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217 results
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Inherited syndrome of microcephaly, dyskinesia and pontocerebellar hypoplasia: a systemic atrophy with early onset.
Barth PG, Vrensen GF, Uylings HB, Oorthuys JW, Stam FC. Barth PG, et al. J Neurol Sci. 1990 Jun;97(1):25-42. doi: 10.1016/0022-510x(90)90096-6. J Neurol Sci. 1990. PMID: 2370559
Disorders of neuronal migration.
Barth PG. Barth PG. Can J Neurol Sci. 1987 Feb;14(1):1-16. doi: 10.1017/s031716710002610x. Can J Neurol Sci. 1987. PMID: 3545413 Review.
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
A sibship with a mild variant of Zellweger syndrome.
Barth PG, Schutgens RB, Wanders RJ, Heymans HS, Moser AE, Moser HW, Bleeker-Wagemakers EM, Jansonius-Schultheiss K, Derix M, Nelck GF. Barth PG, et al. J Inherit Metab Dis. 1987;10(3):253-9. doi: 10.1007/BF01800071. J Inherit Metab Dis. 1987. PMID: 3123783
An X-linked mitochondrial disease affecting cardiac muscle, skeletal muscle and neutrophil leucocytes.
Barth PG, Scholte HR, Berden JA, Van der Klei-Van Moorsel JM, Luyt-Houwen IE, Van 't Veer-Korthof ET, Van der Harten JJ, Sobotka-Plojhar MA. Barth PG, et al. J Neurol Sci. 1983 Dec;62(1-3):327-55. doi: 10.1016/0022-510x(83)90209-5. J Neurol Sci. 1983. PMID: 6142097
Immunophenotyping of congenital myopathies: disorganization of sarcomeric, cytoskeletal and extracellular matrix proteins.
van der Ven PF, Jap PH, ter Laak HJ, Nonaka I, Barth PG, Sengers RC, Stadhouders AM, Ramaekers FC. van der Ven PF, et al. Among authors: barth pg. J Neurol Sci. 1995 Apr;129(2):199-213. doi: 10.1016/0022-510x(94)00282-s. J Neurol Sci. 1995. PMID: 7608737
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
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
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