Zobrazeno 1 - 10 of 29 pro vyhledávání: '"M Ranguin"'
1
Traitement chirurgical des expositions d’implants d’éviscération en hydroxyapatite par greffe d’aponévrose temporale
Autor: P.-J. Pisella, F Boulet, A. Denoyer, M Ranguin
Publikováno v: Journal Français d'Ophtalmologie. 28:976-980
L’avenement des implants biocolonisables en hydroxyapatite a permis une amelioration considerable des resultats fonctionnels et esthetiques des eviscerations. Neanmoins, l’exposition chronique de ces implants demeure la principale complication et
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::1edeab25265fb9f21e14669c09187d06
https://doi.org/10.1016/s0181-5512(05)81124-6
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2
[Repair of exposed hydroxyapatite implants using temporalis fascia: four case reports]
Autor: A, Denoyer, M, Ranguin, F, Boulet, P-J, Pisella
Publikováno v: Journal francais d'ophtalmologie. 28(9)
Using hydroxyapatite porous implants improves the functional and cosmetic results for patients after evisceration. However, exposure is still the most frequent complication and requires various surgical treatments. We present four patients who had an
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::ad7bb40f015e3d4faff2e6c720c753c4
https://pubmed.ncbi.nlm.nih.gov/16395225
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3
Akademický článek
Clinical utility of periodic reinterpretation of CNVs of uncertain significance: an 8-year retrospective study.
Autor: Ravel, Jean-Marie1,2,3 (AUTHOR), Renaud, Mathilde1,3 (AUTHOR), Muller, Jean4,5,6 (AUTHOR), Becker, Aurélie2 (AUTHOR), Renard, Émeline7 (AUTHOR), Remen, Thomas8 (AUTHOR), Lefort, Geneviève2 (AUTHOR), Dexheimer, Mylène2 (AUTHOR), Jonveaux, Philippe3 (AUTHOR), Leheup, Bruno1,3 (AUTHOR), Bonnet, Céline2,3 (AUTHOR) ce.bonnet@chru-nancy.fr, Lambert, Laëtitia1,3 (AUTHOR) l.lambert@chru-nancy.fr
Publikováno v: Genome Medicine. 5/23/2023, Vol. 15 Issue 1, p1-10. 10p.
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4
Akademický článek
hnRNPs: roles in neurodevelopment and implication for brain disorders.
Autor: Tilliole, Pierre, Fix, Simon, Godin, Juliette D.
Publikováno v: Frontiers in Molecular Neuroscience; 2024, p1-24, 24p
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5
Orbital phlebography in the diagnosis of painful ophthalmoplegia
Autor: J. M. Vallat, M. Ranguin, J. Julien, Vallat M, V. Riemens
Publikováno v: Neuroradiology. 9(3)
Three cases of painful ophthalmoplegia have been described in which symptoms suggesting a tumor of the orbit justified neuroradiological assessment. Phlebography in each case revealed stenosis of the superior ophthalmic vein in its third portion, and
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9c6aae253cd9aa3fab8f49e169f1c22e
https://pubmed.ncbi.nlm.nih.gov/1161145
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7
Akademický článek
Circ_TLK1 knockdown alleviates oxygen–glucose deprivation/reoxygenation‐induced PC12 cell injury by regulating microRNA‐136‐5p/follistatin like‐1 axis.
Autor: Zhang, Zhenduo1 (AUTHOR) zdzhang001002@163.com, He, Jinbo2 (AUTHOR), Wang, Baoliang1 (AUTHOR)
Publikováno v: European Journal of Neuroscience. Aug2022, Vol. 56 Issue 4, p4304-4316. 13p. 2 Color Photographs, 2 Black and White Photographs, 2 Graphs.
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8
Akademický článek
Identification of copy-number variants in patients with overgrowth disorders.
