These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

196 related articles for article (PubMed ID: 9763366)

  • 1. Neuroimaging manifestations and classification of congenital muscular dystrophies.
    Barkovich AJ
    AJNR Am J Neuroradiol; 1998 Sep; 19(8):1389-96. PubMed ID: 9763366
    [TBL] [Abstract][Full Text] [Related]  

  • 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. PubMed ID: 9225685
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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. PubMed ID: 8930416
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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. PubMed ID: 10220862
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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; 15(3):182-91. PubMed ID: 8214343
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Congenital muscular dystrophy with complete laminin-alpha2-deficiency, cortical dysplasia, and cerebral white-matter changes in children.
    Tsao CY; Mendell JR; Rusin J; Luquette M
    J Child Neurol; 1998 Jun; 13(6):253-6. PubMed ID: 9660506
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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. PubMed ID: 22790300
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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. PubMed ID: 8730178
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Congenital muscular dystrophies--problems of classification.
    Lenard HG
    Acta Paediatr Jpn; 1991 Apr; 33(2):256-60. PubMed ID: 1957652
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Characteristic Cochlear Hypoplasia in Patients with Walker-Warburg Syndrome: A Radiologic Study of the Inner Ear in α-Dystroglycan-Related Muscular Disorders.
    Talenti G; Robson C; Severino MS; Alves CA; Chitayat D; Dahmoush H; Smith L; Muntoni F; Blaser SI; D'Arco F
    AJNR Am J Neuroradiol; 2021 Jan; 42(1):167-172. PubMed ID: 33122211
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Congenital muscular dystrophies: 1997 update.
    Voit T
    Brain Dev; 1998 Mar; 20(2):65-74. PubMed ID: 9545174
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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. PubMed ID: 17991069
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Walker-Warburg syndrome: diffusion MR imaging.
    Sener RN
    J Neuroradiol; 2005 Jun; 32(3):213-5. PubMed ID: 16134304
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Congenital muscular dystrophy: from muscle to brain.
    Falsaperla R; Praticò AD; Ruggieri M; Parano E; Rizzo R; Corsello G; Vitaliti G; Pavone P
    Ital J Pediatr; 2016 Aug; 42(1):78. PubMed ID: 27576556
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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. PubMed ID: 10667295
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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. PubMed ID: 10724100
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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. PubMed ID: 7847224
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Cerebro-ocular dysplasia-muscular dystrophy syndrome. Report of two cases.
    Heggie P; Grossniklaus HE; Roessmann U; Chou SM; Cruse RP
    Arch Ophthalmol; 1987 Apr; 105(4):520-4. PubMed ID: 3105522
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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
    Neuropediatrics; 1995 Jun; 26(3):148-55. PubMed ID: 7477753
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.