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 *

135 related articles for article (PubMed ID: 34121137)

  • 1. Early diagnosis of lateral meningocele syndrome in an infant without neurological symptoms based on genomic analysis.
    Yamada M; Arimitsu T; Suzuki H; Miwa T; Kosaki K
    Childs Nerv Syst; 2022 Mar; 38(3):659-663. PubMed ID: 34121137
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Truncating mutations in the last exon of NOTCH3 cause lateral meningocele syndrome.
    Gripp KW; Robbins KM; Sobreira NL; Witmer PD; Bird LM; Avela K; Makitie O; Alves D; Hogue JS; Zackai EH; Doheny KF; Stabley DL; Sol-Church K
    Am J Med Genet A; 2015 Feb; 167A(2):271-81. PubMed ID: 25394726
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Neurosurgical Management of Lateral Meningocele Syndrome: A Clinical Update for the Pediatric Neurosurgeon.
    Cuoco JA; Klein BJ; Busch CM; Gosnell HL; Kar A; Marvin EA; Apfel LS
    Pediatr Neurosurg; 2020; 55(1):2-11. PubMed ID: 31838470
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Management of lateral meningocele syndrome in a child without neurological symptoms and literature review.
    Han Y; Chen M; Wang H
    Childs Nerv Syst; 2022 May; 38(5):903-907. PubMed ID: 35128567
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Lateral meningocele (Lehman) syndrome: A child with a novel NOTCH3 mutation.
    Ejaz R; Qin W; Huang L; Blaser S; Tetreault M; Hartley T; Boycott KM; Carter MT;
    Am J Med Genet A; 2016 Apr; 170A(4):1070-5. PubMed ID: 26754023
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Neurosurgical management in lateral meningocele syndrome: case report.
    Brown EC; Gupta K; Sayama C
    J Neurosurg Pediatr; 2017 Feb; 19(2):232-238. PubMed ID: 27911244
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Expansion of the phenotype of lateral meningocele syndrome.
    Cappuccio G; Apuzzo D; Alagia M; Torella A; Pinelli M; Franco B; Corrado B; Del Giudice E; D'Amico A; Nigro V; ; Brunetti-Pierri N
    Am J Med Genet A; 2020 May; 182(5):1259-1262. PubMed ID: 32141180
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Lateral meningocele syndrome: additional report and further evidence supporting a connective tissue basis.
    Alves D; Sampaio M; Figueiredo R; Leão M
    Am J Med Genet A; 2013 Jul; 161A(7):1768-72. PubMed ID: 23696373
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Dural ectasia in Marfan syndrome and other hereditary connective tissue disorders: a 10-year follow-up study.
    Böker T; Vanem TT; Pripp AH; Rand-Hendriksen S; Paus B; Smith HJ; Lundby R
    Spine J; 2019 Aug; 19(8):1412-1421. PubMed ID: 30998996
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A Case of Lateral Meningocele Syndrome without Lateral Meningoceles.
    Rubadeux D; Owens JW; Shillington A
    Mol Syndromol; 2024 Aug; 15(4):328-332. PubMed ID: 39119451
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Lateral meningocele syndrome: vertical transmission and expansion of the phenotype.
    Chen KM; Bird L; Barnes P; Barth R; Hudgins L
    Am J Med Genet A; 2005 Mar; 133A(2):115-21. PubMed ID: 15666314
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Infantile Presentation of Lehman Syndrome with Multiple Lateral Meningoceles, Dural Ectasias, and Herniation of Conus: A Rare Case Report.
    Amuthabarathi M; Harshith K; Nagarajan K
    J Pediatr Neurosci; 2020; 15(2):111-115. PubMed ID: 33042242
    [TBL] [Abstract][Full Text] [Related]  

  • 13. The lateral meningocele syndrome mutation causes marked osteopenia in mice.
    Canalis E; Yu J; Schilling L; Yee SP; Zanotti S
    J Biol Chem; 2018 Sep; 293(36):14165-14177. PubMed ID: 30042232
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Rupture of Giant Anterior Sacral Meningocele in a Patient with Marfan Syndrome: Diagnosis and Management.
    Hollenberg AM; Baldwin AL; Mesfin A; Silberstein H
    World Neurosurg; 2018 Nov; 119():137-141. PubMed ID: 30092475
    [TBL] [Abstract][Full Text] [Related]  

  • 15. An antibody to Notch3 reverses the skeletal phenotype of lateral meningocele syndrome in male mice.
    Yu J; Siebel CW; Schilling L; Canalis E
    J Cell Physiol; 2020 Jan; 235(1):210-220. PubMed ID: 31188489
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Multidisciplinary approach for repair of a large ventral thoracic meningocele in neurofibromatosis-1; a systematic review of the literature and case report.
    Lehner K; Lubelski D; Witham T; Luciano M; Tuffaha S; Yang R; Yang S; Belzberg A
    Clin Neurol Neurosurg; 2021 Nov; 210():106996. PubMed ID: 34739882
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Lateral meningocele syndrome: three new patients and review of the literature.
    Gripp KW; Scott CI; Hughes HE; Wallerstein R; Nicholson L; States L; Bason LD; Kaplan P; Zderic SA; Duhaime AC; Miller F; Magnusson MR; Zackai EH
    Am J Med Genet; 1997 Jun; 70(3):229-39. PubMed ID: 9188658
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Late diagnosis of lateral meningocele syndrome in a 55-year-old woman with symptoms of joint instability and chronic musculoskeletal pain.
    Castori M; Morlino S; Ritelli M; Brancati F; De Bernardo C; Colombi M; Grammatico P
    Am J Med Genet A; 2014 Feb; 164A(2):528-34. PubMed ID: 24311540
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Lehman syndrome: a new syndrome for pierre robin sequence.
    Correia-Sá I; Horta R; Neto T; Amarante J; Marques M
    Cleft Palate Craniofac J; 2015 May; 52(3):369-72. PubMed ID: 23962060
    [TBL] [Abstract][Full Text] [Related]  

  • 20.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 7.