Format
Sort by

Send to

Choose Destination

Links from PubMed

Items: 1 to 20 of 374

1.

Neuroimaging manifestations and classification of congenital muscular dystrophies.

Barkovich AJ.

AJNR Am J Neuroradiol. 1998 Sep;19(8):1389-96.

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.

Ann Neurol. 1997 Jul;42(1):50-9.

PMID:
9225685
3.

Merosin-deficient congenital muscular dystrophy: the spectrum of brain involvement on magnetic resonance imaging.

Philpot J, Cowan F, Pennock J, Sewry C, Dubowitz V, Bydder G, Muntoni F.

Neuromuscul Disord. 1999 Mar;9(2):81-5.

PMID:
10220862
4.

Brain MR in Fukuyama congenital muscular dystrophy.

Aida N, Tamagawa K, Takada K, Yagishita A, Kobayashi N, Chikumaru K, Iwamoto H.

AJNR Am J Neuroradiol. 1996 Apr;17(4):605-13.

5.

Congenital muscular dystrophy: a review of the literature.

Leyten QH, Gabreëls FJ, Renier WO, ter Laak HJ.

Clin Neurol Neurosurg. 1996 Nov;98(4):267-80. Review.

PMID:
8930416
6.

Fukuyama-type congenital muscular dystrophy and the Walker-Warburg syndrome.

Kimura S, Sasaki Y, Kobayashi T, Ohtsuki N, Tanaka Y, Hara M, Miyake S, Yamada M, Iwamoto H, Misugi N.

Brain Dev. 1993 May-Jun;15(3):182-91.

PMID:
8214343
7.

Brain MRI features of merosin-negative congenital muscular dystrophy.

Ibrahim Abdulla JK, Vattoth S, Al Tawari AA, Pandey T, Abubacker S.

Australas Radiol. 2007 Dec;51 Suppl:B221-3.

PMID:
17991069
8.

Congenital muscular dystrophies: 1997 update.

Voit T.

Brain Dev. 1998 Mar;20(2):65-74. Review.

PMID:
9545174
9.

Cerebellar MR in Fukuyama congenital muscular dystrophy: polymicrogyria with cystic lesions.

Aida N, Yagishita A, Takada K, Katsumata Y.

AJNR Am J Neuroradiol. 1994 Oct;15(9):1755-9.

PMID:
7847224
10.

Walker-Warburg syndrome: diffusion MR imaging.

Sener RN.

J Neuroradiol. 2005 Jun;32(3):213-5.

PMID:
16134304
11.

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.

PMID:
17634419
12.

Merosin-deficient congenital muscular dystrophy and cortical dysplasia.

Brett FM, Costigan D, Farrell MA, Heaphy P, Thornton J, King MD.

Eur J Paediatr Neurol. 1998;2(2):77-82.

PMID:
10724100
13.

[Merosin-positive congenital muscular dystrophy, white matter abnormalities, and bilateral posterior occipital cortical dysplasia].

Ribeiro VT, Moreira NC, Teixeira J, Guimarães A, Cruz R, Lima L.

Acta Med Port. 2003 May-Jun;16(3):189-92. Portuguese.

14.

Walker-Warburg syndrome: demonstration of cerebellar cysts with CISS sequence.

Rathod SB, Baheti AD, Dabhade PT, Sankhe SS.

Magn Reson Med Sci. 2012;11(2):137-40.

15.

Congenital muscular dystrophy with adducted thumbs, ptosis, external ophthalmoplegia, mental retardation and cerebellar hypoplasia: a novel form of CMD.

Voit T, Parano E, Straub V, Schröder JM, Schaper J, Pavone P, Falsaperla R, Pavone L, Herrmann R.

Neuromuscul Disord. 2002 Oct;12(7-8):623-30.

PMID:
12207929
16.

Preserved merosin M-chain (or laminin-alpha 2) expression in skeletal muscle distinguishes Walker-Warburg syndrome from Fukuyama muscular dystrophy and merosin-deficient congenital muscular dystrophy.

Voit T, Sewry CA, Meyer K, Hermann R, Straub V, Muntoni F, Kahn T, Unsöld R, Helliwell TR, Appleton R, et al.

Neuropediatrics. 1995 Jun;26(3):148-55.

PMID:
7477753
17.

Walker-Warburg syndrome. Report of two cases.

Vasconcelos MM, Guedes CR, Domingues RC, Vianna RN, Sotero M, Vieira MM.

Arq Neuropsiquiatr. 1999 Sep;57(3A):672-7. Review.

PMID:
10667295
18.

Brain magnetic resonance imaging abnormalities in merosin-positive congenital muscular dystrophy.

Philpot J, Pennock J, Cowan F, Sewry CA, Dubowitz V, Bydder G, Muntoni F.

Eur J Paediatr Neurol. 2000;4(3):109-14.

PMID:
10872105
19.

Fukuyama congenital muscular dystrophy: a neuroradiologic review.

Aida N.

J Magn Reson Imaging. 1998 Mar-Apr;8(2):317-26. Review.

PMID:
9562058
20.

Congenital muscular dystrophy with cerebral and ocular malformations (cerebro-oculo-muscular syndrome).

Heyer R, Ehrich J, Goebel HH, Christen HJ, Hanefeld F.

Brain Dev. 1986;8(6):614-9.

PMID:
3103478
Items per page

Supplemental Content

Support Center