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 *

122 related articles for article (PubMed ID: 9565498)

  • 1. Deletion of thyroid transcription factor-1 gene in an infant with neonatal thyroid dysfunction and respiratory failure.
    Devriendt K; Vanhole C; Matthijs G; de Zegher F
    N Engl J Med; 1998 Apr; 338(18):1317-8. PubMed ID: 9565498
    [No Abstract]   [Full Text] [Related]  

  • 2. Deletion of NKX2.1 gene encoding thyroid transcription factor-1 in two siblings with hypothyroidism and respiratory failure.
    Iwatani N; Mabe H; Devriendt K; Kodama M; Miike T
    J Pediatr; 2000 Aug; 137(2):272-6. PubMed ID: 10931427
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Autosomal dominant transmission of congenital hypothyroidism, neonatal respiratory distress, and ataxia caused by a mutation of NKX2-1.
    Doyle DA; Gonzalez I; Thomas B; Scavina M
    J Pediatr; 2004 Aug; 145(2):190-3. PubMed ID: 15289765
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Novel NKX2.1 mutation associated with hypothyroidism and lethal respiratory failure in a full-term neonate.
    Gillett ES; Deutsch GH; Bamshad MJ; McAdams RM; Mann PC
    J Perinatol; 2013 Feb; 33(2):157-60. PubMed ID: 23361500
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Choreoathetosis, congenital hypothyroidism and neonatal respiratory distress syndrome with intact NKX2-1.
    Barnett CP; Mencel JJ; Gecz J; Waters W; Kirwin SM; Vinette KM; Uppill M; Nicholl J
    Am J Med Genet A; 2012 Dec; 158A(12):3168-73. PubMed ID: 23169673
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. New syndromic form of benign hereditary chorea is associated with a deletion of TITF-1 and PAX-9 contiguous genes.
    Devos D; Vuillaume I; de Becdelievre A; de Martinville B; Dhaenens CM; Cuvellier JC; Cuisset JM; Vallée L; Lemaitre MP; Bourteel H; Hachulla E; Wallaert B; Destée A; Defebvre L; Sablonnière B
    Mov Disord; 2006 Dec; 21(12):2237-40. PubMed ID: 17044090
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Duplication of the pituitary stalk in a patient with a heterozygous deletion of chromosome 14 harboring the thyroid transcription factor-1 gene.
    Accornero S; Danesino C; Bastianello S; D'Errico I; Guala A; Chiovato L
    J Clin Endocrinol Metab; 2010 Aug; 95(8):3595-6. PubMed ID: 20685887
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. ACE gene deletion/deletion polymorphism may be a protective factor for respiratory distress in preterm infants.
    Sivasli E; Yurdakök M; Babaoğlu E; Karabulut H; Yiğit S; Babaoğlu M; Tekinalp G; Tükün A
    Turk J Pediatr; 2007; 49(1):69-74. PubMed ID: 17479647
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A major deletion in the surfactant protein-B gene causing lethal respiratory distress.
    Wegner DJ; Hertzberg T; Heins HB; Elmberger G; MacCoss MJ; Carlson CS; Nogee LM; Cole FS; Hamvas A
    Acta Paediatr; 2007 Apr; 96(4):516-20. PubMed ID: 17391469
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Brain-lung-thyroid disease: clinical features of a kindred with a novel thyroid transcription factor 1 mutation.
    Ferrara JM; Adam OR; Kirwin SM; Houghton DJ; Shepherd C; Vinette KM; Litvan I
    J Child Neurol; 2012 Jan; 27(1):68-73. PubMed ID: 21813802
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A Turkish newborn infant with cerebellar agenesis/neonatal diabetes mellitus and PTF1A mutation.
    Tutak E; Satar M; Yapicioğlu H; Altintaş A; Narli N; Hergüner O; Bayram Y
    Genet Couns; 2009; 20(2):147-52. PubMed ID: 19650412
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Prenatal diagnosis of spinal muscular atrophy with respiratory distress (SMARD1) in a twin pregnancy.
    Sangiuolo F; Filareto A; Giardina E; Nardone AM; Pilu G; Pietropolli A; Bertini E; Novelli G
    Prenat Diagn; 2004 Oct; 24(10):839-41. PubMed ID: 15503272
    [No Abstract]   [Full Text] [Related]  

  • 15. Partial deficiency of thyroid transcription factor 1 produces predominantly neurological defects in humans and mice.
    Pohlenz J; Dumitrescu A; Zundel D; Martiné U; Schönberger W; Koo E; Weiss RE; Cohen RN; Kimura S; Refetoff S
    J Clin Invest; 2002 Feb; 109(4):469-73. PubMed ID: 11854318
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Campomelic syndrome and deletion of SOX9.
    Olney PN; Kean LS; Graham D; Elsas LJ; May KM
    Am J Med Genet; 1999 May; 84(1):20-4. PubMed ID: 10213041
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Mutations in the gene encoding immunoglobulin mu-binding protein 2 cause spinal muscular atrophy with respiratory distress type 1.
    Grohmann K; Schuelke M; Diers A; Hoffmann K; Lucke B; Adams C; Bertini E; Leonhardt-Horti H; Muntoni F; Ouvrier R; Pfeufer A; Rossi R; Van Maldergem L; Wilmshurst JM; Wienker TF; Sendtner M; Rudnik-Schöneborn S; Zerres K; Hübner C
    Nat Genet; 2001 Sep; 29(1):75-7. PubMed ID: 11528396
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Transcription factor haploinsufficiency: when half a loaf is not enough.
    Seidman JG; Seidman C
    J Clin Invest; 2002 Feb; 109(4):451-5. PubMed ID: 11854316
    [No Abstract]   [Full Text] [Related]  

  • 19. Thyroid transcription factor-1 (TTF-1/Nkx2.1/TITF1) gene regulation in the lung.
    Boggaram V
    Clin Sci (Lond); 2009 Jan; 116(1):27-35. PubMed ID: 19037882
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Inherited disorders of neonatal lung diseases.
    Yurdakök M
    Turk J Pediatr; 2004; 46(2):105-14. PubMed ID: 15214737
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.