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.
113 related articles for article (PubMed ID: 10580893)
1. A case in the spectrum of the oculo-encephalo-hepato-renal syndrome. Ehara H; Tamaoki Y; Eda I Pediatr Neurol; 1999 Oct; 21(4):757-62. PubMed ID: 10580893 [TBL] [Abstract][Full Text] [Related]
2. Joubert syndrome with congenital hepatic fibrosis: an entity in the spectrum of oculo-encephalo-hepato-renal disorders. Lewis SM; Roberts EA; Marcon MA; Harvey E; Phillips MJ; Chuang SA; Buncic JR; Clarke JT Am J Med Genet; 1994 Oct; 52(4):419-26. PubMed ID: 7538263 [TBL] [Abstract][Full Text] [Related]
4. [Cerebro-oculo-hepato-renal syndrome (Arima's syndrome) with slowly progressive renal insufficiency and epilepsy]. Kubota M; Shinozaki M; Ishizaki A; Kurata K No To Hattatsu; 1991 Nov; 23(6):596-600. PubMed ID: 1760207 [TBL] [Abstract][Full Text] [Related]
5. Amniotic band syndrome associated with sacral meningocele and anal atresia. Eren E; Buyukyavuz I; Ayata A Pediatr Int; 2010 Jun; 52(3):505-6. PubMed ID: 20723131 [No Abstract] [Full Text] [Related]
6. [A case of arima syndrome (cerebro-oculo-hepato-renal syndrome) in long-term survival with hemodialysis]. Katase K; Hashizume K; Yoneda T; Yoshida T Nihon Jinzo Gakkai Shi; 2006; 48(8):731-5. PubMed ID: 17184024 [TBL] [Abstract][Full Text] [Related]
7. [Magnetic resonance study of a case of alobar holoprosencephaly associated with meningocele]. Magnani F; Tigano G; Nicoletti G; Pero G Radiol Med; 1987 Dec; 74(6):572-4. PubMed ID: 3432618 [No Abstract] [Full Text] [Related]
8. Familial white matter hypoplasia, agenesis of the corpus callosum, mental retardation and growth deficiency: a new distinctive syndrome. Curatolo P; Cilio MR; Del Giudice E; Romano A; Gaggero R; Pessagno A Neuropediatrics; 1993 Apr; 24(2):77-82. PubMed ID: 8327066 [TBL] [Abstract][Full Text] [Related]
12. Cerebello-oculo-hepato-renal syndrome with possible mitochondrial dysfunction. Wakakura M; Hatono N; Tateno S Jpn J Ophthalmol; 1993; 37(1):62-9. PubMed ID: 8320867 [TBL] [Abstract][Full Text] [Related]
13. Currarino syndrome: report of two cases and review of the literature. Amornfa J; Taecholarn C; Khaoroptham S J Med Assoc Thai; 2005 Nov; 88(11):1697-702. PubMed ID: 16471121 [TBL] [Abstract][Full Text] [Related]
14. Aicardi syndrome with holoprosencephaly and cleft lip and palate. Sato N; Matsuishi T; Utsunomiya H; Yamashita Y; Horikoshi T; Okudera T; Hashimoto T Pediatr Neurol; 1987; 3(2):114-6. PubMed ID: 3508052 [TBL] [Abstract][Full Text] [Related]
15. [Neurolipomatosis with encephalo-oculo-cutaneous dysplasia]. Walbaum R; Van de Velde-Staquet MF; Bahon-Le Capon J; Boudiguet B; Dhellemmes P; Krivosic R; Fontaine G Pediatrie; 1979; 34(7):717-23. PubMed ID: 118424 [No Abstract] [Full Text] [Related]
16. New syndrome with the Sakoda complex, bilateral anophthalmia, and cortical dysgenesis. Ehara H; Kurimasa A; Ohno K; Takeshita K Pediatr Neurol; 1998 May; 18(5):445-51. PubMed ID: 9650690 [TBL] [Abstract][Full Text] [Related]
17. Caudal dysplasia, femoral hypoplasia-unusual facies syndrome and absent radius: a new association in infant of diabetic mother? Gupta P; Khatri PC; Agarwal R; Gupta P Indian J Pediatr; 2012 Nov; 79(11):1517-9. PubMed ID: 22382510 [TBL] [Abstract][Full Text] [Related]
18. Lateral meningocele (Lehman) syndrome: A child with a novel NOTCH3 mutation. Ejaz R; Qin W; Huang L; Blaser S; Tetreault M; Hartley T; Boycott KM; Carter MT; Am J Med Genet A; 2016 Apr; 170A(4):1070-5. PubMed ID: 26754023 [TBL] [Abstract][Full Text] [Related]