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Quoted phrase not found in phrase index: "Abnormal seventh cranial physiology"
Page 1
Seventh cranial neuropathy.
Gilchrist JM. Gilchrist JM. Semin Neurol. 2009 Feb;29(1):5-13. doi: 10.1055/s-0028-1124018. Epub 2009 Feb 12. Semin Neurol. 2009. PMID: 19214928 Review.
Facial neuropathy, or seventh cranial neuropathy, is the most common cranial neuropathy. The anatomy of the facial nerve is rather complex for a cranial nerve, with a long intracranial course, in which the nerve takes three bends (or genu). ...
Facial neuropathy, or seventh cranial neuropathy, is the most common cranial neuropathy. The anatomy of the facial nerv …
Long-term outcomes of strabismus surgery in Mobius sequence.
Lueder GT, Galli M. Lueder GT, et al. Strabismus. 2019 Jun;27(2):43-46. doi: 10.1080/09273972.2019.1599402. Epub 2019 Apr 8. Strabismus. 2019. PMID: 30958093
Purpose: Mobius sequence is a rare disorder that results from underdevelopment of the sixth and seventh cranial nerves, with subsequent facial weakness and impairment of ocular abduction. ...Methods: The long-term follow-up results in five children with Mobius seque …
Purpose: Mobius sequence is a rare disorder that results from underdevelopment of the sixth and seventh cranial nerves, with s …
Duraplasty using autologous fascia lata reenforced by on-site pedicled muscle flap: technical note.
Abuzayed B, Kafadar AM, Oğuzoğlu SA, Canbaz B, Kaynar MY. Abuzayed B, et al. J Craniofac Surg. 2009 Mar;20(2):435-8. doi: 10.1097/scs.0b013e31819b968f. J Craniofac Surg. 2009. PMID: 19326487
Besides not applying watertight closure of the duraplasty, the inviability and the poor vascularization of the graft and/or the dura (eg, reoperations, multiple operations, or cranial radiotherapy) may lead to delayed healing of the suture site and resultant persistent CSF …
Besides not applying watertight closure of the duraplasty, the inviability and the poor vascularization of the graft and/or the dura (eg, re …
Pulpal blood flow: effects of corticotomy and midline osteotomy in surgically assisted rapid palatal expansion.
Oztürk M, Doruk C, Ozeç I, Polat S, Babacan H, Biçakci AA. Oztürk M, et al. J Craniomaxillofac Surg. 2003 Apr;31(2):97-100. doi: 10.1016/s1010-5182(02)00188-9. J Craniomaxillofac Surg. 2003. PMID: 12628599
The blood flow was investigated pre- and postoperatively, on the first, third, and seventh postoperative days bilaterally in 13 cases. RESULTS: The results of this study indicate that ischaemia of the pulp can occur following osteotomy at the Le Fort I level. ...
The blood flow was investigated pre- and postoperatively, on the first, third, and seventh postoperative days bilaterally in 13 cases …
Controlled trial of early dexamethasone treatment for the prevention of chronic lung disease in preterm infants: a 3-year follow-up.
Romagnoli C, Zecca E, Luciano R, Torrioli G, Tortorolo G. Romagnoli C, et al. Pediatrics. 2002 Jun;109(6):e85. doi: 10.1542/peds.109.6.e85. Pediatrics. 2002. PMID: 12042579 Clinical Trial.
The original trial included 25 treated neonates who received dexamethasone intravenously from the fourth day of life for 7 days (0.5 mg/kg/d for the first 3 days, 0.25 mg/kg/d the next 3 days, and 0.125 mg/kg/d on the seventh day), and 25 untreated neonates as controls. Fo …
The original trial included 25 treated neonates who received dexamethasone intravenously from the fourth day of life for 7 days (0.5 mg/kg/d …
Predictive value of brain-stem auditory evoked potentials in children with post-traumatic coma produced by diffuse brain injury.
