258 related articles for article (PubMed ID: 18178993)
1. Joubert syndrome: a major brain malformation.
Ray J; Majumder AG; Das D; Mukhopadhyay D; Mondol S
J Indian Med Assoc; 2007 Jul; 105(7):392-4. PubMed ID: 18178993
[TBL] [Abstract][Full Text] [Related]
2. [Joubert's syndrome: report of 12 cases].
Barreirinho MS; Teixeira J; Moreira NC; Bastos S; Gonçalvez S; Barbot MC
Rev Neurol; 2001 May 1-15; 32(9):812-7. PubMed ID: 11424029
[TBL] [Abstract][Full Text] [Related]
3. 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; 86(5):459-69. PubMed ID: 10508989
[TBL] [Abstract][Full Text] [Related]
4. Mitochondrial dysfunction in a patient with Joubert syndrome.
Morava E; Dinopoulos A; Kroes HY; Rodenburg RJ; van Bokhoven H; van den Heuvel LP; Smeitink JA
Neuropediatrics; 2005 Jun; 36(3):214-7. PubMed ID: 15944909
[TBL] [Abstract][Full Text] [Related]
5. [Prenatal suspicion of Joubert syndrome].
Benito-Gutiérrez M; Madurga-Revilla P; González-López A; Martín-García V; Alonso-Torres A; Martínez-Bermejo A
Rev Neurol; 2007 Aug 1-15; 45(3):174. PubMed ID: 17661277
[No Abstract] [Full Text] [Related]
6. Joubert syndrome (and related disorders) (OMIM 213300).
Parisi MA; Doherty D; Chance PF; Glass IA
Eur J Hum Genet; 2007 May; 15(5):511-21. PubMed ID: 17377524
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. Burkitt lymphoma in a child with Joubert syndrome.
Brinkman J; de Nef JJ; Barth PG; Verschuur AC
Pediatr Blood Cancer; 2005 Apr; 44(4):397-9. PubMed ID: 15562502
[TBL] [Abstract][Full Text] [Related]
9. Ophthalmic features of Joubert syndrome.
Khan AO; Oystreck DT; Seidahmed MZ; AlDrees A; Elmalik SA; Alorainy IA; Salih MA
Ophthalmology; 2008 Dec; 115(12):2286-9. PubMed ID: 19041481
[TBL] [Abstract][Full Text] [Related]
10. Neuroepithelial cysts in a patient with Joubert syndrome plus renal cysts.
Marsh SE; Grattan-Smith P; Pereira J; Barkovich AJ; Gleeson JG
J Child Neurol; 2004 Mar; 19(3):227-31. PubMed ID: 15119486
[TBL] [Abstract][Full Text] [Related]
11. 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. PubMed ID: 10511339
[TBL] [Abstract][Full Text] [Related]
12. Genotypes and phenotypes of Joubert syndrome and related disorders.
Valente EM; Brancati F; Dallapiccola B
Eur J Med Genet; 2008; 51(1):1-23. PubMed ID: 18164675
[TBL] [Abstract][Full Text] [Related]
13. [Joubert syndrome: a report of 5 cases].
Calleja-Pérez B; Fernández-Jaén A; Martínez-Bermejo A; Pascual-Castroviejo I
Rev Neurol; 1998 Apr; 26(152):548-50. PubMed ID: 9796002
[TBL] [Abstract][Full Text] [Related]
14. Hypoplasia of deep cerebellar nuclei in joubert syndrome.
Kuchukhidze G; Rauchenzauner M; Gotwald T; Janecke A; Trinka E
Pediatr Neurol; 2009 Jun; 40(6):474-6. PubMed ID: 19433286
[TBL] [Abstract][Full Text] [Related]
15. [Joubert syndrome. Report of a new case and review of literature (author's transl)].
Aparicio Meix JM; Pascual Castroviejo I
An Esp Pediatr; 1980 Jul; 13(7):625-32. PubMed ID: 7416655
[TBL] [Abstract][Full Text] [Related]
16. [Joubert syndrome].
Scheuer E; Lerman-Sagie T; Fattal A; Meir JJ; Harel S
Harefuah; 1995 Dec; 129(12):543-6, 615. PubMed ID: 8682351
[TBL] [Abstract][Full Text] [Related]
17. COACH syndrome: report of two brothers with congenital hepatic fibrosis, cerebellar vermis hypoplasia, oligophrenia, ataxia, and mental retardation.
Gentile M; Di Carlo A; Susca F; Gambotto A; Caruso ML; Panella C; Vajro P; Guanti G
Am J Med Genet; 1996 Aug; 64(3):514-20. PubMed ID: 8862632
[TBL] [Abstract][Full Text] [Related]
18. Clinics in diagnostic imaging (118).
Subramanian S; Hari S; Santosh Kumar S
Singapore Med J; 2007 Sep; 48(9):869-72; quiz 873. PubMed ID: 17728972
[TBL] [Abstract][Full Text] [Related]
19. Joubert syndrome: episodic hyperpnea, abnormal eye movements, retardation and ataxia, associated with dysplasia of the cerebellar vermis.
Boltshauser E; Isler W
Neuropadiatrie; 1977 Feb; 8(1):57-66. PubMed ID: 576733
[TBL] [Abstract][Full Text] [Related]
20. Patterns of fractional anisotropy changes in white matter of cerebellar peduncles distinguish spinocerebellar ataxia-1 from multiple system atrophy and other ataxia syndromes.
Prakash N; Hageman N; Hua X; Toga AW; Perlman SL; Salamon N
Neuroimage; 2009 Aug; 47 Suppl 2():T72-81. PubMed ID: 19446636
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
