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Parabiotic twin syndrome with topical isocortical disruption and gastroschisis.
Barth PG, van der Harten JJ. Barth PG, et al. Acta Neuropathol. 1985;67(3-4):345-9. doi: 10.1007/BF00687825. Acta Neuropathol. 1985. PMID: 3901653
Pontocerebellar hypoplasia type 2: a neuropathological update.
Barth PG, Aronica E, de Vries L, Nikkels PG, Scheper W, Hoozemans JJ, Poll-The BT, Troost D. Barth PG, et al. Acta Neuropathol. 2007 Oct;114(4):373-86. doi: 10.1007/s00401-007-0263-0. Epub 2007 Jul 20. Acta Neuropathol. 2007. PMID: 17641900 Free PMC article.
Aicardi-Goutières syndrome: a genetic microangiopathy?
Barth PG, Walter A, van Gelderen I. Barth PG, et al. Acta Neuropathol. 1999 Aug;98(2):212-6. doi: 10.1007/s004010051071. Acta Neuropathol. 1999. PMID: 10442562
Axonal dystrophy in a case of connatal thalamic and brain stem degeneration.
Jennekens FG, Barth PG, Fleury P, Veldman H, Keuning JF, Westdorp J. Jennekens FG, et al. Among authors: barth pg. Acta Neuropathol. 1984;64(1):68-71. doi: 10.1007/BF00695608. Acta Neuropathol. 1984. PMID: 6089496
Tuberous sclerosis and dysplasia of the corpus callosum. Case report of their combined occurrence in a newborn.
Barth PG, Stam FC, von der Harten JJ. Barth PG, et al. Acta Neuropathol. 1978 Apr 26;42(1):63-4. doi: 10.1007/BF01273269. Acta Neuropathol. 1978. PMID: 654880
Pontocerebellar hypoplasia.
Rudnik-Schöneborn S, Barth PG, Zerres K. Rudnik-Schöneborn S, et al. Among authors: barth pg. Am J Med Genet C Semin Med Genet. 2014 Jun;166C(2):173-83. doi: 10.1002/ajmg.c.31403. Epub 2014 Jun 12. Am J Med Genet C Semin Med Genet. 2014. PMID: 24924738 Review.
Natural course of pontocerebellar hypoplasia type 2A.
Sánchez-Albisua I, Frölich S, Barth PG, Steinlin M, Krägeloh-Mann I. Sánchez-Albisua I, et al. Among authors: barth pg. Orphanet J Rare Dis. 2014 May 5;9:70. doi: 10.1186/1750-1172-9-70. Orphanet J Rare Dis. 2014. PMID: 24886362 Free PMC article.
tRNA splicing endonuclease mutations cause pontocerebellar hypoplasia.
Budde BS, Namavar Y, Barth PG, Poll-The BT, Nürnberg G, Becker C, van Ruissen F, Weterman MA, Fluiter K, te Beek ET, Aronica E, van der Knaap MS, Höhne W, Toliat MR, Crow YJ, Steinling M, Voit T, Roelenso F, Brussel W, Brockmann K, Kyllerman M, Boltshauser E, Hammersen G, Willemsen M, Basel-Vanagaite L, Krägeloh-Mann I, de Vries LS, Sztriha L, Muntoni F, Ferrie CD, Battini R, Hennekam RC, Grillo E, Beemer FA, Stoets LM, Wollnik B, Nürnberg P, Baas F. Budde BS, et al. Among authors: barth pg. Nat Genet. 2008 Sep;40(9):1113-8. doi: 10.1038/ng.204. Nat Genet. 2008. PMID: 18711368
Pontocerebellar hypoplasia type 1: clinical spectrum and relevance of EXOSC3 mutations.
Rudnik-Schöneborn S, Senderek J, Jen JC, Houge G, Seeman P, Puchmajerová A, Graul-Neumann L, Seidel U, Korinthenberg R, Kirschner J, Seeger J, Ryan MM, Muntoni F, Steinlin M, Sztriha L, Colomer J, Hübner C, Brockmann K, Van Maldergem L, Schiff M, Holzinger A, Barth P, Reardon W, Yourshaw M, Nelson SF, Eggermann T, Zerres K. Rudnik-Schöneborn S, et al. Among authors: barth p. Neurology. 2013 Jan 29;80(5):438-46. doi: 10.1212/WNL.0b013e31827f0f66. Epub 2013 Jan 2. Neurology. 2013. PMID: 23284067 Free PMC article.
Cerebellar dentate dysplasia.
Barth PG. Barth PG. Brain Dev. 2011 Sep;33(8):621-6. doi: 10.1016/j.braindev.2011.02.008. Epub 2011 Mar 26. Brain Dev. 2011. PMID: 21441008 Review.
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