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 *

106 related articles for article (PubMed ID: 2471379)

  • 1. [A case of familial congenital analgesia with autosome-dominant type of inheritance].
    Aver'ianov IuN; Nechkina NP; Vinogradova NV; Zakhidov AIa
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1989; 89(3):128-31. PubMed ID: 2471379
    [TBL] [Abstract][Full Text] [Related]  

  • 2. The differential diagnosis of congenital analgesia and other diseases with diminished pain perception in childhood. Case report and review.
    Görke W
    Neuropediatrics; 1981 Feb; 12(1):33-44. PubMed ID: 6166892
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Congenital hereditary lymphedema (Nonne/Milroy).
    Farhud DD; Farhud I; Walizadeh GR; Djaber-Ansari M
    Padiatr Padol; 1989; 24(4):305-7. PubMed ID: 2616174
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [Familial indifference to pain with somatosensory asymmetry: possible central anomaly].
    Bowsher D; Lahuerta J; Peach B; Venn D; Haywar M; Campbell J; Mumford J; Haggett C
    Rev Neurol (Paris); 2002 Feb; 158(2):195-202. PubMed ID: 11965175
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Hereditary hemorrhagic telangiectasia with juvenile polyposis--coincidence or linked autosomal dominant inheritance?
    Ballauff A; Koletzko S
    Z Gastroenterol; 1999 May; 37(5):385-8. PubMed ID: 10413846
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Autosomal dominant insensitivity to pain with hyperplastic myelinopathy and autosomal dominant indifference to pain.
    Comings DE; Amromin GD
    Neurology; 1974 Sep; 24(9):838-48. PubMed ID: 4136553
    [No Abstract]   [Full Text] [Related]  

  • 7. [Congenital generalized analgesia (congenital indifference to pain) in 2 brothers decended from first cousins].
    Lièvre JA; Camus JP; Guillien P; Duclos M
    Bull Mem Soc Med Hop Paris; 1968 Mar; 119(5):447-56. PubMed ID: 4175250
    [No Abstract]   [Full Text] [Related]  

  • 8. Dominantly transmitted congenital indifference to pain.
    Landrieu P; Said G; Allaire C
    Ann Neurol; 1990 May; 27(5):574-8. PubMed ID: 1694419
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Norrbottnian congenital insensitivity to pain.
    Minde JK
    Acta Orthop Suppl; 2006 Apr; 77(321):2-32. PubMed ID: 16768023
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Cumulative familial olivopontocerebellar atrophy type IV].
    Erös E; Czeizel E
    Orv Hetil; 1994 Apr; 135(15):801-4. PubMed ID: 8177597
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Wooly hair].
    Baliaviĕiene GR
    Genetika; 1977; 13(4):739-41. PubMed ID: 892440
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Familial incidence of foramina parietalia permagna.
    Zábek M
    Neurochirurgia (Stuttg); 1987 Jan; 30(1):25-7. PubMed ID: 3561639
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Syndactyly of the ring and small finger.
    De Smet L; Mulier T; Fabry G
    Genet Couns; 1994; 5(1):45-9. PubMed ID: 8031535
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Congenital generalized analgesia in two siblings].
    Horanský V; Zuffová O; Mikulás L
    Kinderarztl Prax; 1968 Nov; 36(11):513-5. PubMed ID: 4181419
    [No Abstract]   [Full Text] [Related]  

  • 15. [Congenital indifference and congenital insensitivity to pain].
    Serratrice G
    Bull Acad Natl Med; 1992 May; 176(5):609-16; discussion 616-8. PubMed ID: 1384939
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Congenital analgesia].
    Finkenwirth H
    Arch Kinderheilkd; 1971; 182(3):272-94. PubMed ID: 4101733
    [No Abstract]   [Full Text] [Related]  

  • 17. [Dowling-Degos disease--an autosomal dominant genetic dermatosis].
    Biltz H; Kiessling M
    Z Hautkr; 1988 Aug; 63(8):642-4. PubMed ID: 3188604
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Familial neonatal and infantile seizures: an autosomal-dominant disorder.
    Zonana J; Silvey K; Strimling B
    Am J Med Genet; 1984 Jul; 18(3):455-9. PubMed ID: 6476007
    [TBL] [Abstract][Full Text] [Related]  

  • 19. On the phenotypic overlap between "severe" oto-palato digital type II syndrome and Larsen syndrome. Variable manifestation of a single autosomal dominant gene.
    Alembik Y; Stoll C; Messer J
    Genet Couns; 1997; 8(2):133-7. PubMed ID: 9219012
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Recurrent familial neuropathy: report of one family].
    Hinault P; Menault F; Le Marec B; Sabouraud O
    J Genet Hum; 1981 Dec; 29(4):409-17. PubMed ID: 7328415
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.