Bosch Blancafort J, Olesti Marco M, Poch Puig JM, Rubio García E, Nogués Bara P, Iglesias Berenguer J. Bosch Blancafort J, et al. Childs Nerv Syst. 1995 Jul;11(7):400-5. doi: 10.1007/BF00717405. Childs Nerv Syst. 1995. PMID: 7585668
On the basis of the results, children were divided into three groups: the first consisted of children with bilateral and normal BAEPs (n = 19); the second of those with asymmetrical BAEPs (n = 6); and the third of those in whom BAEPs has disappeared or in whom only responses of t …
On the basis of the results, children were divided into three groups: the first consisted of children with bilateral and normal BAEPs (n = 1 …
Spectrum of CHD7 mutations in 110 individuals with CHARGE syndrome and genotype-phenotype correlation.
Lalani SR, Safiullah AM, Fernbach SD, Harutyunyan KG, Thaller C, Peterson LE, McPherson JD, Gibbs RA, White LD, Hefner M, Davenport SL, Graham JM, Bacino CA, Glass NL, Towbin JA, Craigen WJ, Neish SR, Lin AE, Belmont JW. Lalani SR, et al. Am J Hum Genet. 2006 Feb;78(2):303-14. doi: 10.1086/500273. Epub 2005 Dec 29. Am J Hum Genet. 2006. PMID: 16400610 Free PMC article.
Characteristic associated anomalies include ocular coloboma, choanal atresia, cranial nerve defects, distinctive external and inner ear abnormalities, hearing loss, cardiovascular malformations, urogenital anomalies, and growth retardation. ...Phenotypically, the mu …
Characteristic associated anomalies include ocular coloboma, choanal atresia, cranial nerve defects, distinctive external and inner e …
Rapp-Hodgkin ectodermal dysplasia syndrome: the clinical and molecular overlap with Hay-Wells syndrome.
Kannu P, Savarirayan R, Ozoemena L, White SM, McGrath JA. Kannu P, et al. Am J Med Genet A. 2006 Apr 15;140(8):887-91. doi: 10.1002/ajmg.a.31187. Am J Med Genet A. 2006. PMID: 16532463
We report on the clinical and molecular abnormalities in a 7-month-old girl and her mother with an ectodermal dysplasia disorder that most closely resembles Rapp-Hodgkin syndrome (RHS). ...This mutation is predicted to disrupt the normal repressive function of the t …
We report on the clinical and molecular abnormalities in a 7-month-old girl and her mother with an ectodermal dysplasia disorder that …
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. Uyguner ZO, et al. Eur J Med Genet. 2015 Jun-Jul;58(6-7):358-63. doi: 10.1016/j.ejmg.2015.05.003. Epub 2015 May 23. Eur J Med Genet. 2015. PMID: 26007620
Moebius syndrome (MBS) is a rare congenital disorder characterized by rhombencephalic mal development, mainly presenting with facial palsy with limited gaze abduction. Most cases are sporadic, possibly caused by a combination of environmental and genetic factors; however, …
Moebius syndrome (MBS) is a rare congenital disorder characterized by rhombencephalic mal development, mainly presenting with facial …
Narrow internal auditory meatus: an idiopathic case confirming the origin and pathway of vestibular evoked myogenic potentials in humans.
Ito K, Ishimoto S, Murofushi T. Ito K, et al. Arch Otolaryngol Head Neck Surg. 2001 Mar;127(3):275-8. doi: 10.1001/archotol.127.3.275. Arch Otolaryngol Head Neck Surg. 2001. PMID: 11255471
MAIN OUTCOME MEASURES: Imaging studies and functional studies concerning the seventh and eighth cranial nerves. RESULTS: Of the 4 nerves in the IAM, all but the cochlear nerve had normal function and normal courses, despite the pronounced narrowing of the IAM …
MAIN OUTCOME MEASURES: Imaging studies and functional studies concerning the seventh and eighth cranial nerves. RESULTS: Of th …