87 related articles for article (PubMed ID: 6858609)
21. [Familial progressive chronic bulbo-pontine paralysis with deafness. A case of Klippel-Trenaunay syndrome in siblings of the same family. Diagnostic and genetic problems].
Van Laere J
Rev Neurol (Paris); 1966 Aug; 115(2):289-95. PubMed ID: 5969547
[No Abstract] [Full Text] [Related]
22. [Familial bilateral facial hypogenesis].
Pérez Gómez JM; Oteo Revuelta JA; Hernández Palacios R; Jiménez López C
An Med Interna; 1989 Feb; 6(2):110. PubMed ID: 2491071
[No Abstract] [Full Text] [Related]
23. [Chronic progressive bulbopontine paralysis with deafness. A clinical syndrome].
van Laere J
Verh K Acad Geneeskd Belg; 1977; 39(3):126-58. PubMed ID: 605657
[No Abstract] [Full Text] [Related]
24. Middle ear adenoma diagnosed by recurrent facial paralysis.
Mori E; Kojima H; Wada K; Moriyama H
Auris Nasus Larynx; 2009 Feb; 36(1):75-8. PubMed ID: 18328653
[TBL] [Abstract][Full Text] [Related]
25. An unusual presentation of peripheral facial paralysis in a family.
Singh H; Singh I
J Assoc Physicians India; 1973 Oct; 21(10):905-7. PubMed ID: 4793281
[No Abstract] [Full Text] [Related]
26. The neuropathology of hereditary congenital facial palsy vs Möbius syndrome.
Verzijl HT; van der Zwaag B; Lammens M; ten Donkelaar HJ; Padberg GW
Neurology; 2005 Feb; 64(4):649-53. PubMed ID: 15728286
[TBL] [Abstract][Full Text] [Related]
27. Johnson-McMillin syndrome: report of another family.
Hennekam RC; Holtus FJ
Am J Med Genet; 1993 Oct; 47(5):714-6. PubMed ID: 8267002
[TBL] [Abstract][Full Text] [Related]
28. [An unusual inaugural form of sarcoidosis: alternating and recurrent facial paralysis].
Arnould G; Weber M; André JM; Brichet B
Rev Otoneuroophtalmol; 1971; 43(4):187-91. PubMed ID: 5113320
[No Abstract] [Full Text] [Related]
29. Refinement of the locus for hereditary congenital facial palsy on chromosome 3q21 in two unrelated families and screening of positional candidate genes.
Michielse CB; Bhat M; Brady A; Jafrid H; van den Hurk JA; Raashid Y; Brunner HG; van Bokhoven H; Padberg GW
Eur J Hum Genet; 2006 Dec; 14(12):1306-12. PubMed ID: 16912702
[TBL] [Abstract][Full Text] [Related]
30. Velopharyngeal closure in patients with facial paralysis: the fiberscopic examination of the velopharyngeal movements.
Ibuki K; Tamaki H; Matsuya T; Miyazaki T
Cleft Palate J; 1981 Apr; 18(2):100-9. PubMed ID: 6939504
[TBL] [Abstract][Full Text] [Related]
31. [Treatment of idiopathic facial nerve paralysis in childhood].
Neuwirth M
Orv Hetil; 1980 Feb; 121(8):447-50. PubMed ID: 7383682
[No Abstract] [Full Text] [Related]
32. Recurrent pleomorphic adenoma of the parotid gland.
Zbären P; Tschumi I; Nuyens M; Stauffer E
Am J Surg; 2005 Feb; 189(2):203-7. PubMed ID: 15720991
[TBL] [Abstract][Full Text] [Related]
33. Familial congenital facial palsy.
Kondev L; Bhadelia RA; Douglass LM
Pediatr Neurol; 2004 May; 30(5):367-70. PubMed ID: 15165644
[TBL] [Abstract][Full Text] [Related]
34. [Congenital facial paralysis in dizygotic twins].
Masaki S
Jibiinkoka; 1970 Jul; 42(7):517-22. PubMed ID: 5466251
[No Abstract] [Full Text] [Related]
35. Facial nerve paralysis secondary to occult malignant neoplasms.
Boahene DO; Olsen KD; Driscoll C; Lewis JE; McDonald TJ
Otolaryngol Head Neck Surg; 2004 Apr; 130(4):459-65. PubMed ID: 15100645
[TBL] [Abstract][Full Text] [Related]
36. Microtia-atresia with unilateral facial palsy.
Parkash H; Grewal MS; Sidhu SS
Indian Pediatr; 1982 May; 19(5):445-8. PubMed ID: 7141660
[No Abstract] [Full Text] [Related]
37. [Therapy of idiopathic facial nerve paralysis].
Klingler D; Bibl D
Wien Med Wochenschr; 1982 Apr; 132(7):149-53. PubMed ID: 7101958
[TBL] [Abstract][Full Text] [Related]
38. [Atypical facial pain in peripheral facial paralysis].
Ochoa-Urdangarain LA; Ramos RO; Garrido-Pérez R; Triana-Pérez I; González-González M; Morillas-Pérez A; Mendiondo-Ramos P; Ochoa-Varela SM
Rev Neurol; 2000 Oct 1-15; 31(7):698-9. PubMed ID: 11082872
[No Abstract] [Full Text] [Related]
39. [Infantile peripheral facial paralysis].
Carbonell J; Calpe A; Bleda C; Cánovas D
Acta Otorrinolaringol Esp; 1996; 47(6):429-33. PubMed ID: 9044580
[TBL] [Abstract][Full Text] [Related]
40. Familial systemic amyloidosis associated with bilateral sensorineural hearing loss and bilateral facial palsies.
Hornigold R; Patel AV; Ward VM; O'Connor AF
J Laryngol Otol; 2006 Sep; 120(9):778-80. PubMed ID: 16870032
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]