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 *

143 related articles for article (PubMed ID: 38306744)

  • 1. Physiopathologic Bases of Moebius Syndrome: Combining Genetic, Vascular, and Teratogenic Theories.
    López Gutierrez D; Luna López I; Medina Mata BA; Moreno Castro S; García Rangel FY
    Pediatr Neurol; 2024 Apr; 153():1-10. PubMed ID: 38306744
    [TBL] [Abstract][Full Text] [Related]  

  • 2. De novo mutations in PLXND1 and REV3L cause Möbius syndrome.
    Tomas-Roca L; Tsaalbi-Shtylik A; Jansen JG; Singh MK; Epstein JA; Altunoglu U; Verzijl H; Soria L; van Beusekom E; Roscioli T; Iqbal Z; Gilissen C; Hoischen A; de Brouwer APM; Erasmus C; Schubert D; Brunner H; Pérez Aytés A; Marin F; Aroca P; Kayserili H; Carta A; de Wind N; Padberg GW; van Bokhoven H
    Nat Commun; 2015 Jun; 6():7199. PubMed ID: 26068067
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Moebius syndrome. Clinical case report].
    Palmer-Morales Y; Zárate-Márquez RE; Prince-Vélez R; González-Méndez R; Zamarripa-Sandoval TA; Verdugo-Salazar N; Torres-Félix VG; Salcido-Daniel R; Valdez-Hernández P; Morfín-Vela A
    Rev Med Inst Mex Seguro Soc; 2013; 51(5):584-6. PubMed ID: 24144154
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A new hereditary congenital facial palsy case supports arg5 in HOX-DNA binding domain as possible hot spot for mutations.
    Uyguner ZO; Toksoy G; Altunoglu U; Ozgur H; Basaran S; Kayserili H
    Eur J Med Genet; 2015; 58(6-7):358-63. PubMed ID: 26007620
    [TBL] [Abstract][Full Text] [Related]  

  • 5. An exome sequencing study of Moebius syndrome including atypical cases reveals an individual with CFEOM3A and a
    Patel RM; Liu D; Gonzaga-Jauregui C; Jhangiani S; Lu JT; Sutton VR; Fernbach SD; Azamian M; White L; Edmond JC; Paysse EA; Belmont JW; Muzny D; Lupski JR; Gibbs RA; Lewis RA; Lee BH; Lalani SR; Campeau PM
    Cold Spring Harb Mol Case Stud; 2017 Mar; 3(2):a000984. PubMed ID: 28299356
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Characterization of ocular motor deficits in congenital facial weakness: Moebius and related syndromes.
    Rucker JC; Webb BD; Frempong T; Gaspar H; Naidich TP; Jabs EW
    Brain; 2014 Apr; 137(Pt 4):1068-79. PubMed ID: 24561559
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Differentiating Moebius syndrome and other congenital facial weakness disorders with electrodiagnostic studies.
    Lehky T; Joseph R; Toro C; Wu T; Van Ryzin C; Gropman A; Facio FM; Webb BD; Jabs EW; Barry BS; Engle EC; Collins FS; Manoli I;
    Muscle Nerve; 2021 Apr; 63(4):516-524. PubMed ID: 33389762
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Neurogenic bladder as a lurking complication in Moebius syndrome.
    Tanaka Y; Maekawa T; Eura R; Hasegawa Y; Kubota M
    Brain Dev; 2022 Jan; 44(1):73-76. PubMed ID: 34400011
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Moebius syndrome and hydrosyringomyelia: description of a new association.
    Losito L; Gennaro L; Cacudi M; De Rinaldis M; Trabacca A
    J Child Neurol; 2013 Jun; 28(6):801-4. PubMed ID: 22832772
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Examining the genetics of congenital facial paralysis--a closer look at Moebius syndrome.
    Kadakia S; Helman SN; Schwedhelm T; Saman M; Azizzadeh B
    Oral Maxillofac Surg; 2015 Jun; 19(2):109-16. PubMed ID: 25663568
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Managing the child with a diagnosis of Moebius syndrome: more than meets the eye.
    McKay VH; Touil LL; Jenkins D; Fattah AY
    Arch Dis Child; 2016 Sep; 101(9):843-6. PubMed ID: 26868039
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Moebius syndrome: clinical features, diagnosis, management and early intervention.
    Picciolini O; Porro M; Cattaneo E; Castelletti S; Masera G; Mosca F; Bedeschi MF
    Ital J Pediatr; 2016 Jun; 42(1):56. PubMed ID: 27260152
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Multigenic truncation of the semaphorin-plexin pathway by a germline chromothriptic rearrangement associated with Moebius syndrome.
    Nazaryan-Petersen L; Oliveira IR; Mehrjouy MM; Mendez JMM; Bak M; Bugge M; Kalscheuer VM; Bache I; Hancks DC; Tommerup N
    Hum Mutat; 2019 Aug; 40(8):1057-1062. PubMed ID: 31033088
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Moebius Syndrome: What We Know So Far.
    Zaidi SMH; Syed IN; Tahir U; Noor T; Choudhry MS
    Cureus; 2023 Feb; 15(2):e35187. PubMed ID: 36960250
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Case report: Identification of a novel variant p.Gly215Arg in the
    Manso-Bazús C; Spataro N; Gabau E; Beltrán-Salazar VP; Trujillo-Quintero JP; Capdevila N; Brunet-Vega A; Baena N; Jeyaprakash AA; Martinez-Glez V; Ruiz A
    Front Genet; 2024; 15():1291063. PubMed ID: 38356699
    [No Abstract]   [Full Text] [Related]  

  • 16. Diagnostic distinctions and genetic analysis of patients diagnosed with moebius syndrome.
    MacKinnon S; Oystreck DT; Andrews C; Chan WM; Hunter DG; Engle EC
    Ophthalmology; 2014 Jul; 121(7):1461-8. PubMed ID: 24612975
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Clinical characteristics and whole exome sequencing results of patients with Möbius syndrome].
    Ma Q; Jia HY; Chang QL; Wang YD; Liang Y; Wang D; Zhang RR; Jiao YH
    Zhonghua Yan Ke Za Zhi; 2022 Jun; 58(6):441-447. PubMed ID: 35692026
    [No Abstract]   [Full Text] [Related]  

  • 18. The epidemiology of Moebius syndrome in Italy.
    Carta A; Favilla S; Calzetti G; Casalini MC; Ferrari PF; Bianchi B; Simonelli MB; Farci R; Gandolfi S; Mora P
    Orphanet J Rare Dis; 2021 Apr; 16(1):162. PubMed ID: 33827605
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Poland-Möbius syndrome: a case report implicating a novel mutation of the PLXND1 gene and literature review.
    Glass GE; Mohammedali S; Sivakumar B; Stotland MA; Abdulkader F; Prosser DO; Love DR
    BMC Pediatr; 2022 Dec; 22(1):745. PubMed ID: 36581828
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Monozygotic twins discordant for a congenital cranial dysinnervation disorder with features of Moebius syndrome.
    Gates RW; Webb BD; Stevenson DA; Jabs EW; DeFilippo C; Ruzhnikov MRZ; Tise CG
    Am J Med Genet A; 2023 Nov; 191(11):2743-2748. PubMed ID: 37675855
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.