Barth PG - Search Results

1

Ependymal abnormalities in lissencephaly/pachygyria.

Sarnat HB, Darwish HZ, Barth PG, Trevenen CL, Pinto A, Kotagal S, Shishikura K, Osawa M, Korobkin R. Sarnat HB, et al. Among authors: barth pg. J Neuropathol Exp Neurol. 1993 Sep;52(5):525-41. doi: 10.1097/00005072-199309000-00011. J Neuropathol Exp Neurol. 1993. PMID: 8360705

2

Magnetic resonance imaging in classification of congenital muscular dystrophies with brain abnormalities.

van der Knaap MS, Smit LM, Barth PG, Catsman-Berrevoets CE, Brouwer OF, Begeer JH, de Coo IF, Valk J. van der Knaap MS, et al. Among authors: barth pg. Ann Neurol. 1997 Jul;42(1):50-9. doi: 10.1002/ana.410420110. Ann Neurol. 1997. PMID: 9225685

3

Diagnostic features and clinical signs of 21 patients with lissencephaly type 1.

de Rijk-van Andel JF, Arts WF, Barth PG, Loonen MC. de Rijk-van Andel JF, et al. Among authors: barth pg. Dev Med Child Neurol. 1990 Aug;32(8):707-17. doi: 10.1111/j.1469-8749.1990.tb08431.x. Dev Med Child Neurol. 1990. PMID: 2210085 Review.

4

Sarcoglycanopathies in Dutch patients with autosomal recessive limb girdle muscular dystrophy.

Ginjaar HB, van der Kooi AJ, Ceelie H, Kneppers AL, van Meegen M, Barth PG, Busch HF, Wokke JH, Anderson LV, Bönnemann CG, Jeanpierre M, Bolhuis PA, Moorman AF, de Visser M, Bakker E, Ommen GJ. Ginjaar HB, et al. Among authors: barth pg. J Neurol. 2000 Jul;247(7):524-9. doi: 10.1007/s004150070151. J Neurol. 2000. PMID: 10993494

5

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

6

Peroxisomal disorders: a review.

Wanders RJ, Schutgens RB, Barth PG. Wanders RJ, et al. Among authors: barth pg. J Neuropathol Exp Neurol. 1995 Sep;54(5):726-39. doi: 10.1097/00005072-199509000-00016. J Neuropathol Exp Neurol. 1995. PMID: 7545216 Review.

7

A new leukoencephalopathy with vanishing white matter.

van der Knaap MS, Barth PG, Gabreëls FJ, Franzoni E, Begeer JH, Stroink H, Rotteveel JJ, Valk J. van der Knaap MS, et al. Among authors: barth pg. Neurology. 1997 Apr;48(4):845-55. doi: 10.1212/wnl.48.4.845. Neurology. 1997. PMID: 9109866 Free article.

8

Discordant infantile encephalopathy with symmetrical thalamic calcifications in identical twins.

van der Knaap MS, Barth PG. van der Knaap MS, et al. Among authors: barth pg. Am J Med Genet. 1994 Aug 15;52(2):218-22. doi: 10.1002/ajmg.1320520218. Am J Med Genet. 1994. PMID: 7802012

9

Central cortico-subcortical involvement: a distinct pattern of brain damage caused by perinatal and postnatal asphyxia in term infants.

Rademakers RP, van der Knaap MS, Verbeeten B Jr, Barth PG, Valk J. Rademakers RP, et al. Among authors: barth pg. J Comput Assist Tomogr. 1995 Mar-Apr;19(2):256-63. J Comput Assist Tomogr. 1995. PMID: 7890852

10

Normal gyration and sulcation in preterm and term neonates: appearance on MR images.

van der Knaap MS, van Wezel-Meijler G, Barth PG, Barkhof F, Adèr HJ, Valk J. van der Knaap MS, et al. Among authors: barth pg. Radiology. 1996 Aug;200(2):389-96. doi: 10.1148/radiology.200.2.8685331. Radiology. 1996. PMID: 8685331

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