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 *

158 related articles for article (PubMed ID: 9309710)

  • 41. Outcomes of infants with idiopathic hypotonia.
    Strubhar AJ; Meranda K; Morgan A
    Pediatr Phys Ther; 2007; 19(3):227-35. PubMed ID: 17700352
    [TBL] [Abstract][Full Text] [Related]  

  • 42. [Joubert's syndrome].
    Vranjesević D; Djukić A; Sekulić N
    Srp Arh Celok Lek; 1989; 117(9-10):669-77. PubMed ID: 18709766
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Clinical and psychosocial follow-up study of children treated with extracorporeal membrane oxygenation.
    Wagner K; Risnes I; Berntsen T; Skarbø AB; Ramberg B; Vandvik IH; Rasmussen M; Nome T; Olsen KB; Svennevig JL
    Ann Thorac Surg; 2007 Oct; 84(4):1349-55. PubMed ID: 17888996
    [TBL] [Abstract][Full Text] [Related]  

  • 44. [Joubert's syndrome].
    Buissonnière RF; Storni V; Robain O; Ponsot G
    Ann Pediatr (Paris); 1990 Mar; 37(3):151-6. PubMed ID: 2190521
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Natural history of trisomy 18 and trisomy 13: II. Psychomotor development.
    Baty BJ; Jorde LB; Blackburn BL; Carey JC
    Am J Med Genet; 1994 Jan; 49(2):189-94. PubMed ID: 7509567
    [TBL] [Abstract][Full Text] [Related]  

  • 46. [Early child morbidity and late development following primary abdominal cesarean section in breech presentation near term].
    Kouam L; Werner-Spangenberg I; Saling E
    Geburtshilfe Frauenheilkd; 1986 Sep; 46(9):609-18. PubMed ID: 2429891
    [TBL] [Abstract][Full Text] [Related]  

  • 47. Familial cerebellar hypoplasia and pancytopenia without chromosomal breakages.
    Mahmood F; King MD; Smyth OP; Farrell MA
    Neuropediatrics; 1998 Dec; 29(6):302-6. PubMed ID: 10029349
    [TBL] [Abstract][Full Text] [Related]  

  • 48. "Joubert syndrome" revisited: key ocular motor signs with magnetic resonance imaging correlation.
    Maria BL; Hoang KB; Tusa RJ; Mancuso AA; Hamed LM; Quisling RG; Hove MT; Fennell EB; Booth-Jones M; Ringdahl DM; Yachnis AT; Creel G; Frerking B
    J Child Neurol; 1997 Oct; 12(7):423-30. PubMed ID: 9373798
    [TBL] [Abstract][Full Text] [Related]  

  • 49. Co-occurrence of distinct ciliopathy diseases in single families suggests genetic modifiers.
    Zaki MS; Sattar S; Massoudi RA; Gleeson JG
    Am J Med Genet A; 2011 Dec; 155A(12):3042-9. PubMed ID: 22002901
    [TBL] [Abstract][Full Text] [Related]  

  • 50. [Congenital oculomotor apraxia. Presentation--developmental problems--differential diagnosis].
    Steinlin M; Thun-Hohenstein L; Boltshauser E
    Klin Monbl Augenheilkd; 1992 May; 200(5):623-5. PubMed ID: 1614174
    [TBL] [Abstract][Full Text] [Related]  

  • 51. Molar tooth sign in Joubert syndrome: clinical, radiologic, and pathologic significance.
    Maria BL; Quisling RG; Rosainz LC; Yachnis AT; Gitten J; Dede D; Fennell E
    J Child Neurol; 1999 Jun; 14(6):368-76. PubMed ID: 10385844
    [TBL] [Abstract][Full Text] [Related]  

  • 52. Joubert syndrome: review and report of seven new cases.
    Kumandas S; Akcakus M; Coskun A; Gumus H
    Eur J Neurol; 2004 Aug; 11(8):505-10. PubMed ID: 15272893
    [TBL] [Abstract][Full Text] [Related]  

  • 53. Cognition, behavior, and development in Joubert syndrome.
    Fennell EB; Gitten JC; Dede DE; Maria BL
    J Child Neurol; 1999 Sep; 14(9):592-6. PubMed ID: 10488904
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Mucopolysaccharidosis type III (Sanfilippo disease) in Sweden: clinical presentation of 22 children diagnosed during a 30-year period.
    Malm G; Månsson JE
    Acta Paediatr; 2010 Aug; 99(8):1253-7. PubMed ID: 20337777
    [TBL] [Abstract][Full Text] [Related]  

  • 55. Joubert syndrome: large clinical variability and a unique neuroimaging aspect.
    Leão EK; Lima MM; Maia OO; Parizotto J; Kok F
    Arq Neuropsiquiatr; 2010 Apr; 68(2):273-6. PubMed ID: 20464299
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Joubert Syndrome and related disorders.
    Brancati F; Dallapiccola B; Valente EM
    Orphanet J Rare Dis; 2010 Jul; 5():20. PubMed ID: 20615230
    [TBL] [Abstract][Full Text] [Related]  

  • 57. Homozygosity mapping of a third Joubert syndrome locus to 6q23.
    Lagier-Tourenne C; Boltshauser E; Breivik N; Gribaa M; Bétard C; Barbot C; Koenig M
    J Med Genet; 2004 Apr; 41(4):273-7. PubMed ID: 15060101
    [TBL] [Abstract][Full Text] [Related]  

  • 58. Variability of outcome in Joubert syndrome.
    Casaer P; Vles JS; Devlieger H; Eggermont E; Boel M; Dom R
    Neuropediatrics; 1985 Feb; 16(1):43-5. PubMed ID: 3974803
    [TBL] [Abstract][Full Text] [Related]  

  • 59. Joubert syndrome is not a cause of classical autism.
    Takahashi TN; Farmer JE; Deidrick KK; Hsu BS; Miles JH; Maria BL
    Am J Med Genet A; 2005 Feb; 132A(4):347-51. PubMed ID: 15633174
    [TBL] [Abstract][Full Text] [Related]  

  • 60. [Neuroradiological aspects of Joubert syndrome: an analysis of two cases].
    Il'ina ES; Mukhin KIu; Alikhanov AA; Generalov VO
    Zh Nevrol Psikhiatr Im S S Korsakova; 2005; 105(10):59-61. PubMed ID: 16281384
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.