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26. Congenital pontocerebellar atrophy and telencephalic defects in three siblings: a new subtype. Leroy JG; Lyon G; Fallet C; Amiel J; De Praeter C; Van Den Broecke C; Vanhaesebrouck P Acta Neuropathol; 2007 Oct; 114(4):387-99. PubMed ID: 17628812 [TBL] [Abstract][Full Text] [Related]
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28. Olivopontocerebellar pathology in multiple system atrophy. Wenning GK; Tison F; Elliott L; Quinn NP; Daniel SE Mov Disord; 1996 Mar; 11(2):157-62. PubMed ID: 8684385 [TBL] [Abstract][Full Text] [Related]
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30. Fatal outcome in a case of pontocerebellar hypoplasia type 2. Grellner W; Rohde K; Wilske J Forensic Sci Int; 2000 Sep; 113(1-3):165-72. PubMed ID: 10978619 [TBL] [Abstract][Full Text] [Related]
31. Severe, fetal-onset form of olivopontocerebellar hypoplasia in three sibs: PCH type 5? Patel MS; Becker LE; Toi A; Armstrong DL; Chitayat D Am J Med Genet A; 2006 Mar; 140(6):594-603. PubMed ID: 16470708 [TBL] [Abstract][Full Text] [Related]
32. Novel mutations in TSEN54 in pontocerebellar hypoplasia type 2. Battini R; D'Arrigo S; Cassandrini D; Guzzetta A; Fiorillo C; Pantaleoni C; Romano A; Alfei E; Cioni G; Santorelli FM J Child Neurol; 2014 Apr; 29(4):520-5. PubMed ID: 23307886 [TBL] [Abstract][Full Text] [Related]
34. Novel homozygous RARS2 mutation in two siblings without pontocerebellar hypoplasia - further expansion of the phenotypic spectrum. Lühl S; Bode H; Schlötzer W; Bartsakoulia M; Horvath R; Abicht A; Stenzel M; Kirschner J; Grünert SC Orphanet J Rare Dis; 2016 Oct; 11(1):140. PubMed ID: 27769281 [TBL] [Abstract][Full Text] [Related]
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36. Clinical, neuroradiological and genetic findings in pontocerebellar hypoplasia. Namavar Y; Barth PG; Kasher PR; van Ruissen F; Brockmann K; Bernert G; Writzl K; Ventura K; Cheng EY; Ferriero DM; Basel-Vanagaite L; Eggens VR; Krägeloh-Mann I; De Meirleir L; King M; Graham JM; von Moers A; Knoers N; Sztriha L; Korinthenberg R; ; Dobyns WB; Baas F; Poll-The BT Brain; 2011 Jan; 134(Pt 1):143-56. PubMed ID: 20952379 [TBL] [Abstract][Full Text] [Related]
37. A mild variant of pontocerebellar hypoplasia type 1 in a 12-year-old Indian boy. Kalpana D; Parvathy L; Ahamed SM; Iype M; Kunju MP Pediatr Neurol; 2009 Apr; 40(4):302-5. PubMed ID: 19302945 [TBL] [Abstract][Full Text] [Related]
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