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Quoted phrase not found in phrase index: "Joubert syndrome 21"
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Total Intravenous Anesthesia in Joubert Syndrome Patient for Otorhinolaryngology Surgery: A Case Report and Mini Review of the Literature.
Kloka J, Blum LV, Piekarski F, Zacharowski K, Raimann FJ. Kloka J, et al. Am J Case Rep. 2020 Aug 7;21:e923018. doi: 10.12659/AJCR.923018. Am J Case Rep. 2020. PMID: 32764531 Free PMC article. Review.
BACKGROUND Joubert syndrome is a rare autosomal recessive disorder first described in 1969, with an estimated prevalence of 1 in 100 000. Joubert syndrome is characterized by partial or complete agenesis of the cerebellar vermis - the structure that co …
BACKGROUND Joubert syndrome is a rare autosomal recessive disorder first described in 1969, with an estimated prevalence of 1 …
Anesthetic management of patients with Joubert syndrome: a retrospective analysis of a single-institutional case series.
Sriganesh K, Vinay B, Jena S, Sudhir V, Saini J, Umamaheswara Rao GS. Sriganesh K, et al. Paediatr Anaesth. 2014 Nov;24(11):1180-4. doi: 10.1111/pan.12472. Epub 2014 Jul 5. Paediatr Anaesth. 2014. PMID: 25040301
OBJECTIVE: To analyze the anesthetic techniques used for sedation during magnetic resonance imaging (MRI) study of patients with Joubert syndrome (JS) and assess the safety and efficacy of these anesthetic regimens in these children. BACKGROUND: Joubert sy …
OBJECTIVE: To analyze the anesthetic techniques used for sedation during magnetic resonance imaging (MRI) study of patients with Joubert …
Joubert syndrome: a haplotype segregation strategy and exclusion of the zinc finger protein of cerebellum 1 (ZIC1) gene.
Bennett CL, Parisi MA, Eckert ML, Huynh HM, Chance PF, Glass IA. Bennett CL, et al. Am J Med Genet A. 2004 Mar 1;125A(2):117-24; discussion 117. doi: 10.1002/ajmg.a.20438. Am J Med Genet A. 2004. PMID: 14981711
Joubert syndrome (JS) is a rare autosomal recessive malformation syndrome, involving dysgenesis of the cerebellar vermis with accompanying brainstem malformations (comprising the molar tooth sign). ...Further, linkage to the ZIC1 genetic locus (3q24) was excluded in …
Joubert syndrome (JS) is a rare autosomal recessive malformation syndrome, involving dysgenesis of the cerebellar vermis with …