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 *

130 related articles for article (PubMed ID: 9188658)

  • 1. 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]  

  • 2. 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]  

  • 3. Multiple lateral meningoceles, distinctive facies and skeletal anomalies: a new case of Lehman syndrome.
    Philip N; Andrac L; Moncla A; Sigaudy S; Zanon N; Lena G; Choux M
    Clin Dysmorphol; 1995 Oct; 4(4):347-51. PubMed ID: 8574426
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. 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]  

  • 6. 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]  

  • 7. 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]  

  • 8. 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]  

  • 9. 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]  

  • 10. Acrofacial dysostoses.
    Le Merrer M; Cikuli M; Ribier J; Briard ML
    Am J Med Genet; 1989 Jul; 33(3):318-22. PubMed ID: 2801764
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Femoral hypoplasia-unusual facies syndrome.
    Singh SK; Chandra D; Ravi RN; Kumari S
    Indian Pediatr; 1997 Aug; 34(8):747-8. PubMed ID: 9492409
    [No Abstract]   [Full Text] [Related]  

  • 12. Joint laxity, vitreoretinal degeneration, facial abnormalities, and generalized skeletal alterations: a new syndrome?
    Nishimura G; Hasegawa T; Sugii K; Tsuyama K; Matsuo N
    J Hum Genet; 1998; 43(3):191-4. PubMed ID: 9747034
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. Oto-facio-osseous-gonadal syndrome: a new form of syndromic deafness?
    da-Silva EO; Duarte AR; Lins TS
    Clin Genet; 1997 Jul; 52(1):51-5. PubMed ID: 9272713
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Familial osteosclerosis with abnormalities of the nervous system and meninges.
    Lehman RA; Stears JC; Wesenberg RL; Nusbaum ED
    J Pediatr; 1977 Jan; 90(1):49-54. PubMed ID: 830893
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. Double meningocele. Case report.
    Durmaz R; Arslantaş A; Ozön YH; Tel E
    Turk J Pediatr; 2000; 42(4):331-3. PubMed ID: 11196754
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Raine syndrome: report of a family with three affected sibs and further delineation of the syndrome.
    Hülskamp G; Wieczorek D; Rieder H; Louwen F; Hörnig-Franz I; Rickert CH; Horst J; Harms E; Rehder H
    Clin Dysmorphol; 2003 Jul; 12(3):153-60. PubMed ID: 14564151
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A boy with choanal atresia and cardiac defect: Burn-McKeown syndrome?
    Toriello HV; Higgins JV
    Clin Dysmorphol; 1999 Apr; 8(2):143-5. PubMed ID: 10319205
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Skeletal changes in a case of Goltz's syndrome (focal dermal hypoplasia).
    Consolo C; Pescatori E; Zorzi R
    Ital J Orthop Traumatol; 1983 Dec; 9(4):541-5. PubMed ID: 6676352
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.