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Results: 1 to 20 of 46

Related Articles by Review for PubMed (Select 11669349)

1.

Quantitative assessment of brainstem development in Joubert syndrome and Dandy-Walker syndrome.

Maria BL, Bozorgmanesh A, Kimmel KN, Theriaque D, Quisling RG.

J Child Neurol. 2001 Oct;16(10):751-8.

PMID:
11669349
2.

Clinical nosologic and genetic aspects of Joubert and related syndromes.

Chance PF, Cavalier L, Satran D, Pellegrino JE, Koenig M, Dobyns WB.

J Child Neurol. 1999 Oct;14(10):660-6; discussion 669-72. Review.

PMID:
10511339
3.

Malformations of the posterior fossa: current perspectives.

Niesen CE.

Semin Pediatr Neurol. 2002 Dec;9(4):320-34. Review.

PMID:
12523556
4.

Recognition of the clinical signs and symptoms of Joubert syndrome.

Merritt L.

Adv Neonatal Care. 2003 Aug;3(4):178-86; quiz 187-8. Review.

PMID:
14502525
5.

Human malformations of the midbrain and hindbrain: review and proposed classification scheme.

Parisi MA, Dobyns WB.

Mol Genet Metab. 2003 Sep-Oct;80(1-2):36-53. Review.

PMID:
14567956
6.

Cerebello-oculo-renal syndromes including Arima, Senior-Löken and COACH syndromes: more than just variants of Joubert syndrome.

Satran D, Pierpont ME, Dobyns WB.

Am J Med Genet. 1999 Oct 29;86(5):459-69. Review.

PMID:
10508989
7.

[Joubert's syndrome].

Buissonnière RF, Storni V, Robain O, Ponsot G.

Ann Pediatr (Paris). 1990 Mar;37(3):151-6. Review. French.

PMID:
2190521
8.

Ritscher-Schinzel (3C) syndrome: documentation of the phenotype.

Kosaki K, Curry CJ, Roeder E, Jones KL.

Am J Med Genet. 1997 Feb 11;68(4):421-7. Review.

PMID:
9021015
9.

Dandy-Walker complex and syringomyelia in an adult: case report and discussion.

Hammond CJ, Chitnavis B, Penny CC, Strong AJ.

Neurosurgery. 2002 Jan;50(1):191-4. Review.

PMID:
11844250
10.

Cerebellar and brainstem development: an overview in relation to Joubert syndrome.

Yachnis AT, Rorke LB.

J Child Neurol. 1999 Sep;14(9):570-3. Review.

PMID:
10488901
11.

[Differential diagnosis of Dandy-Walker syndrome different presentations].

Tobías-González P, Gil Mira M, Valero de Bernabé J, Zapardiel I.

Ginecol Obstet Mex. 2012 Aug;80(8):534-9. Review. Spanish.

PMID:
23088073
12.

Posterior fossa malformations.

Shekdar K.

Semin Ultrasound CT MR. 2011 Jun;32(3):228-41. doi: 10.1053/j.sult.2011.02.003. Review.

PMID:
21596278
13.
14.

Genotypes and phenotypes of Joubert syndrome and related disorders.

Valente EM, Brancati F, Dallapiccola B.

Eur J Med Genet. 2008 Jan-Feb;51(1):1-23. doi: 10.1016/j.ejmg.2007.11.003. Epub 2007 Nov 23. Review.

PMID:
18164675
15.

Neurocutaneous melanosis and the Dandy-Walker complex: an uncommon but not so insignificant association.

Marnet D, Vinchon M, Mostofi K, Catteau B, Kerdraon O, Dhellemmes P.

Childs Nerv Syst. 2009 Dec;25(12):1533-9. doi: 10.1007/s00381-009-0976-6. Epub 2009 Aug 27. Review.

PMID:
19711088
16.

Adult diagnosed Dandy Walker malformation presenting as an acute brainstem event--a case report and review of the literature.

Warwick CT, Reyes BJ, Ayoob MR, Subit M.

W V Med J. 2008 Jan-Feb;104(1):25-7. Review. Erratum in: W V Med J. 2008 Mar-Apr;104(2):table of contents.

PMID:
18335783
17.

The fetal cerebellum. Pitfalls in diagnosis and management.

Malinger G, Lev D, Lerman-Sagie T.

Prenat Diagn. 2009 Apr;29(4):372-80. doi: 10.1002/pd.2196. Review.

PMID:
19194867
18.

Dandy-Walker malformation: analysis of 38 cases.

Pascual-Castroviejo I, Velez A, Pascual-Pascual SI, Roche MC, Villarejo F.

Childs Nerv Syst. 1991 Apr;7(2):88-97. Review.

PMID:
1863935
19.

Joubert syndrome: a clinical and pathological description of an affected male and a female fetus from the same sibship.

van Dorp DB, Palan A, Kwee ML, Barth PG, van der Harten JJ.

Am J Med Genet. 1991 Jul 1;40(1):100-4. Review.

PMID:
1887836
20.

Congenital cutis laxa with ligamentous laxity and delayed development, Dandy-Walker malformation and minor heart and osseous defects.

Biver A, De Rijcke S, Toppet V, Ledoux-Corbusier M, Van Maldergem L.

Clin Genet. 1994 Jun;45(6):318-22. Review.

PMID:
7523003
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