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Items: 1 to 20 of 128

1.

POMT1-associated walker-warburg syndrome: a disorder of dendritic development of neocortical neurons.

Judas M, Sedmak G, Rados M, Sarnavka V, Fumić K, Willer T, Gross C, Hehr U, Strahl S, Cuk M, Barić I.

Neuropediatrics. 2009 Feb;40(1):6-14. doi: 10.1055/s-0029-1224099. Epub 2009 Jul 28.

PMID:
19639522
2.

Abnormal neocortical development in mice lacking cGMP-dependent protein kinase I.

Demyanenko GP, Halberstadt AI, Pryzwansky KB, Werner C, Hofmann F, Maness PF.

Brain Res Dev Brain Res. 2005 Nov 7;160(1):1-8. Epub 2005 Sep 8.

PMID:
16154207
3.

New POMT2 mutations causing congenital muscular dystrophy: identification of a founder mutation.

Yanagisawa A, Bouchet C, Van den Bergh PY, Cuisset JM, Viollet L, Leturcq F, Romero NB, Quijano-Roy S, Fardeau M, Seta N, Guicheney P.

Neurology. 2007 Sep 18;69(12):1254-60. Epub 2007 Jul 18.

PMID:
17634419
5.
6.

Walker-Warburg Syndrome with POMT1 mutations can be associated with cleft lip and cleft palate.

Vajsar J, Baskin B, Swoboda K, Biggar DW, Schachter H, Ray PN.

Neuromuscul Disord. 2008 Aug;18(8):675-7. doi: 10.1016/j.nmd.2008.05.014. Epub 2008 Jul 18.

PMID:
18640039
7.

Dendritic overgrowth and alterations in laminar phenotypes of neocortical neurons in the newborn with semilobar holoprosencephaly.

Judas M, Rasin MR, Kruslin B, Kostović K, Jukić D, Petanjek Z, Kostović I.

Brain Dev. 2003 Jan;25(1):32-9.

PMID:
12536031
8.

An autosomal recessive limb girdle muscular dystrophy (LGMD2) with mild mental retardation is allelic to Walker-Warburg syndrome (WWS) caused by a mutation in the POMT1 gene.

Balci B, Uyanik G, Dincer P, Gross C, Willer T, Talim B, Haliloglu G, Kale G, Hehr U, Winkler J, Topaloğlu H.

Neuromuscul Disord. 2005 Apr;15(4):271-5.

PMID:
15792865
9.

Lifespan alterations of basal dendritic trees of pyramidal neurons in the human prefrontal cortex: a layer-specific pattern.

Petanjek Z, Judas M, Kostović I, Uylings HB.

Cereb Cortex. 2008 Apr;18(4):915-29. Epub 2007 Jul 25.

PMID:
17652464
10.

Dendritic morphology and orientation of pyramidal cells of the neocortex in two groups of early postnatal undernourished-rehabilitated rats.

Cordero ME, Valenzuela CY, Rodriguez A, Aboitiz F.

Brain Res Dev Brain Res. 2003 Apr 14;142(1):37-45.

PMID:
12694943
11.

Alteration in dendritic morphology of cortical neurons in rats with diabetes mellitus induced by streptozotocin.

Martínez-Tellez R, Gómez-Villalobos Mde J, Flores G.

Brain Res. 2005 Jun 28;1048(1-2):108-15.

PMID:
15916754
12.

Dendritic spine "dysgenesis" and mental retardation.

Purpura DP.

Science. 1974 Dec 20;186(4169):1126-8.

PMID:
4469701
14.

Dendritic changes in the hippocampal formation of AIDS patients: a quantitative Golgi study.

Sá MJ, Madeira MD, Ruela C, Volk B, Mota-Miranda A, Paula-Barbosa MM.

Acta Neuropathol. 2004 Feb;107(2):97-110. Epub 2003 Nov 6.

PMID:
14605830
15.

Morphometric Golgi study of cortical locations in WAG/Rij rats: the cortical focus theory.

Karpova AV, Bikbaev AF, Coenen AM, van Luijtelaar G.

Neurosci Res. 2005 Feb;51(2):119-28.

PMID:
15681029
16.
17.
18.

Abnormal dendritic spine characteristics in the temporal and visual cortices of patients with fragile-X syndrome: a quantitative examination.

Irwin SA, Patel B, Idupulapati M, Harris JB, Crisostomo RA, Larsen BP, Kooy F, Willems PJ, Cras P, Kozlowski PB, Swain RA, Weiler IJ, Greenough WT.

Am J Med Genet. 2001 Jan 15;98(2):161-7.

PMID:
11223852
19.
20.

Abnormal neuronal differentiation (functional maturation) in mental retardation.

Marin-Padilla M.

Birth Defects Orig Artic Ser. 1975;11(7):133-53. Review.

PMID:
764896

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