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.
Pubmed for Handhelds
PUBMED FOR HANDHELDS
Journal Abstract Search
160 related items for PubMed ID: 10319197
21. Prevalence of Hand Malformations in Patients With Moebius Syndrome and Their Management. Telich-Tarriba JE, Navarro-Barquin DF, Verdezoto-Gaibor K, Cardenas-Mejia A. Hand (N Y); 2022 Nov; 17(6):1292-1296. PubMed ID: 33641474 [Abstract] [Full Text] [Related]
22. [Moebius syndrome. Apropos of 2 cases]. Speeg C, Lobstein-Henry Y, Ruolt J, Flament J. J Fr Ophtalmol; 1991 Nov; 14(2):103-8. PubMed ID: 1880337 [Abstract] [Full Text] [Related]
23. Poland-Möbius syndrome: evaluation by computerized tomography. Hopper KD, Haas DK, Rice MM, Freeley DA, Taubner RW, Ghaed N. South Med J; 1985 May; 78(5):523-7. PubMed ID: 2986296 [Abstract] [Full Text] [Related]
24. Poland syndrome: a case with a combination of syndromes. Farina D, Gatto G, Leonessa L, Sala U, Gomirato G. Panminerva Med; 1999 Sep; 41(3):259-60. PubMed ID: 10568126 [Abstract] [Full Text] [Related]
25. Childhood psychosis in a case of Moebius syndrome. Gillberg C, Winnergård I. Neuropediatrics; 1984 Aug; 15(3):147-9. PubMed ID: 6483113 [Abstract] [Full Text] [Related]
26. Poland anomaly in mother and daughter. Cobben JM, Robinson PH, van Essen AJ, van der Wiel HL, ten Kate LP. Am J Med Genet; 1989 Aug; 33(4):519-21. PubMed ID: 2556920 [Abstract] [Full Text] [Related]
27. [The role of heredity in the genesis of idiopathic peripheral facial paralysis. A case report]. Pérez González R, Benito Orejas JI, Morais Pérez D, Miyar Villar V, Martín Sigüenza G. Acta Otorrinolaringol Esp; 1997 Aug; 48(5):405-8. PubMed ID: 9376164 [Abstract] [Full Text] [Related]
28. The Moebius sequence--report of a case and a short annotation. Ng SP, Ho NK. J Singapore Paediatr Soc; 1992 Aug; 34(3-4):226-9. PubMed ID: 1305667 [Abstract] [Full Text] [Related]
30. [Familial occurrence of relapsing facial paralysis with paralysis of the oculomotor muscles]. Lisch K. Klin Monbl Augenheilkd; 1969 Sep; 155(3):400-4. PubMed ID: 5354477 [No Abstract] [Full Text] [Related]
31. A three generations family with blepharo-naso-facial malformations suggestive of Pashayan syndrome. Stoll C, Terzic J, Fischbach M. Genet Couns; 1999 Sep; 10(4):337-43. PubMed ID: 10631920 [Abstract] [Full Text] [Related]