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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

150 related items for PubMed ID: 1595429

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  • 23. Analysis of genotype-phenotype correlation in Walker-Warburg syndrome with a novel CRPPA mutation in different clinical manifestations.
    Bayram N, Bayram AK, Per H, Gümüş H, Ozsaygili C, Doğan MS, Çağlayan AO.
    Eur J Ophthalmol; 2022 Sep; 32(5):NP71-NP76. PubMed ID: 33977792
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  • 27. 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. PubMed ID: 7818265
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  • 29. Lissencephaly with extreme cerebral and cerebellar hypoplasia. A magnetic resonance imaging study.
    Kroon AA, Smit BJ, Barth PG, Hennekam RC.
    Neuropediatrics; 1996 Oct; 27(5):273-6. PubMed ID: 8971750
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  • 30. Lissencephaly with congenital muscular dystrophy and ocular abnormalities: cerebro-oculo-muscular syndrome.
    Sasaki M, Yoshioka K, Yanagisawa T, Nemoto A, Takasago Y, Nagano T.
    Childs Nerv Syst; 1989 Feb; 5(1):35-7. PubMed ID: 2495176
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  • 31. Bilateral total retinal detachment at birth: a case report of Walker-Warburg syndrome.
    Hakim N, Soare C, Hakim J.
    Int Med Case Rep J; 2018 Feb; 11():1-4. PubMed ID: 29386918
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  • 33. 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. PubMed ID: 7773974
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  • 34. Walker-Warburg syndrome: A case report of congenital muscular dystrophy with hydrocephalus.
    Aref F, Shaaban A, Ahmed A, Gubari M, Hassan J, Alharbi M, Alsubhi K, Alsalhi K, Albalawi S, Ali M, Ali H, Filfilan N, Shmailah E, Ahmed A.
    Radiol Case Rep; 2024 Nov; 19(11):5063-5065. PubMed ID: 39253050
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  • 37. [Oculocerebral anomalies in Walker's lissencephaly].
    Robain O, Dhermy P, Dufier JL, Blanck MF, Dulac O, Bursztyn J.
    J Fr Ophtalmol; 1985 Nov; 8(1):59-72. PubMed ID: 3923093
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  • 40. 160 kb deletion in ISPD unmasking a recessive mutation in a patient with Walker-Warburg syndrome.
    Czeschik JC, Hehr U, Hartmann B, Lüdecke HJ, Rosenbaum T, Schweiger B, Wieczorek D.
    Eur J Med Genet; 2013 Dec; 56(12):689-94. PubMed ID: 24120487
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