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Quoted phrase not found in phrase index: "Partial absence of cerebellar vermis"
Page 1
Rhomboencephalosynapsis: Review of the Literature.
Fouda MA, Kim TY, Cohen AR. Fouda MA, et al. World Neurosurg. 2022 Mar;159:48-53. doi: 10.1016/j.wneu.2021.12.062. Epub 2021 Dec 22. World Neurosurg. 2022. PMID: 34954057 Review.
Rhombencephalosynapsis is a rare congenital anomaly, characterized by partial or total agenesis of the cerebellar vermis with midline fusion of the cerebellar hemispheres, dentate nuclei, and the superior cerebellar peduncles, creating the disti …
Rhombencephalosynapsis is a rare congenital anomaly, characterized by partial or total agenesis of the cerebellar vermis …
Prenatal diagnosis of rhombencephalosynapsis: neuroimaging features and severity of vermian anomaly.
Krajden Haratz K, Oliveira Szejnfeld P, Govindaswamy M, Leibovitz Z, Gindes L, Severino M, Rossi A, Paladini D, Garcia Rodriguez R, Ben-Sira L, Borkowski Tillman T, Gupta R, Lotem G, Raz N, Hamamoto TENK, Kidron D, Arad A, Birnbaum R, Brussilov M, Pomar L, Vial Y, Leventer RJ, McGillivray G, Fink M, Krzeszowski W, Fernandes Moron A, Lev D, Tamarkin M, Shalev J, Har Toov J, Lerman-Sagie T, Malinger G. Krajden Haratz K, et al. Ultrasound Obstet Gynecol. 2021 Dec;58(6):864-874. doi: 10.1002/uog.23660. Ultrasound Obstet Gynecol. 2021. PMID: 33942916 Free article.
RES was classified, according to the pattern of vermian agenesis and the extent of the fusion of the hemispheres, as complete RES (complete absence of the vermis) or partial RES (further classified according to the part of the vermis that was missing a …
RES was classified, according to the pattern of vermian agenesis and the extent of the fusion of the hemispheres, as complete RES (complete …
Linking inter-subject variability of cerebellar functional connectome to clinical symptoms in major depressive disorder.
Lin J, Xiao Y, Yao C, Sun L, Wang P, Deng Y, Pu J; DIRECT Consortium; Xue SW. Lin J, et al. J Psychiatr Res. 2024 Mar;171:9-16. doi: 10.1016/j.jpsychires.2024.01.006. Epub 2024 Jan 10. J Psychiatr Res. 2024. PMID: 38219285
A partial least squares (PLS) regression analysis was performed to determine the potential dimension linking the IVFC to clinical symptom measures. The results indicated that similar spatial distribution patterns of the cerebellar IVFC were observed between MDD and …
A partial least squares (PLS) regression analysis was performed to determine the potential dimension linking the IVFC to clinical sym …
Rhombencephalosynapsis: a hindbrain malformation associated with incomplete separation of midbrain and forebrain, hydrocephalus and a broad spectrum of severity.
Ishak GE, Dempsey JC, Shaw DW, Tully H, Adam MP, Sanchez-Lara PA, Glass I, Rue TC, Millen KJ, Dobyns WB, Doherty D. Ishak GE, et al. Brain. 2012 May;135(Pt 5):1370-86. doi: 10.1093/brain/aws065. Epub 2012 Mar 26. Brain. 2012. PMID: 22451504 Free PMC article.
Rhombencephalosynapsis is a midline brain malformation characterized by missing cerebellar vermis with apparent fusion of the cerebellar hemispheres. ...Based on a comprehensive evaluation of neuroimaging findings in 42 patients with rhombencephalosynapsis, w …
Rhombencephalosynapsis is a midline brain malformation characterized by missing cerebellar vermis with apparent fusion of the …
Dandy-Walker syndrome and monochorionic twins: insight into a possible etiological mechanism.
Kontopoulos EV, Quintero RA, Salihu HM, Bornick PW, Allen MH. Kontopoulos EV, et al. J Matern Fetal Neonatal Med. 2008 Nov;21(11):839-42. doi: 10.1080/14767050802302967. J Matern Fetal Neonatal Med. 2008. PMID: 18979394
OBJECTIVE: Dandy-Walker syndrome (DWS) is a developmental malformation of the central nervous system characterized by complete or partial absence of the cerebellar vermis, the presence of a posterior fossa cyst, and ventriculomegaly. ...Intrauterine gr …
OBJECTIVE: Dandy-Walker syndrome (DWS) is a developmental malformation of the central nervous system characterized by complete or partial …
Recurrent pseudo-TORCH appearances of the brain presenting as "Dandy-Walker" malformation.
Cohen MC, Karaman I, Squier W, Farrel T, Whitby EH. Cohen MC, et al. Pediatr Dev Pathol. 2012 Jan-Feb;15(1):45-9. doi: 10.2350/10-01-0783-CR.1. Epub 2011 Jul 15. Pediatr Dev Pathol. 2012. PMID: 21762029
Dandy-Walker malformation (DWM) is a developmental abnormality characterized by cystic dilatation of the fourth ventricle, complete or partial agenesis of the cerebellar vermis, and enlarged posterior fossa with upward displacement of the lateral sinuses, ten …
Dandy-Walker malformation (DWM) is a developmental abnormality characterized by cystic dilatation of the fourth ventricle, complete or pa …
Merosin-deficient congenital muscular dystrophy with mental retardation and cerebellar cysts, unlinked to the LAMA2, FCMD, MEB and CMD1B loci, in three Tunisian patients.
Triki C, Louhichi N, Méziou M, Choyakh F, Kéchaou MS, Jlidi R, Mhiri C, Fakhfakh F, Ayadi H. Triki C, et al. Neuromuscul Disord. 2003 Jan;13(1):4-12. doi: 10.1016/s0960-8966(02)00188-8. Neuromuscul Disord. 2003. PMID: 12467726
Brain magnetic resonance imaging showed several cerebellar cysts and vermis hypoplasia in all of the patients. Abnormality of the white matter was present in two patients. ...These patients constituted a particular form of congenital muscular dystrophy with a combin …
Brain magnetic resonance imaging showed several cerebellar cysts and vermis hypoplasia in all of the patients. Abnormality of …
The Dandy-Walker malformation prenatal sonographic diagnosis and its clinical significance.
Nyberg DA, Cyr DR, Mack LA, Fitzsimmons J, Hickok D, Mahony BS. Nyberg DA, et al. J Ultrasound Med. 1988 Feb;7(2):65-71. doi: 10.7863/jum.1988.7.2.65. J Ultrasound Med. 1988. PMID: 3279226
To determine the usual sonographic findings and clinical significance of the Dandy-Walker malformation (DWM) identified in utero, we reviewed seven proven cases diagnosed by prenatal ultrasound during a 6-year period. All patients demonstrated complete or partial absenc …
To determine the usual sonographic findings and clinical significance of the Dandy-Walker malformation (DWM) identified in utero, we reviewe …