama T; Kakisaka Y; Numata Y; Kobayashi T; Hino-Fukuyo N; Fujiwara I; Kure S
    J Neurol Sci; 2012 Apr; 315(1-2):77-81. PubMed ID: 22166853
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Psychosis, short stature in benign hereditary chorea: a novel thyroid transcription factor-1 mutation.
    Glik A; Vuillaume I; Devos D; Inzelberg R
    Mov Disord; 2008 Sep; 23(12):1744-7. PubMed ID: 18661567
    [TBL] [Abstract][Full Text] [Related]  

  • 40.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 9.