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 *

153 related articles for article (PubMed ID: 27640358)

  • 1. Phenotype Differentiation of FOXG1 and MECP2 Disorders: A New Method for Characterization of Developmental Encephalopathies.
    Ma M; Adams HR; Seltzer LE; Dobyns WB; Paciorkowski AR
    J Pediatr; 2016 Nov; 178():233-240.e10. PubMed ID: 27640358
    [TBL] [Abstract][Full Text] [Related]  

  • 2. The core FOXG1 syndrome phenotype consists of postnatal microcephaly, severe mental retardation, absent language, dyskinesia, and corpus callosum hypogenesis.
    Kortüm F; Das S; Flindt M; Morris-Rosendahl DJ; Stefanova I; Goldstein A; Horn D; Klopocki E; Kluger G; Martin P; Rauch A; Roumer A; Saitta S; Walsh LE; Wieczorek D; Uyanik G; Kutsche K; Dobyns WB
    J Med Genet; 2011 Jun; 48(6):396-406. PubMed ID: 21441262
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Novel mutation in forkhead box G1 (FOXG1) gene in an Indian patient with Rett syndrome.
    Das DK; Jadhav V; Ghattargi VC; Udani V
    Gene; 2014 Mar; 538(1):109-12. PubMed ID: 24412290
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Revisiting the phenotype associated with FOXG1 mutations: two novel cases of congenital Rett variant.
    Bahi-Buisson N; Nectoux J; Girard B; Van Esch H; De Ravel T; Boddaert N; Plouin P; Rio M; Fichou Y; Chelly J; Bienvenu T
    Neurogenetics; 2010 May; 11(2):241-9. PubMed ID: 19806373
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Clinical features in Rett syndrome: MECP2-, CDKL5- and FOXG1- related disorders].
    Takahashi S
    No To Hattatsu; 2014 Mar; 46(2):117-20. PubMed ID: 24738188
    [No Abstract]   [Full Text] [Related]  

  • 6. Epilepsy and outcome in FOXG1-related disorders.
    Seltzer LE; Ma M; Ahmed S; Bertrand M; Dobyns WB; Wheless J; Paciorkowski AR
    Epilepsia; 2014 Aug; 55(8):1292-300. PubMed ID: 24836831
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Dystonia as a prominent presenting feature in developmental and epileptic encephalopathies: A case series.
    Dzinovic I; Škorvánek M; Necpál J; Boesch S; Švantnerová J; Wagner M; Havránková P; Pavelekova P; Haň V; Janzarik WG; Berweck S; Diebold I; Kuster A; Jech R; Winkelmann J; Zech M
    Parkinsonism Relat Disord; 2021 Sep; 90():73-78. PubMed ID: 34399161
    [TBL] [Abstract][Full Text] [Related]  

  • 8. The hyperkinetic movement disorder of FOXG1-related epileptic-dyskinetic encephalopathy.
    Cellini E; Vignoli A; Pisano T; Falchi M; Molinaro A; Accorsi P; Bontacchio A; Pinelli L; Giordano L; Guerrini R;
    Dev Med Child Neurol; 2016 Jan; 58(1):93-7. PubMed ID: 26344814
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Comparison of Core Features in Four Developmental Encephalopathies in the Rett Natural History Study.
    Cutri-French C; Armstrong D; Saby J; Gorman C; Lane J; Fu C; Peters SU; Percy A; Neul JL; Marsh ED
    Ann Neurol; 2020 Aug; 88(2):396-406. PubMed ID: 32472944
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Analysis of Hungarian patients with Rett syndrome phenotype for MECP2, CDKL5 and FOXG1 gene mutations.
    Hadzsiev K; Polgar N; Bene J; Komlosi K; Karteszi J; Hollody K; Kosztolanyi G; Renieri A; Melegh B
    J Hum Genet; 2011 Mar; 56(3):183-7. PubMed ID: 21160487
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Early-onset movement disorder as diagnostic marker in genetic syndromes: Three cases of FOXG1-related syndrome.
    Caporali C; Signorini S; De Giorgis V; Pichiecchio A; Zuffardi O; Orcesi S
    Eur J Paediatr Neurol; 2018 Mar; 22(2):336-339. PubMed ID: 29396177
    [TBL] [Abstract][Full Text] [Related]  

  • 12. FOXG1 variants can be associated with milder phenotypes than congenital Rett syndrome with unassisted walking and language development.
    Mazel B; Delanne J; Garde A; Racine C; Bruel AL; Duffourd Y; Lopergolo D; Santorelli FM; Marchi V; Pinto AM; Mencarelli MA; Canitano R; Valentino F; Papa FT; Fallerini C; Mari F; Renieri A; Munnich A; Niclass T; Le Guyader G; Thauvin-Robinet C; Philippe C; Faivre L
    Am J Med Genet B Neuropsychiatr Genet; 2024 Sep; 195(6):e32970. PubMed ID: 38459409
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 14q12 and severe Rett-like phenotypes: new clinical insights and physical mapping of FOXG1-regulatory elements.
    Allou L; Lambert L; Amsallem D; Bieth E; Edery P; Destrée A; Rivier F; Amor D; Thompson E; Nicholl J; Harbord M; Nemos C; Saunier A; Moustaïne A; Vigouroux A; Jonveaux P; Philippe C
    Eur J Hum Genet; 2012 Dec; 20(12):1216-23. PubMed ID: 22739344
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Epilepsy in Rett syndrome, and CDKL5- and FOXG1-gene-related encephalopathies.
    Guerrini R; Parrini E
    Epilepsia; 2012 Dec; 53(12):2067-78. PubMed ID: 22998673
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [FOXG1, a new gene responsible for the congenital form of Rett syndrome].
    Roche-Martinez A; Gerotina E; Armstrong-Moron J; Sans-Capdevila O; Pineda M
    Rev Neurol; 2011 May; 52(10):597-602. PubMed ID: 21488007
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Phenotypic variability in Rett syndrome associated with FOXG1 mutations in females.
    Philippe C; Amsallem D; Francannet C; Lambert L; Saunier A; Verneau F; Jonveaux P
    J Med Genet; 2010 Jan; 47(1):59-65. PubMed ID: 19564653
    [TBL] [Abstract][Full Text] [Related]  

  • 17.
    Wong LC; Singh S; Wang HP; Hsu CJ; Hu SC; Lee WT
    Int J Mol Sci; 2019 Aug; 20(17):. PubMed ID: 31454984
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A case of Lennox-Gastaut syndrome in a patient with FOXG1-related disorder.
    Terrone G; Bienvenu T; Germanaud D; Barthez-Carpentier MA; Diebold B; Delanoe C; Passemard S; Auvin S
    Epilepsia; 2014 Nov; 55(11):e116-9. PubMed ID: 25266269
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Expanding the Clinical and Molecular Spectrum of FOXG1- and ZBTB18-Associated Neurodevelopmental Disorders.
    Brea-Fernández AJ; Souto-Trinei FA; Iglesias E; Caamaño P; Rodríguez Sánchez B; Gómez Lado C; Eiris J; Fernández-Prieto M; Barros F; Brea RJ; Carracedo Á
    Cytogenet Genome Res; 2023; 163(5-6):301-306. PubMed ID: 38056433
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Increased levels of 4HNE-protein plasma adducts in Rett syndrome.
    Pecorelli A; Ciccoli L; Signorini C; Leoncini S; Giardini A; D'Esposito M; Filosa S; Hayek J; De Felice C; Valacchi G
    Clin Biochem; 2011 Apr; 44(5-6):368-71. PubMed ID: 21276437
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.