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 *

117 related articles for article (PubMed ID: 26949683)

  • 1. A Wide Spectrum of Axial Mesodermal Dysplasia Complex With Rhombencephalic Anomaly: A Case Report.
    Kim KW; Seo JH; Ko MH; Won YH; Park SH
    Ann Rehabil Med; 2016 Feb; 40(1):162-7. PubMed ID: 26949683
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Overlap between VACTERL and hemifacial microsomia illustrating a spectrum of malformations seen in axial mesodermal dysplasia complex (AMDC).
    Bergmann C; Zerres K; Peschgens T; Senderek J; Hörnchen H; Rudnik-Schöneborn S
    Am J Med Genet A; 2003 Aug; 121A(2):151-5. PubMed ID: 12910495
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Axial Mesodermal Dysplasia Complex with a Unique Abnormal Course of Vestibulocochlear Nerve.
    Tok Umay S; Özgür A; Görür K; Kömür M; Balcı Y
    J Int Adv Otol; 2019 Aug; 15(2):317-320. PubMed ID: 30431015
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A case of Klippel-Feil syndrome with congenital enlarged Eustachian tube.
    Jovankovičová A; Jakubíková J; Durovčíková D
    Int J Pediatr Otorhinolaryngol; 2012 Apr; 76(4):596-600. PubMed ID: 22301355
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A Novel 12q13.2-q13.3 Microdeletion Syndrome With Combined Features of Diamond Blackfan Anemia, Pierre Robin Sequence and Klippel Feil Deformity.
    Roberti D; Conforti R; Giugliano T; Brogna B; Tartaglione I; Casale M; Piluso G; Perrotta S
    Front Genet; 2018; 9():549. PubMed ID: 30524470
    [TBL] [Abstract][Full Text] [Related]  

  • 6. The axial mesodermal dysplasia spectrum.
    Russell LJ; Weaver DD; Bull MJ
    Pediatrics; 1981 Feb; 67(2):176-82. PubMed ID: 7243441
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Report of a girl with Klippel-feil syndrome and Poland anomaly.
    Erol M; Caksen H; Tan O; Atik B; Unal O; Odabaş D
    Genet Couns; 2004; 15(4):469-72. PubMed ID: 15658624
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Goldenhar, Möbius and hypoglossia-hypodactyly anomalies in a patient: syndrome or association?
    Preis S; Majewski F; Hantschmann R; Schumacher H; Lenard HG
    Eur J Pediatr; 1996 May; 155(5):385-9. PubMed ID: 8741036
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Klippel-Feil syndrome. An unusual association with Sprengel deformity, omovertebral bone, and other skeletal, hematologic, and respiratory disorders. A case report.
    Greenspan A; Cohen J; Szabo RM
    Bull Hosp Jt Dis Orthop Inst; 1991; 51(1):54-62. PubMed ID: 1652319
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Neuroschisis of the cervical spinal cord in a patient with Klippel-Feil syndrome.
    Nagib MG; Larson DA; Maxwell RE; Chou SN
    Neurosurgery; 1987 Apr; 20(4):629-31. PubMed ID: 3587559
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Anesthesia for elective bilateral sagittal slip osteotomy of the mandible and genioplasty in a young man with Klippel-Feil syndrome, Sprengel deformity, and mandibular prognathism.
    Paramaswamy R
    J Dent Anesth Pain Med; 2019 Oct; 19(5):307-312. PubMed ID: 31723672
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Goldenhar-associated conditions (hemifacial microsomia) and congenital deformities of the spine.
    Tsirikos AI; McMaster MJ
    Spine (Phila Pa 1976); 2006 Jun; 31(13):E400-7. PubMed ID: 16741440
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A case of pontine tegmental cap dysplasia with comorbidity of oculoauriculovertebral spectrum.
    Chong PF; Haraguchi K; Torio M; Kirino M; Ogata R; Matsukura M; Sakai Y; Ishizaki Y; Yamamoto T; Kira R
    Brain Dev; 2015 Jan; 37(1):171-4. PubMed ID: 24650581
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Klippel-Feil anomaly with Sprengel anomaly, omovertebral bone, thumb abnormalities, and flexion-crease changes: novel association or syndrome?
    Larson AR; Josephson KD; Pauli RM; Opitz JM; Williams MS
    Am J Med Genet; 2001 Jun; 101(2):158-62. PubMed ID: 11391660
    [TBL] [Abstract][Full Text] [Related]  

  • 15. The association of Chiari type III malformation and Klippel-Feil syndrome with mirror movement: a case report.
    Erol FS; Ucler N; Yakar H
    Turk Neurosurg; 2011; 21(4):655-8. PubMed ID: 22194133
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Klippel-Feil syndrome associated with congenital cervical dislocation: report of an autopsy case.
    Shintaku M; Wada K; Koyama T; Kohno H; Sakamoto T; Hida S
    Clin Neuropathol; 2013; 32(1):51-7. PubMed ID: 22762890
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Report of a new case of axial mesodermal dysplasia complex.
    Bini R; Danti DA; Materassi M; Pela I
    Clin Genet; 1996 Nov; 50(5):407-10. PubMed ID: 9007333
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Axial mesodermal dysplasia spectrum.
    Stewart FJ; Nevin NC; Brown S
    Am J Med Genet; 1993 Feb; 45(4):426-9. PubMed ID: 8465843
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Studies of malformation syndromes of man XXXXI B: nosologic studies in the Hanhart and the Möbius syndrome.
    Herrmann J; Pallister PD; Gilbert EF; Vieseskul C; Bersu E; Pettersen JC; Opitz JM
    Eur J Pediatr; 1976 Apr; 122(1):19-55. PubMed ID: 1261566
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Klippel-Feil syndrome with congenital conductive deafness: report of a case and review of literature.
    Dubey SP; Ghosh LM
    Int J Pediatr Otorhinolaryngol; 1993 Jan; 25(1-3):201-8. PubMed ID: 8436466
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.