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Quoted phrase not found in phrase index: "Molar tooth sign on MRI"
Page 1
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. Maria BL, et al. J Child Neurol. 1999 Jun;14(6):368-76. doi: 10.1177/088307389901400605. J Child Neurol. 1999. PMID: 10385844 Clinical Trial.
In this study, we obtained clinical and developmental data in 61 cases, and radiologic data in 46 of these, to determine the prevalence of the molar tooth sign in a large sample, and to ensure that magnetic resonance images obtained for s …
In this study, we obtained clinical and developmental data in 61 cases, and radiologic data in 46 of these, to determine the prevalen …
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. ...MATERIALS AND M …
OBJECTIVE: To analyze the anesthetic techniques used for sedation during magnetic resonance imaging (MRI) study …
MKS3-related ciliopathy with features of autosomal recessive polycystic kidney disease, nephronophthisis, and Joubert Syndrome.
Gunay-Aygun M, Parisi MA, Doherty D, Tuchman M, Tsilou E, Kleiner DE, Huizing M, Turkbey B, Choyke P, Guay-Woodford L, Heller T, Szymanska K, Johnson CA, Glass I, Gahl WA. Gunay-Aygun M, et al. J Pediatr. 2009 Sep;155(3):386-92.e1. doi: 10.1016/j.jpeds.2009.03.045. Epub 2009 Jun 21. J Pediatr. 2009. PMID: 19540516 Free PMC article. Clinical Trial.
OBJECTIVES: To describe 3 children with mutations in a Meckel syndrome gene (MKS3), with features of autosomal recessive polycystic kidney disease (ARPKD), nephronophthisis, and Joubert syndrome (JS). STUDY DESIGN: Biochemical evaluations, magnetic resonance and ult …
OBJECTIVES: To describe 3 children with mutations in a Meckel syndrome gene (MKS3), with features of autosomal recessive polycystic kidney d …
Neuroleptic malignant syndrome due to risperidone treatment in a child with Joubert syndrome.
Vurucu S, Congologlu A, Altun D, Unay B, Akin R. Vurucu S, et al. J Natl Med Assoc. 2009 Mar;101(3):273-5. doi: 10.1016/s0027-9684(15)30858-0. J Natl Med Assoc. 2009. PMID: 19331262
Joubert syndrome is a rare autosomal recessive disease characterized by hypotonia, ataxia, episodic hyperpnea, psychomotor retardation, abnormal ocular movements, cerebellar vermian hypoplasia, and molar tooth sign on magnetic resonance imagi …
Joubert syndrome is a rare autosomal recessive disease characterized by hypotonia, ataxia, episodic hyperpnea, psychomotor retardation, abno …