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 *

105 related articles for article (PubMed ID: 4045487)

  • 1. Familial syringomyelia.
    Busis NA; Hochberg FH
    J Neurol Neurosurg Psychiatry; 1985 Sep; 48(9):936-8. PubMed ID: 4045487
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Familial syringomyelia: a report of four cases.
    Caraceni T; Giovannini P
    Arch Psychiatr Nervenkr (1970); 1977 Dec; 224(4):331-40. PubMed ID: 305236
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Discordant syringomyelia twins in familial syringomyelia].
    Malessa R; Jörg J
    Nervenarzt; 1986 Jul; 57(7):422-6. PubMed ID: 3748236
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Familial syringomyelia in two siblings: case report.
    Koç K; Anik I; Anik Y; Ceylan S
    Turk Neurosurg; 2007 Oct; 17(4):251-4. PubMed ID: 18050067
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Familial syringomyelia.
    Bentley SJ; Campbell MJ; Kaufmann P
    J Neurol Neurosurg Psychiatry; 1975 Apr; 38(4):346-9. PubMed ID: 1141921
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [4 cases of familial syringomyelia in a single generation].
    Ishchenko MM; Degtiar VV; Komorovskaia IaM
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1976; 76(5):662-5. PubMed ID: 936867
    [No Abstract]   [Full Text] [Related]  

  • 7. Three sisters with Chiari I malformation with and without associated syringomyelia.
    Weisfeld-Adams JD; Carter MR; Likeman MJ; Rankin J
    Pediatr Neurosurg; 2007; 43(6):533-8. PubMed ID: 17992048
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A novel fibroblast growth factor receptor 2 mutation in Crouzon syndrome associated with Chiari type I malformation and syringomyelia.
    Fujisawa H; Hasegawa M; Kida S; Yamashita J
    J Neurosurg; 2002 Aug; 97(2):396-400. PubMed ID: 12186468
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Hereditary features of syringomyelia].
    Shiikina AV
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1969; 69(10):1509-14. PubMed ID: 5369949
    [No Abstract]   [Full Text] [Related]  

  • 10. Craniometric Analysis of the Hindbrain and Craniocervical Junction of Chihuahua, Affenpinscher and Cavalier King Charles Spaniel Dogs With and Without Syringomyelia Secondary to Chiari-Like Malformation.
    Knowler SP; Kiviranta AM; McFadyen AK; Jokinen TS; La Ragione RM; Rusbridge C
    PLoS One; 2017; 12(1):e0169898. PubMed ID: 28121988
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Familial Chiari type I malformation with syringomyelia in two siblings: case report and review of the literature.
    Mavinkurve GG; Sciubba D; Amundson E; Jallo GI
    Childs Nerv Syst; 2005 Nov; 21(11):955-9. PubMed ID: 15821947
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [A familial case of syringomyelia].
    Kuberger MB; Shcherbakova EIa; Nikolaeva NV; Khavkin AI; Kapustin AV
    Pediatriia; 1991; (3):93-5. PubMed ID: 2047194
    [No Abstract]   [Full Text] [Related]  

  • 13. Syringomyelia with syringobulbia presenting as vocal fold paralysis.
    Viswanatha B
    Ear Nose Throat J; 2009 Jul; 88(7):E20. PubMed ID: 19623519
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Treatment of Syringomyelia in Patients with Arachnoiditis at the Craniocervical Junction.
    Davidoff CL; Liu S; Wong JHY; Koustais S; Rogers JM; Stoodley MA
    World Neurosurg; 2017 Nov; 107():565-573. PubMed ID: 28842236
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Use of Morphometric Mapping to Characterise Symptomatic Chiari-Like Malformation, Secondary Syringomyelia and Associated Brachycephaly in the Cavalier King Charles Spaniel.
    Knowler SP; Cross C; Griffiths S; McFadyen AK; Jovanovik J; Tauro A; Kibar Z; Driver CJ; La Ragione RM; Rusbridge C
    PLoS One; 2017; 12(1):e0170315. PubMed ID: 28122014
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Syringomyelia in twin brothers discordant for Chiari I malformation: case report.
    Tubbs RS; Wellons JC; Blount JP; Oakes WJ
    J Child Neurol; 2004 Jun; 19(6):459-62. PubMed ID: 15449382
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [The probable character of heredity in familial syringomyelia].
    Sirotkin VM; Pazoni I; Gimadeeva PM
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1973; 73(6):831-6. PubMed ID: 4753594
    [No Abstract]   [Full Text] [Related]  

  • 18. Chiari Type I malformation and syringomyelia in unrelated patients with blepharophimosis. Report of two cases.
    Paquis P; Lonjon M; Brunet M; Lambert JC; Grellier P
    J Neurosurg; 1998 Nov; 89(5):835-8. PubMed ID: 9817424
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A nationwide survey of familial syringomyelia in Japan.
    Yabe I; Matsushima M; Seki T; Sasaki H
    J Neurol Sci; 2017 Oct; 381():128-129. PubMed ID: 28991663
    [No Abstract]   [Full Text] [Related]  

  • 20. [The heredity of syringomyelia].
    Skvirskaia KB
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1970; 70(9):1281-6. PubMed ID: 5511105
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 6.