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Pontocerebellar hypoplasias. An overview of a group of inherited neurodegenerative disorders with fetal onset.
Barth PG. Barth PG. Brain Dev. 1993 Nov-Dec;15(6):411-22. doi: 10.1016/0387-7604(93)90080-r. Brain Dev. 1993. PMID: 8147499 Review.
Familial lissencephaly with extreme neopallial hypoplasia.
Barth PG, Mullaart R, Stam FC, Slooff JL. Barth PG, et al. Brain Dev. 1982;4(2):145-51. doi: 10.1016/s0387-7604(82)80008-9. Brain Dev. 1982. PMID: 7091570
[3 examples of fetal genetic neuromuscular disorders which lead to hydramnion].
Teeuw AH, Barth PG, van Sonderen L, Zondervan HA. Teeuw AH, et al. Among authors: barth pg. Ned Tijdschr Geneeskd. 1993 May 1;137(18):908-13. Ned Tijdschr Geneeskd. 1993. PMID: 8492834 Dutch.
Gliomatosis cerebri in a newborn.
Barth PG, Stam FC, Hack W, Delemarre-van de Waal HA. Barth PG, et al. Neuropediatrics. 1988 Nov;19(4):197-200. doi: 10.1055/s-2008-1052445. Neuropediatrics. 1988. PMID: 3205377
X-linked myotubular myopathy--a long-term follow-up study.
Barth PG, Dubowitz V. Barth PG, et al. Eur J Paediatr Neurol. 1998;2(1):49-56. doi: 10.1016/1090-3798(98)01004-9. Eur J Paediatr Neurol. 1998. PMID: 10726846
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.
TSEN54 mutations cause pontocerebellar hypoplasia type 5.
Namavar Y, Chitayat D, Barth PG, van Ruissen F, de Wissel MB, Poll-The BT, Silver R, Baas F. Namavar Y, et al. Among authors: barth pg. Eur J Hum Genet. 2011 Jun;19(6):724-6. doi: 10.1038/ejhg.2011.8. Epub 2011 Feb 2. Eur J Hum Genet. 2011. PMID: 21368912 Free PMC article.
Rhabdomyolysis in pontocerebellar hypoplasia type 2 (PCH-2).
Barth PG, Ryan MM, Webster RI, Aronica E, Kan A, Ramkema M, Jardine P, Poll-The BT. Barth PG, et al. Neuromuscul Disord. 2008 Jan;18(1):52-8. doi: 10.1016/j.nmd.2007.08.001. Epub 2007 Sep 6. Neuromuscul Disord. 2008. PMID: 17825555
What's new in pontocerebellar hypoplasia? An update on genes and subtypes.
van Dijk T, Baas F, Barth PG, Poll-The BT. van Dijk T, et al. Among authors: barth pg. Orphanet J Rare Dis. 2018 Jun 15;13(1):92. doi: 10.1186/s13023-018-0826-2. Orphanet J Rare Dis. 2018. PMID: 29903031 Free PMC article. Review.
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