138 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. 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]
11. 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]
12. 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]
13. 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]
14. 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]
15. 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]
16. 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]
17. 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]
18. 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]
19. Differential diagnosis and diagnostic flow chart of joint hypermobility syndrome/ehlers-danlos syndrome hypermobility type compared to other heritable connective tissue disorders.
Colombi M; Dordoni C; Chiarelli N; Ritelli M
Am J Med Genet C Semin Med Genet; 2015 Mar; 169C(1):6-22. PubMed ID: 25821090
[TBL] [Abstract][Full Text] [Related]
20.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
[Next] [New Search]
