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Items: 1 to 20 of 224

1.

Diagnostic criteria for Walker-Warburg syndrome.

Dobyns WB, Pagon RA, Armstrong D, Curry CJ, Greenberg F, Grix A, Holmes LB, Laxova R, Michels VV, Robinow M, et al.

Am J Med Genet. 1989 Feb;32(2):195-210.

PMID:
2494887
2.

Clinical and genetic distinction between Walker-Warburg syndrome and muscle-eye-brain disease.

Cormand B, Pihko H, Bayés M, Valanne L, Santavuori P, Talim B, Gershoni-Baruch R, Ahmad A, van Bokhoven H, Brunner HG, Voit T, Topaloglu H, Dobyns WB, Lehesjoki AE.

Neurology. 2001 Apr 24;56(8):1059-69.

PMID:
11320179
3.

Walker-Warburg syndrome with microtia and absent auditory canals.

Gershoni-Baruch R, Mandel H, Miller B, Sujov P, Braun J.

Am J Med Genet. 1990 Sep;37(1):87-91.

PMID:
2240049
4.

Neurosurgical management of Walker-Warburg syndrome.

Martínez-Lage JF, García Santos JM, Poza M, Puche A, Casas C, Rodriguez Costa T.

Childs Nerv Syst. 1995 Mar;11(3):145-53.

PMID:
7773974
5.

Congenital muscular dystrophy, brain and eye abnormalities: one or more clinical entities?

Laverda AM, Battaglia MA, Drigo P, Battistella PA, Casara GL, Suppiej A, Casellato R.

Childs Nerv Syst. 1993 Apr;9(2):84-7.

PMID:
8319237
6.

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
7.

[Congenital muscular dystrophies: muscle-eye-brain disease].

Meyer S, Struffert T, Uyanik G, Oehl-Jaschkowitz B, Hehr U, Shamdeen MG.

Klin Padiatr. 2005 Mar-Apr;217(2):68-9. German.

PMID:
15770576
8.

[A patient of Walker-Warburg syndrome with a haplotype different from that in Fukuyama-type congenital muscular dystrophy].

Sasaki M, Kondo E, Yamashita Y, Toda T, Nonaka I.

No To Hattatsu. 1999 Sep;31(5):445-51. Japanese.

PMID:
10487070
9.

Hydrocephalus, lissencephaly, ocular abnormalities and congenital muscular dystrophy. A Warburg syndrome variant?

Pavone L, Gullotta F, Grasso S, Vannucchi C.

Neuropediatrics. 1986 Nov;17(4):206-11.

PMID:
3100980
10.

The Walker-Warburg syndrome with cleft lip and palate.

Pratap A, Agrawal A, Tiwari A, Lakshmi R, Rajbanshi S.

Singapore Med J. 2007 Feb;48(2):e66-7.

11.

Ocular malformations and lissencephaly.

Warburg M.

Eur J Pediatr. 1987 Sep;146(5):450-2.

PMID:
3119342
12.

Autosomal recessive eye and brain anomalies: Warburg syndrome.

Pagon RA, Clarren SK, Milam DF Jr, Hendrickson AE.

J Pediatr. 1983 Apr;102(4):542-6.

PMID:
6403688
13.

A case of Walker-Warburg syndrome resulting from a homozygous POMT1 mutation.

Yis U, Uyanik G, Kurul S, Dirik E, Ozer E, Gross C, Hehr U.

Eur J Paediatr Neurol. 2007 Jan;11(1):46-9.

PMID:
17161965
14.

[Walker-Warburg syndrome: experience at the Virgen de la Arrixaca Hospital].

Fernández Martínez MD, Rodríguez Sánchez F, Martínez-Lage Sánchez JF, Rodríguez Costa T, Puche Miras A, Casas Fernández C, Almagro Navarro MJ.

An Esp Pediatr. 1992 Mar;36(3):213-7. Review. Spanish.

PMID:
1580433
15.

Phenotypic spectrum of Fukutinopathy: most severe phenotype of Fukutinopathy.

Yoshioka M.

Brain Dev. 2009 Jun;31(6):419-22. doi: 10.1016/j.braindev.2008.07.012.

PMID:
18834683
16.

Genetic identity of Fukuyama-type congenital muscular dystrophy and Walker-Warburg syndrome.

Toda T, Yoshioka M, Nakahori Y, Kanazawa I, Nakamura Y, Nakagome Y.

Ann Neurol. 1995 Jan;37(1):99-101.

PMID:
7818265
17.

Walker-Warburg syndrome with cleft lip and cleft palate in two sibs.

Burton BK, Dillard RG, Weaver RG.

Am J Med Genet. 1987 Jul;27(3):537-41.

PMID:
3631127
18.

Cobblestone lissencephaly with normal eyes and muscle.

Dobyns WB, Patton MA, Stratton RF, Mastrobattista JM, Blanton SH, Northrup H.

Neuropediatrics. 1996 Apr;27(2):70-5.

PMID:
8737821
19.

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
20.

Walker-Warburg syndrome in a Japanese patient.

Tachi N, Tachi M, Sasaki K, Tanabe C, Minagawa K.

Pediatr Neurol. 1988 Jul-Aug;4(4):236-40. Review.

PMID:
3072008

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