Autor: Parra A; CIBERER, Centro de Investigación Biomédica en Red de Enfermedades Raras, Madrid, Spain.; INGEMM-Idipaz, Institute of Medical and Molecular Genetics, Madrid, Spain.; ITHACA, European Reference Network, Hospital Universitario La Paz, Madrid, Spain., Tenorio-Castano J; CIBERER, Centro de Investigación Biomédica en Red de Enfermedades Raras, Madrid, Spain.; INGEMM-Idipaz, Institute of Medical and Molecular Genetics, Madrid, Spain.; ITHACA, European Reference Network, Hospital Universitario La Paz, Madrid, Spain., Nevado J; CIBERER, Centro de Investigación Biomédica en Red de Enfermedades Raras, Madrid, Spain.; INGEMM-Idipaz, Institute of Medical and Molecular Genetics, Madrid, Spain.; ITHACA, European Reference Network, Hospital Universitario La Paz, Madrid, Spain., Cazalla M; CIBERER, Centro de Investigación Biomédica en Red de Enfermedades Raras, Madrid, Spain.; INGEMM-Idipaz, Institute of Medical and Molecular Genetics, Madrid, Spain.; ITHACA, European Reference Network, Hospital Universitario La Paz, Madrid, Spain., Miranda-Alcaraz L; CIBERER, Centro de Investigación Biomédica en Red de Enfermedades Raras, Madrid, Spain.; INGEMM-Idipaz, Institute of Medical and Molecular Genetics, Madrid, Spain.; ITHACA, European Reference Network, Hospital Universitario La Paz, Madrid, Spain., Gallego-Zazo N; CIBERER, Centro de Investigación Biomédica en Red de Enfermedades Raras, Madrid, Spain.; INGEMM-Idipaz, Institute of Medical and Molecular Genetics, Madrid, Spain.; ITHACA, European Reference Network, Hospital Universitario La Paz, Madrid, Spain., Silván C; INGEMM-Idipaz, Institute of Medical and Molecular Genetics, Madrid, Spain., Arias P; CIBERER, Centro de Investigación Biomédica en Red de Enfermedades Raras, Madrid, Spain.; INGEMM-Idipaz, Institute of Medical and Molecular Genetics, Madrid, Spain.; ITHACA, European Reference Network, Hospital Universitario La Paz, Madrid, Spain., Pozo-Román J; Unit of Pediatric Endocrinology, Department of Pediatrics, Hospital Universitario Infantil Niño Jesús, Madrid, Spain.; Department of Pediatrics, Medical School, Autonomous University of Madrid, Madrid, Spain., Ballesta-Martínez MJ; Sección de Genética Médica, Hospital Clínico Universitario Virgen de la Arrixaca, Murcia, Spain.; Instituto Murciano de Investigación Biosanitaria (IMIB), Murcia, Spain., Guillén-Navarro E; CIBERER, Centro de Investigación Biomédica en Red de Enfermedades Raras, Madrid, Spain.; Instituto Murciano de Investigación Biosanitaria (IMIB), Murcia, Spain., Arroyo I; Pediatrics Department, San Pedro de Alcántara Hospital, Cáceres, Spain., Lotersztein V; Department of Genetics, Centro Nacional de Genética, Buenos Aires, Argentina., Cosentino V; Department of Genetics, CEMIC, Buenos Aires, Argentina., González-Meneses A; Unidad de Dismorfología y Metabolismo, Hospital Universitario Virgen del Rocío, Seville, Spain., Galán E; Pediatrics Department, Hospital Materno-Infantil, Badajoz, Spain., Rosell J; Department of Genetics, Hospital Son Espases, Palma de Mallorca, Spain., Ramos F; Pediatrics Department, Hospital Lozano Blesa, Zaragoza, Spain., Lapunzina P; CIBERER, Centro de Investigación Biomédica en Red de Enfermedades Raras, Madrid, Spain.; INGEMM-Idipaz, Institute of Medical and Molecular Genetics, Madrid, Spain.; ITHACA, European Reference Network, Hospital Universitario La Paz, Madrid, Spain.; Spanish OverGrowth Registry Initiative, La Paz University Hospital, Madrid, Spain.
Publikováno v: Clinical genetics [Clin Genet] 2024 Nov; Vol. 106 (5), pp. 614-624. Date of Electronic Publication: 2024 Aug 01.
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9
Akademický článek
Biological functions and clinic significance of SAF‑A (Review).
Autor: Zhang, Daiquan1 (AUTHOR), Li, Li2 (AUTHOR), Li, Mengni3 (AUTHOR) lzcxm@swmu.edu.cn, Cao, Xinmei2 (AUTHOR) lzcxm@swmu.edu.cn
Publikováno v: Biomedical Reports. Jun2024, Vol. 20 Issue 6, pN.PAG-N.PAG. 1p.
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10
Akademický článek
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