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Biallelic variants in HPDL cause pure and complicated hereditary spastic paraplegia.
Brain. 2021 Jun 22;144(5):1422-1434. doi: 10.1093/brain/awab041.
Brain. 2021.
PMID: 33970200
Free PMC article.
Erratum to: Biallelic variants in HPDL cause pure and complicated hereditary spastic paraplegia.
Wiessner M, Maroofian R, Ni MY, Pedroni A, Müller JS, Stucka R, Beetz C, Efthymiou S, Santorelli FM, Alfares AA, Zhu C, Uhrova Meszarosova A, Alehabib E, Bakhtiari S, Janecke AR, Otero MG, Chen JYH, Peterson JT, Strom TM, De Jonghe P, Deconinck T, De Ridder W, De Winter J, Pasquariello R, Ricca I, Alfadhel M, van de Warrenburg BP, Portier R, Bergmann C, Ghasemi Firouzabadi S, Jin SC, Bilguvar K, Hamed S, Abdelhameed M, Haridy NA, Maqbool S, Rahman F, Anwar N, Carmichael J, Pagnamenta AT, Wood NW, Tran Mau-Them F, Haack T; Genomics England Research Consortium, PREPARE network; Di Rocco M, Ceccherini I, Iacomino M, Zara F, Salpietro V, Scala M, Rusmini M, Xu Y, Wang Y, Suzuki Y, Koh K, Nan H, Ishiura H, Tsuji S, Lambert L, Schmitt E, Lacaze E, Küpper H, Dredge D, Skraban C, Goldstein A, Willis MJH, Grand K, Graham JM, Lewis RA, Millan F, Duman Ö, Olgac Dundar N, Uyanik G, Schöls L, Nürnberg P, Nürnberg G, Català-Bordes A, Seeman P, Kuchar M, Darvish H, Rebelo A, Bouçanova F, Medard JJ, Chrast R, Auer-Grumbach M, Alkuraya FS, Shamseldin H, Al Tala S, Rezazadeh Varaghchi J, Najafi M, Deschner S, Gläser D, Hüttel W, Kruer MC, Kamsteeg EJ, Takiyama Y, Züchner S, Baets J, Synofzik…
See abstract for full author list ➔
Wiessner M, et al. Among authors: dredge d.
Brain. 2021 Sep 4;144(8):e70. doi: 10.1093/brain/awab193.
Brain. 2021.
PMID: 34480796
Free PMC article.
No abstract available.
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Mechanism of KMT5B haploinsufficiency in neurodevelopment in humans and mice.
Sheppard SE, Bryant L, Wickramasekara RN, Vaccaro C, Robertson B, Hallgren J, Hulen J, Watson CJ, Faundes V, Duffourd Y, Lee P, Simon MC, de la Cruz X, Padilla N, Flores-Mendez M, Akizu N, Smiler J, Pellegrino Da Silva R, Li D, March M, Diaz-Rosado A, Peixoto de Barcelos I, Choa ZX, Lim CY, Dubourg C, Journel H, Demurger F, Mulhern M, Akman C, Lippa N, Andrews M, Baldridge D, Constantino J, van Haeringen A, Snoeck-Streef I, Chow P, Hing A, Graham JM Jr, Au M, Faivre L, Shen W, Mao R, Palumbos J, Viskochil D, Gahl W, Tifft C, Macnamara E, Hauser N, Miller R, Maffeo J, Afenjar A, Doummar D, Keren B, Arn P, Macklin-Mantia S, Meerschaut I, Callewaert B, Reis A, Zweier C, Brewer C, Saggar A, Smeland MF, Kumar A, Elmslie F, Deshpande C, Nizon M, Cogne B, van Ierland Y, Wilke M, van Slegtenhorst M, Koudijs S, Chen JY, Dredge D, Pier D, Wortmann S, Kamsteeg EJ, Koch J, Haynes D, Pollack L, Titheradge H, Ranguin K, Denommé-Pichon AS, Weber S, Pérez de la Fuente R, Sánchez Del Pozo J, Lezana Rosales JM, Joset P, Steindl K, Rauch A, Mei D, Mari F, Guerrini R, Lespinasse J, Tran Mau-Them F, Philippe C, Dauriat B, Raymond L, Moutton S, Cueto-González AM, Tan TY, Mignot C, Grotto S, Rena…
See abstract for full author list ➔
Sheppard SE, et al. Among authors: dredge d.
Sci Adv. 2023 Mar 10;9(10):eade1463. doi: 10.1126/sciadv.ade1463. Epub 2023 Mar 10.
Sci Adv. 2023.
PMID: 36897941
Free PMC article.
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Anticonvulsant hypersensitivity syndrome treated with intravenous immunoglobulin.
Dredge DC, Parsons EC, Carter LP, Staley KJ.
Dredge DC, et al.
Pediatr Neurol. 2010 Jul;43(1):65-9. doi: 10.1016/j.pediatrneurol.2010.03.010.
Pediatr Neurol. 2010.
PMID: 20682208
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Bovine parvovirus uses clathrin-mediated endocytosis for cell entry.
Dudleenamjil E, Lin CY, Dredge D, Murray BK, Robison RA, Johnson FB.
Dudleenamjil E, et al. Among authors: dredge d.
J Gen Virol. 2010 Dec;91(Pt 12):3032-41. doi: 10.1099/vir.0.024133-0. Epub 2010 Sep 1.
J Gen Virol. 2010.
PMID: 20810750
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Practical examples and data for upgrading buildings in the health estate.
Rodgers AM, Dredge DS.
Rodgers AM, et al. Among authors: dredge ds.
Hosp Eng. 1978 Aug;32(6):6-10.
Hosp Eng. 1978.
PMID: 10237639
No abstract available.
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