Matyja E - Search Results

1

Light and electron microscopy characteristics of the muscle of patients with SURF1 gene mutations associated with Leigh disease.

Pronicki M, Matyja E, Piekutowska-Abramczuk D, Szymanska-Debinska T, Karkucinska-Wieckowska A, Karczmarewicz E, Grajkowska W, Kmiec T, Popowska E, Sykut-Cegielska J. Pronicki M, et al. Among authors: matyja e. J Clin Pathol. 2008 Apr;61(4):460-6. doi: 10.1136/jcp.2007.051060. Epub 2007 Oct 1. J Clin Pathol. 2008. PMID: 17908801 Free PMC article.

2

Chordoid meningiomas of a different histopathological pattern: a report of two cases.

Matyja E, Grajkowska W, Lazarczyk M, Marchel A, Czernicki T. Matyja E, et al. Folia Neuropathol. 2006;44(1):34-41. Folia Neuropathol. 2006. PMID: 16565929 Free article.

3

Ectopic cerebellum in anterior cranial fossa: Report of a unique case associated with skull congenital malformations and epilepsy.

Matyja E, Grajkowska W, Marchel A, Rysz A, Majkowska-Zwolinska B. Matyja E, et al. Am J Surg Pathol. 2007 Feb;31(2):322-5. doi: 10.1097/01.pas.0000213404.18311.c9. Am J Surg Pathol. 2007. PMID: 17255780

4

Advanced reactive astrogliosis associated with hemangioblastoma versus astroglial-vascular neoplasm ("angioglioma").

Matyja E, Grajkowska W, Taraszewska A, Marchel A, Bojarski P, Nauman P. Matyja E, et al. Folia Neuropathol. 2007;45(3):120-5. Folia Neuropathol. 2007. PMID: 17849362 Free article.

5

Relative expression of mRNAS coding for glutaminase isoforms in CNS tissues and CNS tumors.

Szeliga M, Matyja E, Obara M, Grajkowska W, Czernicki T, Albrecht J. Szeliga M, et al. Among authors: matyja e. Neurochem Res. 2008 May;33(5):808-13. doi: 10.1007/s11064-007-9507-6. Epub 2007 Oct 17. Neurochem Res. 2008. PMID: 17940881

6

G8363A mitochondrial DNA mutation is not a rare cause of Leigh syndrome - clinical, biochemical and pathological study of an affected child.

Pronicki M, Sykut-Cegielska J, Matyja E, Musialowicz J, Karczmarewicz E, Tonska K, Piechota J, Piekutowska-Abramczuk D, Kowalski P, Bartnik E. Pronicki M, et al. Among authors: matyja e. Folia Neuropathol. 2007;45(4):187-91. Folia Neuropathol. 2007. PMID: 18176892 Free article.

7

Expression of tuberin and hamartin in tuberous sclerosis complex-associated and sporadic cortical dysplasia of Taylor's balloon cell type.

Grajkowska W, Kotulska K, Matyja E, Larysz-Brysz M, Mandera M, Roszkowski M, Domańska-Pakieła D, Lewik-Kowalik J, Jóźwiak S. Grajkowska W, et al. Among authors: matyja e. Folia Neuropathol. 2008;46(1):43-8. Folia Neuropathol. 2008. PMID: 18368626 Free article.

8

Remodelling of skeletal muscle cells in children with SCO2 gene mutation - ultrastructural study.

Matyja E, Pronicki M, Kowalski P, Czarnowska E, Taybert J. Matyja E, et al. Folia Neuropathol. 2009;47(1):20-32. Folia Neuropathol. 2009. PMID: 19353431 Free article.

9

Ganglioglioma associated with alterations of NBN gene. A case report.

Grajkowska W, Piekutowska-Abramczuk D, Ciara E, Dembowska-Baginska B, Perek D, Roszkowski M, Daszkiewicz P, Matyja E, Pronicki M, Chrzanowska KH. Grajkowska W, et al. Among authors: matyja e. Folia Neuropathol. 2009;47(3):278-83. Folia Neuropathol. 2009. PMID: 19813148 Free article.

10

Papillary ependymoma with unique superficial cortical location: immunohistochemical and ultrastructural studies. A case report.

Grajkowska W, Matyja E, Pronicki M, Daszkiewicz P, Roszkowski M, Perek D, Drogosiewicz M. Grajkowska W, et al. Among authors: matyja e. Folia Neuropathol. 2009;47(4):354-61. Folia Neuropathol. 2009. PMID: 20054788 Free article.

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