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Quoted phrase not found in phrase index: "Agenesis of the anterior commissure"
Page 1
Tubulin genes and malformations of cortical development.
Romaniello R, Arrigoni F, Fry AE, Bassi MT, Rees MI, Borgatti R, Pilz DT, Cushion TD. Romaniello R, et al. Eur J Med Genet. 2018 Dec;61(12):744-754. doi: 10.1016/j.ejmg.2018.07.012. Epub 2018 Jul 17. Eur J Med Genet. 2018. PMID: 30016746 Review.
Well-known hallmarks of the tubulinopathies include dysmorphism of the basal ganglia (fusion of the caudate nucleus and putamen with absence of the anterior limb of the internal capsule), midline commissural structures hypoplasia and/or agenesis (anterior …
Well-known hallmarks of the tubulinopathies include dysmorphism of the basal ganglia (fusion of the caudate nucleus and putamen with absence …
Bi-allelic ACBD6 variants lead to a neurodevelopmental syndrome with progressive and complex movement disorders.
Kaiyrzhanov R, Rad A, Lin SJ, Bertoli-Avella A, Kallemeijn WW, Godwin A, Zaki MS, Huang K, Lau T, Petree C, Efthymiou S, Karimiani EG, Hempel M, Normand EA, Rudnik-Schöneborn S, Schatz UA, Baggelaar MP, Ilyas M, Sultan T, Alvi JR, Ganieva M, Fowler B, Aanicai R, Tayfun GA, Al Saman A, Alswaid A, Amiri N, Asilova N, Shotelersuk V, Yeetong P, Azam M, Babaei M, Monajemi GB, Mohammadi P, Samie S, Banu SH, Pinto Basto J, Kortüm F, Bauer M, Bauer P, Beetz C, Garshasbi M, Issa AH, Eyaid W, Ahmed H, Hashemi N, Hassanpour K, Herman I, Ibrohimov S, Abdul-Majeed BA, Imdad M, Isrofilov M, Kaiyal Q, Khan S, Kirmse B, Koster J, Lourenço CM, Mitani T, Moldovan O, Murphy D, Najafi M, Pehlivan D, Rocha ME, Salpietro V, Schmidts M, Shalata A, Mahroum M, Talbeya JK, Taylor RW, Vazquez D, Vetro A, Waterham HR, Zaman M, Schrader TA, Chung WK, Guerrini R, Lupski JR, Gleeson J, Suri M, Jamshidi Y, Bhatia KP, Vona B, Schrader M, Severino M, Guille M, Tate EW, Varshney GK, Houlden H, Maroofian R. Kaiyrzhanov R, et al. Brain. 2024 Apr 4;147(4):1436-1456. doi: 10.1093/brain/awad380. Brain. 2024. PMID: 37951597 Free PMC article.
A jerky tremor in the upper limbs (63%), a mild head tremor (59%), parkinsonism/hypokinesia developing with advancing age (32%) and simple motor and vocal tics were among other frequent movement disorders. Midline brain malformations including corpus callosum abnormalities …
A jerky tremor in the upper limbs (63%), a mild head tremor (59%), parkinsonism/hypokinesia developing with advancing age (32%) and simple m …
Mutations in α- and β-tubulin encoding genes: implications in brain malformations.
Romaniello R, Arrigoni F, Bassi MT, Borgatti R. Romaniello R, et al. Brain Dev. 2015 Mar;37(3):273-80. doi: 10.1016/j.braindev.2014.06.002. Epub 2014 Jul 5. Brain Dev. 2015. PMID: 25008804 Review.
In recent years an increasing number of brain malformations has been associated with mutations in tubulin genes: malformations of cortical development such as lissencephaly and various grades of gyral disorganization, focal or diffuse polymicrogyria and open or closed-lips schize …
In recent years an increasing number of brain malformations has been associated with mutations in tubulin genes: malformations of cortical d …
Structure and function of the tricuspid and bicuspid regurgitant aortic valve: an echocardiographic study.
Rönnerfalk M, Tamás É. Rönnerfalk M, et al. Interact Cardiovasc Thorac Surg. 2015 Jul;21(1):71-6. doi: 10.1093/icvts/ivv072. Epub 2015 Apr 2. Interact Cardiovasc Thorac Surg. 2015. PMID: 25840434 Free article.
However, the STJ and maxSiD were significantly related (TAV vs BAV: systole r = 0.9, r = 0.8; diastole r = 0.9, r = 0.7), forming an entity. The conjoined BAV cusps were shorter than the anterior cusps when closed (P = 0.002); the inter-commissural distances of the …
However, the STJ and maxSiD were significantly related (TAV vs BAV: systole r = 0.9, r = 0.8; diastole r = 0.9, r = 0.7), forming an entity. …
Morphologic variability of the mitral valve leaflets.
