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2. Nucleotide variation analysis does not support a causal role for plexin-A1 in hereditary congenital facial paresis. van der Zwaag B; Burbach JP; Brunner HG; van Bokhoven H; Padberg GW Brain Res Dev Brain Res; 2005 Aug; 158(1-2):66-71. PubMed ID: 15996756 [TBL] [Abstract][Full Text] [Related]
5. 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]
7. 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]
8. Identifying new candidate genes for hereditary facial paresis on chromosome 3q21-q22 by RNA in situ hybridization in mouse. van der Zwaag B; Burbach JP; Scharfe C; Oefner PJ; Brunner HG; Padberg GW; van Bokhoven H Genomics; 2005 Jul; 86(1):55-67. PubMed ID: 15953540 [TBL] [Abstract][Full Text] [Related]
14. 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]
15. [A drooping face; the importance of family history in children with recurrent peripheral facial palsy]. Wit MA; de Vos-van Biezenbos JB; de Boe JR Ned Tijdschr Geneeskd; 2007 Feb; 151(6):364-6. PubMed ID: 17352302 [TBL] [Abstract][Full Text] [Related]
16. Delayed presentation of traumatic facial nerve (CN VII) paralysis. Napoli AM; Panagos P J Emerg Med; 2005 Nov; 29(4):421-4. PubMed ID: 16243199 [TBL] [Abstract][Full Text] [Related]
17. [Some problems in the literature of acupuncture treatment of peripheral facial paralysis and suggestions]. Wang SQ; Bai YP; Dong YX Zhongguo Zhen Jiu; 2007 Jun; 27(6):463-6. PubMed ID: 17663115 [TBL] [Abstract][Full Text] [Related]
18. Isolated facial and bulbar paresis: a persistent manifestation of neonatal myasthenia gravis. Jeannet PY; Marcoz JP; Kuntzer T; Roulet-Perez E Neurology; 2008 Jan; 70(3):237-8. PubMed ID: 18195270 [No Abstract] [Full Text] [Related]
19. [Congenital unilateral oculo-facial paralysis with retraction of the eyeball]. ZOLOG N Rev Otoneuroophtalmol; 1962; 34():136-43. PubMed ID: 14003904 [No Abstract] [Full Text] [Related]
20. [Congenital facial diplegia with external oculomotor paralysis (syndrome of Moebius)]. DE GISPERT-VAL M Rev Esp Pediatr; 1961; 17():235-47. PubMed ID: 13720524 [No Abstract] [Full Text] [Related] [Next] [New Search]