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Quoted phrase not found in phrase index: "Polymicrogyria with or without vascular-type Ehlers-Danlos syndrome"
Page 1
Bowel perforation in type IV vascular Ehlers-Danlos syndrome. A systematic review.
El Masri H, Loong TH, Meurette G, Podevin J, Zinzindohoue F, Lehur PA. El Masri H, et al. Tech Coloproctol. 2018 May;22(5):333-341. doi: 10.1007/s10151-018-1783-4. Epub 2018 Apr 26. Tech Coloproctol. 2018. PMID: 29700641 Review.
Spontaneous gastrointestinal (GI) perforation is a well-known complication occurring in patients suffering from Type IV vascular Ehlers-Danlos syndrome (EDS IV). The aim of the present study was to review the current literature on …
Spontaneous gastrointestinal (GI) perforation is a well-known complication occurring in patients suffering from Type IV vas …
Arterial complications of vascular Ehlers-Danlos syndrome.
Eagleton MJ. Eagleton MJ. J Vasc Surg. 2016 Dec;64(6):1869-1880. doi: 10.1016/j.jvs.2016.06.120. Epub 2016 Sep 26. J Vasc Surg. 2016. PMID: 27687326 Free article. Review.
BACKGROUND: Vascular Ehlers-Danlos syndrome (EDS) is a relatively rare genetic syndrome that occurs owing to disorders in the metabolism of fibrillary collagen. ...These findings were cross-referenced using key terms, including endovascular, emb …
BACKGROUND: Vascular Ehlers-Danlos syndrome (EDS) is a relatively rare genetic syndrome that occurs owing …
Neuroendovascular Procedures in Patients with Ehlers-Danlos Type IV: Multicenter Case Series and Systematic Review.
Padmanaban V, Yee PP, Koduri S, Zaidat B, Daou BJ, Chaudhary N, Gemmete JJ, Thompson BG, Kazmierczak CD, Cockroft KM, Pandey AS, Wilkinson DA. Padmanaban V, et al. World Neurosurg. 2023 Feb;170:e529-e541. doi: 10.1016/j.wneu.2022.11.067. Epub 2022 Nov 17. World Neurosurg. 2023. PMID: 36402305
BACKGROUND: Ehlers-Danlos type IV or vascular Ehlers-Danlos syndrome (vEDS) is a rare inherited disorder characterized by profound vascular fragility resulting from defective production of type III procollagen. …
BACKGROUND: Ehlers-Danlos type IV or vascular Ehlers-Danlos syndrome (vEDS) is a rar …
Speech and language in bilateral perisylvian polymicrogyria: a systematic review.
Braden RO, Leventer RJ, Jansen A, Scheffer IE, Morgan AT. Braden RO, et al. Dev Med Child Neurol. 2019 Oct;61(10):1145-1152. doi: 10.1111/dmcn.14153. Epub 2019 Jan 25. Dev Med Child Neurol. 2019. PMID: 30680716 Free article.
AIM: We aimed to systematically review the speech production, language, and oral function phenotype of bilateral perisylvian polymicrogyria (BPP), and examine the correlation between the topography of polymicrogyria and the severity of speech, language, and oral fun …
AIM: We aimed to systematically review the speech production, language, and oral function phenotype of bilateral perisylvian polymicrogyr …
Incomplete hippocampal inversion and epilepsy: A systematic review and meta-analysis.
Mutti C, Riccò M, Bartolini Y, Bernabè G, Trippi I, Melpignano A, Ciliento R, Zinno L, Florindo I, Sasso E, Odone A, Parrino L, Vaudano AE. Mutti C, et al. Epilepsia. 2021 Feb;62(2):383-396. doi: 10.1111/epi.16787. Epub 2020 Dec 16. Epilepsia. 2021. PMID: 33325054
SIGNIFICANCE: The present findings confirm that IHI is commonly observed in patients with MCD especially in periventricular nodular heterotopia or polymicrogyria. However, the estimated OR indicates overall weak increased odds of epilepsy in people with IHI, suggesting tha …
SIGNIFICANCE: The present findings confirm that IHI is commonly observed in patients with MCD especially in periventricular nodular heteroto …
Interictal and seizure-onset EEG patterns in malformations of cortical development: A systematic review.
Shakhatreh L, Janmohamed M, Baker AA, Willard A, Laing J, Rychkova M, Chen Z, Kwan P, O'Brien TJ, Perucca P. Shakhatreh L, et al. Neurobiol Dis. 2022 Nov;174:105863. doi: 10.1016/j.nbd.2022.105863. Epub 2022 Sep 19. Neurobiol Dis. 2022. PMID: 36165814 Free article. Review.
Of the nine interictal EEG patterns, five (three, scalp EEG; two, intracranial EEG) were detected in 2 MCD types, while four (rhythmic epileptiform discharges type 1 and type 2 on scalp EEG; repetitive bursting spikes and sporadic spikes on intracranial EEG) were se …
Of the nine interictal EEG patterns, five (three, scalp EEG; two, intracranial EEG) were detected in 2 MCD types, while four (rhythmic epile …
Fatigue in patients with syndromic heritable thoracic aortic disease: a systematic review of the literature and a qualitative study of patients' experiences and perceptions.
Velvin G, Johansen H, Østertun-Geirdal A, Bathen T. Velvin G, et al. Orphanet J Rare Dis. 2023 May 19;18(1):119. doi: 10.1186/s13023-023-02709-2. Orphanet J Rare Dis. 2023. PMID: 37208760 Free PMC article. Review.
INTRODUCTION: The purpose of this study was to explore the literature on fatigue in patients with syndromic heritable thoracic aortic disease (sHTAD), including Marfan syndrome (MFS), Loeys-Dietz syndrome (LDS), vascular Ehlers Danlos syndrom …
INTRODUCTION: The purpose of this study was to explore the literature on fatigue in patients with syndromic heritable thoracic aortic diseas …
Management of colonic complications of type IV Ehlers-Danlos syndrome: a systematic review and evidence-based management strategy.
Speake D, Dvorkin L, Vaizey CJ, Carlson GL. Speake D, et al. Colorectal Dis. 2020 Feb;22(2):129-135. doi: 10.1111/codi.14749. Epub 2019 Jul 31. Colorectal Dis. 2020. PMID: 31260161
AIM: Type IV Ehlers Danlos Syndrome (EDS) is a connective tissue disorder affecting approximately 1 per 100,000-200,000 people. ...We aim to review the published literature and identify outcome data relating to operative management of colonic pe …
AIM: Type IV Ehlers Danlos Syndrome (EDS) is a connective tissue disorder affecting approximately 1 per 1 …
Neuropathology of genetically defined malformations of cortical development-A systematic literature review.
Brock S, Cools F, Jansen AC. Brock S, et al. Neuropathol Appl Neurobiol. 2021 Aug;47(5):585-602. doi: 10.1111/nan.12696. Epub 2021 Feb 14. Neuropathol Appl Neurobiol. 2021. PMID: 33480109 Free PMC article.
Four groups emerged, consisting of (1) 13 genes with well-defined histological-genotype correlations, (2) 27 genes for which neuropathological reports were limited, (3) 5 genes with conflicting neuropathological features, and (4) 87 genes for which no histological data were avail …
Four groups emerged, consisting of (1) 13 genes with well-defined histological-genotype correlations, (2) 27 genes for which neuropathologic …