Krawczyk-Ożóg A, Hołda MK, Sorysz D, Koziej M, Siudak Z, Dudek D, Klimek-Piotrowska W. Krawczyk-Ożóg A, et al. J Thorac Cardiovasc Surg. 2017 Dec;154(6):1927-1935. doi: 10.1016/j.jtcvs.2017.07.067. Epub 2017 Aug 16. J Thorac Cardiovasc Surg. 2017. PMID: 28893395 Free article.
We also noted the base and the height of the inferoseptal commissure, superolateral commissure, anterior mitral leaflet, and posterior mitral leaflet with their scallops. RESULTS: Variations in posterior mitral leaflet were found in 55 specimens (27.5%), and …
We also noted the base and the height of the inferoseptal commissure, superolateral commissure, anterior mitral leaflet …
Demographic, ocular and associated neurological findings in corpus callosum malformations.
Kızıltunç PB, Şahlı E, İdil A, Atilla H. Kızıltunç PB, et al. Turk J Pediatr. 2021;63(2):291-299. doi: 10.24953/turkjped.2021.02.013. Turk J Pediatr. 2021. PMID: 33929119 Free article.
Patients were divided into 3 groups according to the severity of corpus callosum malformation on MRI (total agenesis, partial agenesis and hypoplasia) and also evaluated as a part of a genetic disorder/syndrome or not. ...RESULTS: Only 35.1% of patients had fixation …
Patients were divided into 3 groups according to the severity of corpus callosum malformation on MRI (total agenesis, partial agen …
Preoperative clinical predictors of difficult laryngeal exposure for microlaryngoscopy: the Laryngoscore.
Piazza C, Mangili S, Bon FD, Paderno A, Grazioli P, Barbieri D, Perotti P, Garofolo S, Nicolai P, Peretti G. Piazza C, et al. Laryngoscope. 2014 Nov;124(11):2561-7. doi: 10.1002/lary.24803. Epub 2014 Jun 26. Laryngoscope. 2014. PMID: 24964904

OBJECTIVES/HYPOTHESIS: To identify a clinical predictor score for difficult laryngeal exposure (DLE) during operative microlaryngoscopy. ...When the Laryngoscore was < 6, good laryngeal exposure was observed in 94% of patients, whereas when 6, DLE was enco

…
OBJECTIVES/HYPOTHESIS: To identify a clinical predictor score for difficult laryngeal exposure (DLE) during operative microlar …
Revisiting brain rewiring and plasticity in children born without corpus callosum.
Siffredi V, Preti MG, Obertino S, Leventer RJ, Wood AG, McIlroy A, Anderson V, Spencer-Smith MM, Van De Ville D. Siffredi V, et al. Dev Sci. 2021 Nov;24(6):e13126. doi: 10.1111/desc.13126. Epub 2021 Jun 1. Dev Sci. 2021. PMID: 34060677 Free PMC article.
In a sample of six adults with CD, they revealed two homotopic bundles crossing the midline via the anterior and posterior commissures and connecting parietal cortices, and the microstructural properties of these aberrant bundles were associated with functional conn …
In a sample of six adults with CD, they revealed two homotopic bundles crossing the midline via the anterior and posterior commiss …
Brain functional connectivity in individuals with callosotomy and agenesis of the corpus callosum: A systematic review.
Mancuso L, Uddin LQ, Nani A, Costa T, Cauda F. Mancuso L, et al. Neurosci Biobehav Rev. 2019 Oct;105:231-248. doi: 10.1016/j.neubiorev.2019.07.004. Epub 2019 Aug 11. Neurosci Biobehav Rev. 2019. PMID: 31412269 Free article.
In the absence of the corpus callosum due to either surgical transection or congenital agenesis, the interhemispheric exchange of information is disrupted, as emphasized by several clinical studies. ...A growing literature has investigated this hypothesis, and a number of …
In the absence of the corpus callosum due to either surgical transection or congenital agenesis, the interhemispheric exchange of inf …
The old and the new: supratentorial MR findings in Chiari II malformation.
Miller E, Widjaja E, Blaser S, Dennis M, Raybaud C. Miller E, et al. Childs Nerv Syst. 2008 May;24(5):563-75. doi: 10.1007/s00381-007-0528-x. Epub 2007 Nov 20. Childs Nerv Syst. 2008. PMID: 18026960
The anterior commissure was in a low position in the lamina terminalis in 38%. Gross abnormalities of the corpus callosum/hippocampal commissure were found in 57%; they were, however, different from the abnormalities seen in classical commiss …
The anterior commissure was in a low position in the lamina terminalis in 38%. Gross abnormalities of the corpus callos …
54 results